151 related articles for article (PubMed ID: 18068337)
1. A novel PTCH1 mutation in a patient of nevoid basal cell carcinoma syndrome.
Honma M; Ohishi Y; Uehara J; Ibe M; Kinouchi M; Ishida-Yamamoto A; Iizuka H
J Dermatol Sci; 2008 Apr; 50(1):73-5. PubMed ID: 18068337
[No Abstract] [Full Text] [Related]
2. A novel missense mutation in the PTCH1 gene in a premature case of nevoid basal cell carcinoma syndrome.
Nakamura M; Tokura Y
Eur J Dermatol; 2009; 19(3):262-3. PubMed ID: 19213655
[No Abstract] [Full Text] [Related]
3. Novel mutation in the PTCH1 gene in a patient with Gorlin syndrome with prominent clinical features.
Valdivielso-Ramos M; Solera J; Mauleon C; Hernanz JM; Amiñoso C; Galiano S; De la Cueva P
Clin Exp Dermatol; 2014 Apr; 39(3):406-7. PubMed ID: 24635088
[No Abstract] [Full Text] [Related]
4. Variable expression of naevoid basal cell carcinoma syndrome in a family with a novel mutation in the PTCH1 gene.
Alonso-González J; Gutiérrez-González E; Fernández-Redondo V; Vega-Gliemmo A; Toribio J
Clin Exp Dermatol; 2012 Apr; 37(3):311-3. PubMed ID: 22007994
[No Abstract] [Full Text] [Related]
5. A novel germ-line mutation of PTCH1 gene in a Japanese family of nevoid basal cell carcinoma syndrome: are the palmoplantar pits associated with true basal cell carcinoma?
Otsubo S; Honma M; Asano K; Takahashi H; Iizuka H
J Dermatol Sci; 2008 Aug; 51(2):144-6. PubMed ID: 18436435
[No Abstract] [Full Text] [Related]
6. Entire PTCH1 deletion is a common event in point mutation-negative cases with nevoid basal cell carcinoma syndrome in Japan.
Nagao K; Fujii K; Saito K; Sugita K; Endo M; Motojima T; Hatsuse H; Miyashita T
Clin Genet; 2011 Feb; 79(2):196-8. PubMed ID: 21210781
[No Abstract] [Full Text] [Related]
7. Coincident two mutations and one single nucleotide polymorphism of the PTCH1 gene in a family with naevoid basal cell carcinoma syndrome.
Abe S; Kabashima K; Sakabe J; Shimauchi T; Yan Z; Okamoto T; Tokura Y
Acta Derm Venereol; 2008; 88(6):635-6. PubMed ID: 19002359
[No Abstract] [Full Text] [Related]
8. Novel PTCH1 Mutation in a Young Child With Gorlin Syndrome and Medulloblastoma.
Gloude NJ; Yoon JM; Crawford JR
Pediatr Blood Cancer; 2016 Jun; 63(6):1128-9. PubMed ID: 26840755
[No Abstract] [Full Text] [Related]
9. Biallelic disruption of the PTCH1 gene in multiple basal cell carcinomas in Japanese patients with nevoid basal cell carcinoma syndrome.
Tate G; Kishimoto K; Mitsuya T
Acta Med Okayama; 2014; 68(3):163-70. PubMed ID: 24942795
[TBL] [Abstract][Full Text] [Related]
10. Early-onset acral basal cell carcinomas in Gorlin syndrome.
Torrelo A; Vicente A; Navarro L; Planaguma M; Bueno E; González-Sarmiento R; Hernández-Martín A; Noguera-Morel L; Requena L; Colmenero I; Parareda A; González-Enseñat MA; Happle R
Br J Dermatol; 2014 Nov; 171(5):1227-9. PubMed ID: 24837096
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].
Mazzuoccolo LD; Martínez MF; Muchnik C; Azurmendi PJ; Stengel F
Medicina (B Aires); 2014; 74(4):307-10. PubMed ID: 25188659
[TBL] [Abstract][Full Text] [Related]
14. New mutation of the PTCH gene in nevoid basal-cell carcinoma syndrome with West syndrome.
Tachi N; Fujii K; Kimura M; Seki K; Hirakai M; Miyashita T
Pediatr Neurol; 2007 Nov; 37(5):363-5. PubMed ID: 17950424
[TBL] [Abstract][Full Text] [Related]
15. Novel patched 1 mutations in patients with nevoid basal cell carcinoma syndrome--case report.
Škodrić-Trifunović V; Stjepanović M; Savić Ž; Ilić M; Kavečan I; Jovanović Privrodski J; Spasovski V; Stojiljković M; Pavlović S
Croat Med J; 2015 Feb; 56(1):63-7. PubMed ID: 25727044
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.
Ponti G; Bertazzoni G; Pastorino L; Monari E; Cuoghi A; Bergamini S; Bellei E; Benassi L; Azzoni P; Petrachi T; Magnoni C; Pellacani G; Loschi P; Pollio A; Witkowski AM; Tomasi A
Biomed Res Int; 2013; 2013():794028. PubMed ID: 24369017
[TBL] [Abstract][Full Text] [Related]
18. Palmar pits associated with the nevoid basal cell carcinoma syndrome.
North JP; McCalmont TH; LeBoit P
J Cutan Pathol; 2012 Aug; 39(8):735-8. PubMed ID: 22845656
[No Abstract] [Full Text] [Related]
19. PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.
Santos DC; Zaphiropoulos PG; Neto CF; Pimentel ER; Sanches JA; Ruiz IR
Int J Dermatol; 2011 Jul; 50(7):838-43. PubMed ID: 21699520
[TBL] [Abstract][Full Text] [Related]
20. Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene.
Kitsiou-Tzeli S; Willems P; Kosmadaki M; Leze E; Vrettou C; Kanavakis E; Katsarou A
J Dermatol; 2011 Dec; 38(12):1205-8. PubMed ID: 21950490
[No Abstract] [Full Text] [Related]
[Next] [New Search]