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Summary Expression Gene Literature (932) GO Terms (3) Nucleotides (145) Proteins (32) Interactants (287) Wiki
XB--1217295

Papers associated with aqp1 (and Disease Ontology)

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Rare heterozygous GDF6 variants in patients with renal anomalies., Martens H, Hennies I, Getwan M, Christians A, Weiss AC, Brand F, Gjerstad AC, Christians A, Gucev Z, Geffers R, Seeman T, Kispert A, Tasic V, Bjerre A, Lienkamp SS, Haffner D, Weber RG., Eur J Hum Genet. December 1, 2020; 28 (12): 1681-1693.                      


Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases., Vilas GL, Loganathan SK, Liu J, Riau AK, Young JD, Mehta JS, Vithana EN, Casey JR., Hum Mol Genet. November 15, 2013; 22 (22): 4579-90.                    


Functional characterization of an AQP0 missense mutation, R33C, that causes dominant congenital lens cataract, reveals impaired cell-to-cell adhesion., Kumari SS, Gandhi J, Mustehsan MH, Eren S, Varadaraj K., Exp Eye Res. November 1, 2013; 116 371-85.                  


Organization of the pronephric kidney revealed by large-scale gene expression mapping., Raciti D, Reggiani L, Geffers L, Jiang Q, Bacchion F, Subrizi AE, Clements D, Tindal C, Davidson DR, Kaissling B, Brändli AW., Genome Biol. January 1, 2008; 9 (5): R84.                                                                        


Water transport across mammalian cell membranes., Verkman AS, van Hoek AN, Ma T, Frigeri A, Skach WR, Mitra A, Tamarappoo BK, Farinas J., Am J Physiol. January 1, 1996; 270 (1 Pt 1): C12-30.

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