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Items: 1 to 20 of 90

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Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis.

Ramoz N, Rueda LA, Bouadjar B, Montoya LS, Orth G, Favre M.

Nat Genet. 2002 Dec;32(4):579-81.

PMID:
12426567
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A homozygous nonsense mutation in the EVER2 gene leads to epidermodysplasia verruciformis.

Sun XK, Chen JF, Xu AE.

Clin Exp Dermatol. 2005 Sep;30(5):573-4.

PMID:
16045695
6.

Epidermodysplasia verruciformis in a HIV-positive patient homozygous for the c917A-->T polymorphism in the TMC8/EVER2 gene.

Hohenstein E, Rady PL, Hergersberg M, Huber AR, Tyring SK, Bregenzer T, Streit M, Itin P.

Dermatology. 2009;218(2):114-8. doi: 10.1159/000174084.

PMID:
19005244
7.
8.

Novel mutations of EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis.

Tate G, Suzuki T, Kishimoto K, Mitsuya T.

J Hum Genet. 2004;49(4):223-5.

PMID:
15042430
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Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.

Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF Jr, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ.

Nat Genet. 2002 Mar;30(3):277-84.

PMID:
11850618
12.

Autosomal dominant epidermodysplasia verruciformis lacking a known EVER1 or EVER2 mutation.

McDermott DF, Gammon B, Snijders PJ, Mbata I, Phifer B, Howland Hartley A, Lee CC, Murphy PM, Hwang ST.

Pediatr Dermatol. 2009 May-Jun;26(3):306-10. doi: 10.1111/j.1525-1470.2008.00853.x.

14.

Epidermodysplasia verruciformis.

Burger B, Itin PH.

Curr Probl Dermatol. 2014;45:123-31. doi: 10.1159/000356068. Review.

PMID:
24643182
15.

Novel homozygous nonsense TMC8 mutation detected in patients with epidermodysplasia verruciformis from a Brazilian family.

Rady PL, De Oliveira WR, He Q, Festa C, Rivitti EA, Tucker SB, Tyring SK.

Br J Dermatol. 2007 Oct;157(4):831-3. No abstract available.

PMID:
17711520
16.

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

Manji SS, Miller KA, Williams LH, Dahl HH.

Am J Pathol. 2012 Apr;180(4):1560-9. doi: 10.1016/j.ajpath.2011.12.034.

PMID:
22330676
17.

TMC8 (EVER2) attenuates intracellular signaling by Zn2+ and Ca2+ and suppresses activation of Cl- currents.

Sirianant L, Ousingsawat J, Tian Y, Schreiber R, Kunzelmann K.

Cell Signal. 2014 Dec;26(12):2826-33. doi: 10.1016/j.cellsig.2014.09.001.

PMID:
25220380
18.

A novel homozygous mutation of the EVER1/TMC6 gene in a Japanese patient with epidermodysplasia verruciformis.

Aochi S, Nakanishi G, Suzuki N, Setsu N, Suzuki D, Aya K, Iwatsuki K.

Br J Dermatol. 2007 Dec;157(6):1265-6. No abstract available.

PMID:
17916203
19.

Molecular cloning and characterization of the mouse Acdp gene family.

Wang CY, Yang P, Shi JD, Purohit S, Guo D, An H, Gu JG, Ling J, Dong Z, She JX.

BMC Genomics. 2004 Jan 15;5(1):7.

20.

Four mutations in Epidermodysplasia verruciformis 1 (EVER1) gene are not contributors to susceptibility in RRP.

Donfack J, Buchinsky FJ, Derkay CS, Steinberg BM, Choi SS, Conley SF, Meyer CM 3rd, McClay JE, Campisi P, Hu FZ, Preston RA, Abramson AL, Ehrlich GD, Post JC.

Int J Pediatr Otorhinolaryngol. 2006 Jul;70(7):1235-40.

PMID:
16487602
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