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Journal Abstract Search

276 related items for PubMed ID: 21699520

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  • 4. 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
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  • 5. Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.
    Reifenberger J, Wolter M, Knobbe CB, Köhler B, Schönicke A, Scharwächter C, Kumar K, Blaschke B, Ruzicka T, Reifenberger G.
    Br J Dermatol; 2005 Jan; 152(1):43-51. PubMed ID: 15656799
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  • 6. Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome.
    Aszterbaum M, Rothman A, Johnson RL, Fisher M, Xie J, Bonifas JM, Zhang X, Scott MP, Epstein EH.
    J Invest Dermatol; 1998 Jun; 110(6):885-8. PubMed ID: 9620294
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  • 9. PTCH1 gene haplotype association with basal cell carcinoma after transplantation.
    Begnini A, Tessari G, Turco A, Malerba G, Naldi L, Gotti E, Boschiero L, Forni A, Rugiu C, Piaserico S, Fortina AB, Brunello A, Cascone C, Girolomoni G, Gomez Lira M.
    Br J Dermatol; 2010 Aug; 163(2):364-70. PubMed ID: 20346027
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  • 11. [Nevoid basal cell carcinoma syndrome with corpus callosum agenesis, PTCH1 mutation and absence of basal cell carcinoma].
    Mazzuoccolo LD, Martínez MF, Muchnik C, Azurmendi PJ, Stengel F.
    Medicina (B Aires); 2014 Aug; 74(4):307-10. PubMed ID: 25188659
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  • 12. 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 28; 59(1):20-24. PubMed ID: 29498494
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  • 14. 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 28; 56(1):63-7. PubMed ID: 25727044
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  • 15. 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 28; 45():151472. PubMed ID: 31982676
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  • 16. 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 28; 6(3):409-415. PubMed ID: 29575684
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  • 17. LOH of PTCH1 region in BCC and ovarian carcinoma: microsatellite vs. HRM analysis.
    Musani V, Sabol M, Car D, Ozretic P, Oreskovic S, Leovic D, Levanat S.
    Front Biosci (Elite Ed); 2012 Jan 01; 4(3):1049-57. PubMed ID: 22201935
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  • 18. The spectrum of patched mutations in a collection of Australian basal cell carcinomas.
    Evans T, Boonchai W, Shanley S, Smyth I, Gillies S, Georgas K, Wainwright B, Chenevix-Trench G, Wicking C.
    Hum Mutat; 2000 Jan 01; 16(1):43-8. PubMed ID: 10874304
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  • 19. PTCH2, a novel human patched gene, undergoing alternative splicing and up-regulated in basal cell carcinomas.
    Zaphiropoulos PG, Undén AB, Rahnama F, Hollingsworth RE, Toftgård R.
    Cancer Res; 1999 Feb 15; 59(4):787-92. PubMed ID: 10029063
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  • 20. Nevoid Basal Cell Carcinoma Syndrome: PTCH1 Mutation Profile and Expression of Genes Involved in the Hedgehog Pathway in Argentinian Patients.
    Martinez MF, Romano MV, Martinez AP, González A, Muchnik C, Stengel FM, Mazzuoccolo LD, Azurmendi PJ.
    Cells; 2019 Feb 11; 8(2):. PubMed ID: 30754660
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