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Summary Expression Phenotypes Gene Literature (235) GO Terms (2) Nucleotides (100) Proteins (27) Interactants (675) Wiki
XB--494036

Papers associated with adm (and Disease Ontology)



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Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM, Krohn P, Baxi AB, Tavares ALP, Sullivan CH, Chillakuru YR, Majumdar HD, Neilson KM, Moody SA., Dis Model Mech. March 3, 2020; 13 (3):                                               


The VAMP-associated protein VAPB is required for cardiac and neuronal pacemaker channel function., Silbernagel N, Walecki M, Schäfer MK, Kessler M, Zobeiri M, Rinné S, Kiper AK, Komadowski MA, Vowinkel KS, Wemhöner K, Fortmüller L, Schewe M, Dolga AM, Scekic-Zahirovic J, Matschke LA, Culmsee C, Baukrowitz T, Monassier L, Ullrich ND, Dupuis L, Just S, Budde T, Fabritz L, Decher N., FASEB J. November 1, 2018; 32 (11): 6159-6173.            


Polycystin 1 loss of function is directly linked to an imbalance in G-protein signaling in the kidney., Zhang B, Tran U, Wessely O., Development. March 22, 2018; 145 (6):                         


Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy., Simons C, Rash LD, Crawford J, Ma L, Cristofori-Armstrong B, Miller D, Ru K, Baillie GJ, Alanay Y, Jacquinet A, Debray FG, Verloes A, Shen J, Yesil G, Guler S, Yuksel A, Cleary JG, Grimmond SM, McGaughran J, King GF, Gabbett MT, Taft RJ., Nat Genet. January 1, 2015; 47 (1): 73-7.      


Fgfr signaling is required as the early eye field forms to promote later patterning and morphogenesis of the eye., Atkinson-Leadbeater K, Hehr CL, McFarlane S., Dev Dyn. May 1, 2014; .              


Disease-associated mutations in CNGB3 promote cytotoxicity in photoreceptor-derived cells., Liu C, Sherpa T, Varnum MD., Mol Vis. June 11, 2013; 19 1268-81.              


Alterations in intracellular potassium concentration by HIV-1 and SIV Nef., Choi B, Fermin CD, Comardelle AM, Haislip AM, Voss TG, Garry RF., Virol J. May 19, 2008; 5 60.      


Molecular mechanism underlying a Cx50-linked congenital cataract., Pal JD, Berthoud VM, Beyer EC, Mackay D, Shiels A, Ebihara L., Am J Physiol. June 1, 1999; 276 (6): C1443-6.

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