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DTSTART;TZID=Europe/Madrid:20180323T100000
DTEND;TZID=Europe/Madrid:20180323T110000
DTSTAMP:20260404T004034
CREATED:20180312T102003Z
LAST-MODIFIED:20180312T102128Z
UID:57989-1521799200-1521802800@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Andreu Matamoros and Maider Badiola
DESCRIPTION:Role of the Cellular Prion Protein in hippocampal neurotransmission\, learning and memory\nAndreu Matamoros\, Molecular and cellular neurobiotechnology\nMisfoldedCellular Prion protein (PrPC) was described as the causative agent of the transmissible spongiform encephalopathies (TSEs)\, independently of its origin (sporadic\, iatrogenic or genetic). PrPC is present at the synaptic terminal\, especially in the cerebral cortex including the hippocampus. It is involved in numerous cellular processes: cell proliferation and differentiation\, copper homeostasis and cell signaling\, among others. Recently has been demonstrated that most of these functions are based in misinterpretation of the mice models and need to be reevaluated. On the other hand\, PrPC protein levels are decreased in TSEs. This opened a new insight in the study of TSEs: understanding the pathology not just as a gain of function due to the prion aggregation\, but as a loss of function due to the reduction of PrPC. \nOur goal is to elucidate the role of PrPC in hippocampal circuitry and its derived functions (i.e. learning and memory) using a new PrPC knockout mice (ZH3). Spontaneous firing and network formation are monitored with Calcium imaging in hippocampus primary cultures. Object Recognition Test and Skinner’s Test are performed to evaluate memory and learning in ZH3 mice. LTP and evocated potentials are also measured in CA3-CA1 connection in vivo. Glutamate neurotransmission is evaluated behaviourally and electrophysiologycally using kainate administration. Finally\, mRNA from ZH3 mice hippocampus has been sequenced to identify differential gene expression compared to Wt mice. \nDissecting the role of PrPC in hippocampus neurotransmission will allow us to better understand alterations in the brain of TSEs patients. \n  \nPaving the way towards an in-vitro 3D mechanosensory-motor circuit on a chip\nMaider Badiola\, Nanobioengineering\nNeuromuscular diseases (NMD) are neurological disorders affecting muscles and their control through nervous system. They often involve afferent and efferent pathways of the Peripheral Nervous System\, and their effects might be reflected in the mechanosensory-motor circuit at different cellular levels (including sensory and motor neurons\, glia and muscle dysfunctions)\, and in the connexion among them. \nThe aim of this research is to create an in-vitro model to mimic the 3D microenvironment of a neural circuit for locomotion to understand and find treatments for NMDs. To that end\, organ-on-a-chip technologies are used for the integration of sensorial and motor neural components together with a functional muscular unit. \nFor that purpose\, we first fabricated a compartmentalised microfluidic device in PDMS using soft lithography techniques. Then the afferent and efferent pathways of the Peripheral Nervous System were mimicked in 2D culturing primary neurons involved in the locomotion circuit (motoneurons and dorsal root ganglia) with Schwann cells in the microdevice. \nBut 2D cultures offer many limitations compared to 3D\, and the assessment of the afferent pathway separately often means a complication. Optogenetics technique can be used in skeletal muscle to induce contraction\, mimicking a natural innervation to some length and facilitating the study of the afferent pathway separately. Therefore\, we propose a study model where primary spinal motor- or dorsal root ganglia sensory- neurons are cultured in 3D in different compartments together with optogenetically sensitive myocytes (a channelrhodopsin-2 positive cell line). This could make possible to evaluate the functionality of efferent and afferent pathways separately. \nThis study provides the basis for future steps towards NMD in-vitro study models.
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-andreu-matamoros-and-maider-badiola/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180323T100000
DTEND;TZID=Europe/Madrid:20180323T110000
DTSTAMP:20260404T004034
CREATED:20180312T102003Z
LAST-MODIFIED:20180312T102003Z
UID:96187-1521799200-1521802800@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Andreu Matamoros and Maider Badiola
DESCRIPTION:Role of the Cellular Prion Protein in hippocampal neurotransmission\, learning and memory\nAndreu Matamoros\, Molecular and cellular neurobiotechnology\nMisfoldedCellular Prion protein (PrPC) was described as the causative agent of the transmissible spongiform encephalopathies (TSEs)\, independently of its origin (sporadic\, iatrogenic or genetic). PrPC is present at the synaptic terminal\, especially in the cerebral cortex including the hippocampus. It is involved in numerous cellular processes: cell proliferation and differentiation\, copper homeostasis and cell signaling\, among others. Recently has been demonstrated that most of these functions are based in misinterpretation of the mice models and need to be reevaluated. On the other hand\, PrPC protein levels are decreased in TSEs. This opened a new insight in the study of TSEs: understanding the pathology not just as a gain of function due to the prion aggregation\, but as a loss of function due to the reduction of PrPC. \nOur goal is to elucidate the role of PrPC in hippocampal circuitry and its derived functions (i.e. learning and memory) using a new PrPC knockout mice (ZH3). Spontaneous firing and network formation are monitored with Calcium imaging in hippocampus primary cultures. Object Recognition Test and Skinner’s Test are performed to evaluate memory and learning in ZH3 mice. LTP and evocated potentials are also measured in CA3-CA1 connection in vivo. Glutamate neurotransmission is evaluated behaviourally and electrophysiologycally using kainate administration. Finally\, mRNA from ZH3 mice hippocampus has been sequenced to identify differential gene expression compared to Wt mice. \nDissecting the role of PrPC in hippocampus neurotransmission will allow us to better understand alterations in the brain of TSEs patients. \n  \nPaving the way towards an in-vitro 3D mechanosensory-motor circuit on a chip\nMaider Badiola\, Nanobioengineering\nNeuromuscular diseases (NMD) are neurological disorders affecting muscles and their control through nervous system. They often involve afferent and efferent pathways of the Peripheral Nervous System\, and their effects might be reflected in the mechanosensory-motor circuit at different cellular levels (including sensory and motor neurons\, glia and muscle dysfunctions)\, and in the connexion among them. \nThe aim of this research is to create an in-vitro model to mimic the 3D microenvironment of a neural circuit for locomotion to understand and find treatments for NMDs. To that end\, organ-on-a-chip technologies are used for the integration of sensorial and motor neural components together with a functional muscular unit. \nFor that purpose\, we first fabricated a compartmentalised microfluidic device in PDMS using soft lithography techniques. Then the afferent and efferent pathways of the Peripheral Nervous System were mimicked in 2D culturing primary neurons involved in the locomotion circuit (motoneurons and dorsal root ganglia) with Schwann cells in the microdevice. \nBut 2D cultures offer many limitations compared to 3D\, and the assessment of the afferent pathway separately often means a complication. Optogenetics technique can be used in skeletal muscle to induce contraction\, mimicking a natural innervation to some length and facilitating the study of the afferent pathway separately. Therefore\, we propose a study model where primary spinal motor- or dorsal root ganglia sensory- neurons are cultured in 3D in different compartments together with optogenetically sensitive myocytes (a channelrhodopsin-2 positive cell line). This could make possible to evaluate the functionality of efferent and afferent pathways separately. \nThis study provides the basis for future steps towards NMD in-vitro study models.
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-andreu-matamoros-and-maider-badiola-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180323T100000
DTEND;TZID=Europe/Madrid:20180323T110000
DTSTAMP:20260404T004034
CREATED:20180312T102003Z
LAST-MODIFIED:20180312T102003Z
UID:96188-1521799200-1521802800@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Andreu Matamoros and Maider Badiola
DESCRIPTION:Role of the Cellular Prion Protein in hippocampal neurotransmission\, learning and memory\nAndreu Matamoros\, Molecular and cellular neurobiotechnology\nMisfoldedCellular Prion protein (PrPC) was described as the causative agent of the transmissible spongiform encephalopathies (TSEs)\, independently of its origin (sporadic\, iatrogenic or genetic). PrPC is present at the synaptic terminal\, especially in the cerebral cortex including the hippocampus. It is involved in numerous cellular processes: cell proliferation and differentiation\, copper homeostasis and cell signaling\, among others. Recently has been demonstrated that most of these functions are based in misinterpretation of the mice models and need to be reevaluated. On the other hand\, PrPC protein levels are decreased in TSEs. This opened a new insight in the study of TSEs: understanding the pathology not just as a gain of function due to the prion aggregation\, but as a loss of function due to the reduction of PrPC. \nOur goal is to elucidate the role of PrPC in hippocampal circuitry and its derived functions (i.e. learning and memory) using a new PrPC knockout mice (ZH3). Spontaneous firing and network formation are monitored with Calcium imaging in hippocampus primary cultures. Object Recognition Test and Skinner’s Test are performed to evaluate memory and learning in ZH3 mice. LTP and evocated potentials are also measured in CA3-CA1 connection in vivo. Glutamate neurotransmission is evaluated behaviourally and electrophysiologycally using kainate administration. Finally\, mRNA from ZH3 mice hippocampus has been sequenced to identify differential gene expression compared to Wt mice. \nDissecting the role of PrPC in hippocampus neurotransmission will allow us to better understand alterations in the brain of TSEs patients. \n  \nPaving the way towards an in-vitro 3D mechanosensory-motor circuit on a chip\nMaider Badiola\, Nanobioengineering\nNeuromuscular diseases (NMD) are neurological disorders affecting muscles and their control through nervous system. They often involve afferent and efferent pathways of the Peripheral Nervous System\, and their effects might be reflected in the mechanosensory-motor circuit at different cellular levels (including sensory and motor neurons\, glia and muscle dysfunctions)\, and in the connexion among them. \nThe aim of this research is to create an in-vitro model to mimic the 3D microenvironment of a neural circuit for locomotion to understand and find treatments for NMDs. To that end\, organ-on-a-chip technologies are used for the integration of sensorial and motor neural components together with a functional muscular unit. \nFor that purpose\, we first fabricated a compartmentalised microfluidic device in PDMS using soft lithography techniques. Then the afferent and efferent pathways of the Peripheral Nervous System were mimicked in 2D culturing primary neurons involved in the locomotion circuit (motoneurons and dorsal root ganglia) with Schwann cells in the microdevice. \nBut 2D cultures offer many limitations compared to 3D\, and the assessment of the afferent pathway separately often means a complication. Optogenetics technique can be used in skeletal muscle to induce contraction\, mimicking a natural innervation to some length and facilitating the study of the afferent pathway separately. Therefore\, we propose a study model where primary spinal motor- or dorsal root ganglia sensory- neurons are cultured in 3D in different compartments together with optogenetically sensitive myocytes (a channelrhodopsin-2 positive cell line). This could make possible to evaluate the functionality of efferent and afferent pathways separately. \nThis study provides the basis for future steps towards NMD in-vitro study models.
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-andreu-matamoros-and-maider-badiola-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180328T100000
DTEND;TZID=Europe/Madrid:20180328T110000
DTSTAMP:20260404T004034
CREATED:20180322T115517Z
LAST-MODIFIED:20180322T115517Z
UID:58142-1522231200-1522234800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Aurélien Bancaud
DESCRIPTION:µLAS technology for DNA processing: setting up elementary functions (concentration\, separation\, purification\, identification) and application in oncology and targeted sequencing\nAurélien Bancaud\, LAAS-CNRS\, Toulouse\, France\nWe recently developed the µLAS technology for nucleic acids processing. Its operating principle relies on the monitoring of DNA transport in a viscoelastic liquid under the combined action of hydrodynamic and electrophoretic forces (1). DNA molecules are dragged toward the walls of microchannels by a transverse force proportional to their contour length. Because the hydrodynamic decreases near the wall\, DNA molecules are sorted according to their molecular weight. Furthermore\, by tailoring the geometry of a channel with a constriction\, we can tune the amplitude of transverse forces and stop molecules to design a concentrator that achieves enrichment rates of 100 to 1000 fold per minute. \nWe will derive a quantitative model of DNA transport in µLAS that relies on 1 fitting parameter and perform rational optimizations of the technology. We will then exploit µLAS for sizing cell-free circulating DNA (cfDNA) in the blood (2)\, and demonstrate that cfDNA profiling is a promissing biomarker for the follow-up of cancer patients. Finally\, we will present the principle of a DNA size-selective valve for the purification and sequencing of target genomic regions by combining µLAS with Cas9 endonuclease. \n(1) Ranchon et al.\, Lab Chip (2016)\n (2) Andriamanampisoa et al.\, Anal Chem (2018)
URL:https://ibecbarcelona.eu/event/ibec-seminar-aurelien-bancaud/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180328T100000
DTEND;TZID=Europe/Madrid:20180328T110000
DTSTAMP:20260404T004034
CREATED:20180322T115517Z
LAST-MODIFIED:20180322T115517Z
UID:96199-1522231200-1522234800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Aurélien Bancaud
DESCRIPTION:µLAS technology for DNA processing: setting up elementary functions (concentration\, separation\, purification\, identification) and application in oncology and targeted sequencing\nAurélien Bancaud\, LAAS-CNRS\, Toulouse\, France\nWe recently developed the µLAS technology for nucleic acids processing. Its operating principle relies on the monitoring of DNA transport in a viscoelastic liquid under the combined action of hydrodynamic and electrophoretic forces (1). DNA molecules are dragged toward the walls of microchannels by a transverse force proportional to their contour length. Because the hydrodynamic decreases near the wall\, DNA molecules are sorted according to their molecular weight. Furthermore\, by tailoring the geometry of a channel with a constriction\, we can tune the amplitude of transverse forces and stop molecules to design a concentrator that achieves enrichment rates of 100 to 1000 fold per minute. \nWe will derive a quantitative model of DNA transport in µLAS that relies on 1 fitting parameter and perform rational optimizations of the technology. We will then exploit µLAS for sizing cell-free circulating DNA (cfDNA) in the blood (2)\, and demonstrate that cfDNA profiling is a promissing biomarker for the follow-up of cancer patients. Finally\, we will present the principle of a DNA size-selective valve for the purification and sequencing of target genomic regions by combining µLAS with Cas9 endonuclease. \n(1) Ranchon et al.\, Lab Chip (2016)\n (2) Andriamanampisoa et al.\, Anal Chem (2018)
URL:https://ibecbarcelona.eu/event/ibec-seminar-aurelien-bancaud-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180404T120000
DTEND;TZID=Europe/Madrid:20180404T130000
DTSTAMP:20260404T004034
CREATED:20180222T110811Z
LAST-MODIFIED:20180222T110811Z
UID:96178-1522843200-1522846800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Fernando López-Gallego
DESCRIPTION:Immobilization of multi-enzyme systems; an avenue to fabricate self-sufficient heterogeneous biocatalysts\nFernando López-Gallego\, Heterogeneous Biocatalysis Lab\, University of Zaragoza (iQSCH-CSIC) / ARAID\, Science Foundation of Aragón\nIn the last decade\, the chemists have been delighted by the catalytic orchestration found in vivo\, and have isolated multi-enzyme system to work ex-vivo in both natural and non-natural tandem reactions creating a new concept: systems biocatalysis. These systems are the pioneers of the cell-free synthetic biology; an emerging discipline that seeks the simplest biology to make the most complex chemistry. We have paid our attention to the heterogenization of multi-enzyme system to catalyze tandem reactions. Co-immobilization of multi-enzyme systems improve: 1) the kinetics of the chemical cascades due to the spatial localization of the different biocatalytic modules that avoids intermediate accumulation and increases cofactor recycling efficiency\, 2) the stability of the biocatalysts due to both structural rigidification and in situ elimination of toxic by-products\, 3) the biocatalyst recycle and 4) the biocatalyst adaptation to continuous processes. Nevertheless\, the co-immobilization of several enzymes to carry out synthetic cascades is challenging because there is no a universal immobilization chemistry that optimally attaches all the enzymes to the same surface. We have recently developed different immobilized multi-enzyme systems formed by a 3-enzyme cascade for oxidizing phenol derivatives with in situ H2O2 supply\, a 3-enzyme cascade for synthesizing 1\,3-dihydroxyacetone with both in situ cofactor recycling and H2O2 elimination\, a 4-enzyme cascade for quantitatively synthesizing pro-chiral ketones starting from racemic esters and a 2-enzyme cascades to synthesize optically pure secondary alcohols integrating the cofactor recycling in the solid-phase. The optimal design of the immobilization protocols enables co-immobilizing several enzymes and cofactors on the porous carrier to optimize their spatial localization across the carrier microstructure and preserve both global activity and stability of the multi-enzyme systems.
URL:https://ibecbarcelona.eu/event/ibec-seminar-fernando-lopez-gallego-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180404T120000
DTEND;TZID=Europe/Madrid:20180404T130000
DTSTAMP:20260404T004034
CREATED:20180222T110811Z
LAST-MODIFIED:20180222T110811Z
UID:96179-1522843200-1522846800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Fernando López-Gallego
DESCRIPTION:Immobilization of multi-enzyme systems; an avenue to fabricate self-sufficient heterogeneous biocatalysts\nFernando López-Gallego\, Heterogeneous Biocatalysis Lab\, University of Zaragoza (iQSCH-CSIC) / ARAID\, Science Foundation of Aragón\nIn the last decade\, the chemists have been delighted by the catalytic orchestration found in vivo\, and have isolated multi-enzyme system to work ex-vivo in both natural and non-natural tandem reactions creating a new concept: systems biocatalysis. These systems are the pioneers of the cell-free synthetic biology; an emerging discipline that seeks the simplest biology to make the most complex chemistry. We have paid our attention to the heterogenization of multi-enzyme system to catalyze tandem reactions. Co-immobilization of multi-enzyme systems improve: 1) the kinetics of the chemical cascades due to the spatial localization of the different biocatalytic modules that avoids intermediate accumulation and increases cofactor recycling efficiency\, 2) the stability of the biocatalysts due to both structural rigidification and in situ elimination of toxic by-products\, 3) the biocatalyst recycle and 4) the biocatalyst adaptation to continuous processes. Nevertheless\, the co-immobilization of several enzymes to carry out synthetic cascades is challenging because there is no a universal immobilization chemistry that optimally attaches all the enzymes to the same surface. We have recently developed different immobilized multi-enzyme systems formed by a 3-enzyme cascade for oxidizing phenol derivatives with in situ H2O2 supply\, a 3-enzyme cascade for synthesizing 1\,3-dihydroxyacetone with both in situ cofactor recycling and H2O2 elimination\, a 4-enzyme cascade for quantitatively synthesizing pro-chiral ketones starting from racemic esters and a 2-enzyme cascades to synthesize optically pure secondary alcohols integrating the cofactor recycling in the solid-phase. The optimal design of the immobilization protocols enables co-immobilizing several enzymes and cofactors on the porous carrier to optimize their spatial localization across the carrier microstructure and preserve both global activity and stability of the multi-enzyme systems.
URL:https://ibecbarcelona.eu/event/ibec-seminar-fernando-lopez-gallego-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180404T120000
DTEND;TZID=Europe/Madrid:20180404T130000
DTSTAMP:20260404T004034
CREATED:20180222T110811Z
LAST-MODIFIED:20180222T110811Z
UID:96180-1522843200-1522846800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Fernando López-Gallego
DESCRIPTION:Immobilization of multi-enzyme systems; an avenue to fabricate self-sufficient heterogeneous biocatalysts\nFernando López-Gallego\, Heterogeneous Biocatalysis Lab\, University of Zaragoza (iQSCH-CSIC) / ARAID\, Science Foundation of Aragón\nIn the last decade\, the chemists have been delighted by the catalytic orchestration found in vivo\, and have isolated multi-enzyme system to work ex-vivo in both natural and non-natural tandem reactions creating a new concept: systems biocatalysis. These systems are the pioneers of the cell-free synthetic biology; an emerging discipline that seeks the simplest biology to make the most complex chemistry. We have paid our attention to the heterogenization of multi-enzyme system to catalyze tandem reactions. Co-immobilization of multi-enzyme systems improve: 1) the kinetics of the chemical cascades due to the spatial localization of the different biocatalytic modules that avoids intermediate accumulation and increases cofactor recycling efficiency\, 2) the stability of the biocatalysts due to both structural rigidification and in situ elimination of toxic by-products\, 3) the biocatalyst recycle and 4) the biocatalyst adaptation to continuous processes. Nevertheless\, the co-immobilization of several enzymes to carry out synthetic cascades is challenging because there is no a universal immobilization chemistry that optimally attaches all the enzymes to the same surface. We have recently developed different immobilized multi-enzyme systems formed by a 3-enzyme cascade for oxidizing phenol derivatives with in situ H2O2 supply\, a 3-enzyme cascade for synthesizing 1\,3-dihydroxyacetone with both in situ cofactor recycling and H2O2 elimination\, a 4-enzyme cascade for quantitatively synthesizing pro-chiral ketones starting from racemic esters and a 2-enzyme cascades to synthesize optically pure secondary alcohols integrating the cofactor recycling in the solid-phase. The optimal design of the immobilization protocols enables co-immobilizing several enzymes and cofactors on the porous carrier to optimize their spatial localization across the carrier microstructure and preserve both global activity and stability of the multi-enzyme systems.
URL:https://ibecbarcelona.eu/event/ibec-seminar-fernando-lopez-gallego-4/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180404T120000
DTEND;TZID=Europe/Madrid:20180404T130000
DTSTAMP:20260404T004034
CREATED:20180222T110811Z
LAST-MODIFIED:20180222T110811Z
UID:57824-1522843200-1522846800@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Fernando López-Gallego
DESCRIPTION:Immobilization of multi-enzyme systems; an avenue to fabricate self-sufficient heterogeneous biocatalysts\nFernando López-Gallego\, Heterogeneous Biocatalysis Lab\, University of Zaragoza (iQSCH-CSIC) / ARAID\, Science Foundation of Aragón\nIn the last decade\, the chemists have been delighted by the catalytic orchestration found in vivo\, and have isolated multi-enzyme system to work ex-vivo in both natural and non-natural tandem reactions creating a new concept: systems biocatalysis. These systems are the pioneers of the cell-free synthetic biology; an emerging discipline that seeks the simplest biology to make the most complex chemistry. We have paid our attention to the heterogenization of multi-enzyme system to catalyze tandem reactions. Co-immobilization of multi-enzyme systems improve: 1) the kinetics of the chemical cascades due to the spatial localization of the different biocatalytic modules that avoids intermediate accumulation and increases cofactor recycling efficiency\, 2) the stability of the biocatalysts due to both structural rigidification and in situ elimination of toxic by-products\, 3) the biocatalyst recycle and 4) the biocatalyst adaptation to continuous processes. Nevertheless\, the co-immobilization of several enzymes to carry out synthetic cascades is challenging because there is no a universal immobilization chemistry that optimally attaches all the enzymes to the same surface. We have recently developed different immobilized multi-enzyme systems formed by a 3-enzyme cascade for oxidizing phenol derivatives with in situ H2O2 supply\, a 3-enzyme cascade for synthesizing 1\,3-dihydroxyacetone with both in situ cofactor recycling and H2O2 elimination\, a 4-enzyme cascade for quantitatively synthesizing pro-chiral ketones starting from racemic esters and a 2-enzyme cascades to synthesize optically pure secondary alcohols integrating the cofactor recycling in the solid-phase. The optimal design of the immobilization protocols enables co-immobilizing several enzymes and cofactors on the porous carrier to optimize their spatial localization across the carrier microstructure and preserve both global activity and stability of the multi-enzyme systems.
URL:https://ibecbarcelona.eu/event/ibec-seminar-fernando-lopez-gallego/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20180411
DTEND;VALUE=DATE:20180414
DTSTAMP:20260404T004034
CREATED:20180405T131107Z
LAST-MODIFIED:20180405T131107Z
UID:58257-1523404800-1523663999@ibecbarcelona.eu
SUMMARY:Leadership in Action
DESCRIPTION:Every organisation needs great leadership. Dynamic and purposeful leaders can literally change the world. In academia the very best leaders are self-aware\, skilful communicators with excellent people skills. This course is designed to develop leadership skills for postdocs and focusses on identifying and honing everyone’ personal leadership style. It will bring leadership to all aspects of your personal and professional life. \nDates:  \nFrom 11th  to 13th  April \nResidential course at: \nMontserrat Hotel & Training Center \nCollbató (35 min. from BCN) \nTarget Group: \nEarly postdocs. 1st  and 2nd  year Postdoctoral researchers. \n54 places in total for all BIST centres.
URL:https://ibecbarcelona.eu/event/leadership-in-action/
CATEGORIES:Professional and Personal Development
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20180411
DTEND;VALUE=DATE:20180414
DTSTAMP:20260404T004034
CREATED:20180405T131107Z
LAST-MODIFIED:20180405T131107Z
UID:96214-1523404800-1523663999@ibecbarcelona.eu
SUMMARY:Leadership in Action
DESCRIPTION:Every organisation needs great leadership. Dynamic and purposeful leaders can literally change the world. In academia the very best leaders are self-aware\, skilful communicators with excellent people skills. This course is designed to develop leadership skills for postdocs and focusses on identifying and honing everyone’ personal leadership style. It will bring leadership to all aspects of your personal and professional life. \nDates:  \nFrom 11th  to 13th  April \nResidential course at: \nMontserrat Hotel & Training Center \nCollbató (35 min. from BCN) \nTarget Group: \nEarly postdocs. 1st  and 2nd  year Postdoctoral researchers. \n54 places in total for all BIST centres.
URL:https://ibecbarcelona.eu/event/leadership-in-action-2/
CATEGORIES:Professional and Personal Development
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180411T100000
DTEND;TZID=Europe/Madrid:20180414T150000
DTSTAMP:20260404T004034
CREATED:20180405T070513Z
LAST-MODIFIED:20180406T092822Z
UID:58242-1523440800-1523718000@ibecbarcelona.eu
SUMMARY:Fira de Recerca en Directe 2018
DESCRIPTION:Posa’t a la pell d’un científic!\nDe l’11 al 14 d’abril i en el marc de la 16a edició de la Fira Recerca en Directe –organitzada pel Parc Científic de Barcelona i Obra Social “la Caixa”– més de 75 investigadors d’onze centres capdavanters de Catalunya traslladaran els seus laboratoris a CosmoCaixa Barcelona per convidar als ciutadans a participar en els seus projectes de recerca i resoldre enigmes tot seguint el mètode científic. \nEnguany l’IBEC participa amb l’activitat: La mecànica cel·lular\, la membrana de més a prop.\n \nEls participants coneixeran com s’adapta la membrana cel·lular als estímuls del seu entorn acompanyats dels investigadors del grup de Mecanobiologia Cel·lular i Molecular i Dinàmica Integrativa de Cèl·lules i Teixits de l’IBEC. \nLa Xarxa Quiroga\, el Carlos Pérez\, l’Ariadna Marín i el Macià Esteve us explicaran quins són els mecanismes que utilitzen les cèl·lules per detectar i respondre a estímuls mecànics i  com les forces i el control molecular cooperen per aconseguir que els teixits duguin a terme la seva funció biològica. \nACTIVITAT: 16a edició de la Fira Recerca en Directe\nLLOC: CosmoCaixa Barcelona · Carrer d’Isaac Newton\, 26 · 08022 Barcelona\nDIES: Escoles: De l’11 al 13 d’abril (Entrada gratuïta prèvia reserva).\nPúblic general: Dissabte 14 d’abril (Visita inclosa amb l’entrada de CosmoCaixa Barcelona).\nHORARI: De l’11 al 13 d’abril: de 10.00 h a 15.00 h\nDissabte 14 d’abril: de 10.00 h a 14.00 h / A les 12.00 h: Activitat conduïda per Francesc Orella (Protagonista de la sèrie Merlí).\nAforament limitat. Reserves: 934 031 134 / difusiociencia@pcb.ub.cat
URL:https://ibecbarcelona.eu/event/fira-de-recerca-en-directe-2018/
LOCATION:CosmoCaixa Barcelona\, Carrer d'Isaac Newton\, 08022 Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180411T100000
DTEND;TZID=Europe/Madrid:20180414T150000
DTSTAMP:20260404T004034
CREATED:20180405T070513Z
LAST-MODIFIED:20180405T070513Z
UID:96211-1523440800-1523718000@ibecbarcelona.eu
SUMMARY:Fira de Recerca en Directe 2018
DESCRIPTION:Posa’t a la pell d’un científic!\nDe l’11 al 14 d’abril i en el marc de la 16a edició de la Fira Recerca en Directe –organitzada pel Parc Científic de Barcelona i Obra Social “la Caixa”– més de 75 investigadors d’onze centres capdavanters de Catalunya traslladaran els seus laboratoris a CosmoCaixa Barcelona per convidar als ciutadans a participar en els seus projectes de recerca i resoldre enigmes tot seguint el mètode científic. \nEnguany l’IBEC participa amb l’activitat: La mecànica cel·lular\, la membrana de més a prop.\n \nEls participants coneixeran com s’adapta la membrana cel·lular als estímuls del seu entorn acompanyats dels investigadors del grup de Mecanobiologia Cel·lular i Molecular i Dinàmica Integrativa de Cèl·lules i Teixits de l’IBEC. \nLa Xarxa Quiroga\, el Carlos Pérez\, l’Ariadna Marín i el Macià Esteve us explicaran quins són els mecanismes que utilitzen les cèl·lules per detectar i respondre a estímuls mecànics i  com les forces i el control molecular cooperen per aconseguir que els teixits duguin a terme la seva funció biològica. \nACTIVITAT: 16a edició de la Fira Recerca en Directe\nLLOC: CosmoCaixa Barcelona · Carrer d’Isaac Newton\, 26 · 08022 Barcelona\nDIES: Escoles: De l’11 al 13 d’abril (Entrada gratuïta prèvia reserva).\nPúblic general: Dissabte 14 d’abril (Visita inclosa amb l’entrada de CosmoCaixa Barcelona).\nHORARI: De l’11 al 13 d’abril: de 10.00 h a 15.00 h\nDissabte 14 d’abril: de 10.00 h a 14.00 h / A les 12.00 h: Activitat conduïda per Francesc Orella (Protagonista de la sèrie Merlí).\nAforament limitat. Reserves: 934 031 134 / difusiociencia@pcb.ub.cat
URL:https://ibecbarcelona.eu/event/fira-de-recerca-en-directe-2018-2/
LOCATION:CosmoCaixa Barcelona\, Carrer d'Isaac Newton\, 08022 Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180411T100000
DTEND;TZID=Europe/Madrid:20180414T150000
DTSTAMP:20260404T004034
CREATED:20180405T070513Z
LAST-MODIFIED:20180405T070513Z
UID:96213-1523440800-1523718000@ibecbarcelona.eu
SUMMARY:Fira de Recerca en Directe 2018
DESCRIPTION:Posa’t a la pell d’un científic!\nDe l’11 al 14 d’abril i en el marc de la 16a edició de la Fira Recerca en Directe –organitzada pel Parc Científic de Barcelona i Obra Social “la Caixa”– més de 75 investigadors d’onze centres capdavanters de Catalunya traslladaran els seus laboratoris a CosmoCaixa Barcelona per convidar als ciutadans a participar en els seus projectes de recerca i resoldre enigmes tot seguint el mètode científic. \nEnguany l’IBEC participa amb l’activitat: La mecànica cel·lular\, la membrana de més a prop.\n \nEls participants coneixeran com s’adapta la membrana cel·lular als estímuls del seu entorn acompanyats dels investigadors del grup de Mecanobiologia Cel·lular i Molecular i Dinàmica Integrativa de Cèl·lules i Teixits de l’IBEC. \nLa Xarxa Quiroga\, el Carlos Pérez\, l’Ariadna Marín i el Macià Esteve us explicaran quins són els mecanismes que utilitzen les cèl·lules per detectar i respondre a estímuls mecànics i  com les forces i el control molecular cooperen per aconseguir que els teixits duguin a terme la seva funció biològica. \nACTIVITAT: 16a edició de la Fira Recerca en Directe\nLLOC: CosmoCaixa Barcelona · Carrer d’Isaac Newton\, 26 · 08022 Barcelona\nDIES: Escoles: De l’11 al 13 d’abril (Entrada gratuïta prèvia reserva).\nPúblic general: Dissabte 14 d’abril (Visita inclosa amb l’entrada de CosmoCaixa Barcelona).\nHORARI: De l’11 al 13 d’abril: de 10.00 h a 15.00 h\nDissabte 14 d’abril: de 10.00 h a 14.00 h / A les 12.00 h: Activitat conduïda per Francesc Orella (Protagonista de la sèrie Merlí).\nAforament limitat. Reserves: 934 031 134 / difusiociencia@pcb.ub.cat
URL:https://ibecbarcelona.eu/event/fira-de-recerca-en-directe-2018-4/
LOCATION:CosmoCaixa Barcelona\, Carrer d'Isaac Newton\, 08022 Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180411T100000
DTEND;TZID=Europe/Madrid:20180414T150000
DTSTAMP:20260404T004034
CREATED:20180405T070513Z
LAST-MODIFIED:20180405T070513Z
UID:96212-1523440800-1523718000@ibecbarcelona.eu
SUMMARY:Fira de Recerca en Directe 2018
DESCRIPTION:Posa’t a la pell d’un científic!\nDe l’11 al 14 d’abril i en el marc de la 16a edició de la Fira Recerca en Directe –organitzada pel Parc Científic de Barcelona i Obra Social “la Caixa”– més de 75 investigadors d’onze centres capdavanters de Catalunya traslladaran els seus laboratoris a CosmoCaixa Barcelona per convidar als ciutadans a participar en els seus projectes de recerca i resoldre enigmes tot seguint el mètode científic. \nEnguany l’IBEC participa amb l’activitat: La mecànica cel·lular\, la membrana de més a prop.\n \nEls participants coneixeran com s’adapta la membrana cel·lular als estímuls del seu entorn acompanyats dels investigadors del grup de Mecanobiologia Cel·lular i Molecular i Dinàmica Integrativa de Cèl·lules i Teixits de l’IBEC. \nLa Xarxa Quiroga\, el Carlos Pérez\, l’Ariadna Marín i el Macià Esteve us explicaran quins són els mecanismes que utilitzen les cèl·lules per detectar i respondre a estímuls mecànics i  com les forces i el control molecular cooperen per aconseguir que els teixits duguin a terme la seva funció biològica. \nACTIVITAT: 16a edició de la Fira Recerca en Directe\nLLOC: CosmoCaixa Barcelona · Carrer d’Isaac Newton\, 26 · 08022 Barcelona\nDIES: Escoles: De l’11 al 13 d’abril (Entrada gratuïta prèvia reserva).\nPúblic general: Dissabte 14 d’abril (Visita inclosa amb l’entrada de CosmoCaixa Barcelona).\nHORARI: De l’11 al 13 d’abril: de 10.00 h a 15.00 h\nDissabte 14 d’abril: de 10.00 h a 14.00 h / A les 12.00 h: Activitat conduïda per Francesc Orella (Protagonista de la sèrie Merlí).\nAforament limitat. Reserves: 934 031 134 / difusiociencia@pcb.ub.cat
URL:https://ibecbarcelona.eu/event/fira-de-recerca-en-directe-2018-3/
LOCATION:CosmoCaixa Barcelona\, Carrer d'Isaac Newton\, 08022 Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180412T090000
DTEND;TZID=Europe/Madrid:20180413T150000
DTSTAMP:20260404T004034
CREATED:20180412T101128Z
LAST-MODIFIED:20180412T101409Z
UID:58371-1523523600-1523631600@ibecbarcelona.eu
SUMMARY:hPSCs training course
DESCRIPTION:Reprogramming\, Differentiation and Molecular Genetics\nThis two-day course comprises lectures and practical hands-on workshops run by specialized trainers from academia and industry. The course will provide an overview of reprogramming techniques\, molecular genetics (including CRISPR/Cas9 and hPSCs)\, differentiation\, and organoid derivation. It will be of particular interest to PhD students and postdoctoral fellows aiming to work or already trained in the field of hPSCs. \nRegister: http://events.ibecbarcelona.eu/hPSCs-training-course/
URL:https://ibecbarcelona.eu/event/hpscs-training-course/
LOCATION:IBEC\, Baldiri Reixac 10-12\, Barcelona\, 08028\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180412T090000
DTEND;TZID=Europe/Madrid:20180413T150000
DTSTAMP:20260404T004034
CREATED:20180412T101128Z
LAST-MODIFIED:20180412T101128Z
UID:96224-1523523600-1523631600@ibecbarcelona.eu
SUMMARY:hPSCs training course
DESCRIPTION:Reprogramming\, Differentiation and Molecular Genetics\nThis two-day course comprises lectures and practical hands-on workshops run by specialized trainers from academia and industry. The course will provide an overview of reprogramming techniques\, molecular genetics (including CRISPR/Cas9 and hPSCs)\, differentiation\, and organoid derivation. It will be of particular interest to PhD students and postdoctoral fellows aiming to work or already trained in the field of hPSCs. \nRegister: http://events.ibecbarcelona.eu/hPSCs-training-course/
URL:https://ibecbarcelona.eu/event/hpscs-training-course-2/
LOCATION:IBEC\, Baldiri Reixac 10-12\, Barcelona\, 08028\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180413T100000
DTEND;TZID=Europe/Madrid:20180413T110000
DTSTAMP:20260404T004034
CREATED:20180226T153414Z
LAST-MODIFIED:20180226T153414Z
UID:96181-1523613600-1523617200@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Joan Seoane
DESCRIPTION:Intratumor heterogeneity in brain cancer\nJoan Seoane\, Group Leader / Director of Translational Research at Vall d’Hebron Institute of Oncology (VHIO)\nJoan Seoane is a Group Leader and Director of the Translational Research program at the Vall d’Hebron Institute of Oncology (VHIO) within the Vall d’Hebron University Hospital since 2011. \nIn 1998\, Joan obtained his PhD in Biochemistry and Molecular Biology from the University of Barcelona. Previously\, in 1993\, he obtained his BSc degree in Chemistry. Joan joined the Memorial Sloan-Kettering Cancer Center (MSKCC) in New York as a post-doctoral fellow in 1998. \nFrom 1998 to 2001\, he worked as a Research Fellow and subsequently\, from 2001 to 2003\, as a Research Associate. He was appointed ICREA Research Professor in 2004 and joined VHIO. \nIn 2007\, he became a member of the EMBO Young Investigator program and the recipient of a European Research Council (ERC) grant in 2008. Later\, he obtained two ERC Proof of Concept grants (2011\, 2013). In 2008\, he became Board member of the European Association of Cancer Research (EACR) and Professor of the Autonomous University of Barcelona. \nIn 2012\, founded Mosaic Biomedicals as a spin-off company from his lab and\, in 2013\, he was the recipient of the Dr. Josef Steiner Award. In 2016\, he became Secretary General of the EACR.
URL:https://ibecbarcelona.eu/event/ibec-seminar-joan-seoane-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180413T100000
DTEND;TZID=Europe/Madrid:20180413T110000
DTSTAMP:20260404T004034
CREATED:20180226T153414Z
LAST-MODIFIED:20180226T153414Z
UID:96193-1523613600-1523617200@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Joan Seoane
DESCRIPTION:Intratumor heterogeneity in brain cancer\nJoan Seoane\, Group Leader / Director of Translational Research at Vall d’Hebron Institute of Oncology (VHIO)\nJoan Seoane is a Group Leader and Director of the Translational Research program at the Vall d’Hebron Institute of Oncology (VHIO) within the Vall d’Hebron University Hospital since 2011. \nIn 1998\, Joan obtained his PhD in Biochemistry and Molecular Biology from the University of Barcelona. Previously\, in 1993\, he obtained his BSc degree in Chemistry. Joan joined the Memorial Sloan-Kettering Cancer Center (MSKCC) in New York as a post-doctoral fellow in 1998. \nFrom 1998 to 2001\, he worked as a Research Fellow and subsequently\, from 2001 to 2003\, as a Research Associate. He was appointed ICREA Research Professor in 2004 and joined VHIO. \nIn 2007\, he became a member of the EMBO Young Investigator program and the recipient of a European Research Council (ERC) grant in 2008. Later\, he obtained two ERC Proof of Concept grants (2011\, 2013). In 2008\, he became Board member of the European Association of Cancer Research (EACR) and Professor of the Autonomous University of Barcelona. \nIn 2012\, founded Mosaic Biomedicals as a spin-off company from his lab and\, in 2013\, he was the recipient of the Dr. Josef Steiner Award. In 2016\, he became Secretary General of the EACR.
URL:https://ibecbarcelona.eu/event/ibec-seminar-joan-seoane-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180413T100000
DTEND;TZID=Europe/Madrid:20180413T110000
DTSTAMP:20260404T004034
CREATED:20180226T153414Z
LAST-MODIFIED:20180226T153414Z
UID:96194-1523613600-1523617200@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Joan Seoane
DESCRIPTION:Intratumor heterogeneity in brain cancer\nJoan Seoane\, Group Leader / Director of Translational Research at Vall d’Hebron Institute of Oncology (VHIO)\nJoan Seoane is a Group Leader and Director of the Translational Research program at the Vall d’Hebron Institute of Oncology (VHIO) within the Vall d’Hebron University Hospital since 2011. \nIn 1998\, Joan obtained his PhD in Biochemistry and Molecular Biology from the University of Barcelona. Previously\, in 1993\, he obtained his BSc degree in Chemistry. Joan joined the Memorial Sloan-Kettering Cancer Center (MSKCC) in New York as a post-doctoral fellow in 1998. \nFrom 1998 to 2001\, he worked as a Research Fellow and subsequently\, from 2001 to 2003\, as a Research Associate. He was appointed ICREA Research Professor in 2004 and joined VHIO. \nIn 2007\, he became a member of the EMBO Young Investigator program and the recipient of a European Research Council (ERC) grant in 2008. Later\, he obtained two ERC Proof of Concept grants (2011\, 2013). In 2008\, he became Board member of the European Association of Cancer Research (EACR) and Professor of the Autonomous University of Barcelona. \nIn 2012\, founded Mosaic Biomedicals as a spin-off company from his lab and\, in 2013\, he was the recipient of the Dr. Josef Steiner Award. In 2016\, he became Secretary General of the EACR.
URL:https://ibecbarcelona.eu/event/ibec-seminar-joan-seoane-4/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180413T100000
DTEND;TZID=Europe/Madrid:20180413T110000
DTSTAMP:20260404T004034
CREATED:20180226T153414Z
LAST-MODIFIED:20180409T075629Z
UID:57830-1523613600-1523617200@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Joan Seoane
DESCRIPTION:Intratumor heterogeneity in brain cancer\nJoan Seoane\, Group Leader / Director of Translational Research at Vall d’Hebron Institute of Oncology (VHIO)\nJoan Seoane is a Group Leader and Director of the Translational Research program at the Vall d’Hebron Institute of Oncology (VHIO) within the Vall d’Hebron University Hospital since 2011. \nIn 1998\, Joan obtained his PhD in Biochemistry and Molecular Biology from the University of Barcelona. Previously\, in 1993\, he obtained his BSc degree in Chemistry. Joan joined the Memorial Sloan-Kettering Cancer Center (MSKCC) in New York as a post-doctoral fellow in 1998. \nFrom 1998 to 2001\, he worked as a Research Fellow and subsequently\, from 2001 to 2003\, as a Research Associate. He was appointed ICREA Research Professor in 2004 and joined VHIO. \nIn 2007\, he became a member of the EMBO Young Investigator program and the recipient of a European Research Council (ERC) grant in 2008. Later\, he obtained two ERC Proof of Concept grants (2011\, 2013). In 2008\, he became Board member of the European Association of Cancer Research (EACR) and Professor of the Autonomous University of Barcelona. \nIn 2012\, founded Mosaic Biomedicals as a spin-off company from his lab and\, in 2013\, he was the recipient of the Dr. Josef Steiner Award. In 2016\, he became Secretary General of the EACR.
URL:https://ibecbarcelona.eu/event/ibec-seminar-joan-seoane/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180418T080000
DTEND;TZID=Europe/Madrid:20180419T170000
DTSTAMP:20260404T004034
CREATED:20180413T131426Z
LAST-MODIFIED:20180413T131426Z
UID:96227-1524038400-1524157200@ibecbarcelona.eu
SUMMARY:International PhD Programme interviews
DESCRIPTION:In 2018\, four fellowships will be funded by the Spanish Ministry of Economy\, Industry and Competitiveness through the ‘Ayudas para contratos predoctorales para la formación de doctores’ 2018 call. Three additional fellowships will be funded by IBEC through the Severo Ochoa Excellence Award (IBEC Severo Ochoa Fellowship)\, Fundación Bancaria La Caixa and Fundación Cellex. \nApril 18th-19th 2018: Interviews in Barcelona with selection committee and group leaders responsible for research projects. \nApril 27th 2018: Publication of final list of selected candidates. Letter of acceptance to be signed by candidates. \nMay-October 2018: Start of the fellowships funded by Fundación Bancaria La Caixa and Fundación Cellex\, to be agreed with the Group Leader responsible. \nBeginning of 2019 (To be confirmed\, based on the resolution of the call ‘Ayudas para contratos predoctorales para la formación de doctores’ by the Spanish Ministry of Economy\, Industry and Competitivity): Start of the rest of the fellowships. \nhttp://ibecbarcelona.eu/phd/IIPPfellowships
URL:https://ibecbarcelona.eu/event/international-phd-programme-interviews-3/
LOCATION:PCB\, Baldiri Reixa 4-8\, 10-12\, 15-21\, Barcelona\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180418T080000
DTEND;TZID=Europe/Madrid:20180419T170000
DTSTAMP:20260404T004034
CREATED:20180413T131426Z
LAST-MODIFIED:20180413T131426Z
UID:96228-1524038400-1524157200@ibecbarcelona.eu
SUMMARY:International PhD Programme interviews
DESCRIPTION:In 2018\, four fellowships will be funded by the Spanish Ministry of Economy\, Industry and Competitiveness through the ‘Ayudas para contratos predoctorales para la formación de doctores’ 2018 call. Three additional fellowships will be funded by IBEC through the Severo Ochoa Excellence Award (IBEC Severo Ochoa Fellowship)\, Fundación Bancaria La Caixa and Fundación Cellex. \nApril 18th-19th 2018: Interviews in Barcelona with selection committee and group leaders responsible for research projects. \nApril 27th 2018: Publication of final list of selected candidates. Letter of acceptance to be signed by candidates. \nMay-October 2018: Start of the fellowships funded by Fundación Bancaria La Caixa and Fundación Cellex\, to be agreed with the Group Leader responsible. \nBeginning of 2019 (To be confirmed\, based on the resolution of the call ‘Ayudas para contratos predoctorales para la formación de doctores’ by the Spanish Ministry of Economy\, Industry and Competitivity): Start of the rest of the fellowships. \nhttp://ibecbarcelona.eu/phd/IIPPfellowships
URL:https://ibecbarcelona.eu/event/international-phd-programme-interviews-4/
LOCATION:PCB\, Baldiri Reixa 4-8\, 10-12\, 15-21\, Barcelona\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180418T080000
DTEND;TZID=Europe/Madrid:20180419T170000
DTSTAMP:20260404T004034
CREATED:20180413T131426Z
LAST-MODIFIED:20180413T132059Z
UID:58380-1524038400-1524157200@ibecbarcelona.eu
SUMMARY:International PhD Programme interviews
DESCRIPTION:In 2018\, four fellowships will be funded by the Spanish Ministry of Economy\, Industry and Competitiveness through the ‘Ayudas para contratos predoctorales para la formación de doctores’ 2018 call. Three additional fellowships will be funded by IBEC through the Severo Ochoa Excellence Award (IBEC Severo Ochoa Fellowship)\, Fundación Bancaria La Caixa and Fundación Cellex. \nApril 18th-19th 2018: Interviews in Barcelona with selection committee and group leaders responsible for research projects. \nApril 27th 2018: Publication of final list of selected candidates. Letter of acceptance to be signed by candidates. \nMay-October 2018: Start of the fellowships funded by Fundación Bancaria La Caixa and Fundación Cellex\, to be agreed with the Group Leader responsible. \nBeginning of 2019 (To be confirmed\, based on the resolution of the call ‘Ayudas para contratos predoctorales para la formación de doctores’ by the Spanish Ministry of Economy\, Industry and Competitivity): Start of the rest of the fellowships. \nhttps://ibecbarcelona.eu/phd/IIPPfellowships
URL:https://ibecbarcelona.eu/event/international-phd-programme-interviews/
LOCATION:PCB\, Baldiri Reixa 4-8\, 10-12\, 15-21\, Barcelona\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180418T080000
DTEND;TZID=Europe/Madrid:20180419T170000
DTSTAMP:20260404T004034
CREATED:20180413T131426Z
LAST-MODIFIED:20180413T131426Z
UID:96226-1524038400-1524157200@ibecbarcelona.eu
SUMMARY:International PhD Programme interviews
DESCRIPTION:In 2018\, four fellowships will be funded by the Spanish Ministry of Economy\, Industry and Competitiveness through the ‘Ayudas para contratos predoctorales para la formación de doctores’ 2018 call. Three additional fellowships will be funded by IBEC through the Severo Ochoa Excellence Award (IBEC Severo Ochoa Fellowship)\, Fundación Bancaria La Caixa and Fundación Cellex. \nApril 18th-19th 2018: Interviews in Barcelona with selection committee and group leaders responsible for research projects. \nApril 27th 2018: Publication of final list of selected candidates. Letter of acceptance to be signed by candidates. \nMay-October 2018: Start of the fellowships funded by Fundación Bancaria La Caixa and Fundación Cellex\, to be agreed with the Group Leader responsible. \nBeginning of 2019 (To be confirmed\, based on the resolution of the call ‘Ayudas para contratos predoctorales para la formación de doctores’ by the Spanish Ministry of Economy\, Industry and Competitivity): Start of the rest of the fellowships. \nhttp://ibecbarcelona.eu/phd/IIPPfellowships
URL:https://ibecbarcelona.eu/event/international-phd-programme-interviews-2/
LOCATION:PCB\, Baldiri Reixa 4-8\, 10-12\, 15-21\, Barcelona\, Spain
CATEGORIES:Other
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180420T100000
DTEND;TZID=Europe/Madrid:20180420T110000
DTSTAMP:20260404T004034
CREATED:20180403T074519Z
LAST-MODIFIED:20180403T074519Z
UID:96202-1524218400-1524222000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: (David) Dagan Feng
DESCRIPTION:Biomedical Engineering and Technology Research at USYD and beyond\n(David) Dagan Feng\, PhD\, FACS\, FATSE\, FHKIE\, FIEEE\, & FIET\nRecent advances in engineering\, information technology and imaging have revolutionized biotechnology\, biomedical research and healthcare. This talk will initially focus on some of his core theories and enabling techniques research in molecular imaging for E-Healthcare and its impact to clinical practice\, in particular in cancer and metabolic diseases. This talk will then give an overview of the Biomedical Engineering and Technology research at the University of Sydney and beyond\, in particular several University new initiatives and the USYD-SJTU Joint Research Alliance.
URL:https://ibecbarcelona.eu/event/ibec-seminar-david-dagan-feng-4/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180420T100000
DTEND;TZID=Europe/Madrid:20180420T110000
DTSTAMP:20260404T004034
CREATED:20180403T074519Z
LAST-MODIFIED:20180403T074519Z
UID:96200-1524218400-1524222000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: (David) Dagan Feng
DESCRIPTION:Biomedical Engineering and Technology Research at USYD and beyond\n(David) Dagan Feng\, PhD\, FACS\, FATSE\, FHKIE\, FIEEE\, & FIET\nRecent advances in engineering\, information technology and imaging have revolutionized biotechnology\, biomedical research and healthcare. This talk will initially focus on some of his core theories and enabling techniques research in molecular imaging for E-Healthcare and its impact to clinical practice\, in particular in cancer and metabolic diseases. This talk will then give an overview of the Biomedical Engineering and Technology research at the University of Sydney and beyond\, in particular several University new initiatives and the USYD-SJTU Joint Research Alliance.
URL:https://ibecbarcelona.eu/event/ibec-seminar-david-dagan-feng-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180420T100000
DTEND;TZID=Europe/Madrid:20180420T110000
DTSTAMP:20260404T004034
CREATED:20180403T074519Z
LAST-MODIFIED:20180403T074519Z
UID:58189-1524218400-1524222000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: (David) Dagan Feng
DESCRIPTION:Biomedical Engineering and Technology Research at USYD and beyond\n(David) Dagan Feng\, PhD\, FACS\, FATSE\, FHKIE\, FIEEE\, & FIET\nRecent advances in engineering\, information technology and imaging have revolutionized biotechnology\, biomedical research and healthcare. This talk will initially focus on some of his core theories and enabling techniques research in molecular imaging for E-Healthcare and its impact to clinical practice\, in particular in cancer and metabolic diseases. This talk will then give an overview of the Biomedical Engineering and Technology research at the University of Sydney and beyond\, in particular several University new initiatives and the USYD-SJTU Joint Research Alliance.
URL:https://ibecbarcelona.eu/event/ibec-seminar-david-dagan-feng/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180420T100000
DTEND;TZID=Europe/Madrid:20180420T110000
DTSTAMP:20260404T004034
CREATED:20180403T074519Z
LAST-MODIFIED:20180403T074519Z
UID:96201-1524218400-1524222000@ibecbarcelona.eu
SUMMARY:IBEC Seminar: (David) Dagan Feng
DESCRIPTION:Biomedical Engineering and Technology Research at USYD and beyond\n(David) Dagan Feng\, PhD\, FACS\, FATSE\, FHKIE\, FIEEE\, & FIET\nRecent advances in engineering\, information technology and imaging have revolutionized biotechnology\, biomedical research and healthcare. This talk will initially focus on some of his core theories and enabling techniques research in molecular imaging for E-Healthcare and its impact to clinical practice\, in particular in cancer and metabolic diseases. This talk will then give an overview of the Biomedical Engineering and Technology research at the University of Sydney and beyond\, in particular several University new initiatives and the USYD-SJTU Joint Research Alliance.
URL:https://ibecbarcelona.eu/event/ibec-seminar-david-dagan-feng-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20180426T190000
DTEND;TZID=Europe/Madrid:20180426T213000
DTSTAMP:20260404T004034
CREATED:20180417T121153Z
LAST-MODIFIED:20180417T133508Z
UID:58427-1524769200-1524778200@ibecbarcelona.eu
SUMMARY:SciDF@Bars: "Del Laboratorio al Parlamento: Asesoramiento Científico"
DESCRIPTION:Many political issues are related to science and technology: climate change\, vaccines\, ciber-security or the use of glyphosate are some examples of how science gets onto the politic agenda. \nFor all those issues scientific advice is needed: How does it work? Which different models exist? How is science advice organised in different regions of the world and\, specially\, in Spain and Catalunya? \nIn this SciDF@Bars\, we will discuss with experts and perform a study case to talk about it while having some beers and networking with friends. \nJoin us next Thursday\, 26th April at 19:15h in Mau Mau! \nThe entrance fee is 5€\, with one beer included*. Event language: SPANISH \n*The fee for the event helps to finance the activities of Scientists Dating Forum\, whose complete spectrum of activities you can find on www.scientistsdatingforum.org.
URL:https://ibecbarcelona.eu/event/scidfbars-del-laboratorio-al-parlamento-asesoramiento-cientifico/
LOCATION:Mau Mau\, 35 Calle de Fontrodona\, 08004 Barcelona\, Spain
CATEGORIES:Other
END:VEVENT
END:VCALENDAR