The Mitochondrial SDHD Gene Is Required for Early Embryogenesis, and Its Partial Deficiency Results in Persistent Carotid Body Glomus Cell Activation with Full Responsiveness to Hypoxia

The SDHD gene encodes one of the two membrane-anchoring proteins of the succinate dehydrogenase (complex II) of the mitochondrial electron transport chain. This gene has recently been proposed to be involved in oxygen sensing because mutations that cause loss of its function produce hereditary famil...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Piruat, José I., Pintado, C. Oscar, Ortega-Sáenz, Patricia, Roche, Marta, López-Barneo, José
التنسيق: Artigo
اللغة:Inglês
منشور في: American Society for Microbiology 2004
الموضوعات:
Mammalian Genetic Models with Minimal or Complex Phenotypes
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC533988/
https://ncbi.nlm.nih.gov/pubmed/15572694
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.24.24.10933-10940.2004
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