Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Deng F Guo"'
Autor:
Xitiz Chamling, Seongjin Seo, Kevin Bugge, Charles Searby, Deng F Guo, Arlene V Drack, Kamal Rahmouni, Val C Sheffield
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59101 (2013)
Bardet-Biedl syndrome (BBS) is a genetically heterogeneous autosomal recessive disorder characterized by obesity, retinal degeneration, polydactyly, hypogenitalism and renal defects. Recent findings have associated the etiology of the disease with ci
Externí odkaz:
https://doaj.org/article/e119a92897b34b91ab3a970c80b7f651
Publikováno v:
The FASEB Journal. 36
Publikováno v:
Hypertension. 68
Bardet-Biedl syndrome (BBS) is a pleiotropic autosomal recessive human disorder associated with several clinical features including obesity and hypertension. We previously demonstrated that Bbs1 gene deletion from the central nervous system caused ob
Abstract 083: Metabolic and Cardiovascular Effects of BBS1 Ablation From the POMC-containing Neurons
Publikováno v:
Hypertension. 66
Bardet-Biedl syndrome (BBS) is a pleiotropic autosomal recessive disorder associated with several features including obesity and hypertension. Deletion of Bbs genes globally, in the nervous system or in the leptin receptor-expressing cells recapitula
Publikováno v:
Hypertension. 64
Genetic defects that cause ciliary dysfunction are associated with obesity and cardiovascular diseases in humans and animal models suggesting that functional cilia are important for metabolism and cardiovascular regulation. Cilia are membrane-bound,
Autor:
Deng F Guo, Donald A Morgan, Justin L Grobe, Darryl Nishimura, Charles Searby, Val C Sheffield, Kamal Rahmouni
Publikováno v:
Hypertension. 64
Bardet-Biedl syndrome (BBS) is a pleiotropic autosomal recessive disorder associated with several features including obesity and hypertension. Deletion of BBS genes globally or in the nervous system recapitulated many of the BBS phenotypes including
Autor:
Kamal Rahmouni, Xitiz Chamling, Kevin Bugge, Val C. Sheffield, Charles Searby, Arlene V. Drack, Seongjin Seo, Deng F. Guo
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e59101 (2013)
PLoS ONE, Vol 8, Iss 3, p e59101 (2013)
Bardet-Biedl syndrome (BBS) is a genetically heterogeneous autosomal recessive disorder characterized by obesity, retinal degeneration, polydactyly, hypogenitalism and renal defects. Recent findings have associated the etiology of the disease with ci