157 related articles for article (PubMed ID: 10982183)
1. Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13.
Takahashi M; Rapley E; Biggs PJ; Lakhani SR; Cooke D; Hansen J; Blair E; Hofmann B; Siebert R; Turner G; Evans DG; Schrander-Stumpel C; Beemer FA; van Vloten WA; Breuning MH; van den Ouweland A; Halley D; Delpech B; Cleveland M; Leigh I; Chapman P; Burn J; Hohl D; Görög JP; Seal S; Mangion J
Hum Genet; 2000 Jan; 106(1):58-65. PubMed ID: 10982183
[TBL] [Abstract][Full Text] [Related]
2. Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene.
Biggs PJ; Wooster R; Ford D; Chapman P; Mangion J; Quirk Y; Easton DF; Burn J; Stratton MR
Nat Genet; 1995 Dec; 11(4):441-3. PubMed ID: 7493027
[TBL] [Abstract][Full Text] [Related]
3. The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas.
Biggs PJ; Chapman P; Lakhani SR; Burn J; Stratton MR
Oncogene; 1996 Mar; 12(6):1375-7. PubMed ID: 8649842
[TBL] [Abstract][Full Text] [Related]
4. A new hereditary cylindromatosis family associated with CYLD1 on chromosome 16.
Thomson SA; Rasmussen SA; Zhang J; Wallace MR
Hum Genet; 1999; 105(1-2):171-3. PubMed ID: 10480375
[TBL] [Abstract][Full Text] [Related]
5. Multiple familial trichoepithelioma caused by mutations in the cylindromatosis tumor suppressor gene.
Salhi A; Bornholdt D; Oeffner F; Malik S; Heid E; Happle R; Grzeschik KH
Cancer Res; 2004 Aug; 64(15):5113-7. PubMed ID: 15289313
[TBL] [Abstract][Full Text] [Related]
6. Familial cylindromatosis mimicking tuberous sclerosis complex and confirmation of the cylindromatosis locus, CYLD1, in a large family.
Verhoef S; Schrander-Stumpel CT; Vuzevski VD; Tempelaars A; Jansen LA; Malfeyt GA; Ceelen TL; Lindhout D; Halley DJ; van den Ouweland AM
J Med Genet; 1998 Oct; 35(10):841-5. PubMed ID: 9783709
[TBL] [Abstract][Full Text] [Related]
7. Fine-mapping chromosome 20 in 230 systemic lupus erythematosus sib pair and multiplex families: evidence for genetic epistasis with chromosome 16q12.
Gaffney PM; Langefeld CD; Graham RR; Ortmann WA; Williams AH; Rodine PR; Moser KL; Behrens TW
Am J Hum Genet; 2006 May; 78(5):747-758. PubMed ID: 16642431
[TBL] [Abstract][Full Text] [Related]
8. Identification of the familial cylindromatosis tumour-suppressor gene.
Bignell GR; Warren W; Seal S; Takahashi M; Rapley E; Barfoot R; Green H; Brown C; Biggs PJ; Lakhani SR; Jones C; Hansen J; Blair E; Hofmann B; Siebert R; Turner G; Evans DG; Schrander-Stumpel C; Beemer FA; van Den Ouweland A; Halley D; Delpech B; Cleveland MG; Leigh I; Leisti J; Rasmussen S
Nat Genet; 2000 Jun; 25(2):160-5. PubMed ID: 10835629
[TBL] [Abstract][Full Text] [Related]
9. Loss of heterozygosity at cylindromatosis gene locus, CYLD, in sporadic skin adnexal tumours.
Leonard N; Chaggar R; Jones C; Takahashi M; Nikitopoulou A; Lakhani SR
J Clin Pathol; 2001 Sep; 54(9):689-92. PubMed ID: 11533075
[TBL] [Abstract][Full Text] [Related]
10. Identification of a recurrent mutation in the CYLD gene in Brooke-Spiegler syndrome.
Scheinfeld N; Hu G; Gill M; Austin C; Celebi JT
Clin Exp Dermatol; 2003 Sep; 28(5):539-41. PubMed ID: 12950348
[TBL] [Abstract][Full Text] [Related]
11. Molecular analysis of chromosome 16q regions in dermal analogue tumors of salivary glands: a genetic link to dermal cylindroma?
Choi HR; Batsakis JG; Callender DL; Prieto VG; Luna MA; El-Naggar AK
Am J Surg Pathol; 2002 Jun; 26(6):778-83. PubMed ID: 12023583
[TBL] [Abstract][Full Text] [Related]
12. Five new CYLD mutations in skin appendage tumors and evidence that aspartic acid 681 in CYLD is essential for deubiquitinase activity.
Almeida S; Maillard C; Itin P; Hohl D; Huber M
J Invest Dermatol; 2008 Mar; 128(3):587-93. PubMed ID: 17851586
[TBL] [Abstract][Full Text] [Related]
13. A novel missense mutation in CYLD in a family with Brooke-Spiegler syndrome.
Hu G; Onder M; Gill M; Aksakal B; Oztas M; Gürer MA; Celebi JT
J Invest Dermatol; 2003 Oct; 121(4):732-4. PubMed ID: 14632188
[TBL] [Abstract][Full Text] [Related]
14. Diverse phenotype of Brooke-Spiegler syndrome associated with a nonsense mutation in the CYLD tumor suppressor gene.
Zhang G; Huang Y; Yan K; Li W; Fan X; Liang Y; Sun L; Li H; Zhang S; Gao M; Du W; Yang S; Liu J; Zhang X
Exp Dermatol; 2006 Dec; 15(12):966-70. PubMed ID: 17083363
[TBL] [Abstract][Full Text] [Related]
15. Phenotype variability in tumor disorders of the skin appendages associated with mutations in the CYLD gene.
Parren LJMT; Giehl K; van Geel M; Frank J
Arch Dermatol Res; 2018 Sep; 310(7):599-606. PubMed ID: 29974194
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 15024746
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 15541090
[TBL] [Abstract][Full Text] [Related]
18. Paroxysmal kinesigenic choreoathetosis: evidence of linkage to the pericentromeric region of chromosome 16 in four Chinese families.
Wang X; Sun W; Zhu X; Li L; Du T; Mao W; Wu X; Wei H; Zhu S; Sun Y; Liu Y; Niu N; Wang Y; Liu Y
Eur J Neurol; 2010 Jun; 17(6):800-7. PubMed ID: 20158512
[TBL] [Abstract][Full Text] [Related]
19. Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.
Rajan N; Langtry JA; Ashworth A; Roberts C; Chapman P; Burn J; Trainer AH
Arch Dermatol; 2009 Nov; 145(11):1277-84. PubMed ID: 19917957
[TBL] [Abstract][Full Text] [Related]
20. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
Winkelmann J; Lichtner P; Pütz B; Trenkwalder C; Hauk S; Meitinger T; Strom T; Muller-Myhsok B
Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]