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X-WR-CALNAME:Institute for Bioengineering of Catalonia
X-ORIGINAL-URL:https://ibecbarcelona.eu
X-WR-CALDESC:Events for Institute for Bioengineering of Catalonia
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BEGIN:VTIMEZONE
TZID:Europe/Madrid
BEGIN:DAYLIGHT
TZOFFSETFROM:+0100
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TZNAME:CEST
DTSTART:20160327T010000
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DTSTART:20161030T010000
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DTSTART:20170326T010000
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BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170512T110000
DTEND;TZID=Europe/Madrid:20170512T140000
DTSTAMP:20260406T013922
CREATED:20170224T122921Z
LAST-MODIFIED:20170801T105113Z
UID:27780-1494586800-1494597600@ibecbarcelona.eu
SUMMARY:reSearch4Talent 2017
DESCRIPTION:reSearch4Talent 2017\nOn Friday 12th May 2017 we’ll open our doors again to undergraduate and masters students interested in a research career. \nThis will be the third edition of reSearch4Talent. \n\nPROGRAMME:\n11:00 Welcome\n11:15 Director’s talk\, “What is IBEC?” and overview of research groups\n11:50 HR Speech\n12:00 Careers Fair: a chance for participants to mingle and chat with our researchers\n13:00 – 14:00 Lab visits \n\nVENUE:\nInstitute for Bioengineering of Catalonia (IBEC)\nDolors Aleu Room\nParc Científic de Barcelona (PCB)\nC. Baldiri Reixac\, 4-8\, Barcelona \nMore details here.
URL:https://ibecbarcelona.eu/event/research4talent-2017/
LOCATION:Sala Dolors Aleu\, Cluster II\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170512T110000
DTEND;TZID=Europe/Madrid:20170512T140000
DTSTAMP:20260406T013922
CREATED:20170224T122921Z
LAST-MODIFIED:20170224T122921Z
UID:96005-1494586800-1494597600@ibecbarcelona.eu
SUMMARY:reSearch4Talent 2017
DESCRIPTION:reSearch4Talent 2017\nOn Friday 12th May 2017 we’ll open our doors again to undergraduate and masters students interested in a research career. \nThis will be the third edition of reSearch4Talent. \n\nPROGRAMME:\n11:00 Welcome\n11:15 Director’s talk\, “What is IBEC?” and overview of research groups\n11:50 HR Speech\n12:00 Careers Fair: a chance for participants to mingle and chat with our researchers\n13:00 – 14:00 Lab visits \n\nVENUE:\nInstitute for Bioengineering of Catalonia (IBEC)\nDolors Aleu Room\nParc Científic de Barcelona (PCB)\nC. Baldiri Reixac\, 4-8\, Barcelona \nMore details here.
URL:https://ibecbarcelona.eu/event/research4talent-2017-2/
LOCATION:Sala Dolors Aleu\, Cluster II\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170512T110000
DTEND;TZID=Europe/Madrid:20170512T140000
DTSTAMP:20260406T013922
CREATED:20170224T122921Z
LAST-MODIFIED:20170224T122921Z
UID:96012-1494586800-1494597600@ibecbarcelona.eu
SUMMARY:reSearch4Talent 2017
DESCRIPTION:reSearch4Talent 2017\nOn Friday 12th May 2017 we’ll open our doors again to undergraduate and masters students interested in a research career. \nThis will be the third edition of reSearch4Talent. \n\nPROGRAMME:\n11:00 Welcome\n11:15 Director’s talk\, “What is IBEC?” and overview of research groups\n11:50 HR Speech\n12:00 Careers Fair: a chance for participants to mingle and chat with our researchers\n13:00 – 14:00 Lab visits \n\nVENUE:\nInstitute for Bioengineering of Catalonia (IBEC)\nDolors Aleu Room\nParc Científic de Barcelona (PCB)\nC. Baldiri Reixac\, 4-8\, Barcelona \nMore details here.
URL:https://ibecbarcelona.eu/event/research4talent-2017-3/
LOCATION:Sala Dolors Aleu\, Cluster II\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170512T110000
DTEND;TZID=Europe/Madrid:20170512T140000
DTSTAMP:20260406T013922
CREATED:20170224T122921Z
LAST-MODIFIED:20170224T122921Z
UID:96013-1494586800-1494597600@ibecbarcelona.eu
SUMMARY:reSearch4Talent 2017
DESCRIPTION:reSearch4Talent 2017\nOn Friday 12th May 2017 we’ll open our doors again to undergraduate and masters students interested in a research career. \nThis will be the third edition of reSearch4Talent. \n\nPROGRAMME:\n11:00 Welcome\n11:15 Director’s talk\, “What is IBEC?” and overview of research groups\n11:50 HR Speech\n12:00 Careers Fair: a chance for participants to mingle and chat with our researchers\n13:00 – 14:00 Lab visits \n\nVENUE:\nInstitute for Bioengineering of Catalonia (IBEC)\nDolors Aleu Room\nParc Científic de Barcelona (PCB)\nC. Baldiri Reixac\, 4-8\, Barcelona \nMore details here.
URL:https://ibecbarcelona.eu/event/research4talent-2017-4/
LOCATION:Sala Dolors Aleu\, Cluster II\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170508
DTEND;VALUE=DATE:20170509
DTSTAMP:20260406T013922
CREATED:20170324T075403Z
LAST-MODIFIED:20170324T075403Z
UID:96011-1494201600-1494287999@ibecbarcelona.eu
SUMMARY:Say it so it stays : Oral presentation skills training for scientists
DESCRIPTION:Training activity in transferable skills. \nThe course’s aim is to improve scientists’ effectiveness and confidence when presenting their research to peers and public. \nDates: \nMonday 8th May 9.30 – 5.30\, \nTuesday 9th May 9.30 -1pm\, \nand Friday 12th May 9.30 to 1.30 \nIn person class sessions = 14 hours. One whole day and two half days. \nTarget group: \nPhD students and post-docs. \nProvider: Elinor Thompson.
URL:https://ibecbarcelona.eu/event/say-it-so-it-stays-oral-presentation-skills-training-for-scientists-4/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170508
DTEND;VALUE=DATE:20170509
DTSTAMP:20260406T013922
CREATED:20170324T075403Z
LAST-MODIFIED:20170324T102545Z
UID:28624-1494201600-1494287999@ibecbarcelona.eu
SUMMARY:Say it so it stays : Oral presentation skills training for scientists
DESCRIPTION:Training activity in transferable skills. \nThe course’s aim is to improve scientists’ effectiveness and confidence when presenting their research to peers and public. \nDates: \nMonday 8th May 9.30 – 5.30\, \nTuesday 9th May 9.30 -1pm\, \nand Friday 12th May 9.30 to 1.30 \nIn person class sessions = 14 hours. One whole day and two half days. \nTarget group: \nPhD students and post-docs. \nProvider: Elinor Thompson.
URL:https://ibecbarcelona.eu/event/say-it-so-it-stays-oral-presentation-skills-training-for-scientists/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170504T093000
DTEND;TZID=Europe/Madrid:20170504T133000
DTSTAMP:20260406T013922
CREATED:20170324T091407Z
LAST-MODIFIED:20170425T125552Z
UID:28640-1493890200-1493904600@ibecbarcelona.eu
SUMMARY:Mindfulness for improved self-mastery & resilience
DESCRIPTION:Training activity in Leadership&management skills. \nWorkshop of two ½ day sessions will feature the benefits of mindfulness\, a tool to develop self-efficacy and improve stress management and resilience. This training is based on the MBSR (Mindfulness-based Stress Reduction\, Center for Mindfulness\, Univ. Massachusetts) program. \nDates:  \n4th and 11th May from 9.30 -1:30pm. \nIn person class sessions = 8 hours + Pre-reading material \nTarget group: \nAll IBEC members \nProvider: Andrés Martín.
URL:https://ibecbarcelona.eu/event/mindfulness-for-improved-self-mastery-resilience/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170504T093000
DTEND;TZID=Europe/Madrid:20170504T133000
DTSTAMP:20260406T013922
CREATED:20170324T091407Z
LAST-MODIFIED:20170324T091407Z
UID:96018-1493890200-1493904600@ibecbarcelona.eu
SUMMARY:Mindfulness for improved self-mastery & resilience
DESCRIPTION:Training activity in Leadership&management skills. \nWorkshop of two ½ day sessions will feature the benefits of mindfulness\, a tool to develop self-efficacy and improve stress management and resilience. This training is based on the MBSR (Mindfulness-based Stress Reduction\, Center for Mindfulness\, Univ. Massachusetts) program. \nDates:  \n4th and 11th May from 9.30 -1:30pm. \nIn person class sessions = 8 hours + Pre-reading material \nTarget group: \nAll IBEC members \nProvider: Andrés Martín.
URL:https://ibecbarcelona.eu/event/mindfulness-for-improved-self-mastery-resilience-4/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T120000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170403T100450Z
LAST-MODIFIED:20170403T100450Z
UID:96031-1493294400-1493298000@ibecbarcelona.eu
SUMMARY:IBEC-IRB Barcelona joint seminar: Erik Sahai
DESCRIPTION:Imaging therapy response and failure\nErik Sahai\, The Francis Crick Institute\, London\nMany tumors show an initial response to targeted therapies before genetic resistance emerges\, however little is known about how tumor cells tolerate therapy before genetic resistance dominates. We present data that shows how the ECM generates a ‘safe haven’ in which melanoma cells can tolerate targeted therapy.  This supports the population of cancer cells from which genetically resistance emerges. We are now studying the emergence of resistant clones and clonal competition in the context of ‘safe havens’. Finally\, we present analysis of organ specific responses to targeted therapy in melanoma.
URL:https://ibecbarcelona.eu/event/ibec-irb-barcelona-joint-seminar-erik-sahai-3/
LOCATION:Sala Félix Serratossa\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T120000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170403T100450Z
LAST-MODIFIED:20170403T100450Z
UID:96038-1493294400-1493298000@ibecbarcelona.eu
SUMMARY:IBEC-IRB Barcelona joint seminar: Erik Sahai
DESCRIPTION:Imaging therapy response and failure\nErik Sahai\, The Francis Crick Institute\, London\nMany tumors show an initial response to targeted therapies before genetic resistance emerges\, however little is known about how tumor cells tolerate therapy before genetic resistance dominates. We present data that shows how the ECM generates a ‘safe haven’ in which melanoma cells can tolerate targeted therapy.  This supports the population of cancer cells from which genetically resistance emerges. We are now studying the emergence of resistant clones and clonal competition in the context of ‘safe havens’. Finally\, we present analysis of organ specific responses to targeted therapy in melanoma.
URL:https://ibecbarcelona.eu/event/ibec-irb-barcelona-joint-seminar-erik-sahai-4/
LOCATION:Sala Félix Serratossa\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T120000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170403T100450Z
LAST-MODIFIED:20170801T105123Z
UID:28744-1493294400-1493298000@ibecbarcelona.eu
SUMMARY:IBEC-IRB Barcelona joint seminar: Erik Sahai
DESCRIPTION:Imaging therapy response and failure\nErik Sahai\, The Francis Crick Institute\, London\nMany tumors show an initial response to targeted therapies before genetic resistance emerges\, however little is known about how tumor cells tolerate therapy before genetic resistance dominates. We present data that shows how the ECM generates a ‘safe haven’ in which melanoma cells can tolerate targeted therapy.  This supports the population of cancer cells from which genetically resistance emerges. We are now studying the emergence of resistant clones and clonal competition in the context of ‘safe havens’. Finally\, we present analysis of organ specific responses to targeted therapy in melanoma.
URL:https://ibecbarcelona.eu/event/ibec-irb-barcelona-joint-seminar-erik-sahai/
LOCATION:Sala Félix Serratossa\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T120000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170403T100450Z
LAST-MODIFIED:20170403T100450Z
UID:96030-1493294400-1493298000@ibecbarcelona.eu
SUMMARY:IBEC-IRB Barcelona joint seminar: Erik Sahai
DESCRIPTION:Imaging therapy response and failure\nErik Sahai\, The Francis Crick Institute\, London\nMany tumors show an initial response to targeted therapies before genetic resistance emerges\, however little is known about how tumor cells tolerate therapy before genetic resistance dominates. We present data that shows how the ECM generates a ‘safe haven’ in which melanoma cells can tolerate targeted therapy.  This supports the population of cancer cells from which genetically resistance emerges. We are now studying the emergence of resistant clones and clonal competition in the context of ‘safe havens’. Finally\, we present analysis of organ specific responses to targeted therapy in melanoma.
URL:https://ibecbarcelona.eu/event/ibec-irb-barcelona-joint-seminar-erik-sahai-2/
LOCATION:Sala Félix Serratossa\, Parc Científic de Barcelona\, Barcelona\, Spain
CATEGORIES:Joint seminar / workshop / symposium
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T110000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170425T112649Z
LAST-MODIFIED:20170425T112649Z
UID:96044-1493290800-1493298000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Anna Crespo
DESCRIPTION:“Estudi transcripcional i funcional de les ribonucleotidil reductases de Pseudomonas aeruginosa“\nAnna Crespo\, Bacterial infections and antimicrobial therapies group\nAnna will be defending her PhD thesis on Thursday 27th April at 11:00 in the Aula Magna of the UB’s Facultat de Farmàcia i Ciències de l’Alimentació. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-anna-crespo-4/
LOCATION:Aula Magna\, Faculty of Pharmacy\, Av. Joan XXIII s/n\, Barcelona\, Spain
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T110000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170425T112649Z
LAST-MODIFIED:20170425T112833Z
UID:28860-1493290800-1493298000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Anna Crespo
DESCRIPTION:“Estudi transcripcional i funcional de les ribonucleotidil reductases de Pseudomonas aeruginosa“\nAnna Crespo\, Bacterial infections and antimicrobial therapies group\nAnna will be defending her PhD thesis on Thursday 27th April at 11:00 in the Aula Magna of the UB’s Facultat de Farmàcia i Ciències de l’Alimentació. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-anna-crespo/
LOCATION:Aula Magna\, Faculty of Pharmacy\, Av. Joan XXIII s/n\, Barcelona\, Spain
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T110000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170425T112649Z
LAST-MODIFIED:20170425T112649Z
UID:96042-1493290800-1493298000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Anna Crespo
DESCRIPTION:“Estudi transcripcional i funcional de les ribonucleotidil reductases de Pseudomonas aeruginosa“\nAnna Crespo\, Bacterial infections and antimicrobial therapies group\nAnna will be defending her PhD thesis on Thursday 27th April at 11:00 in the Aula Magna of the UB’s Facultat de Farmàcia i Ciències de l’Alimentació. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-anna-crespo-2/
LOCATION:Aula Magna\, Faculty of Pharmacy\, Av. Joan XXIII s/n\, Barcelona\, Spain
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170427T110000
DTEND;TZID=Europe/Madrid:20170427T130000
DTSTAMP:20260406T013922
CREATED:20170425T112649Z
LAST-MODIFIED:20170425T112649Z
UID:96043-1493290800-1493298000@ibecbarcelona.eu
SUMMARY:PhD Thesis Defence: Anna Crespo
DESCRIPTION:“Estudi transcripcional i funcional de les ribonucleotidil reductases de Pseudomonas aeruginosa“\nAnna Crespo\, Bacterial infections and antimicrobial therapies group\nAnna will be defending her PhD thesis on Thursday 27th April at 11:00 in the Aula Magna of the UB’s Facultat de Farmàcia i Ciències de l’Alimentació. \nEverybody is welcome to attend. \n—\nIf you’re an IBEC PhD student and would like to advertise your PhD defence on the IBEC calendar\, please contact vleigh@ibecbarcelona.eu
URL:https://ibecbarcelona.eu/event/phd-thesis-defence-anna-crespo-3/
LOCATION:Aula Magna\, Faculty of Pharmacy\, Av. Joan XXIII s/n\, Barcelona\, Spain
CATEGORIES:PhD Thesis Defence
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170426T090000
DTEND;TZID=Europe/Madrid:20170426T130000
DTSTAMP:20260406T013922
CREATED:20170327T094639Z
LAST-MODIFIED:20170327T094639Z
UID:96029-1493197200-1493211600@ibecbarcelona.eu
SUMMARY:Curso de Primeros Auxilios
DESCRIPTION:El objetivo del curso es ser una ayuda para adquirir los conocimientos necesarios de cara a prestar los primeros auxilios a aquellas personas que sufran un accidente o enfermedad repentina\, hasta la llegada del personal sanitario. De esta primera actuación va a depender\, en gran medida\, el estado general y la posterior evolución de la persona. Con este curso conoceremos los tratamientos que están a nuestro alcance y sabremos lo que NO debemos hacer nunca para no agravar el estado del lesionado. \nFechas: \n26 de Abril. 4 horas\, de 9 a 13h. \nParticipantes: \nToda la comunidad IBEC
URL:https://ibecbarcelona.eu/event/curso-de-primeros-auxilios-3/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170426T090000
DTEND;TZID=Europe/Madrid:20170426T130000
DTSTAMP:20260406T013922
CREATED:20170327T094639Z
LAST-MODIFIED:20170327T094639Z
UID:28694-1493197200-1493211600@ibecbarcelona.eu
SUMMARY:Curso de Primeros Auxilios
DESCRIPTION:El objetivo del curso es ser una ayuda para adquirir los conocimientos necesarios de cara a prestar los primeros auxilios a aquellas personas que sufran un accidente o enfermedad repentina\, hasta la llegada del personal sanitario. De esta primera actuación va a depender\, en gran medida\, el estado general y la posterior evolución de la persona. Con este curso conoceremos los tratamientos que están a nuestro alcance y sabremos lo que NO debemos hacer nunca para no agravar el estado del lesionado. \nFechas: \n26 de Abril. 4 horas\, de 9 a 13h. \nParticipantes: \nToda la comunidad IBEC
URL:https://ibecbarcelona.eu/event/curso-de-primeros-auxilios/
CATEGORIES:Professional and Personal Development
ORGANIZER;CN="IBEC":MAILTO:www.ibecbarcelona.eu
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170426T090000
DTEND;TZID=Europe/Madrid:20170426T130000
DTSTAMP:20260406T013922
CREATED:20170324T111018Z
LAST-MODIFIED:20170324T111018Z
UID:96028-1493197200-1493211600@ibecbarcelona.eu
SUMMARY:Curso de primeros auxilios
DESCRIPTION:El objetivo del curso es ser una ayuda para adquirir los conocimientos necesarios de cara a prestar los primeros auxilios a aquellas personas que sufran un accidente o enfermedad repentina\, hasta la llegada del personal sanitario. De esta primera actuación va a depender\, en gran medida\, el estado general y la posterior evolución de la persona. Con este curso conoceremos los tratamientos que están a nuestro alcance y sabremos lo que NO debemos hacer nunca para no agravar el estado del lesionado. \nFechas: \n26 de Abril. 4 horas\, de 9 a 13h. \nParticipantes: \nToda la comunidad IBEC \nFormador: ASEM.
URL:https://ibecbarcelona.eu/event/curso-de-primeros-auxilios-2/
CATEGORIES:Professional and Personal Development
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170425T000000
DTEND;TZID=Europe/Madrid:20170426T235959
DTSTAMP:20260406T013922
CREATED:20170404T102254Z
LAST-MODIFIED:20170404T102254Z
UID:96037-1493078400-1493251199@ibecbarcelona.eu
SUMMARY:II Festival de la Nanociencia (10alamenos9)
DESCRIPTION:IBEC is an organiser of this year’s Festival de la Nanociencia (10alamenos9)\, funded by FECYT.\nThe festival will take place simultaneously in Barcelona\, Saragossa\, Bellaterra\, San Sebastian and Madrid. \nThe programme will include seminars by Gabriel Gomila and Samuel Sanchez and a Workshop on Drug Delivery (Cosmocaixa 26/04/2017)\, visits to IBEC and workshop for students (March and April at IBEC)\, and a Nano Workshop in collaborations with Il·lustraciència (Cosmocaixa 25/04/2017 and 26/04/2017). \nMore details here.
URL:https://ibecbarcelona.eu/event/ii-festival-de-la-nanociencia-10alamenos9-4/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170425
DTEND;VALUE=DATE:20170427
DTSTAMP:20260406T013922
CREATED:20170404T102254Z
LAST-MODIFIED:20170801T105133Z
UID:28771-1493078400-1493251199@ibecbarcelona.eu
SUMMARY:II Festival de la Nanociencia (10alamenos9)
DESCRIPTION:IBEC is an organiser of this year’s Festival de la Nanociencia (10alamenos9)\, funded by FECYT.\nThe festival will take place simultaneously in Barcelona\, Saragossa\, Bellaterra\, San Sebastian and Madrid. \nThe programme will include seminars by Gabriel Gomila and Samuel Sanchez and a Workshop on Drug Delivery (Cosmocaixa 26/04/2017)\, visits to IBEC and workshop for students (March and April at IBEC)\, and a Nano Workshop in collaborations with Il·lustraciència (Cosmocaixa 25/04/2017 and 26/04/2017). \nMore details here.
URL:https://ibecbarcelona.eu/event/ii-festival-de-la-nanociencia-10alamenos9/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20170425
DTEND;VALUE=DATE:20170427
DTSTAMP:20260406T013922
CREATED:20170404T102254Z
LAST-MODIFIED:20170404T102254Z
UID:96035-1493078400-1493251199@ibecbarcelona.eu
SUMMARY:II Festival de la Nanociencia (10alamenos9)
DESCRIPTION:IBEC is an organiser of this year’s Festival de la Nanociencia (10alamenos9)\, funded by FECYT.\nThe festival will take place simultaneously in Barcelona\, Saragossa\, Bellaterra\, San Sebastian and Madrid. \nThe programme will include seminars by Gabriel Gomila and Samuel Sanchez and a Workshop on Drug Delivery (Cosmocaixa 26/04/2017)\, visits to IBEC and workshop for students (March and April at IBEC)\, and a Nano Workshop in collaborations with Il·lustraciència (Cosmocaixa 25/04/2017 and 26/04/2017). \nMore details here.
URL:https://ibecbarcelona.eu/event/ii-festival-de-la-nanociencia-10alamenos9-2/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170425T000000
DTEND;TZID=Europe/Madrid:20170426T235959
DTSTAMP:20260406T013922
CREATED:20170404T102254Z
LAST-MODIFIED:20170404T102254Z
UID:96036-1493078400-1493251199@ibecbarcelona.eu
SUMMARY:II Festival de la Nanociencia (10alamenos9)
DESCRIPTION:IBEC is an organiser of this year’s Festival de la Nanociencia (10alamenos9)\, funded by FECYT.\nThe festival will take place simultaneously in Barcelona\, Saragossa\, Bellaterra\, San Sebastian and Madrid. \nThe programme will include seminars by Gabriel Gomila and Samuel Sanchez and a Workshop on Drug Delivery (Cosmocaixa 26/04/2017)\, visits to IBEC and workshop for students (March and April at IBEC)\, and a Nano Workshop in collaborations with Il·lustraciència (Cosmocaixa 25/04/2017 and 26/04/2017). \nMore details here.
URL:https://ibecbarcelona.eu/event/ii-festival-de-la-nanociencia-10alamenos9-3/
CATEGORIES:Outreach / Fair / Festival
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170331T100000
DTEND;TZID=Europe/Madrid:20170331T230000
DTSTAMP:20260406T013922
CREATED:20170202T093241Z
LAST-MODIFIED:20170202T093241Z
UID:95983-1490954400-1491001200@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Aida Garrido and Marina Uroz
DESCRIPTION:Optical control of endogenous receptors and cellular excitability using targeted covalent photoswitches\nAida Garrido\, Nanoprobes and nanoswitches group\nLight-regulated drugs allow remotely photoswitching biological activity and enable plausible therapies based on small molecules. However\, only freely diffusible photochromic ligands have been shown to work directly in endogenous receptors and methods for covalent attachment depend on genetic manipulation. Here we introduce a chemical strategy to covalently conjugate and photoswitch the activity of endogenous proteins and demonstrate its application to the kainate receptor channel GluK1. The approach is based on photoswitchable ligands containing a short-lived\, highly reactive anchoring group that is targeted at the protein of interest by ligand affinity. These targeted covalent photoswitches (TCPs) constitute a new class of light-regulated drugs and act as prosthetic molecules that photocontrol the activity of GluK1-expressing neurons\, and restore photoresponses in degenerated retina. The modularity of TCPs enables the application to different ligands and opens the way to new therapeutic opportunities. \n  \nTraction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium\nMarina Uroz\, Integrative Cell and Tissue Dynamics group\nEpithelial repair and regeneration are driven by collective cell migration and division. Both cellular functions involve tightly controlled mechanical events. Mechanics of collective cell migration is increasingly well understood\, but physical forces associated with cell division in cohesive epithelia have escaped experimental observation. Using the zebrafish epicardium as a model system\, we show that cells dividing in a migrating epithelium exert large cell-extracellular matrix (ECM) forces during cytokinesis. These forces point towards the midbody and are exerted through paxillin-rich focal adhesions that connect the cytokinetic ring to the underlying extracellular matrix. Large forces at these adhesions are associated with failure of cytokinesis and polyploidy\, indicating that abnormal cell-matrix adhesion at the cleavage furrow impedes the latest stages of abscission. Mechanical interaction between the cytokinetic ring and the ECM thus provide a new mechanism for the regulation of cell division and polyploidy.  \n 
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-aida-garrido-and-marina-uroz-2/
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170331T100000
DTEND;TZID=Europe/Madrid:20170331T230000
DTSTAMP:20260406T013922
CREATED:20170202T093241Z
LAST-MODIFIED:20170202T093241Z
UID:95989-1490954400-1491001200@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Aida Garrido and Marina Uroz
DESCRIPTION:Optical control of endogenous receptors and cellular excitability using targeted covalent photoswitches\nAida Garrido\, Nanoprobes and nanoswitches group\nLight-regulated drugs allow remotely photoswitching biological activity and enable plausible therapies based on small molecules. However\, only freely diffusible photochromic ligands have been shown to work directly in endogenous receptors and methods for covalent attachment depend on genetic manipulation. Here we introduce a chemical strategy to covalently conjugate and photoswitch the activity of endogenous proteins and demonstrate its application to the kainate receptor channel GluK1. The approach is based on photoswitchable ligands containing a short-lived\, highly reactive anchoring group that is targeted at the protein of interest by ligand affinity. These targeted covalent photoswitches (TCPs) constitute a new class of light-regulated drugs and act as prosthetic molecules that photocontrol the activity of GluK1-expressing neurons\, and restore photoresponses in degenerated retina. The modularity of TCPs enables the application to different ligands and opens the way to new therapeutic opportunities. \n  \nTraction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium\nMarina Uroz\, Integrative Cell and Tissue Dynamics group\nEpithelial repair and regeneration are driven by collective cell migration and division. Both cellular functions involve tightly controlled mechanical events. Mechanics of collective cell migration is increasingly well understood\, but physical forces associated with cell division in cohesive epithelia have escaped experimental observation. Using the zebrafish epicardium as a model system\, we show that cells dividing in a migrating epithelium exert large cell-extracellular matrix (ECM) forces during cytokinesis. These forces point towards the midbody and are exerted through paxillin-rich focal adhesions that connect the cytokinetic ring to the underlying extracellular matrix. Large forces at these adhesions are associated with failure of cytokinesis and polyploidy\, indicating that abnormal cell-matrix adhesion at the cleavage furrow impedes the latest stages of abscission. Mechanical interaction between the cytokinetic ring and the ECM thus provide a new mechanism for the regulation of cell division and polyploidy.  \n 
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-aida-garrido-and-marina-uroz-3/
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170331T100000
DTEND;TZID=Europe/Madrid:20170331T230000
DTSTAMP:20260406T013922
CREATED:20170202T093241Z
LAST-MODIFIED:20170202T093241Z
UID:95990-1490954400-1491001200@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Aida Garrido and Marina Uroz
DESCRIPTION:Optical control of endogenous receptors and cellular excitability using targeted covalent photoswitches\nAida Garrido\, Nanoprobes and nanoswitches group\nLight-regulated drugs allow remotely photoswitching biological activity and enable plausible therapies based on small molecules. However\, only freely diffusible photochromic ligands have been shown to work directly in endogenous receptors and methods for covalent attachment depend on genetic manipulation. Here we introduce a chemical strategy to covalently conjugate and photoswitch the activity of endogenous proteins and demonstrate its application to the kainate receptor channel GluK1. The approach is based on photoswitchable ligands containing a short-lived\, highly reactive anchoring group that is targeted at the protein of interest by ligand affinity. These targeted covalent photoswitches (TCPs) constitute a new class of light-regulated drugs and act as prosthetic molecules that photocontrol the activity of GluK1-expressing neurons\, and restore photoresponses in degenerated retina. The modularity of TCPs enables the application to different ligands and opens the way to new therapeutic opportunities. \n  \nTraction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium\nMarina Uroz\, Integrative Cell and Tissue Dynamics group\nEpithelial repair and regeneration are driven by collective cell migration and division. Both cellular functions involve tightly controlled mechanical events. Mechanics of collective cell migration is increasingly well understood\, but physical forces associated with cell division in cohesive epithelia have escaped experimental observation. Using the zebrafish epicardium as a model system\, we show that cells dividing in a migrating epithelium exert large cell-extracellular matrix (ECM) forces during cytokinesis. These forces point towards the midbody and are exerted through paxillin-rich focal adhesions that connect the cytokinetic ring to the underlying extracellular matrix. Large forces at these adhesions are associated with failure of cytokinesis and polyploidy\, indicating that abnormal cell-matrix adhesion at the cleavage furrow impedes the latest stages of abscission. Mechanical interaction between the cytokinetic ring and the ECM thus provide a new mechanism for the regulation of cell division and polyploidy.  \n 
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-aida-garrido-and-marina-uroz-4/
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170331T100000
DTEND;TZID=Europe/Madrid:20170331T230000
DTSTAMP:20260406T013922
CREATED:20170202T093241Z
LAST-MODIFIED:20170323T102457Z
UID:27406-1490954400-1491001200@ibecbarcelona.eu
SUMMARY:PhD Discussions Sessions: Aida Garrido and Marina Uroz
DESCRIPTION:Optical control of endogenous receptors and cellular excitability using targeted covalent photoswitches\nAida Garrido\, Nanoprobes and nanoswitches group\nLight-regulated drugs allow remotely photoswitching biological activity and enable plausible therapies based on small molecules. However\, only freely diffusible photochromic ligands have been shown to work directly in endogenous receptors and methods for covalent attachment depend on genetic manipulation. Here we introduce a chemical strategy to covalently conjugate and photoswitch the activity of endogenous proteins and demonstrate its application to the kainate receptor channel GluK1. The approach is based on photoswitchable ligands containing a short-lived\, highly reactive anchoring group that is targeted at the protein of interest by ligand affinity. These targeted covalent photoswitches (TCPs) constitute a new class of light-regulated drugs and act as prosthetic molecules that photocontrol the activity of GluK1-expressing neurons\, and restore photoresponses in degenerated retina. The modularity of TCPs enables the application to different ligands and opens the way to new therapeutic opportunities. \n  \nTraction forces at the cytokinetic ring regulate cell division and polyploidy in the migrating zebrafish epicardium\nMarina Uroz\, Integrative Cell and Tissue Dynamics group\nEpithelial repair and regeneration are driven by collective cell migration and division. Both cellular functions involve tightly controlled mechanical events. Mechanics of collective cell migration is increasingly well understood\, but physical forces associated with cell division in cohesive epithelia have escaped experimental observation. Using the zebrafish epicardium as a model system\, we show that cells dividing in a migrating epithelium exert large cell-extracellular matrix (ECM) forces during cytokinesis. These forces point towards the midbody and are exerted through paxillin-rich focal adhesions that connect the cytokinetic ring to the underlying extracellular matrix. Large forces at these adhesions are associated with failure of cytokinesis and polyploidy\, indicating that abnormal cell-matrix adhesion at the cleavage furrow impedes the latest stages of abscission. Mechanical interaction between the cytokinetic ring and the ECM thus provide a new mechanism for the regulation of cell division and polyploidy.  \n 
URL:https://ibecbarcelona.eu/event/phd-discussions-sessions-aida-garrido-and-marina-uroz/
CATEGORIES:PhD Discussions Session
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170329T120000
DTEND;TZID=Europe/Madrid:20170329T130000
DTSTAMP:20260406T013922
CREATED:20170308T135727Z
LAST-MODIFIED:20170308T135727Z
UID:96007-1490788800-1490792400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Aranzazu Villasante
DESCRIPTION:Cancer Engineering: Strategies to Engineer Predictable Tumor Models\nDr. Aranzazu Villasante\, Department of Biomedical Engineering\, Columbia University\, New York\nAlthough many drugs show promise in monolayer or in animal models systems\, most fail to translate in humans and this is because they lack of ability to replicate the human microenvironment in patients. In response to these limitations\, I have generated a set of predictable tissue-engineered (TE) models of cancer by using different strategies. Today\, I am going to focus on some of these approaches to engineer pediatric tumors in vitro. Firstly\, I will show a TE model of Ewing’s sarcoma (ES) within its bone niche. This particular strategy is based on engineered human bone by introducing osteoclasts in co-culture with osteoblasts in the 3-dimensional bone niche. This model mimics bone remodeling and recapitulates some of the features observed in the osteolytic process in cancer and also\, the effects of the therapeutic reagent Zoledronic acid observed in patients. The second strategy consists in designing biomaterials with the same tumor composition to mimic the biological and mechanical properties of tumors from patients. I have developed 3D porous collagen 1-hyaluronic acid scaffolds (Col1-HA scaffolds) for studies of tumor derivedexosomes\, which are known to be initiators of pre-metastatic niche formation in certain sites. Interestingly\, I found high levels of a critical mediator of ES growth and metastasis (EZH2) in exosomes isolated from both patients and TE model of ES. Alternatively\, we cultured TE models based on Col1-HA scaffolds into a mechanical loading bioreactor for better mimicking biomechanical forces in ES. We found that biomechanical stimuli modulate osteolytic-related proteins (i.e. RUNX2) and sensitivity to anticancer drugs\, such as Sorafenib. I will also explain the use of perfusion bioreactors and cell sheet engineering to develop a novel model of Neuroblastoma (NB) to study the effect of consolidative drugs\, such as Isotretinoin\, on tumor vasculature and stem-like cells. Here\, I will show the existence of sub-populations of NB cells with different levels of stemness properties; these levels are related to the capacity of stem-like cells to transdifferentiate and also\, to chemoresistance and relapse. Finally\, the take-home message of my talk will be that TE models can bridge the gap between 2D in vitro cultures and in vivo animal models in a predictive\, inexpensive and low timeconsuming fashion for successfully understand cancer biology and improve cancer treatments.
URL:https://ibecbarcelona.eu/event/ibec-seminar-aranzazu-villasante-2/
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170329T120000
DTEND;TZID=Europe/Madrid:20170329T130000
DTSTAMP:20260406T013922
CREATED:20170308T135727Z
LAST-MODIFIED:20170308T135727Z
UID:96009-1490788800-1490792400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Aranzazu Villasante
DESCRIPTION:Cancer Engineering: Strategies to Engineer Predictable Tumor Models\nDr. Aranzazu Villasante\, Department of Biomedical Engineering\, Columbia University\, New York\nAlthough many drugs show promise in monolayer or in animal models systems\, most fail to translate in humans and this is because they lack of ability to replicate the human microenvironment in patients. In response to these limitations\, I have generated a set of predictable tissue-engineered (TE) models of cancer by using different strategies. Today\, I am going to focus on some of these approaches to engineer pediatric tumors in vitro. Firstly\, I will show a TE model of Ewing’s sarcoma (ES) within its bone niche. This particular strategy is based on engineered human bone by introducing osteoclasts in co-culture with osteoblasts in the 3-dimensional bone niche. This model mimics bone remodeling and recapitulates some of the features observed in the osteolytic process in cancer and also\, the effects of the therapeutic reagent Zoledronic acid observed in patients. The second strategy consists in designing biomaterials with the same tumor composition to mimic the biological and mechanical properties of tumors from patients. I have developed 3D porous collagen 1-hyaluronic acid scaffolds (Col1-HA scaffolds) for studies of tumor derivedexosomes\, which are known to be initiators of pre-metastatic niche formation in certain sites. Interestingly\, I found high levels of a critical mediator of ES growth and metastasis (EZH2) in exosomes isolated from both patients and TE model of ES. Alternatively\, we cultured TE models based on Col1-HA scaffolds into a mechanical loading bioreactor for better mimicking biomechanical forces in ES. We found that biomechanical stimuli modulate osteolytic-related proteins (i.e. RUNX2) and sensitivity to anticancer drugs\, such as Sorafenib. I will also explain the use of perfusion bioreactors and cell sheet engineering to develop a novel model of Neuroblastoma (NB) to study the effect of consolidative drugs\, such as Isotretinoin\, on tumor vasculature and stem-like cells. Here\, I will show the existence of sub-populations of NB cells with different levels of stemness properties; these levels are related to the capacity of stem-like cells to transdifferentiate and also\, to chemoresistance and relapse. Finally\, the take-home message of my talk will be that TE models can bridge the gap between 2D in vitro cultures and in vivo animal models in a predictive\, inexpensive and low timeconsuming fashion for successfully understand cancer biology and improve cancer treatments.
URL:https://ibecbarcelona.eu/event/ibec-seminar-aranzazu-villasante-3/
CATEGORIES:IBEC Seminar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Madrid:20170329T120000
DTEND;TZID=Europe/Madrid:20170329T130000
DTSTAMP:20260406T013922
CREATED:20170308T135727Z
LAST-MODIFIED:20170308T135727Z
UID:28031-1490788800-1490792400@ibecbarcelona.eu
SUMMARY:IBEC Seminar: Aranzazu Villasante
DESCRIPTION:Cancer Engineering: Strategies to Engineer Predictable Tumor Models\nDr. Aranzazu Villasante\, Department of Biomedical Engineering\, Columbia University\, New York\nAlthough many drugs show promise in monolayer or in animal models systems\, most fail to translate in humans and this is because they lack of ability to replicate the human microenvironment in patients. In response to these limitations\, I have generated a set of predictable tissue-engineered (TE) models of cancer by using different strategies. Today\, I am going to focus on some of these approaches to engineer pediatric tumors in vitro. Firstly\, I will show a TE model of Ewing’s sarcoma (ES) within its bone niche. This particular strategy is based on engineered human bone by introducing osteoclasts in co-culture with osteoblasts in the 3-dimensional bone niche. This model mimics bone remodeling and recapitulates some of the features observed in the osteolytic process in cancer and also\, the effects of the therapeutic reagent Zoledronic acid observed in patients. The second strategy consists in designing biomaterials with the same tumor composition to mimic the biological and mechanical properties of tumors from patients. I have developed 3D porous collagen 1-hyaluronic acid scaffolds (Col1-HA scaffolds) for studies of tumor derivedexosomes\, which are known to be initiators of pre-metastatic niche formation in certain sites. Interestingly\, I found high levels of a critical mediator of ES growth and metastasis (EZH2) in exosomes isolated from both patients and TE model of ES. Alternatively\, we cultured TE models based on Col1-HA scaffolds into a mechanical loading bioreactor for better mimicking biomechanical forces in ES. We found that biomechanical stimuli modulate osteolytic-related proteins (i.e. RUNX2) and sensitivity to anticancer drugs\, such as Sorafenib. I will also explain the use of perfusion bioreactors and cell sheet engineering to develop a novel model of Neuroblastoma (NB) to study the effect of consolidative drugs\, such as Isotretinoin\, on tumor vasculature and stem-like cells. Here\, I will show the existence of sub-populations of NB cells with different levels of stemness properties; these levels are related to the capacity of stem-like cells to transdifferentiate and also\, to chemoresistance and relapse. Finally\, the take-home message of my talk will be that TE models can bridge the gap between 2D in vitro cultures and in vivo animal models in a predictive\, inexpensive and low timeconsuming fashion for successfully understand cancer biology and improve cancer treatments.
URL:https://ibecbarcelona.eu/event/ibec-seminar-aranzazu-villasante/
CATEGORIES:IBEC Seminar
END:VEVENT
END:VCALENDAR