Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Matthieu Hamlin"'
Autor:
Flavie Ader, Laetitia Duboscq-Bidot, Sibylle Marteau, Matthieu Hamlin, Pascale Richard, Vincent Fontaine, Eric Villard
Publikováno v:
Stem Cell Research, Vol 58, Iss , Pp 102616- (2022)
Loss-of-function (LoF) mutations in FLNC are strongly associated with dilated cardiomyopathy (DCM). Using CRISPR/Cas9 mediated edition in an healthy donor derived iPSC (ICAN-403.3) we subcloned 1 iPSC line harboring LoF mutation in FLNC. All lines ar
Externí odkaz:
https://doaj.org/article/6ad0daf2ebc44666815a1ba145185d3f
Autor:
Vincent Fontaine, Laetitia Duboscq-Bidot, Charlène Jouve, Matthieu Hamlin, Angélique Curjol, Véronique Briand, Philip Janiak, Jean-Sébastien Hulot, Marie-Pierre Pruniaux-Harnist, Philippe Charron, Eric Villard
Publikováno v:
Stem Cell Research, Vol 52, Iss , Pp 102245- (2021)
MYH7 is a major gene responsible for hypertrophic cardiomyopathy (HCM). From patient’s skin fibroblasts, we derived an iPSC line (CDGEN1.16) harboring the heterozygous MYH7 R403L mutation, a hot-spot codon in HCM. We subsequently corrected the muta
Externí odkaz:
https://doaj.org/article/897d8d238b4d403f92be9515966e4b13
Autor:
Eddy Quelennec, Celine Banal, Matthieu Hamlin, Dimartino Clémantine, Marie Michael, Nathalie Lefort
Publikováno v:
Stem Cell Research, Vol 48, Iss , Pp 101959- (2020)
Human pluripotent stem cells offer a limitless source of cells for regenerative medicine. They are also highly valuable as tools to study development and pathologies or as cellular substrates to screen and test new drugs. We generated human induced p
Externí odkaz:
https://doaj.org/article/83ebef62695246fb9477798d6a2eafd9
Autor:
Flavie Ader, Laetitia Duboscq-Bidot, Sibylle Marteau, Matthieu Hamlin, Pascale Richard, Vincent Fontaine, Eric Villard
Publikováno v:
Stem Cell Research
Stem Cell Research, Elsevier, 2021, 58, pp.102616. ⟨10.1016/j.scr.2021.102616⟩
Stem Cell Research, 2021, 58, pp.102616. ⟨10.1016/j.scr.2021.102616⟩
Stem Cell Research, Vol 58, Iss, Pp 102616-(2022)
Stem Cell Research, Elsevier, 2021, 58, pp.102616. ⟨10.1016/j.scr.2021.102616⟩
Stem Cell Research, 2021, 58, pp.102616. ⟨10.1016/j.scr.2021.102616⟩
Stem Cell Research, Vol 58, Iss, Pp 102616-(2022)
International audience; Loss-of-function (LoF) mutations in FLNC are strongly associated with dilated cardiomyopathy (DCM). Using CRISPR/Cas9 mediated edition in an healthy donor derived iPSC (ICAN-403.3) we subcloned 1 iPSC line harboring LoF mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d4dad27abe9f468a66fa61fa96c1632
https://pubmed.ncbi.nlm.nih.gov/34883448
https://pubmed.ncbi.nlm.nih.gov/34883448
Autor:
Véronique Briand, Matthieu Hamlin, Eric Villard, Marie-Pierre Pruniaux-Harnist, Philippe Charron, Charlène Jouve, Angélique Curjol, Jean-Sébastien Hulot, Philip Janiak, L. Duboscq-Bidot, Vincent Fontaine
Publikováno v:
Stem Cell Research
Stem Cell Research, Elsevier, 2021, 52, pp.102245. ⟨10.1016/j.scr.2021.102245⟩
Stem Cell Research, Vol 52, Iss, Pp 102245-(2021)
Stem Cell Research, Elsevier, 2021, 52, pp.102245. ⟨10.1016/j.scr.2021.102245⟩
Stem Cell Research, Vol 52, Iss, Pp 102245-(2021)
International audience; MYH7 is a major gene responsible for hypertrophic cardiomyopathy (HCM). From patient’s skin fibroblasts, we derived an iPSC line (CDGEN1.16) harboring the heterozygous MYH7 R403L mutation, a hot-spot codon in HCM. We subsequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ac7cadd7458ad175a0542c557980fd7
https://doi.org/10.1016/j.scr.2021.102245
https://doi.org/10.1016/j.scr.2021.102245