144 related articles for article (PubMed ID: 38354379)
1. Gorlin-Like Phenotype in a Young Girl With a De Novo PTCH2 Variant Mutation of Uncertain Significance.
Garcia-Garcia M; García-González S; Cabañuz C; Prieto-Torres L
Am J Dermatopathol; 2024 Apr; 46(4):247-251. PubMed ID: 38354379
[TBL] [Abstract][Full Text] [Related]
2. Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.
Casano K; Meddaugh H; Zambrano RM; Marble M; Torres JI; Lacassie Y
Eur J Med Genet; 2020 Apr; 63(4):103842. PubMed ID: 31945512
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. PTCH2 is not a strong candidate gene for gorlin syndrome predisposition.
Smith MJ; Evans DG
Fam Cancer; 2022 Jul; 21(3):343-346. PubMed ID: 34170463
[TBL] [Abstract][Full Text] [Related]
6. Basal cell nevus syndrome: From DNA to therapeutics.
Lin MJ; Dubin DP; Khorasani H; Giordano CN
Clin Dermatol; 2020; 38(4):467-476. PubMed ID: 32972605
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Conjunctival ganglioglioma as a feature of basal cell nevus syndrome.
Sauer A; Blavin J; Lhermitte B; Speeg-Schatz C
J AAPOS; 2011 Aug; 15(4):387-8. PubMed ID: 21907124
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. [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]
13. Gorlin syndrome (nevoid basal cell carcinoma syndrome): update and literature review.
Fujii K; Miyashita T
Pediatr Int; 2014 Oct; 56(5):667-74. PubMed ID: 25131638
[TBL] [Abstract][Full Text] [Related]
14. Basal cell nevus syndrome: clinical and genetic diagnosis.
García de Marcos JA; Dean-Ferrer A; Arroyo Rodríguez S; Calderón-Polanco J; Alamillos Granados FJ; Poblet E
Oral Maxillofac Surg; 2009 Dec; 13(4):225-30. PubMed ID: 19795138
[TBL] [Abstract][Full Text] [Related]
15. PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.
Santos DC; Zaphiropoulos PG; Neto CF; Pimentel ER; Sanches JA; Ruiz IR
Int J Dermatol; 2011 Jul; 50(7):838-43. PubMed ID: 21699520
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Early-onset acral basal cell carcinomas in Gorlin syndrome.
Torrelo A; Vicente A; Navarro L; Planaguma M; Bueno E; González-Sarmiento R; Hernández-Martín A; Noguera-Morel L; Requena L; Colmenero I; Parareda A; González-Enseñat MA; Happle R
Br J Dermatol; 2014 Nov; 171(5):1227-9. PubMed ID: 24837096
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Gorlin syndrome or basal cell nevus syndrome (BCNS): A case report.
Shivaswamy KN; Sumathy TK; Shyamprasad AL; Ranganathan C
Dermatol Online J; 2010 Sep; 16(9):6. PubMed ID: 20875327
[TBL] [Abstract][Full Text] [Related]
20. Patching together the genetics of Gorlin syndrome.
Bale SJ; Falk RT; Rogers GR
J Cutan Med Surg; 1998 Jul; 3(1):31-4. PubMed ID: 9677257
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
