Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Christiaan H. Arendzen"'
Autor:
Viviana Meraviglia, Sravya Ganesh, Christiaan H. Arendzen, Christian Freund, Elena Sommariva, Alessandra Rossini, Milena Bellin
Publikováno v:
Stem Cell Research, Vol 54, Iss , Pp 102426- (2021)
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with mutations in genes of the desmosomes and characterized by arrhythmia and fibro-fatty replacement of the myocardium. We generated human induced pluripo
Externí odkaz:
https://doaj.org/article/8582f8f1cc1745cea5b803e330c4f30f
Autor:
Viviana Meraviglia, Christiaan H. Arendzen, Merve Tok, Christian Freund, Angela Serena Maione, Elena Sommariva, Milena Bellin
Publikováno v:
Stem Cell Research, Vol 46, Iss , Pp 101835- (2020)
Arrhythmogenic Cardiomyopathy (ACM) is a rare inherited heart muscle disease characterised by progressive fibro-fatty replacement of the ventricular myocardium leading to life-threatening arrhythmias. We generated human induced pluripotent stem cells
Externí odkaz:
https://doaj.org/article/83bf51a2312947fc89fe29c2685411d1
Autor:
Viviana Meraviglia, Christiaan H. Arendzen, Christian Freund, Douwe E. Atsma, Christine L. Mummery, Milena Bellin
Publikováno v:
Stem Cell Research, Vol 45, Iss , Pp - (2020)
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is a malignant channelopathy associated with exercise- and stress-induced cardiac sudden death. The autosomal dominant form of CPVT is due to mutations in the ryanodine receptor 2 (RYR2) ge
Externí odkaz:
https://doaj.org/article/04f096cec0ac49378a48a48f736017ae
Autor:
Nanda Boon, Xuefei Lu, Charlotte A. Andriessen, Ioannis Moustakas, Thilo M. Buck, Christian Freund, Christiaan H. Arendzen, Stefan Böhringer, Camiel J.F. Boon, Hailiang Mei, Jan Wijnholds
Publikováno v:
Stem Cell Reports, 18, 1123-1137. Cell Press
Retinitis pigmentosa and Leber congenital amaurosis are inherited retinal dystrophies that can be caused by mutations in the Crumbs homolog 1 (CRB1) gene. CRB1 is required for organizing apical-basal polarity and adhesion between photoreceptors and M
Autor:
U Chaudhari, A Ranga, Christiaan H. Arendzen, Christian Freund, O Pourquie, Harald Mikkers, Christine L. Mummery, S J Cramer
Publikováno v:
Stem Cell Research, Vol 57, Iss, Pp 102592-(2021)
Stem Cell Research, 57. ELSEVIER
Stem Cell Research, 57. ELSEVIER
An induced pluripotent stem cell (iPSC) line, in which a H2B-fluorescent protein fusion is temporally expressed, is a valuable tool to track cells and study cell divisions and apoptosis. To this end we introduced a 3rd generation "all-in-one" doxycyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d315ab315879becb2125f470c0dab47
https://hdl.handle.net/1887/3276395
https://hdl.handle.net/1887/3276395
Autor:
Milena Bellin, Christiaan H. Arendzen, Alessandra Rossini, Christian Freund, Sravya Ganesh, Elena Sommariva, Viviana Meraviglia
Publikováno v:
Stem Cell Research
Stem Cell Research, 54. ELSEVIER
Stem Cell Research, Vol 54, Iss, Pp 102426-(2021)
Stem Cell Research, 54. ELSEVIER
Stem Cell Research, Vol 54, Iss, Pp 102426-(2021)
Arrhythmogenic Cardiomyopathy (ACM) is a rare genetic cardiac disease predominantly associated with mutations in genes of the desmosomes and characterized by arrhythmia and fibro-fatty replacement of the myocardium. We generated human induced pluripo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d55c2d4cc2d75835cb5f2e849c55a1
https://hdl.handle.net/1887/3221405
https://hdl.handle.net/1887/3221405
Autor:
Marga J. Bouma, Christine L. Mummery, Christiaan H. Arendzen, Christian Freund, Harald Mikkers
Publikováno v:
Current Protocols in Stem Cell Biology
We describe a protocol for efficient generation of human‐induced pluripotent stem cells (hiPSCs) from urine‐derived cells (UDCs) obtained from adult donors using self‐replicative RNA containing the reprogramming factors OCT3/4, SOX2, KLF4, GLIS
Autor:
Christine L. Mummery, Milena Bellin, Christiaan H. Arendzen, Christian Freund, Douwe E. Atsma, Viviana Meraviglia
Publikováno v:
Stem Cell Research, Vol 45, Iss, Pp-(2020)
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) is a malignant channelopathy associated with exercise- and stress -induced cardiac sudden death. The autosomal dominant form of CPVT is due to mutations in the ryanodine receptor 2 ( RYR2 )