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Benjamin G Neel

Showing results (121-130 of 223) with videos related to

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Biochemistry|February 5, 2011
Substrate specificity of protein tyrosine phosphatases 1B, RPTPα, SHP-1, and SHP-2Lige Ren, Xianwen Chen, Rinrada Luechapanichkul, et al.
Nature Communications|May 12, 2021
Selective and noncovalent targeting of RAS mutants for inhibition and degradationKai Wen Teng, Steven T Tsai, Takamitsu Hattori, et al.
Nature|July 19, 2013
Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signallingWentian Yang, Jianguo Wang, Douglas C Moore, et al.
Journal of Cell Science|September 15, 2012
Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangementFrancis J Alenghat, Quentin J Baca, Nooreen T Rubin, et al.
Circulation|March 5, 2008
Deletion of Ptpn11 (Shp2) in cardiomyocytes causes dilated cardiomyopathy via effects on the extracellular signal-regulated kinase/mitogen-activated protein kinase and RhoA signaling pathwaysMaria I Kontaridis, Wentian Yang, Kendra K Bence, et al.
Cell Systems|April 15, 2019
N-Glycoproteomics of Patient-Derived Xenografts: A Strategy to Discover Tumor-Associated Proteins in High-Grade Serous Ovarian CancerAnkit Sinha, Ali Hussain, Vladimir Ignatchenko, et al.
The Journal of Biological Chemistry|September 16, 2010
Altered glucose homeostasis in mice with liver-specific deletion of Src homology phosphatase 2Kosuke Matsuo, Mirela Delibegovic, Izumi Matsuo, et al.
Plos One|June 2, 2012
Regulation of signaling at regions of cell-cell contact by endoplasmic reticulum-bound protein-tyrosine phosphatase 1BFawaz G Haj, Ola Sabet, Ali Kinkhabwala, et al.
Human Molecular Genetics|April 17, 2018
Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growthMylène Tajan, Julie Pernin-Grandjean, Nicolas Beton, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 6, 2015
Oncogenic and RASopathy-associated K-RAS mutations relieve membrane-dependent occlusion of the effector-binding siteMohammad T Mazhab-Jafari, Christopher B Marshall, Matthew J Smith, et al.
Pageof 23

Showing results (121-130 of 223) with videos related to

Sort By:
Pageof 23
Biochemistry|February 5, 2011
Substrate specificity of protein tyrosine phosphatases 1B, RPTPα, SHP-1, and SHP-2Lige Ren, Xianwen Chen, Rinrada Luechapanichkul, et al.
Nature Communications|May 12, 2021
Selective and noncovalent targeting of RAS mutants for inhibition and degradationKai Wen Teng, Steven T Tsai, Takamitsu Hattori, et al.
Nature|July 19, 2013
Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signallingWentian Yang, Jianguo Wang, Douglas C Moore, et al.
Journal of Cell Science|September 15, 2012
Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangementFrancis J Alenghat, Quentin J Baca, Nooreen T Rubin, et al.
Circulation|March 5, 2008
Deletion of Ptpn11 (Shp2) in cardiomyocytes causes dilated cardiomyopathy via effects on the extracellular signal-regulated kinase/mitogen-activated protein kinase and RhoA signaling pathwaysMaria I Kontaridis, Wentian Yang, Kendra K Bence, et al.
Cell Systems|April 15, 2019
N-Glycoproteomics of Patient-Derived Xenografts: A Strategy to Discover Tumor-Associated Proteins in High-Grade Serous Ovarian CancerAnkit Sinha, Ali Hussain, Vladimir Ignatchenko, et al.
The Journal of Biological Chemistry|September 16, 2010
Altered glucose homeostasis in mice with liver-specific deletion of Src homology phosphatase 2Kosuke Matsuo, Mirela Delibegovic, Izumi Matsuo, et al.
Plos One|June 2, 2012
Regulation of signaling at regions of cell-cell contact by endoplasmic reticulum-bound protein-tyrosine phosphatase 1BFawaz G Haj, Ola Sabet, Ali Kinkhabwala, et al.
Human Molecular Genetics|April 17, 2018
Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growthMylène Tajan, Julie Pernin-Grandjean, Nicolas Beton, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 6, 2015
Oncogenic and RASopathy-associated K-RAS mutations relieve membrane-dependent occlusion of the effector-binding siteMohammad T Mazhab-Jafari, Christopher B Marshall, Matthew J Smith, et al.
Pageof 23