Transmembrane water-flux through SLC4A11: A route defective in genetic corneal diseases

Human Molecular Genetics

Volumn 22, Issue 22, 2013, Pages 4579-4590

  Vilas, Gonzalo L ^a   Loganathan, Sampath K ^a   Liu, Jun ^b   Riau, Andri K ^b   Young, James D ^a   Mehta, Jodhbir S ^b,c,d   Vithana, Eranga N ^b,c   Casey, Joseph R ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b SINGAPORE EYE RESEARCH INSTITUTE   (Singapore)

^c NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^d DUKE NUS MEDICAL SCHOOL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

AQUAPORIN; NUCLEOSIDE TRANSPORTER; PROTEIN PATCHED 2; STILBENE; WATER;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APICAL MEMBRANE; ARTICLE; BASOLATERAL MEMBRANE; CELL STRAIN HEK293; CELL SWELLING; CONTROLLED STUDY; CORNEA DISEASE; CORNEA EDEMA; CORNEA ENDOTHELIUM; ENDOTHELIUM CELL; GENE; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; HETEROZYGOTE; HUMAN; HUMAN CELL; MOUSE; MUTANT; NONHUMAN; OOCYTE; OSMOSIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN FAMILY; SLC4A11 GENE; SOLUTE; WATER ABSORPTION; WATER FLOW; WATER PERMEABILITY; XENOPUS LAEVIS;

ANIMALS; AQUAPORIN 1; AQUAPORINS; CORNEA; CORNEAL DYSTROPHIES, HEREDITARY; CORNEAL STROMA; HEARING LOSS, SENSORINEURAL; HEK293 CELLS; HUMANS; MEMBRANE TRANSPORT PROTEINS; MICE; MICE, KNOCKOUT; MODELS, ANIMAL; OOCYTES; PHENOTYPE; SIGNAL TRANSDUCTION; SLC4A PROTEINS; WATER; XENOPUS LAEVIS;

EID: 84887008661     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt307     Document Type: Article

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