These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

73 related articles for article (PubMed ID: 17554363)

  • 1. 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. PubMed ID: 17554363
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes.
    Richards FM; Goudie DR; Cooper WN; Jene Q; Barroso I; Wicking C; Wainwright BJ; Ferguson-Smith MA
    Hum Genet; 1997 Dec; 101(3):317-22. PubMed ID: 9439661
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The "sins" of the fathers: self-healing squamous epithelioma in Scotland.
    Bale SJ
    J Cutan Med Surg; 1999 Apr; 3(4):207-10. PubMed ID: 10366398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 24747516
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 18176752
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 25(5):806-12. PubMed ID: 16170343
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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; 174(17):1149-51. PubMed ID: 22533930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Multiple Self-Healing Squamous Epithelioma (MSSE): A Digenic Trait Associated with Loss of Function Mutations in
    Goudie D
    Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33256177
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple self-healing squamous epithelioma.
    Ferguson-Smith MA; Wallace DC; James ZH; Renwick JH
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):157-63. PubMed ID: 5173258
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 43(4):365-9. PubMed ID: 21358634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestry.
    Lang J; Hayward N; Goldgar D; Tsao H; Hogg D; Palmer J; Stark M; Tobias ES; MacKie R
    Genes Chromosomes Cancer; 2007 Mar; 46(3):277-87. PubMed ID: 17171691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata.
    Chuang GS; Martinez-Mir A; Geyer A; Engler DE; Glaser B; Cserhalmi-Friedman PB; Gordon D; Horev L; Lukash B; Herman E; Cid MP; Brenner S; Landau M; Sprecher E; Garcia Muret MP; Christiano AM; Zlotogorski A
    J Am Acad Dermatol; 2005 Mar; 52(3 Pt 1):410-6. PubMed ID: 15761418
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect.
    Garritano S; Gemignani F; Palmero EI; Olivier M; Martel-Planche G; Le Calvez-Kelm F; Brugiéres L; Vargas FR; Brentani RR; Ashton-Prolla P; Landi S; Tavtigian SV; Hainaut P; Achatz MI
    Hum Mutat; 2010 Feb; 31(2):143-50. PubMed ID: 19877175
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Desmoglein in multiple self-healing squamous epithelioma of Ferguson-Smith--comparison of staining patterns with actinic keratoacanthoma and squamous cell carcinoma of the skin.
    Krunic AL; Garrod DR; Hunter JA; Clark RE
    Arch Dermatol Res; 1998 Jun; 290(6):319-24. PubMed ID: 9705163
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.
    Goudie DR; Yuille MA; Leversha MA; Furlong RA; Carter NP; Lush MJ; Affara NA; Ferguson-Smith MA
    Nat Genet; 1993 Feb; 3(2):165-9. PubMed ID: 8499949
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MYOC gene mutations in Spanish patients with autosomal dominant primary open-angle glaucoma: a founder effect in southeast Spain.
    Campos-Mollo E; Sánchez-Sánchez F; López-Garrido MP; López-Sánchez E; López-Martínez F; Escribano J
    Mol Vis; 2007 Sep; 13():1666-73. PubMed ID: 17893668
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families.
    Oros KK; Leblanc G; Arcand SL; Shen Z; Perret C; Mes-Masson AM; Foulkes WD; Ghadirian P; Provencher D; Tonin PN
    BMC Med Genet; 2006 Mar; 7():23. PubMed ID: 16539696
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 23358096
    [No Abstract]   [Full Text] [Related]  

  • 19. Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping.
    Kibar Z; Dubé MP; Powell J; McCuaïg C; Hayflick SJ; Zonana J; Hovnanian A; Radhakrishna U; Antonarakis SE; Benohanian A; Sheeran AD; Stephan ML; Gosselin R; Kelsell DP; Christianson AL; Fraser FC; Der Kaloustian VM; Rouleau GA
    Eur J Hum Genet; 2000 May; 8(5):372-80. PubMed ID: 10854098
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.
    Cavaco BM; Guerra L; Bradley KJ; Carvalho D; Harding B; Oliveira A; Santos MA; Sobrinho LG; Thakker RV; Leite V
    J Clin Endocrinol Metab; 2004 Apr; 89(4):1747-52. PubMed ID: 15070940
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.