Search research articles
Contact Us
Filters
Showing results (61-70 of 78) with videos related to
Page
of 8
Sort By:
The Journal of Biological Chemistry
|
October 15, 2013
A substrate access tunnel in the cytosolic domain is not an essential feature of the solute carrier 4 (SLC4) family of bicarbonate transporters
Volodymyr Shnitsar, Jing Li, Xuyao Li, et al.
Plos One
|
September 6, 2007
Blindness caused by deficiency in AE3 chloride/bicarbonate exchanger
Bernardo V Alvarez, Gregory S Gilmour, Silvina C Mema, et al.
Life Sciences
|
February 7, 2006
Involvement of AE3 isoform of Na(+)-independent Cl(-)/HCO(3)(-) exchanger in myocardial pH(i) recovery from intracellular alkalization
Gladys E Chiappe de Cingolani, Irene L Ennis, Patricio E Morgan, et al.
Human Molecular Genetics
|
July 2, 2013
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases
Gonzalo L Vilas, Sampath K Loganathan, Jun Liu, et al.
Human Molecular Genetics
|
November 7, 2019
Defective cell adhesion function of solute transporter, SLC4A11, in endothelial corneal dystrophies
Darpan Malhotra, Martin Jung, Claudia Fecher-Trost, et al.
Blood
|
February 28, 2018
A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis
Elizabeth Yang, Patricia Seo-Mayer, Kimberly Lezon-Geyda, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 27, 2004
The bicarbonate transport metabolon
Heather L McMurtrie, Haley J Cleary, Bernardo V Alvarez, et al.
British Journal of Pharmacology
|
May 21, 2011
Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
Verónica C De Giusti, Alejandro Orlowski, María C Villa-Abrille, et al.
Scientific Reports
|
June 5, 2015
Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification
Didier Zoccola, Philippe Ganot, Anthony Bertucci, et al.
Journal of Human Genetics
|
July 11, 2014
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy
Nagasamy Soumittra, Sampath K Loganathan, Dharanija Madhavan, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 78) with videos related to
Sort By:
Page
of 8
The Journal of Biological Chemistry
|
October 15, 2013
A substrate access tunnel in the cytosolic domain is not an essential feature of the solute carrier 4 (SLC4) family of bicarbonate transporters
Volodymyr Shnitsar, Jing Li, Xuyao Li, et al.
Plos One
|
September 6, 2007
Blindness caused by deficiency in AE3 chloride/bicarbonate exchanger
Bernardo V Alvarez, Gregory S Gilmour, Silvina C Mema, et al.
Life Sciences
|
February 7, 2006
Involvement of AE3 isoform of Na(+)-independent Cl(-)/HCO(3)(-) exchanger in myocardial pH(i) recovery from intracellular alkalization
Gladys E Chiappe de Cingolani, Irene L Ennis, Patricio E Morgan, et al.
Human Molecular Genetics
|
July 2, 2013
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases
Gonzalo L Vilas, Sampath K Loganathan, Jun Liu, et al.
Human Molecular Genetics
|
November 7, 2019
Defective cell adhesion function of solute transporter, SLC4A11, in endothelial corneal dystrophies
Darpan Malhotra, Martin Jung, Claudia Fecher-Trost, et al.
Blood
|
February 28, 2018
A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis
Elizabeth Yang, Patricia Seo-Mayer, Kimberly Lezon-Geyda, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
October 27, 2004
The bicarbonate transport metabolon
Heather L McMurtrie, Haley J Cleary, Bernardo V Alvarez, et al.
British Journal of Pharmacology
|
May 21, 2011
Antibodies against the cardiac sodium/bicarbonate co-transporter (NBCe1) as pharmacological tools
Verónica C De Giusti, Alejandro Orlowski, María C Villa-Abrille, et al.
Scientific Reports
|
June 5, 2015
Bicarbonate transporters in corals point towards a key step in the evolution of cnidarian calcification
Didier Zoccola, Philippe Ganot, Anthony Bertucci, et al.
Journal of Human Genetics
|
July 11, 2014
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy
Nagasamy Soumittra, Sampath K Loganathan, Dharanija Madhavan, et al.
Page
of 8