Search research articles
Contact Us
Filters
Showing results (121-130 of 223) with videos related to
Page
of 23
Sort By:
Biochemistry
|
February 5, 2011
Substrate specificity of protein tyrosine phosphatases 1B, RPTPα, SHP-1, and SHP-2
Lige Ren, Xianwen Chen, Rinrada Luechapanichkul, et al.
Nature Communications
|
May 12, 2021
Selective and noncovalent targeting of RAS mutants for inhibition and degradation
Kai Wen Teng, Steven T Tsai, Takamitsu Hattori, et al.
Nature
|
July 19, 2013
Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signalling
Wentian Yang, Jianguo Wang, Douglas C Moore, et al.
Journal of Cell Science
|
September 15, 2012
Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangement
Francis 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 pathways
Maria 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 Cancer
Ankit 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 2
Kosuke 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 1B
Fawaz 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 growth
Mylène 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 site
Mohammad T Mazhab-Jafari, Christopher B Marshall, Matthew J Smith, et al.
Page
of 23
Search research articles
Search
Showing results (121-130 of 223) with videos related to
Sort By:
Page
of 23
Biochemistry
|
February 5, 2011
Substrate specificity of protein tyrosine phosphatases 1B, RPTPα, SHP-1, and SHP-2
Lige Ren, Xianwen Chen, Rinrada Luechapanichkul, et al.
Nature Communications
|
May 12, 2021
Selective and noncovalent targeting of RAS mutants for inhibition and degradation
Kai Wen Teng, Steven T Tsai, Takamitsu Hattori, et al.
Nature
|
July 19, 2013
Ptpn11 deletion in a novel progenitor causes metachondromatosis by inducing hedgehog signalling
Wentian Yang, Jianguo Wang, Douglas C Moore, et al.
Journal of Cell Science
|
September 15, 2012
Macrophages require Skap2 and Sirpα for integrin-stimulated cytoskeletal rearrangement
Francis 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 pathways
Maria 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 Cancer
Ankit 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 2
Kosuke 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 1B
Fawaz 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 growth
Mylène 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 site
Mohammad T Mazhab-Jafari, Christopher B Marshall, Matthew J Smith, et al.
Page
of 23