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Proceedings of the National Academy of Sciences of the United States of America|May 7, 2014
Mutation of mouse Samd4 causes leanness, myopathy, uncoupled mitochondrial respiration, and dysregulated mTORC1 signalingZhe Chen, William Holland, John M Shelton, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2016
Insulin resistance and diabetes caused by genetic or diet-induced KBTBD2 deficiency in miceZhao Zhang, Emre Turer, Xiaohong Li, et al.
Nature Communications|November 6, 2014
An epigenetic switch induced by Shh signalling regulates gene activation during development and medulloblastoma growthXuanming Shi, Zilai Zhang, Xiaoming Zhan, et al.
Molecular Biology of the Cell|April 11, 2008
R-Spondin family members regulate the Wnt pathway by a common mechanismKyung-Ah Kim, Marie Wagle, Karolyn Tran, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 2017
Creatine maintains intestinal homeostasis and protects against colitisEmre Turer, William McAlpine, Kuan-Wen Wang, et al.
Blood Advances|August 8, 2020
Adenosine monophosphate deaminase 3 null mutation causes reduction of naive T cells in mouse peripheral bloodXiaoming Zhan, Xue Zhong, Jin Huk Choi, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 20, 2020
Essential requirement for nicastrin in marginal zone and B-1 B cell developmentJin Huk Choi, Jonghee Han, Panayotis C Theodoropoulos, et al.
Nature Communications|March 3, 2021
N4BP1 negatively regulates NF-κB by binding and inhibiting NEMO oligomerizationHexin Shi, Lei Sun, Ying Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2015
Mutation of the ER retention receptor KDELR1 leads to cell-intrinsic lymphopenia and a failure to control chronic viral infectionOwen M Siggs, Daniel L Popkin, Philippe Krebs, et al.
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