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Journal Abstract Search

294 related items for PubMed ID: 26356331

  • 21.
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  • 22. [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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  • 23. Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosis.
    Hubacek M, Kripnerova T, Nemcikova M, Krepelová A, Puchmajerova A, Malikova M, Havlovicová M, Cadova J, Kodet R, Macek M, Dostalova T.
    Neuro Endocrinol Lett; 2016 Sep 08; 37(4):269-276. PubMed ID: 27857042
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  • 28. Relation between sonic hedgehog pathway gene polymorphisms and basal cell carcinoma development in the Polish population.
    Lesiak A, Sobolewska-Sztychny D, Majak P, Sobjanek M, Wodz K, Sygut KP, Majsterek I, Wozniacka A, Narbutt J.
    Arch Dermatol Res; 2016 Jan 08; 308(1):39-47. PubMed ID: 26590974
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  • 29. Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.
    Reifenberger J, Wolter M, Weber RG, Megahed M, Ruzicka T, Lichter P, Reifenberger G.
    Cancer Res; 1998 May 01; 58(9):1798-803. PubMed ID: 9581815
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  • 32. Treatment of multiple unresectable basal cell carcinomas from Gorlin-Goltz syndrome: a case report.
    Ojevwe FO, Ojevwe CD, Zacny JP, Dudek AZ, Lin A, Kohlitz P.
    Anticancer Res; 2015 Mar 01; 35(3):1777-81. PubMed ID: 25750342
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  • 33. 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 01; 54(2):69-78. PubMed ID: 32816116
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  • 37. Genetic and clinicopathologic aspects of Gorlin-Goltz syndrome (NBCCS): presentation of two case reports and literature review.
    Acocella A, Sacco R, Bertolai R, Sacco N.
    Minerva Stomatol; 2009 Jun 01; 58(1-2):43-53. PubMed ID: 19234436
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  • 38. Unexpected manifestation of naevoid basal cell carcinoma (Gorlin) syndrome with a novel mutation in the PTCH1 gene in a female patient with long-lasting pemphigus vulgaris.
    Goetze S, Raessler F, Hipler UC, Schulz S, Kohlhase J, Elsner P.
    J Eur Acad Dermatol Venereol; 2016 Mar 01; 30(3):493-4. PubMed ID: 25600101
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  • 39. Gorlin syndrome-derived induced pluripotent stem cells are hypersensitive to hedgehog-mediated osteogenic induction.
    Hasegawa D, Ochiai-Shino H, Onodera S, Nakamura T, Saito A, Onda T, Watanabe K, Nishimura K, Ohtaka M, Nakanishi M, Kosaki K, Yamaguchi A, Shibahara T, Azuma T.
    PLoS One; 2017 Mar 01; 12(10):e0186879. PubMed ID: 29088246
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  • 40. 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 15; 56(20):4562-5. PubMed ID: 8840960
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