BEGIN:VCALENDAR
VERSION:2.0
PRODID:-//Institute for Bioengineering of Catalonia - ECPv6.18.3.1//NONSGML v1.0//EN
CALSCALE:GREGORIAN
METHOD:PUBLISH
X-WR-CALNAME:Institute for Bioengineering of Catalonia
X-ORIGINAL-URL:https://ibecbarcelona.eu
X-WR-CALDESC:Events for Institute for Bioengineering of Catalonia
REFRESH-INTERVAL;VALUE=DURATION:PT1H
X-Robots-Tag:noindex
X-PUBLISHED-TTL:PT1H
BEGIN:VTIMEZONE
TZID:Europe/Madrid
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20210328T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20211031T010000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20220327T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20221030T010000
END:STANDARD
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
TZOFFSETTO:+0200
TZNAME:CEST
DTSTART:20230326T010000
END:DAYLIGHT
BEGIN:STANDARD
TZOFFSETFROM:+0200
TZOFFSETTO:+0100
TZNAME:CET
DTSTART:20231029T010000
END:STANDARD
END:VTIMEZONE
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220512T101500
DTEND;TZID=Europe/Madrid:20220512T140000
DTSTAMP:20220419T073953Z
CREATED:20220419T073953Z
LAST-MODIFIED:20220419T073953Z
UID:96584-1652350500-1652364000@ibecbarcelona.eu
SUMMARY:Research4Talent 2022
DESCRIPTION:On Thursday 12th May 2022 we’ll open our doors to UNDERGRADUATE & MASTER’s students interested in a research career\n \nThe day is a chance for you to talk to our researchers and ask them questions about their day-to-day work in the lab\, career paths\, work-life balance\, mobility etc. \nIn 2021 IBEC signed more that 165 internship agreements for Undergraduate and Master Students with a wide range of national and international universities. If you are interested in IBEC’s eighth edition of reSEARCH4TALENT\, please register now.
URL:https://ibecbarcelona.eu/event/research4talent-2022/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220512T101500
DTEND;TZID=Europe/Madrid:20220512T140000
DTSTAMP:20220419T073953Z
CREATED:20220419T073953Z
LAST-MODIFIED:20220419T073953Z
UID:96585-1652350500-1652364000@ibecbarcelona.eu
SUMMARY:Research4Talent 2022
DESCRIPTION:On Thursday 12th May 2022 we’ll open our doors to UNDERGRADUATE & MASTER’s students interested in a research career\n \nThe day is a chance for you to talk to our researchers and ask them questions about their day-to-day work in the lab\, career paths\, work-life balance\, mobility etc. \nIn 2021 IBEC signed more that 165 internship agreements for Undergraduate and Master Students with a wide range of national and international universities. If you are interested in IBEC’s eighth edition of reSEARCH4TALENT\, please register now.
URL:https://ibecbarcelona.eu/event/research4talent-2022-2/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220512T101500
DTEND;TZID=Europe/Madrid:20220512T140000
DTSTAMP:20220419T073953Z
CREATED:20220419T073953Z
LAST-MODIFIED:20220419T073953Z
UID:96588-1652350500-1652364000@ibecbarcelona.eu
SUMMARY:Research4Talent 2022
DESCRIPTION:On Thursday 12th May 2022 we’ll open our doors to UNDERGRADUATE & MASTER’s students interested in a research career\n \nThe day is a chance for you to talk to our researchers and ask them questions about their day-to-day work in the lab\, career paths\, work-life balance\, mobility etc. \nIn 2021 IBEC signed more that 165 internship agreements for Undergraduate and Master Students with a wide range of national and international universities. If you are interested in IBEC’s eighth edition of reSEARCH4TALENT\, please register now.
URL:https://ibecbarcelona.eu/event/research4talent-2022-3/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220509T183000
DTEND;TZID=Europe/Madrid:20220511T210000
DTSTAMP:20220504T115535Z
CREATED:20220504T115535Z
LAST-MODIFIED:20220504T115535Z
UID:96611-1652121000-1652302800@ibecbarcelona.eu
SUMMARY:Pint of Science 2022
DESCRIPTION:Monica Mir de Nanobioengineering\,  Agustín Gutierrez de Signal and Information Processing for Sensing Systems y  Silvia Pujals de Nanoscopy for nanomedicine participarán en el evento global de divulgación científica Pint of Science. \nEl festival Pint of Science\, que se celebrará del 09 al 11 de mayo\, tiene como objetivo ofrecer charlas interesantes\, divertidas y relevantes sobre las últimas investigaciones científicas de la mano de las personas que las llevan a cabo. \n  \nLunes\, 9 de mayo:  \n\nMonica Mir “¿Como funcionan los test para detección de COVID?”\nAgustín Gutierrez “Una nueva inteligencia para controlar el mundo”\n\nMartes 10 de mayo: \n\nSilvia Pujals “Nanopartículas para la medicina. ¿Promesa o realidad?”\n\n  \n\n\n\n\nSi quieres más información\, visita: Eventos de Barcelona | Pint of Science ES. \nPodéis ver el cartel aquí.
URL:https://ibecbarcelona.eu/event/pint-of-science-2022/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220509T183000
DTEND;TZID=Europe/Madrid:20220511T210000
DTSTAMP:20220504T115535Z
CREATED:20220504T115535Z
LAST-MODIFIED:20220504T115535Z
UID:96612-1652121000-1652302800@ibecbarcelona.eu
SUMMARY:Pint of Science 2022
DESCRIPTION:Monica Mir de Nanobioengineering\,  Agustín Gutierrez de Signal and Information Processing for Sensing Systems y  Silvia Pujals de Nanoscopy for nanomedicine participarán en el evento global de divulgación científica Pint of Science. \nEl festival Pint of Science\, que se celebrará del 09 al 11 de mayo\, tiene como objetivo ofrecer charlas interesantes\, divertidas y relevantes sobre las últimas investigaciones científicas de la mano de las personas que las llevan a cabo. \n  \nLunes\, 9 de mayo:  \n\nMonica Mir “¿Como funcionan los test para detección de COVID?”\nAgustín Gutierrez “Una nueva inteligencia para controlar el mundo”\n\nMartes 10 de mayo: \n\nSilvia Pujals “Nanopartículas para la medicina. ¿Promesa o realidad?”\n\n  \n\n\n\n\nSi quieres más información\, visita: Eventos de Barcelona | Pint of Science ES. \nPodéis ver el cartel aquí.
URL:https://ibecbarcelona.eu/event/pint-of-science-2022/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220509T183000
DTEND;TZID=Europe/Madrid:20220511T210000
DTSTAMP:20220504T115535Z
CREATED:20220504T115535Z
LAST-MODIFIED:20220504T115535Z
UID:96608-1652121000-1652302800@ibecbarcelona.eu
SUMMARY:Pint of Science 2022
DESCRIPTION:Monica Mir de Nanobioengineering\,  Agustín Gutierrez de Signal and Information Processing for Sensing Systems y  Silvia Pujals de Nanoscopy for nanomedicine participarán en el evento global de divulgación científica Pint of Science. \nEl festival Pint of Science\, que se celebrará del 09 al 11 de mayo\, tiene como objetivo ofrecer charlas interesantes\, divertidas y relevantes sobre las últimas investigaciones científicas de la mano de las personas que las llevan a cabo. \n  \nLunes\, 9 de mayo:  \n\nMonica Mir “¿Como funcionan los test para detección de COVID?”\nAgustín Gutierrez “Una nueva inteligencia para controlar el mundo”\n\nMartes 10 de mayo: \n\nSilvia Pujals “Nanopartículas para la medicina. ¿Promesa o realidad?”\n\n  \n\n\n\n\nSi quieres más información\, visita: Eventos de Barcelona | Pint of Science ES. \nPodéis ver el cartel aquí.
URL:https://ibecbarcelona.eu/event/pint-of-science-2022/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220429T100000
DTEND;TZID=Europe/Madrid:20220429T120000
DTSTAMP:20220422T065109Z
CREATED:20220422T065109Z
LAST-MODIFIED:20220422T065109Z
UID:96589-1651226400-1651233600@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\nSefora Conti\, Integrative cell and tissue dynamics group \nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti-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:20220429T100000
DTEND;TZID=Europe/Madrid:20220429T120000
DTSTAMP:20220422T065109Z
CREATED:20220422T065109Z
LAST-MODIFIED:20220422T065109Z
UID:96592-1651226400-1651233600@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\nSefora Conti\, Integrative cell and tissue dynamics group \nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti-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:20220429T100000
DTEND;TZID=Europe/Madrid:20220429T120000
DTSTAMP:20220422T065109Z
CREATED:20220422T065109Z
LAST-MODIFIED:20220422T065109Z
UID:96593-1651226400-1651233600@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\nSefora Conti\, Integrative cell and tissue dynamics group \nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti-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:20220427T120000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220503T143818Z
CREATED:20220503T143816Z
LAST-MODIFIED:20220503T143818Z
UID:94013-1651060800-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\n\n\n\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \n\n\n\nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\n\n\n\n\n\n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T120000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220503T143816Z
CREATED:20220503T143816Z
LAST-MODIFIED:20220503T143816Z
UID:94014-1651060800-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\n\n\n\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \n\n\n\nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\n\n\n\n\n\n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T120000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220503T143816Z
CREATED:20220503T143816Z
LAST-MODIFIED:20220503T143816Z
UID:94015-1651060800-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\n\n\n\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \n\n\n\nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\n\n\n\n\n\n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T100000
DTEND;TZID=Europe/Madrid:20220430T150000
DTSTAMP:20220503T144700Z
CREATED:20220503T144700Z
LAST-MODIFIED:20220503T144700Z
UID:94018-1651053600-1651330800@ibecbarcelona.eu
SUMMARY:Fira Recerca en Directe 2022
DESCRIPTION:Fira Recerca en Directe\n\n\n\n\n\n\n\nLa Fira Recerca en Directe es planteja com a un tastet de projectes de recerca que estan en curs sobre diferents disciplines amb un format de proximitat\, on es presenta l’oportunitat de parlar cara a cara amb els mateixos investigadors\, així com de realitzar petits experiments amb la instrumentació científica i part del laboratori que desplacen fins a la Fira. \n\n\n\nVa néixer el 2003 per establir un canal de comunicació on es pogués transmetre a la població el mètode científic i la recerca que es porta a terme als laboratoris de tot Catalunya. \n\n\n\nParticipa el grup de “Nanobioenginyeria” amb un stand on parlaràn sobre les nanopartícules i com viatgen pel nostre cos.
URL:https://ibecbarcelona.eu/event/fira-recerca-en-directe-2022/
LOCATION:CosmoCaixa
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T100000
DTEND;TZID=Europe/Madrid:20220430T150000
DTSTAMP:20220503T144700Z
CREATED:20220503T144700Z
LAST-MODIFIED:20220503T144700Z
UID:94019-1651053600-1651330800@ibecbarcelona.eu
SUMMARY:Fira Recerca en Directe 2022
DESCRIPTION:Fira Recerca en Directe\n\n\n\n\n\n\n\nLa Fira Recerca en Directe es planteja com a un tastet de projectes de recerca que estan en curs sobre diferents disciplines amb un format de proximitat\, on es presenta l’oportunitat de parlar cara a cara amb els mateixos investigadors\, així com de realitzar petits experiments amb la instrumentació científica i part del laboratori que desplacen fins a la Fira. \n\n\n\nVa néixer el 2003 per establir un canal de comunicació on es pogués transmetre a la població el mètode científic i la recerca que es porta a terme als laboratoris de tot Catalunya. \n\n\n\nParticipa el grup de “Nanobioenginyeria” amb un stand on parlaràn sobre les nanopartícules i com viatgen pel nostre cos.
URL:https://ibecbarcelona.eu/event/fira-recerca-en-directe-2022/
LOCATION:CosmoCaixa
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T100000
DTEND;TZID=Europe/Madrid:20220430T150000
DTSTAMP:20220503T144701Z
CREATED:20220503T144700Z
LAST-MODIFIED:20220503T144701Z
UID:94016-1651053600-1651330800@ibecbarcelona.eu
SUMMARY:Fira Recerca en Directe 2022
DESCRIPTION:Fira Recerca en Directe\n\n\n\n\n\n\n\nLa Fira Recerca en Directe es planteja com a un tastet de projectes de recerca que estan en curs sobre diferents disciplines amb un format de proximitat\, on es presenta l’oportunitat de parlar cara a cara amb els mateixos investigadors\, així com de realitzar petits experiments amb la instrumentació científica i part del laboratori que desplacen fins a la Fira. \n\n\n\nVa néixer el 2003 per establir un canal de comunicació on es pogués transmetre a la població el mètode científic i la recerca que es porta a terme als laboratoris de tot Catalunya. \n\n\n\nParticipa el grup de “Nanobioenginyeria” amb un stand on parlaràn sobre les nanopartícules i com viatgen pel nostre cos.
URL:https://ibecbarcelona.eu/event/fira-recerca-en-directe-2022/
LOCATION:CosmoCaixa
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T000000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220314T110017Z
CREATED:20220314T110017Z
LAST-MODIFIED:20220314T110017Z
UID:96556-1651017600-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T000000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220314T110017Z
CREATED:20220314T110017Z
LAST-MODIFIED:20220314T110017Z
UID:96560-1651017600-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski-3/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220427T000000
DTEND;TZID=Europe/Madrid:20220427T130000
DTSTAMP:20220314T110017Z
CREATED:20220314T110017Z
LAST-MODIFIED:20220314T110017Z
UID:90931-1651017600-1651064400@ibecbarcelona.eu
SUMMARY:Open BIST Seminar: Dr. Wiktor Szymanski
DESCRIPTION:Molecular basis for the use of light in medicine\nWiktor Szymanski\, Medical Imaging Center\, University Medical Center Groningen \nLight is a unique control element in chemistry and biology\, because it can be safely delivered with very high precision to modulate processes in space and time. In this educational lecture\, aimed at Master students but hopefully of interest to all academics\, I will discuss the main processes that a molecule can undergo once it has been promoted to the excited state under light irradiation. Using the Jablonski diagram as the starting point\, I will outline how these processes are or could be used in the clinic for diagnostics (optical and optoacoustic imaging) and therapy (photodynamic therapy and photopharmacology). \n\nWiktor Szymanski received his PhD degree from The Warsaw University of Technology\, Poland\, in 2008\, working under the supervision of Prof. Ryszard Ostaszewski. He spent two years working on the use of biotransformations in organic chemistry with Prof. Ben L. Feringa and Prof. Dick B. Janssen at the University of Groningen. Since 2010 he has been working on the construction of photoactive protein- peptide- and DNA-bioconjugates and photopharmacology in the Feringa Labs. In 2014\, he joined the Medical Imaging Center\, University Medical Center Groningen\, where he was appointed in 2015 as tenure track assistant professor and in 2019 as associate professor (adjunct hoogleraar).
URL:https://ibecbarcelona.eu/event/open-bist-seminar-dr-wiktor-szymanski-2/
LOCATION:IBEC\, floor 11\, Tower I\, Baldiri Reixac 4-8\, 08028 Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220415T100000
DTEND;TZID=Europe/Madrid:20220415T120000
DTSTAMP:20230301T140903Z
CREATED:20220503T144933Z
LAST-MODIFIED:20230301T140903Z
UID:94022-1650016800-1650024000@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\n\n\n\nSefora Conti\, Integrative cell and tissue dynamics group \n\n\n\nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \n\n\n\nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \n\n\n\nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \n\n\n\nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \n\n\n\nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \n\n\n\nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220415T100000
DTEND;TZID=Europe/Madrid:20220415T120000
DTSTAMP:20230301T140902Z
CREATED:20220503T144933Z
LAST-MODIFIED:20230301T140902Z
UID:94020-1650016800-1650024000@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\n\n\n\nSefora Conti\, Integrative cell and tissue dynamics group \n\n\n\nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \n\n\n\nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \n\n\n\nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \n\n\n\nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \n\n\n\nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \n\n\n\nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220415T100000
DTEND;TZID=Europe/Madrid:20220415T120000
DTSTAMP:20230301T140902Z
CREATED:20220503T144933Z
LAST-MODIFIED:20230301T140902Z
UID:94021-1650016800-1650024000@ibecbarcelona.eu
SUMMARY:PhD Discussions: Sefora Conti
DESCRIPTION:Mechanical phenotyping of colorectal cancer patient derived organoids based on LGR5 expression\n\n\n\nSefora Conti\, Integrative cell and tissue dynamics group \n\n\n\nColorectal cancer (CRC) tumors are composed by heterogeneous cell populations comprising differentiated cells and a small pool of cancer stem cells (CSCs). The link between cancer cell differentiation states and their metastatic potential has been the focus of extensive investigation\, with some studies pointing to microenvironmentally defined plasticity as a mechanism indispensable for metastasis formation. Another aspect that might be determinant in tumor cells ability to successfully disseminate\, intravasate\, survive in the blood stream\, extravasate\, colonize distant organs and form secondary tumors is their mechanical phenotype. \n\n\n\nAdopting a bottom-up approach\, we performed a broad biophysical characterization of CRC patient derived organoids (PDOs)\, engineered to fluorescently label cells expressing LGR5\, a well-established marker for CSCs. We show that CRC cells differentiation states are associated with distinct biomechanical phenotypes\, with potential repercussions on their metastatic ability. \n\n\n\nAt the single cell level\, LGR5+ cells display a more elongated and polarized shape while the LGR5- cells exhibit higher roundness and a smaller asymmetry in the stress field. LGR5+ are stiffer compared to their differentiated counterparts and more prone to adopt a fast amoeboid-like migration under confinement.  At the molecular level\, cancer stemness is related to differential expression of the ERM protein family\, responsible of tethering the cell membrane to the underlying actin cortex. \n\n\n\nThese distinct mechanical phenotypes translate to different migratory and morphological phenotypes at a cluster level. Clusters expressing high levels of LGR5 showed a more spread and flattened shape compared to more differentiated clusters. Moreover\, LGR5 expression in clusters is negatively correlated with their migration speed and their polarization state. Hence\, clusters containing more differentiated cells migrate faster\, display higher roundness and higher polarization state. \n\n\n\nAt higher complexity levels\, such as interactions with endothelial cells\, LGR5 expression in CRC clusters affects their ability to adhere to an endothelial monolayer and form a gap through which they attach to the underlying collagen coating. Notably\, we found that clusters expressing more LGR5 have an advantage while attaching to the endothelium as indicated by higher attachment rate and shorter time to form a gap. \n\n\n\nBased on these findings relating distinct mechanical phenotypes to LGR5 expression\, we speculate that mechanical adaptability coupled with cancer plasticity may be an indispensable mechanism for cancer progression.
URL:https://ibecbarcelona.eu/event/phd-discussions-sefora-conti/
LOCATION:IBEC\, floor 11\, tower i
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220503T142713Z
CREATED:20220503T142713Z
LAST-MODIFIED:20220503T142713Z
UID:94012-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\n\n\n\nIgnasi Casanellas\, Nanobioengineering Group \n\n\n\nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \n\n\n\nMore information here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas/
LOCATION:Sala de Graus Eduard Fontseré
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220503T142714Z
CREATED:20220503T142713Z
LAST-MODIFIED:20220503T142714Z
UID:94009-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\n\n\n\nIgnasi Casanellas\, Nanobioengineering Group \n\n\n\nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \n\n\n\nMore information here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas/
LOCATION:Sala de Graus Eduard Fontseré
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220503T142713Z
CREATED:20220503T142713Z
LAST-MODIFIED:20220503T142713Z
UID:94011-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\n\n\n\nIgnasi Casanellas\, Nanobioengineering Group \n\n\n\nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \n\n\n\nMore information here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas/
LOCATION:Sala de Graus Eduard Fontseré
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220309T132156Z
CREATED:20220309T132156Z
LAST-MODIFIED:20220309T132156Z
UID:96545-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\nIgnasi Casanellas\, Nanobioengineering Group \nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \nMore information here \n 
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas-2/
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220309T132156Z
CREATED:20220309T132156Z
LAST-MODIFIED:20220309T132156Z
UID:96549-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\nIgnasi Casanellas\, Nanobioengineering Group \nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \nMore information here \n 
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas-4/
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220413T150000
DTEND;TZID=Europe/Madrid:20220413T170000
DTSTAMP:20220309T132156Z
CREATED:20220309T132156Z
LAST-MODIFIED:20220309T132156Z
UID:96548-1649862000-1649869200@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Ignasi Casanellas
DESCRIPTION:Cell-adhesive nanopatterns for musculoskeletal tissue engineering\nIgnasi Casanellas\, Nanobioengineering Group \nThis thesis defence will take place at “Sala de Graus Eduard Fontseré\, Facultat de Física\, Universitat de Barcelona” at 3PM. If you wish to follow this defence online\, you can contact Ignasi here. \nMore information here \n 
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-ignasi-casanellas-3/
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220401T110000
DTEND;TZID=Europe/Madrid:20220401T130000
DTSTAMP:20220503T142336Z
CREATED:20220503T142336Z
LAST-MODIFIED:20220503T142336Z
UID:94007-1648810800-1648818000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Francina Mesquida Veny
DESCRIPTION:Activity-dependent mechanisms of axonal growth\n\n\n\nFrancina Mesquida Veny\, Molecular and cellular neurobiotechnology  \n\n\n\nThis thesis defence will take place at “Aula de Graus” Facultat de Biologia\, Universitat de Barcelona” at 11AM. \n\n\n\nIf anyone is interested in attending online\, you can contact Francina here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-francina-mesquida-veny/
LOCATION:Aula de Graus\, Faculty of Biology
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220401T110000
DTEND;TZID=Europe/Madrid:20220401T130000
DTSTAMP:20220503T142337Z
CREATED:20220503T142336Z
LAST-MODIFIED:20220503T142337Z
UID:94005-1648810800-1648818000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Francina Mesquida Veny
DESCRIPTION:Activity-dependent mechanisms of axonal growth\n\n\n\nFrancina Mesquida Veny\, Molecular and cellular neurobiotechnology  \n\n\n\nThis thesis defence will take place at “Aula de Graus” Facultat de Biologia\, Universitat de Barcelona” at 11AM. \n\n\n\nIf anyone is interested in attending online\, you can contact Francina here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-francina-mesquida-veny/
LOCATION:Aula de Graus\, Faculty of Biology
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20220401T110000
DTEND;TZID=Europe/Madrid:20220401T130000
DTSTAMP:20220503T142336Z
CREATED:20220503T142336Z
LAST-MODIFIED:20220503T142336Z
UID:94008-1648810800-1648818000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Francina Mesquida Veny
DESCRIPTION:Activity-dependent mechanisms of axonal growth\n\n\n\nFrancina Mesquida Veny\, Molecular and cellular neurobiotechnology  \n\n\n\nThis thesis defence will take place at “Aula de Graus” Facultat de Biologia\, Universitat de Barcelona” at 11AM. \n\n\n\nIf anyone is interested in attending online\, you can contact Francina here
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-francina-mesquida-veny/
LOCATION:Aula de Graus\, Faculty of Biology
CATEGORIES:PhD Thesis Defence
END:VEVENT
END:VCALENDAR