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The Journal of Biological Chemistry
|
September 10, 2017
Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca<sup>2+</sup> in knock-out mouse models of polycystic kidney disease
Murali K Yanda, Qiangni Liu, Valeriu Cebotaru, et al.
Plos One
|
July 19, 2011
A novel role of protein tyrosine kinase2 in mediating chloride secretion in human airway epithelial cells
Lihua Liang, Owen M Woodward, Zhaohui Chen, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
June 24, 2016
STIM1fl/fl Ksp-Cre Mouse has Impaired Renal Water Balance
Liudmila Cebotaru, Valeriu Cebotaru, Hua Wang, et al.
Plos One
|
April 5, 2013
Insulin-like growth factor 1 (IGF-1) enhances the protein expression of CFTR
Ha Won Lee, Jie Cheng, Olga Kovbasnjuk, et al.
Cell Calcium
|
November 25, 2021
The Mitochondrial Ca<sup>2+</sup> import complex is altered in ADPKD
Murali K Yanda, Vartika Tomar, Robert Cole, et al.
Cellular Signalling
|
October 9, 2018
Role of calcium in adult onset polycystic kidney disease
Murali K Yanda, Qiangni Liu, Valeriu Cebotaru, et al.
The Journal of Biological Chemistry
|
August 15, 2002
Characterization of aquaporin-6 as a nitrate channel in mammalian cells. Requirement of pore-lining residue threonine 63
Masahiro Ikeda, Eric Beitz, David Kozono, et al.
The Journal of Biological Chemistry
|
October 15, 2005
Polycystin 2 interacts with type I inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling
Yun Li, Jerry M Wright, Feng Qian, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
April 27, 2019
Restoration of F508-del Function by Transcomplementation: The Partners Meet in the Endoplasmic Reticulum
Emily Anne Smith Bergbower, Inna Sabirzhanova, Clément Boinot, et al.
Human Mutation
|
October 28, 2008
Localization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships
Kristina V Krasnov, Maria Tzetis, Jie Cheng, et al.
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of 12
Search research articles
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Showing results (31-40 of 119) with videos related to
Sort By:
Page
of 12
The Journal of Biological Chemistry
|
September 10, 2017
Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca<sup>2+</sup> in knock-out mouse models of polycystic kidney disease
Murali K Yanda, Qiangni Liu, Valeriu Cebotaru, et al.
Plos One
|
July 19, 2011
A novel role of protein tyrosine kinase2 in mediating chloride secretion in human airway epithelial cells
Lihua Liang, Owen M Woodward, Zhaohui Chen, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
June 24, 2016
STIM1fl/fl Ksp-Cre Mouse has Impaired Renal Water Balance
Liudmila Cebotaru, Valeriu Cebotaru, Hua Wang, et al.
Plos One
|
April 5, 2013
Insulin-like growth factor 1 (IGF-1) enhances the protein expression of CFTR
Ha Won Lee, Jie Cheng, Olga Kovbasnjuk, et al.
Cell Calcium
|
November 25, 2021
The Mitochondrial Ca<sup>2+</sup> import complex is altered in ADPKD
Murali K Yanda, Vartika Tomar, Robert Cole, et al.
Cellular Signalling
|
October 9, 2018
Role of calcium in adult onset polycystic kidney disease
Murali K Yanda, Qiangni Liu, Valeriu Cebotaru, et al.
The Journal of Biological Chemistry
|
August 15, 2002
Characterization of aquaporin-6 as a nitrate channel in mammalian cells. Requirement of pore-lining residue threonine 63
Masahiro Ikeda, Eric Beitz, David Kozono, et al.
The Journal of Biological Chemistry
|
October 15, 2005
Polycystin 2 interacts with type I inositol 1,4,5-trisphosphate receptor to modulate intracellular Ca2+ signaling
Yun Li, Jerry M Wright, Feng Qian, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology
|
April 27, 2019
Restoration of F508-del Function by Transcomplementation: The Partners Meet in the Endoplasmic Reticulum
Emily Anne Smith Bergbower, Inna Sabirzhanova, Clément Boinot, et al.
Human Mutation
|
October 28, 2008
Localization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships
Kristina V Krasnov, Maria Tzetis, Jie Cheng, et al.
Page
of 12