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RAS interaction with Sin1 is dispensable for mTORC2 assembly and activity.
Castel, Pau; Dharmaiah, Srisathiyanarayanan; Sale, Matthew J; Messing, Simon; Rizzuto, Gabrielle; Cuevas-Navarro, Antonio; Cheng, Alice; Trnka, Michael J; Urisman, Anatoly; Esposito, Dominic; Simanshu, Dhirendra K; McCormick, Frank.
Afiliação
  • Castel P; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94158.
  • Dharmaiah S; National Cancer Institute (NCI) RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD 21702.
  • Sale MJ; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94158.
  • Messing S; National Cancer Institute (NCI) RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD 21702.
  • Rizzuto G; Department of Anatomic Pathology, University of California, San Francisco, CA 94158.
  • Cuevas-Navarro A; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94158.
  • Cheng A; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94158.
  • Trnka MJ; Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158.
  • Urisman A; Department of Anatomic Pathology, University of California, San Francisco, CA 94158.
  • Esposito D; National Cancer Institute (NCI) RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD 21702.
  • Simanshu DK; National Cancer Institute (NCI) RAS Initiative, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, MD 21702; Frank.mccormick@ucsf.edu dhirendra.simanshu@nih.gov.
  • McCormick F; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA 94158; Frank.mccormick@ucsf.edu dhirendra.simanshu@nih.gov.
Proc Natl Acad Sci U S A ; 118(33)2021 08 17.
Article em En | MEDLINE | ID: mdl-34380736
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas p21(ras) / Proteínas Adaptadoras de Transdução de Sinal / Alvo Mecanístico do Complexo 2 de Rapamicina Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas p21(ras) / Proteínas Adaptadoras de Transdução de Sinal / Alvo Mecanístico do Complexo 2 de Rapamicina Idioma: En Ano de publicação: 2021 Tipo de documento: Article