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Items: 1 to 20 of 79

1.

Digenic/multilocus aetiology of multiple self-healing squamous epithelioma (Ferguson-Smith disease): TGFBR1 and a second linked locus.

Ferguson-Smith MA, Goudie DR.

Int J Biochem Cell Biol. 2014 Aug;53:520-5. doi: 10.1016/j.biocel.2014.04.007. Epub 2014 Apr 18. Review.

PMID:
24747516
2.

Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1.

Goudie DR, D'Alessandro M, Merriman B, Lee H, Szeverényi I, Avery S, O'Connor BD, Nelson SF, Coats SE, Stewart A, Christie L, Pichert G, Friedel J, Hayes I, Burrows N, Whittaker S, Gerdes AM, Broesby-Olsen S, Ferguson-Smith MA, Verma C, Lunny DP, Reversade B, Lane EB.

Nat Genet. 2011 Feb 27;43(4):365-9. doi: 10.1038/ng.780.

PMID:
21358634
3.

[Multiple self-healing squamous epithelioma is an inherited self-healing skin cancer condition].

Broesby-Olsen S, Frandsen SK, Thomassen M, Brandrup F, Gerdes AM.

Ugeskr Laeger. 2012 Apr 23;174(17):1149-51. Danish.

PMID:
22533930
4.

Multiple self-healing squamous epithelioma (MSSE): rare variants in an adjacent region of chromosome 9q22.3 to known TGFBR1 mutations suggest a digenic or multilocus etiology.

Kang HC, Quigley DA, Kim IJ, Wakabayashi Y, Ferguson-Smith MA, D'Alessandro M, Birgitte Lane E, Akhurst RJ, Goudie DR, Balmain A.

J Invest Dermatol. 2013 Jul;133(7):1907-10. doi: 10.1038/jid.2013.45. Epub 2013 Jan 28. No abstract available.

5.

A puzzling case: SCC or not?

Simpkin S, Lamont D, Yung A.

Australas J Dermatol. 2013 Aug;54(3):e74-7. doi: 10.1111/j.1440-0960.2012.00919.x. Epub 2012 Jul 3.

PMID:
22758773
6.

[Multiple self-healing squamous epithelioma, or Ferguson-Smith disease: demonstration of mutations in the TGFβ-receptor].

Dereure O.

Ann Dermatol Venereol. 2011 Nov;138(11):790-1. doi: 10.1016/j.annder.2011.09.005. Epub 2011 Oct 5. French. No abstract available.

PMID:
22078045
7.

The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosity.

Bose S, Morgan LJ, Booth DR, Goudie DR, Ferguson-Smith MA, Richards FM.

Oncogene. 2006 Feb 2;25(5):806-12.

PMID:
16170343
8.

Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?

D'Alessandro M, Coats SE, Morley SM, Mackintosh L, Tessari G, Turco A, Gerdes AM, Pichert G, Whittaker S, Brandrup F, Broesby-Olsen S, Gomez-Lira M, Girolomoni G, Maize JC, Feldman RJ, Kato N, Koga Y, Ferguson-Smith MA, Goudie DR, Lane EB.

J Invest Dermatol. 2007 Oct;127(10):2336-44. Epub 2007 Jun 7.

9.

Multiple self-healing squamous epithelioma of Ferguson-Smith: observations in a Danish family covering four generations.

Broesby-Olsen S, Bygum A, Gerdes AM, Brandrup F.

Acta Derm Venereol. 2008;88(1):52-6. doi: 10.2340/00015555-0359.

10.
11.

The "sins" of the fathers: self-healing squamous epithelioma in Scotland.

Bale SJ.

J Cutan Med Surg. 1999 Apr;3(4):207-10.

PMID:
10366398
13.

[Familial epithelioma of Ferguson-Smith about two familial cases].

Schnitzler L, Schubert B, Verret JL, Emeriau M, Brunet A.

Ann Dermatol Venereol. 1977 Mar;104(3):206-16. French.

PMID:
869463
14.

Severe exacerbation of multiple self-healing squamous epithelioma (Ferguson-Smith disease) with radiotherapy, which was successfully treated with acitretin.

Robertson SJ, Bashir SJ, Pichert G, Robson A, Whittaker S.

Clin Exp Dermatol. 2010 Jun;35(4):e100-2. doi: 10.1111/j.1365-2230.2009.03668.x. Epub 2009 Oct 23.

PMID:
19874360
15.

TGFBR1 intralocus epistatic interaction as a risk factor for colorectal cancer.

Martinez-Canto A, Castillejo A, Mata-Balaguer T, Castillejo MI, Hernandez-Illan E, Irles E, Barbera VM, Egoavil C, Guarinos C, Alenda C, Ochoa E, Lazaro R, Fajardo S, Lacueva J, Calpena R, Soto JL.

PLoS One. 2012;7(1):e30812. doi: 10.1371/journal.pone.0030812. Epub 2012 Jan 23.

16.

Is TGFBR1*6A a susceptibility allele for nonsyndromic familial colorectal neoplasia?

Daley D, Morgan W, Lewis S, Willis J, Elston RC, Markowitz SD, Wiesner GL.

Cancer Epidemiol Biomarkers Prev. 2007 May;16(5):892-4.

17.

A haplotype of TGFBR1 is predominantly found in non-small cell lung cancer patients displaying TGFBR1 allelic-specific expression.

Sun J, Lei Z, Liu RY, Lu Y, Zhuang Z, Jiang X, Qian Q, Liu Z, Zhao J, Zhang HT.

Oncol Rep. 2011 Mar;25(3):685-91. doi: 10.3892/or.2011.1135. Epub 2011 Jan 10.

PMID:
21225232
18.

The chromosome 9q genes TGFBR1, TSC1, and ZNF189 are rarely mutated in bladder cancer.

van Tilborg AA, de Vries A, Zwarthoff EC.

J Pathol. 2001 May;194(1):76-80.

PMID:
11329144
19.

Skin tumors induced by sorafenib; paradoxic RAS-RAF pathway activation and oncogenic mutations of HRAS, TP53, and TGFBR1.

Arnault JP, Mateus C, Escudier B, Tomasic G, Wechsler J, Hollville E, Soria JC, Malka D, Sarasin A, Larcher M, André J, Kamsu-Kom N, Boussemart L, Lacroix L, Spatz A, Eggermont AM, Druillennec S, Vagner S, Eychène A, Dumaz N, Robert C.

Clin Cancer Res. 2012 Jan 1;18(1):263-72. doi: 10.1158/1078-0432.CCR-11-1344. Epub 2011 Nov 17.

20.

Losses of heterozygosity on chromosomes 17p and 9p/18q may play important roles in early and advanced phases of gallbladder carcinogenesis.

Hidaka E, Yanagisawa A, Sakai Y, Seki M, Kitagawa T, Setoguchi T, Kato Y.

J Cancer Res Clin Oncol. 1999 Aug-Sep;125(8-9):439-43.

PMID:
10480335

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