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Items: 1 to 20 of 90

1.
2.

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. Epub 2002 Nov 11.

PMID:
12426567
3.
4.

TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins.

Keresztes G, Mutai H, Heller S.

BMC Genomics. 2003 Jun 17;4(1):24. Epub 2003 Jun 17.

5.

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. Epub 2008 Nov 13.

PMID:
19005244
7.

Identification of a novel mutation and a genetic polymorphism of EVER1 gene in two families with epidermodysplasia verruciformis.

Zuo YG, Ma D, Zhang Y, Qiao J, Wang B.

J Dermatol Sci. 2006 Dec;44(3):153-9. Epub 2006 Sep 27.

PMID:
17008061
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. Epub 2004 Mar 23.

PMID:
15042430
9.

Genetics of epidermodysplasia verruciformis: Insights into host defense against papillomaviruses.

Orth G.

Semin Immunol. 2006 Dec;18(6):362-74. Epub 2006 Oct 2. Review.

PMID:
17011789
10.
11.

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. Epub 2002 Feb 19.

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. Epub 2014 Mar 17. 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. Epub 2007 Aug 17. 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. Epub 2012 Feb 11.

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. Epub 2014 Sep 15.

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. Epub 2007 Oct 4. 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. Epub 2006 Feb 17.

PMID:
16487602

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