190 related articles for article (PubMed ID: 35932013)
1. Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndrome.
Ye L; Wang L; Peng K; Fang O; Tian Z; Li C; Fu X; Chen Q; Chen J; Luan J; Zhang Z; Zhang Q
BMC Med Genomics; 2022 Aug; 15(1):172. PubMed ID: 35932013
[TBL] [Abstract][Full Text] [Related]
2. Nevoid Basal Cell Carcinoma Syndrome:
Martinez MF; Romano MV; Martinez AP; González A; Muchnik C; Stengel FM; Mazzuoccolo LD; Azurmendi PJ
Cells; 2019 Feb; 8(2):. PubMed ID: 30754660
[TBL] [Abstract][Full Text] [Related]
3. Genomic profiling of late-onset basal cell carcinomas from two brothers with nevoid basal cell carcinoma syndrome.
Hasan Ali O; Yurchenko AA; Pavlova O; Sartori A; Bomze D; Higgins R; Ring SS; Hartmann F; Bühler D; Fritzsche FR; Jochum W; Navarini AA; Kim A; French LE; Dermitzakis E; Christiano AM; Hohl D; Bickers DR; Nikolaev SI; Flatz L
J Eur Acad Dermatol Venereol; 2021 Feb; 35(2):396-402. PubMed ID: 32564428
[TBL] [Abstract][Full Text] [Related]
4. Novel alterations in IFT172 and KIFAP3 may induce basal cell carcinoma.
Onodera S; Morita N; Nakamura Y; Takahashi S; Hashimoto K; Nomura T; Katakura A; Kosaki K; Azuma T
Orphanet J Rare Dis; 2021 Oct; 16(1):443. PubMed ID: 34674729
[TBL] [Abstract][Full Text] [Related]
5. Novel PTCH1 Mutation Causes Gorlin-Goltz Syndrome.
Yue HT; Cao HY; He M
Chin J Dent Res; 2024 Mar; 27(1):83-88. PubMed ID: 38546523
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. The Role of Dermal Fibroblasts in Nevoid Basal Cell Carcinoma Syndrome Patients: An Overview.
Bellei B; Caputo S; Carbone A; Silipo V; Papaccio F; Picardo M; Eibenschutz L
Int J Mol Sci; 2020 Jan; 21(3):. PubMed ID: 31979112
[TBL] [Abstract][Full Text] [Related]
8. Linear basal cell nevus with a novel mosaic PTCH1 mutation.
Saeidian AH; Cohen-Nowak A; O'Donnell M; Shalabi D; McGuinn KP; Youssefian L; Vahidnezhad H; Niaziorimi F; Dasgeb B; Kasper DA; Lee JB; Uitto J; Nikbakht N
Exp Dermatol; 2020 Jun; 29(6):531-534. PubMed ID: 32298489
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Loss of Primary Cilia Drives Switching from Hedgehog to Ras/MAPK Pathway in Resistant Basal Cell Carcinoma.
Kuonen F; Huskey NE; Shankar G; Jaju P; Whitson RJ; Rieger KE; Atwood SX; Sarin KY; Oro AE
J Invest Dermatol; 2019 Jul; 139(7):1439-1448. PubMed ID: 30707899
[TBL] [Abstract][Full Text] [Related]
11. Proteomic analysis of PTCH1+/- fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients.
Ponti G; Bertazzoni G; Pastorino L; Monari E; Cuoghi A; Bergamini S; Bellei E; Benassi L; Azzoni P; Petrachi T; Magnoni C; Pellacani G; Loschi P; Pollio A; Witkowski AM; Tomasi A
Biomed Res Int; 2013; 2013():794028. PubMed ID: 24369017
[TBL] [Abstract][Full Text] [Related]
12. Keratinocytes from Gorlin Syndrome-induced pluripotent stem cells are resistant against UV radiation.
Morita N; Onodera S; Nakamura Y; Nakamura T; Takahashi SI; Nomura T; Azuma T
Med Mol Morphol; 2021 Jun; 54(2):69-78. PubMed ID: 32816116
[TBL] [Abstract][Full Text] [Related]
13. AKT1 Activation is Obligatory for Spontaneous BCC Tumor Growth in a Murine Model that Mimics Some Features of Basal Cell Nevus Syndrome.
Kim AL; Back JH; Zhu Y; Tang X; Yardley NP; Kim KJ; Athar M; Bickers DR
Cancer Prev Res (Phila); 2016 Oct; 9(10):794-802. PubMed ID: 27388747
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Unique features of PTCH1 mutation spectrum in Chinese sporadic basal cell carcinoma.
Huang YS; Bu DF; Li XY; Ma ZH; Yang Y; Lin ZM; Lu FM; Tu P; Li H
J Eur Acad Dermatol Venereol; 2013 Feb; 27(2):235-41. PubMed ID: 22313357
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Biallelic disruption of the PTCH1 gene in multiple basal cell carcinomas in Japanese patients with nevoid basal cell carcinoma syndrome.
Tate G; Kishimoto K; Mitsuya T
Acta Med Okayama; 2014; 68(3):163-70. PubMed ID: 24942795
[TBL] [Abstract][Full Text] [Related]
19. Shh and p50/Bcl3 signaling crosstalk drives pathogenesis of BCCs in Gorlin syndrome.
Chaudhary SC; Tang X; Arumugam A; Li C; Srivastava RK; Weng Z; Xu J; Zhang X; Kim AL; McKay K; Elmets CA; Kopelovich L; Bickers DR; Athar M
Oncotarget; 2015 Nov; 6(34):36789-814. PubMed ID: 26413810
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
