148 related articles for article (PubMed ID: 26782978)
1. Gorlin syndrome with an ovarian leiomyoma associated with a PTCH1 second hit.
Akizawa Y; Miyashita T; Sasaki R; Nagata R; Aoki R; Ishitani K; Nagashima Y; Matsui H; Saito K
Am J Med Genet A; 2016 Apr; 170A(4):1029-34. PubMed ID: 26782978
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Multiple keratocystic odontogenic tumors associated with nevoid basal cell carcinoma syndrome having distinct PTCH1 mutations: a case report.
Sasaki R; Miyashita T; Matsumoto N; Fujii K; Saito K; Ando T
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 Aug; 110(2):e41-6. PubMed ID: 20659694
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.
Musani V; Ozretić P; Trnski D; Sabol M; Poduje S; Tošić M; Šitum M; Levanat S
Croat Med J; 2018 Feb; 59(1):20-24. PubMed ID: 29498494
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular analysis of keratocystic odontogenic tumor cell lines derived from sporadic and basal cell nevus syndrome patients.
Noguchi K; Wakai K; Kiyono T; Kawabe M; Yoshikawa K; Hashimoto-Tamaoki T; Kishimoto H; Nakano Y
Int J Oncol; 2017 Dec; 51(6):1731-1738. PubMed ID: 29039452
[TBL] [Abstract][Full Text] [Related]
9. Integrated genotypic analysis of hedgehog-related genes identifies subgroups of keratocystic odontogenic tumor with distinct clinicopathological features.
Shimada Y; Katsube K; Kabasawa Y; Morita K; Omura K; Yamaguchi A; Sakamoto K
PLoS One; 2013; 8(8):e70995. PubMed ID: 23951062
[TBL] [Abstract][Full Text] [Related]
10. Is loss of heterozygosity at 9q22.3 (PTCH gene) and 19p13.3 (STK11 gene) involved in the pathogenesis of ovarian stromal tumors?
Tsuji T; Catasus L; Prat J
Hum Pathol; 2005 Jul; 36(7):792-6. PubMed ID: 16084949
[TBL] [Abstract][Full Text] [Related]
11. [Gorlin syndrome in the paediatric age].
Roncalés-Samanes P; Peña-Segura JL; Fernando-Martínez R; Fuertes-Rodrigo C; García-Oguiza A; López-Pisón J
Rev Neurol; 2014 Apr; 58(7):303-7. PubMed ID: 24677153
[TBL] [Abstract][Full Text] [Related]
12. Biallelic PTCH1 Inactivation Is a Dominant Genomic Change in Sporadic Keratocystic Odontogenic Tumors.
Stojanov IJ; Schaefer IM; Menon RS; Wasman J; Gokozan HN; Garcia EP; Baur DA; Woo SB; Sholl LM
Am J Surg Pathol; 2020 Apr; 44(4):553-560. PubMed ID: 31725470
[TBL] [Abstract][Full Text] [Related]
13. Bilateral ovarian fibromas as the sole manifestation of Gorlin syndrome in a 22-year-old woman: a case report and literature review.
Zhu M; Li J; Duan J; Yang J; Gu W; Jiang W
Diagn Pathol; 2023 Oct; 18(1):118. PubMed ID: 37907964
[TBL] [Abstract][Full Text] [Related]
14. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.
Smith MJ; Beetz C; Williams SG; Bhaskar SS; O'Sullivan J; Anderson B; Daly SB; Urquhart JE; Bholah Z; Oudit D; Cheesman E; Kelsey A; McCabe MG; Newman WG; Evans DG
J Clin Oncol; 2014 Dec; 32(36):4155-61. PubMed ID: 25403219
[TBL] [Abstract][Full Text] [Related]
15. First evidence of genotype-phenotype correlations in Gorlin syndrome.
Evans DG; Oudit D; Smith MJ; Rutkowski D; Allan E; Newman WG; Lear JT
J Med Genet; 2017 Aug; 54(8):530-536. PubMed ID: 28596197
[TBL] [Abstract][Full Text] [Related]
16. Ovarian preservation in a young patient with Gorlin syndrome and multiple bilateral ovarian masses.
Morse CB; McLaren JF; Roy D; Siegelman ES; Livolsi VA; Gracia CR
Fertil Steril; 2011 Jul; 96(1):e47-50. PubMed ID: 21565340
[TBL] [Abstract][Full Text] [Related]
17. New mutations and an updated database for the patched-1 (PTCH1) gene.
Reinders MG; van Hout AF; Cosgun B; Paulussen AD; Leter EM; Steijlen PM; Mosterd K; van Geel M; Gille JJ
Mol Genet Genomic Med; 2018 May; 6(3):409-415. PubMed ID: 29575684
[TBL] [Abstract][Full Text] [Related]
18. Current recommendations for cancer surveillance in Gorlin syndrome: a report from the SIOPE host genome working group (SIOPE HGWG).
Guerrini-Rousseau L; Smith MJ; Kratz CP; Doergeloh B; Hirsch S; Hopman SMJ; Jorgensen M; Kuhlen M; Michaeli O; Milde T; Ridola V; Russo A; Salvador H; Waespe N; Claret B; Brugieres L; Evans DG
Fam Cancer; 2021 Oct; 20(4):317-325. PubMed ID: 33860896
[TBL] [Abstract][Full Text] [Related]
19. Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.
Goetze S; Raessler F; Hipler UC; Schulz S; Kohlhase J; Elsner P
J Eur Acad Dermatol Venereol; 2016 Mar; 30(3):493-4. PubMed ID: 25600101
[No Abstract] [Full Text] [Related]
20. Conservative treatment of recurrent ovarian fibromas in a young patient affected by Gorlin syndrome.
Seracchioli R; Bagnoli A; Colombo FM; Missiroli S; Venturoli S
Hum Reprod; 2001 Jun; 16(6):1261-3. PubMed ID: 11387302
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
