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Genetic and Pharmacological Strategies to Refunctionalize the von Hippel Lindau R167Q Mutant Protein

Aberrant von Hippel Lindau (VHL) protein function is the underlying driver of VHL-related diseases, including both sporadic and inherited clear cell renal cell carcinoma (ccRCC). About one third of VHL mutations are missense point mutations, with R167Q being the most common VHL point mutation in her...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ding, Zhiyong, German, Peter, Bai, Shanshan, Reddy, A. Srinivas, Liu, Xian-De, Sun, Mianen, Zhou, Lijun, Chen, Xiaohua, Zhao, Xiaobei, Wu, Chengbiao, Zhang, Shuxing, Mills, Gordon B., Jonasch, Eric
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2014
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4047720/
https://ncbi.nlm.nih.gov/pubmed/24755468
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-13-3213
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