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pro vyhledávání: '"Kerry Bean"'
Autor:
Sonja Strang‐Karlsson, Sylvia Keigwin, Anna‐Kaisa Anttonen, Duncan Baker, Kerry Bean, Eveliina Jakkula
Publikováno v:
Clinical Case Reports, Vol 10, Iss 10, Pp n/a-n/a (2022)
Abstract Classical Ehlers–Danlos syndrome (cEDS) is a rare inherited autosomal dominant connective tissue disorder with core clinical features including skin hyperextensibility, abnormal scarring, and generalized joint hypermobility. Classical EDS
Externí odkaz:
https://doaj.org/article/48f9b9be2ce34085a51286125321affa
Autor:
Duncan Baker, Adam J. Hirst, Paul J. Gokhale, Miguel A. Juarez, Steve Williams, Mark Wheeler, Kerry Bean, Thomas F. Allison, Harry D. Moore, Peter W. Andrews, Ivana Barbaric
Publikováno v:
Stem Cell Reports, Vol 7, Iss 5, Pp 998-1012 (2016)
Genetic changes in human pluripotent stem cells (hPSCs) gained during culture can confound experimental results and potentially jeopardize the outcome of clinical therapies. Particularly common changes in hPSCs are trisomies of chromosomes 1, 12, 17,
Externí odkaz:
https://doaj.org/article/b5a76d73b9de425994a516a51d117bcb
Autor:
Kerry Bean, Harry Moore, Peter W. Andrews, Miguel A. Juárez, Paul J. Gokhale, Mark Wheeler, Ivana Barbaric, Thomas F. Allison, Steve Williams, Adam J. Hirst, Duncan Baker
Publikováno v:
Stem Cell Reports
Stem Cell Reports, Vol 7, Iss 5, Pp 998-1012 (2016)
Stem Cell Reports, Vol 7, Iss 5, Pp 998-1012 (2016)
Summary Genetic changes in human pluripotent stem cells (hPSCs) gained during culture can confound experimental results and potentially jeopardize the outcome of clinical therapies. Particularly common changes in hPSCs are trisomies of chromosomes 1,