193 related articles for article (PubMed ID: 19795138)
21. 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]
22. 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]
23. 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]
24. 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]
25. 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]
26. PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts.
Gu XM; Zhao HS; Sun LS; Li TJ
J Dent Res; 2006 Sep; 85(9):859-63. PubMed ID: 16931872
[TBL] [Abstract][Full Text] [Related]
27. The immunoprofile of odontogenic keratocyst (keratocystic odontogenic tumor) that includes expression of PTCH, SMO, GLI-1 and bcl-2 is similar to ameloblastoma but different from odontogenic cysts.
Vered M; Peleg O; Taicher S; Buchner A
J Oral Pathol Med; 2009 Aug; 38(7):597-604. PubMed ID: 19473442
[TBL] [Abstract][Full Text] [Related]
28. Genetic screening for nevoid basal cell carcinoma syndrome in patients with a solitary keratocystic odontogenic tumour is not useful.
Karagozoglu KH; Van Hagen JM; Baart JA; Van Der Waal I
Minerva Stomatol; 2011; 60(1-2):1-4. PubMed ID: 21252844
[TBL] [Abstract][Full Text] [Related]
29. "PTCH"-ing it together: a basal cell nevus syndrome review.
Lam C; Ou JC; Billingsley EM
Dermatol Surg; 2013 Nov; 39(11):1557-72. PubMed ID: 23725561
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Spectrum of PTCH mutations in Italian nevoid basal cell-carcinoma syndrome patients: identification of thirteen novel alleles.
Savino M; d'Apolito M; Formica V; Baorda F; Mari F; Renieri A; Carabba E; Tarantino E; Andreucci E; Belli S; Lo Muzio L; Dallapiccola B; Zelante L; Savoia A
Hum Mutat; 2004 Nov; 24(5):441. PubMed ID: 15459969
[TBL] [Abstract][Full Text] [Related]
32. [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]
33. 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]
34. An oral clinical approach to Gorlin-Goltz syndrome.
Abreu LG; Paiva SM; Pretti H; Bastos Lages EM; Castro WH
Gen Dent; 2015; 63(2):e9-e12. PubMed ID: 25734295
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. A novel polymorphism in the PTC gene allows easy identification of allelic loss in basal cell nevus syndrome lesions.
Zedan W; Robinson PA; High AS
Diagn Mol Pathol; 2001 Mar; 10(1):41-5. PubMed ID: 11277394
[TBL] [Abstract][Full Text] [Related]
37. Expression of calretinin in odontogenic keratocysts and basal cell carcinomas: A study of sporadic and Gorlin-Goltz syndrome-related cases.
Cesinaro AM; Burtini G; Maiorana A; Rossi G; Migaldi M
Ann Diagn Pathol; 2020 Apr; 45():151472. PubMed ID: 31982676
[TBL] [Abstract][Full Text] [Related]
38. Syndrome in question: Gorlin-Goltz syndrome.
Ribeiro PL; Souza JB; Abreu KD; Brezinscki MS; Pignaton CC
An Bras Dermatol; 2016; 91(4):541-3. PubMed ID: 27579759
[TBL] [Abstract][Full Text] [Related]
39. Basal cell nevus syndrome: clinical and molecular review and case report.
Pino LC; Balassiano LK; Sessim M; de Almeida AP; Empinotti VD; Semenovitch I; Treu C; Lupi O
Int J Dermatol; 2016 Apr; 55(4):367-75. PubMed ID: 26356331
[TBL] [Abstract][Full Text] [Related]
40. Unexpected phenotype in a frameshift mutation of PTCH1.
Beltrami B; Prada E; Tolva G; Scuvera G; Silipigni R; Graziani D; Bulfamante G; Gervasini C; Marchisio P; Milani D
Mol Genet Genomic Med; 2020 Jan; 8(1):e987. PubMed ID: 31578813
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
