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Journal Abstract Search

143 related items for PubMed ID: 15042702

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  • 25. Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.
    Boutet N, Bignon YJ, Drouin-Garraud V, Sarda P, Longy M, Lacombe D, Gorry P.
    J Invest Dermatol; 2003 Sep; 121(3):478-81. PubMed ID: 12925203
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  • 26. 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 15; 16(2):442-50. PubMed ID: 20068110
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  • 27. The patched signaling pathway in tumorigenesis and development: lessons from animal models.
    Hahn H, Wojnowski L, Miller G, Zimmer A.
    J Mol Med (Berl); 1999 Jun 15; 77(6):459-68. PubMed ID: 10475061
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  • 30. 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 15; 35(2):396-402. PubMed ID: 32564428
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  • 32. Novel clinical and molecular findings in Spanish patients with naevoid basal cell carcinoma syndrome.
    Alonso N, Cañueto J, Ciria S, Bueno E, Palacios-Alvarez I, Alegre M, Badenas C, Barreiro A, Pena L, Maldonado C, Nespeira-Jato MV, Peña-Penabad C, Azon A, Gavrilova M, Ferrer I, Sanmartin O, Robles L, Hernandez-Martin A, Urioste M, Puig S, Puig L, Gonzalez-Sarmiento R.
    Br J Dermatol; 2018 Jan 15; 178(1):198-206. PubMed ID: 28733979
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  • 35. Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.
    Kijima C, Miyashita T, Suzuki M, Oka H, Fujii K.
    Fam Cancer; 2012 Dec 15; 11(4):565-70. PubMed ID: 22829011
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  • 36. [From gene to disease: basal cell naevus syndrome].
    de Meij TG, Baars MJ, Gille JJ, Hack WW, Haasnoot K, van Hagen JM.
    Ned Tijdschr Geneeskd; 2005 Jan 08; 149(2):78-81. PubMed ID: 15688838
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  • 38. Germline mutations of the PTCH gene in Japanese patients with nevoid basal cell carcinoma syndrome.
    Tanioka M, Takahashi K, Kawabata T, Kosugi S, Murakami K, Miyachi Y, Nishigori C, Iizuka T.
    Arch Dermatol Res; 2005 Jan 08; 296(7):303-8. PubMed ID: 15565302
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