These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
371 related articles for article (PubMed ID: 25117323)
1. 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]
2. [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]
3. A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome. Durmaz CD; Evans G; Smith MJ; Ertop P; Akay BN; Tuncalı T Cytogenet Genome Res; 2018; 154(2):57-61. PubMed ID: 29544218 [TBL] [Abstract][Full Text] [Related]
4. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome. Fujii K; Ohashi H; Suzuki M; Hatsuse H; Shiohama T; Uchikawa H; Miyashita T Fam Cancer; 2013 Dec; 12(4):611-4. PubMed ID: 23479190 [TBL] [Abstract][Full Text] [Related]
5. Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation. Kijima C; Miyashita T; Suzuki M; Oka H; Fujii K Fam Cancer; 2012 Dec; 11(4):565-70. PubMed ID: 22829011 [TBL] [Abstract][Full Text] [Related]
6. PTCH1 and SMO gene alterations in keratocystic odontogenic tumors. Sun LS; Li XF; Li TJ J Dent Res; 2008 Jun; 87(6):575-9. PubMed ID: 18502968 [TBL] [Abstract][Full Text] [Related]
7. [Skeletal and dermatological manifestations of the nevoid Basal cell carcinoma syndrome (Gorlin-Goltz syndrome). Results of 8 patients in 12 years]. Rupprecht M; Mensing CH; Barvencik F; Ittrich H; Heiland M; Rueger JM; Amling M; Pogoda P Rofo; 2007 Jun; 179(6):618-26. PubMed ID: 17492539 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci. Garavelli L; Piemontese MR; Cavazza A; Rosato S; Wischmeijer A; Gelmini C; Albertini E; Albertini G; Forzano F; Franchi F; Carella M; Zelante L; Superti-Furga A Am J Med Genet A; 2013 Nov; 161A(11):2894-901. PubMed ID: 24124115 [TBL] [Abstract][Full Text] [Related]
11. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome. Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428 [TBL] [Abstract][Full Text] [Related]
12. Novel PTCH1 mutations in patients with keratocystic odontogenic tumors screened for nevoid basal cell carcinoma (NBCC) syndrome. Pastorino L; Pollio A; Pellacani G; Guarneri C; Ghiorzo P; Longo C; Bruno W; Giusti F; Bassoli S; Bianchi-Scarrà G; Ruini C; Seidenari S; Tomasi A; Ponti G PLoS One; 2012; 7(8):e43827. PubMed ID: 22952776 [TBL] [Abstract][Full Text] [Related]
13. Skeletal and cranio-facial signs in Gorlin syndrome from ancient Egypt to the modern age: sphenoid asymmetry in a patient with a novel PTCH1 mutation. Ponti G; Ruini C; Pastorino L; Loschi P; Pecchi A; Malagoli M; Mandel VD; Boano R; Conti A; Pellacani G; Tomasi A Future Oncol; 2014 May; 10(6):917-25. PubMed ID: 24941978 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome. Ponti G; Pastorino L; Pollio A; Nasti S; Pellacani G; Mignogna MD; Tomasi A; Del Forno C; Longo C; Bianchi-Scarrà G; Ficarra G; Seidenari S Fam Cancer; 2012 Sep; 11(3):411-8. PubMed ID: 22565648 [TBL] [Abstract][Full Text] [Related]
19. Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis. Pan S; Dong Q; Sun LS; Li TJ Clin Cancer Res; 2010 Jan; 16(2):442-50. PubMed ID: 20068110 [TBL] [Abstract][Full Text] [Related]
20. A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome. Zhou J; Zhang G; Shi M; Liu Z; Xiao M; Fu S; Gong X; Shi X Med Mol Morphol; 2019 Dec; 52(4):235-237. PubMed ID: 30997576 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]