222 related articles for article (PubMed ID: 18302678)
1. 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]
2. 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]
3. [PTCH2 gene alterations in keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome].
Xu LL; Li TJ
Beijing Da Xue Xue Bao Yi Xue Ban; 2008 Feb; 40(1):15-8. PubMed ID: 18278130
[TBL] [Abstract][Full Text] [Related]
4. One germline mutation of PTCH gene in a Chinese family with non-syndromic keratocystic odontogenic tumours.
Wang X; Lu Y; Shen G; Chen W
Int J Oral Maxillofac Surg; 2011 Aug; 40(8):829-33. PubMed ID: 21507611
[TBL] [Abstract][Full Text] [Related]
5. Germline mutations of the PTCH gene in families with odontogenic keratocysts and nevoid basal cell carcinoma syndrome.
Song YL; Zhang WF; Peng B; Wang CN; Wang Q; Bian Z
Tumour Biol; 2006; 27(4):175-80. PubMed ID: 16675912
[TBL] [Abstract][Full Text] [Related]
6. [PTCH gene mutations in odontogenic keratocysts].
Yuan JW; Li TJ; Zhong HH; Zhao HS
Zhonghua Kou Qiang Yi Xue Za Zhi; 2006 Jan; 41(1):41-4. PubMed ID: 16620627
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Identification of known and novel PTCH mutations in both syndromic and non-syndromic keratocystic odontogenic tumors.
Pan S; Xu LL; Sun LS; Li TJ
Int J Oral Sci; 2009 Mar; 1(1):34-8. PubMed ID: 20690502
[TBL] [Abstract][Full Text] [Related]
10. Molecular characterization of Italian nevoid basal cell carcinoma syndrome patients.
Pastorino L; Cusano R; Nasti S; Faravelli F; Forzano F; Baldo C; Barile M; Gliori S; Muggianu M; Ghigliotti G; Lacaita MG; Lo Muzio L; Bianchi-Scarra G
Hum Mutat; 2005 Mar; 25(3):322-3. PubMed ID: 15712338
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. PTCH mutations and deletions in patients with typical nevoid basal cell carcinoma syndrome and in patients with a suspected genetic predisposition to basal cell carcinoma: a French study.
Soufir N; Gerard B; Portela M; Brice A; Liboutet M; Saiag P; Descamps V; Kerob D; Wolkenstein P; Gorin I; Lebbe C; Dupin N; Crickx B; Basset-Seguin N; Grandchamp B
Br J Cancer; 2006 Aug; 95(4):548-53. PubMed ID: 16909134
[TBL] [Abstract][Full Text] [Related]
15. 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-ScarrĂ G; Ruini C; Seidenari S; Tomasi A; Ponti G
PLoS One; 2012; 7(8):e43827. PubMed ID: 22952776
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. New mutation of the patched homologue 1 gene in a Chinese family with naevoid basal cell carcinoma syndrome.
Wang W; Wang J; Li J; Mao L; Guo F; Zhang B
Br J Oral Maxillofac Surg; 2009 Jul; 47(5):366-9. PubMed ID: 19008023
[TBL] [Abstract][Full Text] [Related]
18. [Detection of PTCH gene mutations in odontogenic keratocysts by SSCP and DNA sequencing].
Gu XM; Li TJ
Hua Xi Kou Qiang Yi Xue Za Zhi; 2006 Aug; 24(4):293-6. PubMed ID: 16999341
[TBL] [Abstract][Full Text] [Related]
19. 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-ScarrĂ G; Ficarra G; Seidenari S
Fam Cancer; 2012 Sep; 11(3):411-8. PubMed ID: 22565648
[TBL] [Abstract][Full Text] [Related]
20. Immunolocalization of PTCH protein in odontogenic cysts and tumors.
Barreto DC; Bale AE; De Marco L; Gomez RS
J Dent Res; 2002 Nov; 81(11):757-60. PubMed ID: 12407090
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]