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R de Jonge

Showing results (241-250 of 298) with videos related to

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Molecular Pharmacology|March 5, 2010
Correction of the Delta phe508 cystic fibrosis transmembrane conductance regulator trafficking defect by the bioavailable compound glafenineRenaud Robert, Graeme W Carlile, Jie Liao, et al.
BMC Genetics|April 11, 2008
Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis miceBalázs Tóth, Martina Wilke, Frauke Stanke, et al.
The Journal of Biological Chemistry|May 24, 2003
Autophosphorylation of cGMP-dependent protein kinase type IIArie B Vaandrager, Boris M Hogema, Marcel Edixhoven, et al.
Journal of Medicinal Chemistry|June 13, 2003
SYNOPSIS: SYNthesize and OPtimize System in SilicoH Maarten Vinkers, Marc R de Jonge, Frederik F D Daeyaert, et al.
Gastroenterology|October 28, 2010
D-glucose acts via sodium/glucose cotransporter 1 to increase NHE3 in mouse jejunal brush border by a Na+/H+ exchange regulatory factor 2-dependent processRong Lin, Rakhilya Murtazina, Boyoung Cha, et al.
The Journal of Biological Chemistry|February 14, 1997
cGMP stimulation of cystic fibrosis transmembrane conductance regulator Cl- channels co-expressed with cGMP-dependent protein kinase type II but not type IbetaA B Vaandrager, B C Tilly, A Smolenski, et al.
Gastroenterology|October 6, 2009
Lysophosphatidic acid stimulates the intestinal brush border Na(+)/H(+) exchanger 3 and fluid absorption via LPA(5) and NHERF2Songbai Lin, Sunil Yeruva, Peijian He, et al.
Neurogastroenterology and Motility|August 19, 2011
The role of rectal chloride secretion in childhood constipationN Bekkali, H R de Jonge, R M J G J van den Wijngaard, et al.
Life Science Alliance|January 20, 2019
Folding-function relationship of the most common cystic fibrosis-causing CFTR conductance mutantsMarcel van Willigen, Annelotte M Vonk, Hui Ying Yeoh, et al.
Human Molecular Genetics|February 2, 2002
The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectricsPaul Dickinson, Stephen N Smith, Sheila Webb, et al.
Pageof 30

Showing results (241-250 of 298) with videos related to

Sort By:
Pageof 30
Molecular Pharmacology|March 5, 2010
Correction of the Delta phe508 cystic fibrosis transmembrane conductance regulator trafficking defect by the bioavailable compound glafenineRenaud Robert, Graeme W Carlile, Jie Liao, et al.
BMC Genetics|April 11, 2008
Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis miceBalázs Tóth, Martina Wilke, Frauke Stanke, et al.
The Journal of Biological Chemistry|May 24, 2003
Autophosphorylation of cGMP-dependent protein kinase type IIArie B Vaandrager, Boris M Hogema, Marcel Edixhoven, et al.
Journal of Medicinal Chemistry|June 13, 2003
SYNOPSIS: SYNthesize and OPtimize System in SilicoH Maarten Vinkers, Marc R de Jonge, Frederik F D Daeyaert, et al.
Gastroenterology|October 28, 2010
D-glucose acts via sodium/glucose cotransporter 1 to increase NHE3 in mouse jejunal brush border by a Na+/H+ exchange regulatory factor 2-dependent processRong Lin, Rakhilya Murtazina, Boyoung Cha, et al.
The Journal of Biological Chemistry|February 14, 1997
cGMP stimulation of cystic fibrosis transmembrane conductance regulator Cl- channels co-expressed with cGMP-dependent protein kinase type II but not type IbetaA B Vaandrager, B C Tilly, A Smolenski, et al.
Gastroenterology|October 6, 2009
Lysophosphatidic acid stimulates the intestinal brush border Na(+)/H(+) exchanger 3 and fluid absorption via LPA(5) and NHERF2Songbai Lin, Sunil Yeruva, Peijian He, et al.
Neurogastroenterology and Motility|August 19, 2011
The role of rectal chloride secretion in childhood constipationN Bekkali, H R de Jonge, R M J G J van den Wijngaard, et al.
Life Science Alliance|January 20, 2019
Folding-function relationship of the most common cystic fibrosis-causing CFTR conductance mutantsMarcel van Willigen, Annelotte M Vonk, Hui Ying Yeoh, et al.
Human Molecular Genetics|February 2, 2002
The severe G480C cystic fibrosis mutation, when replicated in the mouse, demonstrates mistrafficking, normal survival and organ-specific bioelectricsPaul Dickinson, Stephen N Smith, Sheila Webb, et al.
Pageof 30