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of 5
pro vyhledávání: '"Jeanette Feder"'
Autor:
Sarit Suissa, Zhibo Wang, Jason Poole, Sharine Wittkopp, Jeanette Feder, Timothy E Shutt, Douglas C Wallace, Gerald S Shadel, Dan Mishmar
Publikováno v:
PLoS Genetics, Vol 5, Iss 5, p e1000474 (2009)
Although the functional consequences of mitochondrial DNA (mtDNA) genetic backgrounds (haplotypes, haplogroups) have been demonstrated by both disease association studies and cell culture experiments, it is not clear which of the mutations within the
Externí odkaz:
https://doaj.org/article/1a91ccc462a54c74b4362e6148a5d28e
Publikováno v:
European Journal of Human Genetics. 15:498-500
The quest for genes associated with diseases is widely recognized as an essential task in the effort to investigate the genetic basis of complex human disorders and traits. A basic stage in association studies is the careful choice of the model popul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b2e7b92f08c270ae3febf91349b557d
https://doi.org/10.1038/sj.ejhg.5201764
https://doi.org/10.1038/sj.ejhg.5201764
Autor:
Timothy E. Shutt, Dan Mishmar, Zhibo Wang, Sarit Suissa, Jason C. Poole, Jeanette Feder, Gerald S. Shadel, Douglas C. Wallace, Sharine Wittkopp
Publikováno v:
PLoS Genetics, Vol 5, Iss 5, p e1000474 (2009)
Suissa, Sarit; Wang, Zhibo; Poole, Jason; Wittkopp, Sharine; Feder, Jeanette; Shutt, Timothy E; et al.(2009). Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication. PLoS Genetics, 5(5), e1000474. doi: 10.1371/journal.pgen.1000474. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/57f7h98m
PLoS Genetics
Suissa, Sarit; Wang, Zhibo; Poole, Jason; Wittkopp, Sharine; Feder, Jeanette; Shutt, Timothy E; et al.(2009). Ancient mtDNA Genetic Variants Modulate mtDNA Transcription and Replication. PLoS Genetics, 5(5), e1000474. doi: 10.1371/journal.pgen.1000474. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/57f7h98m
PLoS Genetics
Although the functional consequences of mitochondrial DNA (mtDNA) genetic backgrounds (haplotypes, haplogroups) have been demonstrated by both disease association studies and cell culture experiments, it is not clear which of the mutations within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9613044a9ce6704e2a6976170ea336
http://europepmc.org/articles/PMC2673036?pdf=render
http://europepmc.org/articles/PMC2673036?pdf=render
Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes
Autor:
Julio Wainstein, Dan Mishmar, Ilana Harman-Boehm, Jeanette Feder, Ilana Blech, Ofer Ovadia, Josef Cohen, Benjamin Glaser
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 10, Iss 1, p 60 (2009)
BMC Medical Genetics, Vol 10, Iss 1, p 60 (2009)
Background Although mitochondrial dysfunction is consistently manifested in patients with Type 2 Diabetes mellitus (T2DM), the association of mitochondrial DNA (mtDNA) sequence variants with T2DM varies among populations. These differences might stem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e06df4c5186c8932b7a0cff8d47f6c61
http://europepmc.org/articles/PMC2706816
http://europepmc.org/articles/PMC2706816
Autor:
Ilana Blech, Jeanette Feder, Itamar Raz, Dan E. Arking, Dan Mishmar, Julio Wainstein, Sarah Dadon, Shirly Amar, Ofer Ovadia, Benjamin Glaser
Publikováno v:
BMC Genomics
BMC Genomics, Vol 9, Iss 1, p 198 (2008)
BMC Genomics, Vol 9, Iss 1, p 198 (2008)
Background Recent genome-wide association studies searching for candidate susceptibility loci for common complex diseases such as type 2 diabetes mellitus (T2DM) and its common complications have uncovered novel disease-associated genes. Nevertheless
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::367e91aff9b5d1298c6018461606d536
http://europepmc.org/articles/PMC2386827
http://europepmc.org/articles/PMC2386827