143 related articles for article (PubMed ID: 18436435)
1. 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]
2. Germline PTCH1 mutations in Japanese basal cell nevus syndrome patients.
Takahashi C; Kanazawa N; Yoshikawa Y; Yoshikawa R; Saitoh Y; Chiyo H; Tanizawa T; Hashimoto-Tamaoki T; Nakano Y
J Hum Genet; 2009 Jul; 54(7):403-8. PubMed ID: 19557015
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. PTCH germline mutations in Chinese nevoid basal cell carcinoma syndrome patients.
Li TJ; Yuan JW; Gu XM; Sun LS; Zhao HS
Oral Dis; 2008 Mar; 14(2):174-9. PubMed ID: 18302678
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identification of a novel mutation in the PTCH gene in a Korean family with naevoid basal cell carcinoma syndrome.
Lee YW; Roh BH; Ki CS; Park YL; Shin HB; Lee YK; Choi TY; Whang KU
Clin Exp Dermatol; 2007 Mar; 32(2):202-3. PubMed ID: 16780502
[No Abstract] [Full Text] [Related]
11. 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]
12. Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.
Tanioka M; Takahashi K; Kawabata T; Kosugi S; Murakami K; Miyachi Y; Nishigori C; Iizuka T
Arch Dermatol Res; 2005 Jan; 296(7):303-8. PubMed ID: 15565302
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Splicing aberration in naevoid basal cell carcinoma syndrome.
Ishitsuka Y; Furuta J; Miyashita T; Otsuka F
Acta Derm Venereol; 2012 Nov; 92(6):619-20. PubMed ID: 22434048
[No Abstract] [Full Text] [Related]
15.
Ponti G; Manfredini M; Pastorino L; Maccaferri M; Tomasi A; Pellacani G
Anticancer Res; 2018 Jan; 38(1):471-476. PubMed ID: 29277811
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [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]
18. A novel mutation of the PTCH1 gene activates the Shh/Gli signaling pathway in a Chinese family with nevoid basal cell carcinoma syndrome.
Zhang T; Chen M; Lü Y; Xing Q; Chen W
Biochem Biophys Res Commun; 2011 Jun; 409(2):166-70. PubMed ID: 21514272
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
