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pro vyhledávání: '"Sherine S L Chan"'
Correction: Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish.
Autor:
Anna M Sokol, Barbara Uszczynska-Ratajczak, Michelle M Collins, Michal Bazala, Ulrike Topf, Pia R Lundegaard, Sreedevi Sugunan, Stefan Guenther, Carsten Kuenne, Johannes Graumann, Sherine S L Chan, Didier Y R Stainier, Agnieszka Chacinska
Publikováno v:
PLoS Genetics, Vol 15, Iss 1, p e1007972 (2019)
[This corrects the article DOI: 10.1371/journal.pgen.1007743.].
Externí odkaz:
https://doaj.org/article/7b73b7d754a74cebb5b5c4b59e3956f3
Autor:
Anna M Sokol, Barbara Uszczynska-Ratajczak, Michelle M Collins, Michal Bazala, Ulrike Topf, Pia R Lundegaard, Sreedevi Sugunan, Stefan Guenther, Carsten Kuenne, Johannes Graumann, Sherine S L Chan, Didier Y R Stainier, Agnieszka Chacinska
Publikováno v:
PLoS Genetics, Vol 14, Iss 11, p e1007743 (2018)
Development and function of tissues and organs are powered by the activity of mitochondria. In humans, inherited genetic mutations that lead to progressive mitochondrial pathology often manifest during infancy and can lead to death, reflecting the in
Externí odkaz:
https://doaj.org/article/23383a47843e48fcb904a69659560535
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137710 (2015)
Organismal metabolic rate, a fundamental metric in biology, demonstrates an allometric scaling relationship with body size. Fractal-like vascular distribution networks of biological systems are proposed to underlie metabolic rate allometric scaling l
Externí odkaz:
https://doaj.org/article/92862958f2844f22a28b166d1798c9b8
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59218 (2013)
Opa1 catalyzes fusion of inner mitochondrial membranes and formation of the cristae. OPA1 mutations in humans lead to autosomal dominant optic atrophy. OPA1 knockout mice lose viability around embryonic day 9 from unknown reasons, indicating that OPA
Externí odkaz:
https://doaj.org/article/d5fc080521d74891a7610b99f9922bec
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e25652 (2011)
Many debilitating conditions are linked to bioenergetic defects. Developing screens to probe the genetic and/or chemical basis for such links has proved intractable. Furthermore, there is a need for a physiologically relevant assay of bioenergetics i
Externí odkaz:
https://doaj.org/article/9ed4560aeb7d42c594becd9289075565
Publikováno v:
Archives of pathologylaboratory medicine. 135(7)
Context.—Primary mitochondrial dysfunction is one of the most common causes of inherited disorders predominantly involving the neuromuscular system. Advances in the molecular study of mitochondrial DNA have changed our vision and our approach to pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a9c9d5f9eb131ce423fe956f9a80194
https://pubmed.ncbi.nlm.nih.gov/21732785
https://pubmed.ncbi.nlm.nih.gov/21732785
Autor:
Kasiviswanathan, Rajesh1, Longley, Matthew J.1, Sherine S. L. Chan1, Copeland, William C.1 copelanl@niehs.nih.gov
Publikováno v:
Journal of Biological Chemistry. 7/17/2009, Vol. 284 Issue 29, p19501-19510. 10p. 3 Charts, 3 Graphs.
Autor:
Thomas Cahill, Willian Abraham da Silveira, Ludivine Renaud, Tucker Williamson, Hao Wang, Dongjun Chung, Ian Overton, Sherine S. L. Chan, Gary Hardiman
Publikováno v:
Cells, Vol 10, Iss 4, p 906 (2021)
The development of the Artemis programme with the goal of returning to the moon is spurring technology advances that will eventually take humans to Mars and herald a new era of interplanetary space travel. However, long-term space travel poses unique
Externí odkaz:
https://doaj.org/article/33392384a8014d88b3d6906ae6e995c6