Showing 41 - 60 results of 321 for search '"STK11"', query time: 0.69s Refine Results
  1. 41

    Association between STK11 Gene Polymorphisms and Coronary Artery Disease in Type 2 Diabetes in Han Population in China by Xiaowei Ma, Ge Bai, Difei Lu, Linjuan Huang, Jianwei Zhang, Ruifen Deng, Shan Ding, Nan Gu, Xiaohui Guo

    Published 2017-01-01
    “…Recent studies indicated that the Serine threonine kinase 11 (STK11), which is a key regulator of the AMP-activated protein kinase (AMPK), plays a crucial role in cardiovascular system. …”
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    Article
  2. 42

    Identification of a novel mRNA species of the LKB1/STK11 Peutz-Jeghers serine/threonine kinase. by Churchman, M, Dowling, B, Tomlinson, I

    Published 1999
    “…Germline mutations in the LKB1/STK11 serine/threonine kinase cause Peutz-Jeghers syndrome and this gene is also mutated at a moderate frequency in a wide variety of sporadic tumours. …”
    Journal article
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    Quantitative phosphoproteomic analyses identify STK11IP as a lysosome-specific substrate of mTORC1 that regulates lysosomal acidification by Zhenzhen Zi, Zhuzhen Zhang, Qiang Feng, Chiho Kim, Xu-Dong Wang, Philipp E. Scherer, Jinming Gao, Beth Levine, Yonghao Yu

    Published 2022-04-01
    “…Here the authors show STK11IP is a substrate of mTORC1 that regulates lysosomal acidification through V-ATPase and represses autophagy.…”
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    Article
  13. 53

    A novel <it>de novo </it>mutation in the serine-threonine kinase <it>STK11 </it>gene in a Korean patient with Peutz-Jeghers syndrome by Ki Chang-Seok, Sun Young-Kyu, Kang Jung-Gu, Choi Yoon-Jung, Yoo Jee-Hyoung, Yoo Jong-Ha, Lee Kyung-A, Choi Jong-Rak

    Published 2008-05-01
    “…Germline mutation of the <it>STK11 </it>gene, which encodes a serine-threonine kinase, is responsible for PJS.…”
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    Article
  14. 54

    Generation of an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome due to STK11 mutation by Teng Wang, Kongxi Zhu, Weihua Yu, Lei Peng, Hongjuan Wang, Qiong Wu

    Published 2023-09-01
    “…We established an iPSC line (TSHSUi001-A) from a patient with Peutz-Jeghers syndrome, carrying heterozygous c.290 + 1G > A mutation in STK11 gene. Peripheral blood mononuclear cells were reprogrammed using non-integrating delivery of OCT4, SOX2, KFL4, BCL-XL and c-MYC. …”
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    Article
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