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Summary Expression Phenotypes Gene Literature (37) GO Terms (7) Nucleotides (213) Proteins (72) Interactants (538) Wiki
XB-GENEPAGE-950379

Papers associated with slc26a4.3



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Activation of 2-oxoglutarate receptor 1 (OXGR1) by α-ketoglutarate (αKG) does not detectably stimulate Pendrin-mediated anion exchange in Xenopus oocytes., Heneghan JF, Majmundar AJ, Rivera A, Wohlgemuth JG, Dlott JS, Snyder LM, Hildebrandt F, Alper SL., Physiol Rep. July 1, 2022; 10 (14): e15362.

Noncanonical mechanism of voltage sensor coupling to pore revealed by tandem dimers of Shaker., Carvalho-de-Souza JL, Bezanilla F., Nat Commun. August 8, 2019; 10 (1): 3584.                                  

Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome., Zhang F, Bai X, Xiao Y, Zhang X, Zhang G, Li J, Xu L, Wang H., Int J Pediatr Otorhinolaryngol. June 1, 2016; 85 75-9.

RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D, Powers TR, van Velkinburgh JC, Trujillo-Provencio C, Schilkey F, Serrano EE., BMC Res Notes. November 18, 2015; 8 691.      

BMP signalling controls the construction of vertebrate mucociliary epithelia., Cibois M, Luxardi G, Chevalier B, Thomé V, Mercey O, Zaragosi LE, Barbry P, Pasini A, Marcet B, Kodjabachian L., Development. July 1, 2015; 142 (13): 2352-63.                        

mab21-l3 regulates cell fate specification of multiciliate cells and ionocytes., Takahashi C, Kusakabe M, Suzuki T, Miyatake K, Nishida E., Nat Commun. January 19, 2015; 6 6017.      

Interfacial gating triad is crucial for electromechanical transduction in voltage-activated potassium channels., Chowdhury S, Haehnel BM, Chanda B., J Gen Physiol. November 1, 2014; 144 (5): 457-67.            

Protein phosphatase 1 inhibitor-1 deficiency reduces phosphorylation of renal NaCl cotransporter and causes arterial hypotension., Picard N, Trompf K, Yang CL, Miller RL, Carrel M, Loffing-Cueni D, Fenton RA, Ellison DH, Loffing J., J Am Soc Nephrol. March 1, 2014; 25 (3): 511-22.

Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN, Blackiston DJ, Rea AC, Dore TM, Levin M., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809.                

Embryonic frog epidermis: a model for the study of cell-cell interactions in the development of mucociliary disease., Dubaissi E, Papalopulu N., Dis Model Mech. March 1, 2011; 4 (2): 179-92.                        

Specification of ion transport cells in the Xenopus larval skin., Quigley IK, Stubbs JL, Kintner C., Development. February 1, 2011; 138 (4): 705-14.                                          

Pendrin function and regulation in Xenopus oocytes., Reimold FR, Heneghan JF, Stewart AK, Zelikovic I, Vandorpe DH, Shmukler BE, Alper SL., Cell Physiol Biochem. January 1, 2011; 28 (3): 435-50.

Pendrin modulates ENaC function by changing luminal HCO3-., Pech V, Pham TD, Hong S, Weinstein AM, Spencer KB, Duke BJ, Walp E, Kim YH, Sutliff RL, Bao HF, Eaton DC, Wall SM., J Am Soc Nephrol. November 1, 2010; 21 (11): 1928-41.

The Na+-dependent chloride-bicarbonate exchanger SLC4A8 mediates an electroneutral Na+ reabsorption process in the renal cortical collecting ducts of mice., Leviel F, Hübner CA, Houillier P, Morla L, El Moghrabi S, Brideau G, Hassan H, Hatim H, Parker MD, Kurth I, Kougioumtzes A, Sinning A, Pech V, Riemondy KA, Miller RL, Hummler E, Shull GE, Aronson PS, Doucet A, Wall SM, Chambrey R, Eladari D., J Clin Invest. May 1, 2010; 120 (5): 1627-35.

Efficient molecular genetic diagnosis of enlarged vestibular aqueducts in East Asians., Choi BY, Stewart AK, Nishimura KK, Cha WJ, Seong MW, Park SS, Kim SW, Chun YS, Chung JW, Park SN, Chang SO, Kim CS, Alper SL, Griffith AJ, Oh SH., Genet Test Mol Biomarkers. October 1, 2009; 13 (5): 679-87.

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss., Dai P, Stewart AK, Chebib F, Hsu A, Rozenfeld J, Huang D, Kang D, Lip V, Fang H, Shao H, Liu X, Yu F, Yuan H, Kenna M, Miller DT, Shen Y, Yang W, Zelikovic I, Platt OS, Han D, Alper SL, Wu BL., Physiol Genomics. August 7, 2009; 38 (3): 281-90.

Multiple intermediate states precede pore block during N-type inactivation of a voltage-gated potassium channel., Prince-Carter A, Pfaffinger PJ., J Gen Physiol. July 1, 2009; 134 (1): 15-34.                              

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome., Yang T, Gurrola JG, Wu H, Chiu SM, Wangemann P, Snyder PM, Smith RJ., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.      

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?, Choi BY, Stewart AK, Madeo AC, Pryor SP, Lenhard S, Kittles R, Eisenman D, Kim HJ, Niparko J, Thomsen J, Arnos KS, Nance WE, King KA, Zalewski CK, Brewer CC, Shawker T, Reynolds JC, Butman JA, Karniski LP, Alper SL, Griffith AJ., Hum Mutat. April 1, 2009; 30 (4): 599-608.

KCNQ1 and KCNE1 in the IKs channel complex make state-dependent contacts in their extracellular domains., Xu X, Jiang M, Hsu KL, Zhang M, Tseng GN., J Gen Physiol. June 1, 2008; 131 (6): 589-603.                    

Panulirus interruptus Ih-channel gene PIIH: modification of channel properties by alternative splicing and role in rhythmic activity., Ouyang Q, Goeritz M, Harris-Warrick RM., J Neurophysiol. June 1, 2007; 97 (6): 3880-92.

Regulation of anion exchanger Slc26a6 by protein kinase C., Hassan HA, Mentone S, Karniski LP, Rajendran VM, Aronson PS., Am J Physiol Cell Physiol. April 1, 2007; 292 (4): C1485-92.

[Evidence of a novel gene for the LAV-syndrome]., Birkenhäger R, Zimmer AJ, Maier W, Klenzner T, Aschendorff A, Schipper J., Laryngorhinootologie. February 1, 2007; 86 (2): 102-6.

PSD-95 and PKC converge in regulating NMDA receptor trafficking and gating., Lin Y, Jover-Mengual T, Wong J, Bennett MV, Zukin RS., Proc Natl Acad Sci U S A. December 26, 2006; 103 (52): 19902-7.              

[Identification of two heterozygous mutations in the SLC26A4/PDS gene in a family with Pendred-syndrome]., Birkenhäger R, Knapp FB, Klenzner T, Aschendorff A, Schipper J., Laryngorhinootologie. December 1, 2004; 83 (12): 831-5.

Mechanisms of regulation of epithelial sodium channel by SGK1 in A6 cells., Alvarez de la Rosa D, Paunescu TG, Els WJ, Helman SI, Canessa CM., J Gen Physiol. October 1, 2004; 124 (4): 395-407.                    

Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux., Gillam MP, Sidhaye AR, Lee EJ, Rutishauser J, Stephan CW, Kopp P., J Biol Chem. March 26, 2004; 279 (13): 13004-10.

WNK4 regulates apical and basolateral Cl- flux in extrarenal epithelia., Kahle KT, Gimenez I, Hassan H, Wilson FH, Wong RD, Forbush B, Aronson PS, Lifton RP., Proc Natl Acad Sci U S A. February 17, 2004; 101 (7): 2064-9.

Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells., Yoshida A, Taniguchi S, Hisatome I, Royaux IE, Green ED, Kohn LD, Suzuki K., J Clin Endocrinol Metab. July 1, 2002; 87 (7): 3356-61.

Identification of an apical Cl(-)/HCO3(-) exchanger in the small intestine., Wang Z, Petrovic S, Mann E, Soleimani M., Am J Physiol Gastrointest Liver Physiol. March 1, 2002; 282 (3): G573-9.

Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells., Knauf F, Yang CL, Thomson RB, Mentone SA, Giebisch G, Aronson PS., Proc Natl Acad Sci U S A. July 31, 2001; 98 (16): 9425-30.

Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family., Waldegger S, Moschen I, Ramirez A, Smith RJ, Ayadi H, Lang F, Kubisch C., Genomics. February 15, 2001; 72 (1): 43-50.

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4)., Scott DA, Wang R, Kreman TM, Andrews M, McDonald JM, Bishop JR, Smith RJ, Karniski LP, Sheffield VC., Hum Mol Genet. July 1, 2000; 9 (11): 1709-15.

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange., Scott DA, Karniski LP., Am J Physiol Cell Physiol. January 1, 2000; 278 (1): C207-11.

An ion transporter involved in congenital deafness focus on "human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange"., Cuppoletti J., Am J Physiol Cell Physiol. January 1, 2000; 278 (1): C11-2.

The Pendred syndrome gene encodes a chloride-iodide transport protein., Scott DA, Wang R, Kreman TM, Sheffield VC, Karniski LP., Nat Genet. April 1, 1999; 21 (4): 440-3.

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