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Structural Basis of the Interaction between Tuberous Sclerosis Complex 1 (TSC1) and Tre2-Bub2-Cdc16 Domain Family Member 7 (TBC1D7)

Mutations in TSC1 or TSC2 cause tuberous sclerosis complex (TSC), an autosomal dominant disorder characterized by the occurrence of benign tumors in various vital organs and tissues. TSC1 and TSC2, the TSC1 and TSC2 gene products, form the TSC protein complex that senses specific cellular growth con...

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Detaylı Bibliyografya
Yayımlandı:J Biol Chem
Asıl Yazarlar: Qin, Jiayue, Wang, Zhizhi, Hoogeveen-Westerveld, Marianne, Shen, Guobo, Gong, Weimin, Nellist, Mark, Xu, Wenqing
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Biochemistry and Molecular Biology 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4861430/
https://ncbi.nlm.nih.gov/pubmed/26893383
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M115.701870
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