158 related articles for article (PubMed ID: 19213655)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome.
Ponti G; Pollio A; Mignogna MD; Pellacani G; Pastorino L; Bianchi-Scarrà G; Di Gregorio C; Magnoni C; Azzoni P; Greco M; Seidenari S
Cancer Genet; 2012 Apr; 205(4):177-81. PubMed ID: 22559979
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Molecular evidence of type 2 mosaicism in Gorlin syndrome.
Torrelo A; Hernández-Martín A; Bueno E; Colmenero I; Rivera I; Requena L; Happle R; González-Sarmiento R
Br J Dermatol; 2013 Dec; 169(6):1342-5. PubMed ID: 23746055
[TBL] [Abstract][Full Text] [Related]
10. The dermoscopy of Gorlin syndrome: pursuit of the pits revisited.
Jarrett R; Walker L; Bowling J
Arch Dermatol; 2010 May; 146(5):582. PubMed ID: 20479325
[No Abstract] [Full Text] [Related]
11. DHPLC analysis of patients with Nevoid Basal Cell Carcinoma Syndrome reveals novel PTCH missense mutations in the sterol-sensing domain.
Marsh A; Wicking C; Wainwright B; Chenevix-Trench G
Hum Mutat; 2005 Sep; 26(3):283. PubMed ID: 16088933
[TBL] [Abstract][Full Text] [Related]
12. Pediatric nevoid basal cell carcinoma syndrome.
Pilkington S; McKinley LH; Miller RA
Cutis; 2017 Dec; 100(6):423-426. PubMed ID: 29360891
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome.
Le Brun Keris Y; Jouk PS; Saada-Sebag G; Roux JJ; Mattei B; Bagait L; Paoloni-Giacobino A; Grandchamp B; Soufir N; Lespinasse J
Eur J Med Genet; 2008; 51(5):472-8. PubMed ID: 18539553
[TBL] [Abstract][Full Text] [Related]
16. Multiple nevoid basal cell carcinoma syndrome associated with congenital orbital teratoma, caused by a PTCH1 frameshift mutation.
Rodrigues AL; Carvalho A; Cabral R; Carneiro V; Gilardi P; Duarte CP; Puente-Prieto J; Santos P; Mota-Vieira L
Genet Mol Res; 2014 Jul; 13(3):5654-63. PubMed ID: 25117323
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome.
Matsuzawa N; Nagao T; Shimozato K; Niikawa N; Yoshiura KI
J Clin Pathol; 2006 Oct; 59(10):1084-6. PubMed ID: 17021131
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
