Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ruben W.J. van Helden"'
On-chip analysis of glycolysis and mitochondrial respiration in human induced pluripotent stem cells
Autor:
Stefanie Fuchs, Ruben W.J. van Helden, Maury Wiendels, Mees N.S. de Graaf, Valeria V. Orlova, Christine L. Mummery, Berend J. van Meer, Torsten Mayr
Publikováno v:
Materials Today Bio, Vol 17, Iss , Pp 100475- (2022)
Recent advances in microfluidic engineering allow the creation of microenvironments in which human cells can be cultured under (patho-)physiological conditions with greater reality than standard plastic tissue culture plates. Microfluidic devices, al
Externí odkaz:
https://doaj.org/article/cd0291a830874cb4afd8c49614c6b254
Autor:
Ruben W.J. van Helden, Matthew J. Birket, Christian Freund, Christaan H. Arendzen, Harald M. Mikkers, Valeria Orlova, René I. de Coo, Christine L. Mummery, Milena Bellin
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102374- (2021)
Combined Oxidative Phosphorylation Deficiency 8 (COXPD8) is an autosomal recessive disorder causing lethal childhood-onset hypertrophic cardiomyopathy. Homozygous or compound heterozygous mutations in the nuclear-encoded mitochondrial alanyl-tRNA syn
Externí odkaz:
https://doaj.org/article/e9be3e0eb06f46b2aeab5553c8f64016
Autor:
Viviana Meraviglia, Christine L. Mummery, Valeria V. Orlova, Elisa Giacomelli, Giulia Campostrini, Richard P. Davis, Ruben W.J. van Helden, Milena Bellin, Loukia Yiangou
Publikováno v:
Nature Protocols, 16(4), 2213-2256. NATURE RESEARCH
Nature Protocols
Nat Protoc
Nature Protocols
Nat Protoc
Tissue-like structures from human pluripotent stem cells containing multiple cell types are transforming our ability to model and understand human development and disease. Here we describe a protocol to generate cardiomyocytes (CMs), cardiac fibrobla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4d0b270178dbf2f6bb1803e642c5c4
https://hdl.handle.net/11577/3402156
https://hdl.handle.net/11577/3402156
Autor:
Christian Freund, Christaan H. Arendzen, Milena Bellin, Ruben W.J. van Helden, Valeria V. Orlova, Christine L. Mummery, René I. de Coo, Matthew J. Birket, Harald Mikkers
Publikováno v:
Stem Cell Research, 53. ELSEVIER
Stem Cell Research, 53:102374. Elsevier Inc.
Stem Cell Research, Vol 53, Iss, Pp 102374-(2021)
Stem Cell Research, 53:102374. Elsevier Inc.
Stem Cell Research, Vol 53, Iss, Pp 102374-(2021)
Combined Oxidative Phosphorylation Deficiency 8 (COXPD8) is an autosomal recessive disorder causing lethal childhood-onset hypertrophic cardiomyopathy. Homozygous or compound heterozygous mutations in the nuclear-encoded mitochondrial alanyl-tRNA syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2638dc85a5c69d5fa9b6e1ea32c3a707
https://doi.org/10.1016/j.scr.2021.102374
https://doi.org/10.1016/j.scr.2021.102374