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Michael Kulik

Showing results (11-20 of 19) with videos related to

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Genome Research|December 3, 2009
Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesisIchiro Hiratani, Tyrone Ryba, Mari Itoh, et al.
Frontiers in Bioengineering and Biotechnology|November 26, 2020
The StemCellFactory: A Modular System Integration for Automated Generation and Expansion of Human Induced Pluripotent Stem CellsAndreas Elanzew, Bastian Nießing, Daniel Langendoerfer, et al.
The Journal of Experimental Medicine|August 1, 2007
Human hepatic stem cells from fetal and postnatal donorsEva Schmelzer, Lili Zhang, Andrew Bruce, et al.
Journal of Geriatric Oncology|July 26, 2018
Health status, emergency department visits, and oncologists' feedback: An analysis of secondary endpoints from a randomized phase II geriatric assessment trialSchroder Sattar, Shabbir M H Alibhai, Sarah Brennenstuhl, et al.
Bioengineering & Translational Medicine|September 30, 2022
Needle to needle robot-assisted manufacture of cell therapy productsJelena Ochs, Mariana P Hanga, Georgina Shaw, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|July 26, 2017
A randomized phase II trial of geriatric assessment and management for older cancer patientsMartine T E Puts, Schroder Sattar, Michael Kulik, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|November 11, 2016
Chemotherapy treatment decision-making experiences of older adults with cancer, their family members, oncologists and family physicians: a mixed methods studyMartine T E Puts, Schroder Sattar, Kara McWatters, et al.
Nature|July 31, 2020
Landscape of cohesin-mediated chromatin loops in the human genomeFabian Grubert, Rohith Srivas, Damek V Spacek, et al.
American Journal of Human Genetics|May 8, 2021
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunctionBobby G Ng, Paulina Sosicka, François Fenaille, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Genome Research|December 3, 2009
Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesisIchiro Hiratani, Tyrone Ryba, Mari Itoh, et al.
Frontiers in Bioengineering and Biotechnology|November 26, 2020
The StemCellFactory: A Modular System Integration for Automated Generation and Expansion of Human Induced Pluripotent Stem CellsAndreas Elanzew, Bastian Nießing, Daniel Langendoerfer, et al.
The Journal of Experimental Medicine|August 1, 2007
Human hepatic stem cells from fetal and postnatal donorsEva Schmelzer, Lili Zhang, Andrew Bruce, et al.
Journal of Geriatric Oncology|July 26, 2018
Health status, emergency department visits, and oncologists' feedback: An analysis of secondary endpoints from a randomized phase II geriatric assessment trialSchroder Sattar, Shabbir M H Alibhai, Sarah Brennenstuhl, et al.
Bioengineering & Translational Medicine|September 30, 2022
Needle to needle robot-assisted manufacture of cell therapy productsJelena Ochs, Mariana P Hanga, Georgina Shaw, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|July 26, 2017
A randomized phase II trial of geriatric assessment and management for older cancer patientsMartine T E Puts, Schroder Sattar, Michael Kulik, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|November 11, 2016
Chemotherapy treatment decision-making experiences of older adults with cancer, their family members, oncologists and family physicians: a mixed methods studyMartine T E Puts, Schroder Sattar, Kara McWatters, et al.
Nature|July 31, 2020
Landscape of cohesin-mediated chromatin loops in the human genomeFabian Grubert, Rohith Srivas, Damek V Spacek, et al.
American Journal of Human Genetics|May 8, 2021
A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunctionBobby G Ng, Paulina Sosicka, François Fenaille, et al.
Pageof 2