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Summary Anatomy Item Literature (6783) Expression Attributions Wiki
XB-ANAT-730

Papers associated with visual system (and slc4a1)

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The appearance of neural and glial cell markers during early development of the nervous system in the amphibian embryo., Messenger NJ., Development. September 1, 1989; 107 (1): 43-54.                      

Distinct regions of human glycophorin A enhance human red cell anion exchanger (band 3; AE1) transport function and surface trafficking., Young MT., J Biol Chem. August 29, 2003; 278 (35): 32954-61.

Cloning of a Na+-driven Cl/HCO3 exchanger from squid giant fiber lobe., Virkki LV., Am J Physiol Cell Physiol. October 1, 2003; 285 (4): C771-80.

A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells., Rungroj N., J Biol Chem. April 2, 2004; 279 (14): 13833-8.

Identification of asymmetrically localized transcripts along the animal-vegetal axis of the Xenopus egg., Kataoka K., Dev Growth Differ. October 1, 2005; 47 (8): 511-21.        

Molecular physiology of SLC4 anion exchangers., Alper SL., Exp Physiol. January 1, 2006; 91 (1): 153-61.

A novel Xenopus laevis larval keratin gene, xlk2: its gene structure and expression during regeneration and metamorphosis of limb and tail., Tazawa I., Biochim Biophys Acta. May 1, 2006; 1759 (5): 216-24.          

Electrogenic Na/HCO3 cotransporter (NBCe1) variants expressed in Xenopus oocytes: functional comparison and roles of the amino and carboxy termini., McAlear SD., J Gen Physiol. June 1, 2006; 127 (6): 639-58.                              

Consequences of point mutations in trout anion exchanger 1 (tAE1) transmembrane domains: evidence that tAE1 can behave as a chloride channel., Martial S., J Cell Physiol. June 1, 2006; 207 (3): 829-35.

Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle., Ito D., J Cell Sci. September 1, 2006; 119 (Pt 17): 3602-12.

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL., Hum Mol Genet. November 15, 2013; 22 (22): 4579-90.                    

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