148 related articles for article (PubMed ID: 26782978)
21. PTCH1 gene mutations in Keratocystic odontogenic tumors: a study of 43 Chinese patients and a systematic review.
Guo YY; Zhang JY; Li XF; Luo HY; Chen F; Li TJ
PLoS One; 2013; 8(10):e77305. PubMed ID: 24204797
[TBL] [Abstract][Full Text] [Related]
22. Molecular pathogenesis of keratocystic odontogenic tumors developing in nevoid basal cell carcinoma syndrome.
Suzuki M; Nagao K; Hatsuse H; Sasaki R; Saito K; Fujii K; Miyashita T
Oral Surg Oral Med Oral Pathol Oral Radiol; 2013 Sep; 116(3):348-53. PubMed ID: 23953420
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome.
Ozcan G; Balta B; Sekerci AE; Etoz OA; Martinuzzi C; Kara O; Pastorino L; Kocoglu F; Ulker O; Erdogan M
Indian J Pathol Microbiol; 2016; 59(3):335-8. PubMed ID: 27510672
[TBL] [Abstract][Full Text] [Related]
25. Gorlin syndrome patient with large deletion in 9q22.32-q22.33 detected by quantitative multiplex fluorescent PCR.
Musani V; Cretnik M; Situm M; Basta-Juzbasic A; Levanat S
Dermatology; 2009; 219(2):111-8. PubMed ID: 19439922
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. Gorlin syndrome-induced pluripotent stem cells form medulloblastoma with loss of heterozygosity in
Ikemoto Y; Miyashita T; Nasu M; Hatsuse H; Kajiwara K; Fujii K; Motojima T; Kokido I; Toyoda M; Umezawa A
Aging (Albany NY); 2020 May; 12(10):9935-9947. PubMed ID: 32436863
[TBL] [Abstract][Full Text] [Related]
28. Gorlin Syndrome Associated With a Solitary Circumscribed Retinal Astrocytic Proliferation in a Pediatric Patient.
Lopez-Cañizares A; Al-Khersan H; Carletti P; Shields CL; Berrocal AM
Ophthalmic Surg Lasers Imaging Retina; 2022 Sep; 53(9):514-516. PubMed ID: 36107625
[TBL] [Abstract][Full Text] [Related]
29. Novel PTCH1 Gene Mutation in Nevoid Basal Cell Carcinoma Syndrome.
Sim YC; Kim GH; Choi SW; Ahn KM
J Craniofac Surg; 2018 May; 29(3):e252-e255. PubMed ID: 29381605
[TBL] [Abstract][Full Text] [Related]
30. Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
Bholah Z; Smith MJ; Byers HJ; Miles EK; Evans DG; Newman WG
Fam Cancer; 2014 Sep; 13(3):477-80. PubMed ID: 24659465
[TBL] [Abstract][Full Text] [Related]
31. Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.
Ewing AD; Cheetham SW; McGill JJ; Sharkey M; Walker R; West JA; West MJ; Summers KM
Am J Med Genet A; 2021 Jul; 185(7):2070-2083. PubMed ID: 33960642
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. [PTCH1 gene analysis in 25 Japanese patients with Gorlin syndrome].
Endo M; Fujii K; Miyashita T; Uchikawa H; Tanabe R; Sugita K; Arai H; Kohno Y
No To Hattatsu; 2009 Jul; 41(4):259-63. PubMed ID: 19618880
[TBL] [Abstract][Full Text] [Related]
34. Severe PATCHED1 Deficiency in Cancer-Prone Gorlin Patient Cells Results in Intrinsic Radiosensitivity.
Vulin A; Sedkaoui M; Moratille S; Sevenet N; Soularue P; Rigaud O; Guibbal L; Dulong J; Jeggo P; Deleuze JF; Lamartine J; Martin MT
Int J Radiat Oncol Biol Phys; 2018 Oct; 102(2):417-425. PubMed ID: 30191873
[TBL] [Abstract][Full Text] [Related]
35. Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.
Huq AJ; Walsh M; Rajagopalan B; Finlay M; Trainer AH; Bonnet F; Sevenet N; Winship IM
Fam Cancer; 2018 Oct; 17(4):601-606. PubMed ID: 29356994
[TBL] [Abstract][Full Text] [Related]
36. Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.
Onodera S; Saito A; Hasegawa D; Morita N; Watanabe K; Nomura T; Shibahara T; Ohba S; Yamaguchi A; Azuma T
PLoS One; 2017; 12(9):e0184702. PubMed ID: 28915250
[TBL] [Abstract][Full Text] [Related]
37. Surprising genetic and pathological findings in a patient with giant bilateral periadrenal tumours: PEComas and mutations of
Igaz P; Toth G; Nagy P; Dezső K; Turai PI; Medvecz M; Wikonkal N; Huszty G; Piros L; Toth E; Bozsik A; Likó I; Patócs A; Butz H
J Med Genet; 2022 Sep; 59(9):916-919. PubMed ID: 34916233
[TBL] [Abstract][Full Text] [Related]
38. SHH desmoplastic/nodular medulloblastoma and Gorlin syndrome in the setting of Down syndrome: case report, molecular profiling, and review of the literature.
Mangum R; Varga E; Boué DR; Capper D; Benesch M; Leonard J; Osorio DS; Pierson CR; Zumberge N; Sahm F; Schrimpf D; Pfister SM; Finlay JL
Childs Nerv Syst; 2016 Dec; 32(12):2439-2446. PubMed ID: 27444290
[TBL] [Abstract][Full Text] [Related]
39. Underestimated PTCH1 mutation rate in sporadic keratocystic odontogenic tumors.
Qu J; Yu F; Hong Y; Guo Y; Sun L; Li X; Zhang J; Zhang H; Shi R; Chen F; Li T
Oral Oncol; 2015 Jan; 51(1):40-5. PubMed ID: 25458233
[TBL] [Abstract][Full Text] [Related]
40. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
Muller EA; Aradhya S; Atkin JF; Carmany EP; Elliott AM; Chudley AE; Clark RD; Everman DB; Garner S; Hall BD; Herman GE; Kivuva E; Ramanathan S; Stevenson DA; Stockton DW; Hudgins L
Am J Med Genet A; 2012 Feb; 158A(2):391-9. PubMed ID: 22190277
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
