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The Journal of Biological Chemistry
|
December 18, 2001
Inhibition of the calcium release-activated calcium (CRAC) current in Jurkat T cells by the HIV-1 envelope protein gp160
Olivier Dellis, Sophie C Gangloff, Marc Paulais, et al.
American Journal of Physiology. Renal Physiology
|
March 28, 2008
Kir4.1/Kir5.1 channel forms the major K+ channel in the basolateral membrane of mouse renal collecting duct principal cells
Sahran Lachheb, Françoise Cluzeaud, Marcelle Bens, et al.
Human Mutation
|
December 6, 2019
Analysis of CLCNKB mutations at dimer-interface, calcium-binding site, and pore reveals a variety of functional alterations in ClC-Kb channel leading to Bartter syndrome
Yohan Bignon, Imene Sakhi, Sara Bitam, et al.
Human Mutation
|
February 10, 2011
Heterogeneity in the processing of CLCN5 mutants related to Dent disease
Teddy Grand, Sébastien L'Hoste, David Mordasini, et al.
Plos Pathogens
|
September 26, 2014
Identification and functional expression of a glutamate- and avermectin-gated chloride channel from Caligus rogercresseyi, a southern Hemisphere sea louse affecting farmed fish
Isabel Cornejo, Olga Andrini, María Isabel Niemeyer, et al.
Scientific Reports
|
August 5, 2017
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening
Maxime Louet, Sara Bitam, Naziha Bakouh, et al.
Kidney International
|
August 7, 2009
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing
Teddy Grand, David Mordasini, Sébastien L'Hoste, et al.
Journal of the American Society of Nephrology : JASN
|
November 4, 2005
Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis
Stéphane Lourdel, Johannes Loffing, Guillaume Favre, et al.
Human Mutation
|
March 19, 2005
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype
Jérôme Clain, Jacqueline Lehmann-Che, Ingrid Duguépéroux, et al.
Biochimica Et Biophysica Acta
|
June 25, 2013
Characterization of the mouse ClC-K1/Barttin chloride channel
Sébastien L'Hoste, Alexei Diakov, Olga Andrini, et al.
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of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
The Journal of Biological Chemistry
|
December 18, 2001
Inhibition of the calcium release-activated calcium (CRAC) current in Jurkat T cells by the HIV-1 envelope protein gp160
Olivier Dellis, Sophie C Gangloff, Marc Paulais, et al.
American Journal of Physiology. Renal Physiology
|
March 28, 2008
Kir4.1/Kir5.1 channel forms the major K+ channel in the basolateral membrane of mouse renal collecting duct principal cells
Sahran Lachheb, Françoise Cluzeaud, Marcelle Bens, et al.
Human Mutation
|
December 6, 2019
Analysis of CLCNKB mutations at dimer-interface, calcium-binding site, and pore reveals a variety of functional alterations in ClC-Kb channel leading to Bartter syndrome
Yohan Bignon, Imene Sakhi, Sara Bitam, et al.
Human Mutation
|
February 10, 2011
Heterogeneity in the processing of CLCN5 mutants related to Dent disease
Teddy Grand, Sébastien L'Hoste, David Mordasini, et al.
Plos Pathogens
|
September 26, 2014
Identification and functional expression of a glutamate- and avermectin-gated chloride channel from Caligus rogercresseyi, a southern Hemisphere sea louse affecting farmed fish
Isabel Cornejo, Olga Andrini, María Isabel Niemeyer, et al.
Scientific Reports
|
August 5, 2017
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening
Maxime Louet, Sara Bitam, Naziha Bakouh, et al.
Kidney International
|
August 7, 2009
Novel CLCN5 mutations in patients with Dent's disease result in altered ion currents or impaired exchanger processing
Teddy Grand, David Mordasini, Sébastien L'Hoste, et al.
Journal of the American Society of Nephrology : JASN
|
November 4, 2005
Hyperaldosteronemia and activation of the epithelial sodium channel are not required for sodium retention in puromycin-induced nephrosis
Stéphane Lourdel, Johannes Loffing, Guillaume Favre, et al.
Human Mutation
|
March 19, 2005
Misprocessing of the CFTR protein leads to mild cystic fibrosis phenotype
Jérôme Clain, Jacqueline Lehmann-Che, Ingrid Duguépéroux, et al.
Biochimica Et Biophysica Acta
|
June 25, 2013
Characterization of the mouse ClC-K1/Barttin chloride channel
Sébastien L'Hoste, Alexei Diakov, Olga Andrini, et al.
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of 4