310 related articles for article (PubMed ID: 8840960)
1. Mutations in the human homologue of Drosophila patched (PTCH) in basal cell carcinomas and the Gorlin syndrome: different in vivo mechanisms of PTCH inactivation.
Unden AB; Holmberg E; Lundh-Rozell B; Stähle-Bäckdahl M; Zaphiropoulos PG; Toftgård R; Vorechovsky I
Cancer Res; 1996 Oct; 56(20):4562-5. PubMed ID: 8840960
[TBL] [Abstract][Full Text] [Related]
2. Somatic mutations in the human homologue of Drosophila patched in primitive neuroectodermal tumours.
Vorechovský I; Tingby O; Hartman M; Strömberg B; Nister M; Collins VP; Toftgård R
Oncogene; 1997 Jul; 15(3):361-6. PubMed ID: 9233770
[TBL] [Abstract][Full Text] [Related]
3. Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.
Wicking C; Shanley S; Smyth I; Gillies S; Negus K; Graham S; Suthers G; Haites N; Edwards M; Wainwright B; Chenevix-Trench G
Am J Hum Genet; 1997 Jan; 60(1):21-6. PubMed ID: 8981943
[TBL] [Abstract][Full Text] [Related]
4. Mutations in the human homologue of Drosophila patched in Japanese nevoid basal cell carcinoma syndrome patients.
Fujii K; Kohno Y; Sugita K; Nakamura M; Moroi Y; Urabe K; Furue M; Yamada M; Miyashita T
Hum Mutat; 2003 Apr; 21(4):451-2. PubMed ID: 12655573
[TBL] [Abstract][Full Text] [Related]
5. PTCH gene mutations in odontogenic keratocysts.
Barreto DC; Gomez RS; Bale AE; Boson WL; De Marco L
J Dent Res; 2000 Jun; 79(6):1418-22. PubMed ID: 10890722
[TBL] [Abstract][Full Text] [Related]
6. Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases.
Situm M; Levanat S; Crnic I; Pavelic B; Macan D; Grgurević J; Mubrin-Koncar M; Lipozencić J
Croat Med J; 1999 Dec; 40(4):533-8. PubMed ID: 10554356
[TBL] [Abstract][Full Text] [Related]
7. Gorlin syndrome: identification of 4 novel germ-line mutations of the human patched (PTCH) gene. Mutations in brief no. 137. Online.
Hasenpusch-Theil K; Bataille V; Laehdetie J; Obermayr F; Sampson JR; Frischauf AM
Hum Mutat; 1998; 11(6):480. PubMed ID: 10200051
[TBL] [Abstract][Full Text] [Related]
8. Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.
Minami M; Urano Y; Ishigami T; Tsuda H; Kusaka J; Arase S
J Dermatol Sci; 2001 Sep; 27(1):21-6. PubMed ID: 11457640
[TBL] [Abstract][Full Text] [Related]
9. [From gene to disease: basal cell naevus syndrome].
de Meij TG; Baars MJ; Gille JJ; Hack WW; Haasnoot K; van Hagen JM
Ned Tijdschr Geneeskd; 2005 Jan; 149(2):78-81. PubMed ID: 15688838
[TBL] [Abstract][Full Text] [Related]
10. PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
Soufir N; Gerard B; Portela M; Brice A; Liboutet M; Saiag P; Descamps V; Kerob D; Wolkenstein P; Gorin I; Lebbe C; Dupin N; Crickx B; Basset-Seguin N; Grandchamp B
Br J Cancer; 2006 Aug; 95(4):548-53. PubMed ID: 16909134
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the human homologue of the Drosophila patched gene in Caucasian and African-American nevoid basal cell carcinoma syndrome patients.
Chidambaram A; Goldstein AM; Gailani MR; Gerrard B; Bale SJ; DiGiovanna JJ; Bale AE; Dean M
Cancer Res; 1996 Oct; 56(20):4599-601. PubMed ID: 8840969
[TBL] [Abstract][Full Text] [Related]
12. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
Pastorino L; Cusano R; Nasti S; Faravelli F; Forzano F; Baldo C; Barile M; Gliori S; Muggianu M; Ghigliotti G; Lacaita MG; Lo Muzio L; Bianchi-Scarra G
Hum Mutat; 2005 Mar; 25(3):322-3. PubMed ID: 15712338
[TBL] [Abstract][Full Text] [Related]
13. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.
Boutet N; Bignon YJ; Drouin-Garraud V; Sarda P; Longy M; Lacombe D; Gorry P
J Invest Dermatol; 2003 Sep; 121(3):478-81. PubMed ID: 12925203
[TBL] [Abstract][Full Text] [Related]
14. Sporadic medulloblastomas contain PTCH mutations.
Raffel C; Jenkins RB; Frederick L; Hebrink D; Alderete B; Fults DW; James CD
Cancer Res; 1997 Mar; 57(5):842-5. PubMed ID: 9041183
[TBL] [Abstract][Full Text] [Related]
15. Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome.
Song YL; Zhang WF; Peng B; Wang CN; Wang Q; Bian Z
Tumour Biol; 2006; 27(4):175-80. PubMed ID: 16675912
[TBL] [Abstract][Full Text] [Related]
16. PTCH mutations: distribution and analyses.
Lindström E; Shimokawa T; Toftgård R; Zaphiropoulos PG
Hum Mutat; 2006 Mar; 27(3):215-9. PubMed ID: 16419085
[TBL] [Abstract][Full Text] [Related]
17. Trichoepitheliomas contain somatic mutations in the overexpressed PTCH gene: support for a gatekeeper mechanism in skin tumorigenesis.
Vorechovský I; Undén AB; Sandstedt B; Toftgård R; Ståhle-Bäckdahl M
Cancer Res; 1997 Nov; 57(21):4677-81. PubMed ID: 9354420
[TBL] [Abstract][Full Text] [Related]
18. A new germline mutation of the PTCH gene in a Japanese patient with nevoid basal cell carcinoma syndrome associated with meningioma.
Tate G; Li M; Suzuki T; Mitsuya T
Jpn J Clin Oncol; 2003 Jan; 33(1):47-50. PubMed ID: 12604725
[TBL] [Abstract][Full Text] [Related]
19. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas.
Gailani MR; Ståhle-Bäckdahl M; Leffell DJ; Glynn M; Zaphiropoulos PG; Pressman C; Undén AB; Dean M; Brash DE; Bale AE; Toftgård R
Nat Genet; 1996 Sep; 14(1):78-81. PubMed ID: 8782823
[TBL] [Abstract][Full Text] [Related]
20. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
Aszterbaum M; Rothman A; Johnson RL; Fisher M; Xie J; Bonifas JM; Zhang X; Scott MP; Epstein EH
J Invest Dermatol; 1998 Jun; 110(6):885-8. PubMed ID: 9620294
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]