Nonsynonymous Mutations within APOB in Human Familial Hypobetalipoproteinemia: EVIDENCE FOR FEEDBACK INHIBITION OF LIPOGENESIS AND POSTENDOPLASMIC RETICULUM DEGRADATION OF APOLIPOPROTEIN B

Five nontruncating missense APOB mutations, namely A31P, G275S, L324M, G912D, and G945S, were identified in heterozygous carriers of familial hypobetalipoproteinemia (FHBL) in the Italian population. To test that the FHBL phenotype was a result of impaired hepatic secretion of mutant apoB proteins,...

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Detalhes bibliográficos
Main Authors: Zhong, Shumei, Magnolo, Antonia Lucia, Sundaram, Meenakshi, Zhou, Hu, Yao, Erik F., Di Leo, Enza, Loria, Paola, Wang, Shuai, Bamji-Mirza, Michelle, Wang, Lisheng, McKnight, C. Jamie, Figeys, Daniel, Wang, Yuwei, Tarugi, Patrizia, Yao, Zemin
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2010
Assuntos:
Molecular Bases of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2825441/
https://ncbi.nlm.nih.gov/pubmed/20032471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.060467
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