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The Journal of Physiology
|
November 17, 2017
K<sub>2P</sub> TASK-2 and KCNQ1-KCNE3 K<sup>+</sup> channels are major players contributing to intestinal anion and fluid secretion
Francisca Julio-Kalajzić, Sandra Villanueva, Johanna Burgos, et al.
Plos One
|
February 2, 2011
Gating of a pH-sensitive K(2P) potassium channel by an electrostatic effect of basic sensor residues on the selectivity filter
Leandro Zúñiga, Valeria Márquez, Fernando D González-Nilo, et al.
Frontiers in Physiology
|
August 3, 2013
TASK-2: a K2P K(+) channel with complex regulation and diverse physiological functions
L Pablo Cid, Hugo A Roa-Rojas, María I Niemeyer, et al.
The Journal of Physiology
|
September 14, 2011
Sexual dimorphism and oestrogen regulation of KCNE3 expression modulates the functional properties of KCNQ1 K⁺ channels
Rodrigo Alzamora, Fiona O'Mahony, Viviana Bustos, et al.
Scientific Reports
|
June 20, 2018
Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse
Amber R Philp, Texia T Riquelme, Pamela Millar-Büchner, et al.
Plos One
|
September 25, 2015
Cleft Palate, Moderate Lung Developmental Retardation and Early Postnatal Lethality in Mice Deficient in the Kir7.1 Inwardly Rectifying K+ Channel
Sandra Villanueva, Johanna Burgos, Karen I López-Cayuqueo, 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.
Journal of Cell Science
|
September 13, 2005
Basolateral localization of native ClC-2 chloride channels in absorptive intestinal epithelial cells and basolateral sorting encoded by a CBS-2 domain di-leucine motif
Gaspar Peña-Münzenmayer, Marcelo Catalán, Isabel Cornejo, et al.
Human Mutation
|
May 25, 2013
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression
Mathilde Keck, Olga Andrini, Olivier Lahuna, et al.
Nature Genetics
|
September 12, 2006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
Alfredo Ramirez, André Heimbach, Jan Gründemann, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 40) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 40 results.
The Journal of Physiology
|
November 17, 2017
K<sub>2P</sub> TASK-2 and KCNQ1-KCNE3 K<sup>+</sup> channels are major players contributing to intestinal anion and fluid secretion
Francisca Julio-Kalajzić, Sandra Villanueva, Johanna Burgos, et al.
Plos One
|
February 2, 2011
Gating of a pH-sensitive K(2P) potassium channel by an electrostatic effect of basic sensor residues on the selectivity filter
Leandro Zúñiga, Valeria Márquez, Fernando D González-Nilo, et al.
Frontiers in Physiology
|
August 3, 2013
TASK-2: a K2P K(+) channel with complex regulation and diverse physiological functions
L Pablo Cid, Hugo A Roa-Rojas, María I Niemeyer, et al.
The Journal of Physiology
|
September 14, 2011
Sexual dimorphism and oestrogen regulation of KCNE3 expression modulates the functional properties of KCNQ1 K⁺ channels
Rodrigo Alzamora, Fiona O'Mahony, Viviana Bustos, et al.
Scientific Reports
|
June 20, 2018
Kcnn4 is a modifier gene of intestinal cystic fibrosis preventing lethality in the Cftr-F508del mouse
Amber R Philp, Texia T Riquelme, Pamela Millar-Büchner, et al.
Plos One
|
September 25, 2015
Cleft Palate, Moderate Lung Developmental Retardation and Early Postnatal Lethality in Mice Deficient in the Kir7.1 Inwardly Rectifying K+ Channel
Sandra Villanueva, Johanna Burgos, Karen I López-Cayuqueo, 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.
Journal of Cell Science
|
September 13, 2005
Basolateral localization of native ClC-2 chloride channels in absorptive intestinal epithelial cells and basolateral sorting encoded by a CBS-2 domain di-leucine motif
Gaspar Peña-Münzenmayer, Marcelo Catalán, Isabel Cornejo, et al.
Human Mutation
|
May 25, 2013
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expression
Mathilde Keck, Olga Andrini, Olivier Lahuna, et al.
Nature Genetics
|
September 12, 2006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
Alfredo Ramirez, André Heimbach, Jan Gründemann, et al.
Page
of 4