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Items: 1 to 20 of 123

1.

Mutation analysis of the CYLD gene in two Chinese families with multiple familial Trichoepithelioma.

Chen M, Liu H, Fu X, Yu Y, Yu G, Liu H, Tian H, Zhou G, Zhang D, Wang G, Zhang F.

Australas J Dermatol. 2011 May;52(2):146-7. doi: 10.1111/j.1440-0960.2011.00763.x. No abstract available.

PMID:
21605102
2.

A novel missense mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.

Lv HL, Huang YJ, Zhou D, Du YF, Zhao XY, Liang YH, Quan C, Zhang H, Zhou FS, Gao M, Zhou L, Yang S, Zhang XJ.

J Dermatol Sci. 2008 May;50(2):143-6. doi: 10.1016/j.jdermsci.2007.11.012. Epub 2008 Feb 1. No abstract available.

PMID:
18242958
3.

A novel mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.

Qian F, Zhai Y, Yuan X, Li P, Wang W, Ding Y, Wang J, Wu B, Cheng H, Sun L, Yang S, Zhang X.

Australas J Dermatol. 2014 Aug;55(3):232-4. doi: 10.1111/ajd.12210. No abstract available.

PMID:
25117167
4.

Novel and recurrent germline and somatic mutations in a cohort of 67 patients from 48 families with Brooke-Spiegler syndrome including the phenotypic variant of multiple familial trichoepitheliomas and correlation with the histopathologic findings in 379 biopsy specimens.

Grossmann P, Vanecek T, Steiner P, Kacerovska D, Spagnolo DV, Cribier B, Rose C, Vazmitel M, Carlson JA, Emberger M, Martinek P, Pearce RL, Pearn J, Michal M, Kazakov DV.

Am J Dermatopathol. 2013 Feb;35(1):34-44. doi: 10.1097/DAD.0b013e31824e7658.

PMID:
23249834
5.

A recurrent R936X mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.

Zhang QG, Liang YH.

Indian J Dermatol Venereol Leprol. 2015 Mar-Apr;81(2):192-4. doi: 10.4103/0378-6323.152298. No abstract available.

6.

Basal cell carcinoma arising in association with trichoepithelioma in a case of Brooke-Spiegler syndrome with a novel genetic mutation in CYLD.

Melly L, Lawton G, Rajan N.

J Cutan Pathol. 2012 Oct;39(10):977-8. doi: 10.1111/j.1600-0560.2012.01952.x. Epub 2012 Aug 9. No abstract available.

PMID:
22882113
7.

Three mutations of CYLD gene in Chinese families with multiple familial trichoepithelioma.

Lv H, Li C, Li Y, Tang J, Zhang Z.

Am J Dermatopathol. 2014 Jul;36(7):605-7. doi: 10.1097/DAD.0b013e318297f825. No abstract available.

PMID:
24247569
8.

Novel substitution and frameshift mutations of CYLD in two Chinese families with multiple familial trichoepithelioma.

Liang YH, Sun CS, Ye XY, Zhang W, Yang S, Zhang XJ.

Br J Dermatol. 2008 May;158(5):1156-8. doi: 10.1111/j.1365-2133.2008.08491.x. Epub 2008 Mar 20. No abstract available.

PMID:
18363762
9.

Mild phenotype of familial cylindromatosis associated with an R758X nonsense mutation in the CYLD tumour suppressor gene.

Oiso N, Mizuno N, Fukai K, Nakagawa K, Ishii M.

Br J Dermatol. 2004 Nov;151(5):1084-6.

PMID:
15541090
10.

A novel frameshift mutation in the cylindromatosis (CYLD) gene in a Chinese family with multiple familial trichoepithelioma.

Wu JW, Xiao SX, Huo J, An JG, Ren JW.

Arch Dermatol Res. 2014 Nov;306(9):857-60. doi: 10.1007/s00403-014-1499-x. Epub 2014 Sep 19.

PMID:
25234269
11.

CYLD mutation causes multiple familial trichoepithelioma in three Chinese families.

Zheng G, Hu L, Huang W, Chen K, Zhang X, Yang S, Sun J, Jiang Y, Luo G, Kong X.

Hum Mutat. 2004 Apr;23(4):400.

PMID:
15024746
12.

Germline mutation analysis in the CYLD gene in Chinese patients with multiple trichoepitheliomas.

Li ZL, Guan HH, Xiao XM, Hui Y, Jia WX, Yu RX, Chen H, Li CR.

Genet Mol Res. 2014 Nov 14;13(4):9650-5. doi: 10.4238/2014.November.14.10.

13.

Trichoepithelioma.

Johnson H, Robles M, Kamino H, Walters RF, Lee A, Sanchez M.

Dermatol Online J. 2008 Oct 15;14(10):5.

PMID:
19061604
14.

A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma and no CYLD protein expression in the tumour tissue.

Zuo YG, Xu Y, Wang B, Liu YH, Qu T, Fang K, Ho MG.

Br J Dermatol. 2007 Oct;157(4):818-21. Epub 2007 Jul 27. No abstract available.

PMID:
17662085
15.

Multiple trichoepitheliomas associated with a novel heterozygous mutation in the CYLD gene as an adjunct to the histopathological diagnosis.

Reuven B, Margarita I, Dov H, Ziad K.

Am J Dermatopathol. 2013 Jun;35(4):445-7. doi: 10.1097/DAD.0b013e31827132af.

PMID:
23694822
16.

A novel missense mutation of CYLD gene in a Chinese family with multiple familial trichoepithelioma.

Wang FX, Yang LJ, Li M, Zhang SL, Zhu XH.

Arch Dermatol Res. 2010 Jan;302(1):67-70. doi: 10.1007/s00403-009-1003-1. Epub 2009 Nov 13.

PMID:
19911186
17.

Large germline deletions of the CYLD gene in patients with Brooke-Spiegler syndrome and multiple familial trichoepithelioma.

Vanecek T, Halbhuber Z, Kacerovska D, Martinek P, Sedivcova M, Carr RA, Slouka D, Michal M, Kazakov DV.

Am J Dermatopathol. 2014 Nov;36(11):868-74. doi: 10.1097/DAD.0000000000000068.

PMID:
25347032
18.

A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome.

Bessis D, Giraud S, Richard S.

Br J Dermatol. 2006 Nov;155(5):1067-9. No abstract available.

PMID:
17034545
19.

Two novel CYLD gene mutations in Chinese families with trichoepithelioma and a literature review of 16 families with trichoepithelioma reported in China.

Liang YH, Gao M, Sun LD, Liu LJ, Cui Y, Yang S, Fan X, Wang J, Xiao FL, Zhang XJ.

Br J Dermatol. 2005 Dec;153(6):1213-5. Review. No abstract available.

PMID:
16307661
20.

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.

Nagy N, Rajan N, Farkas K, Kinyó A, Kemény L, Széll M.

Acta Derm Venereol. 2013 Nov;93(6):743-5. doi: 10.2340/00015555-1590. No abstract available.

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