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688 related items for PubMed ID: 23249834
21. Multiple trichoepitheliomas associated with a novel heterozygous mutation in the CYLD gene as an adjunct to the histopathological diagnosis. Reuven B, Margarita I, Dov H, Ziad K. Am J Dermatopathol; 2013 Jun; 35(4):445-7. PubMed ID: 23694822 [Abstract] [Full Text] [Related]
24. Mild phenotype of familial cylindromatosis associated with an R758X nonsense mutation in the CYLD tumour suppressor gene. Oiso N, Mizuno N, Fukai K, Nakagawa K, Ishii M. Br J Dermatol; 2004 Nov; 151(5):1084-6. PubMed ID: 15541090 [Abstract] [Full Text] [Related]
25. A novel germline mutation in the CYLD gene in a Slovak patient with Brooke-Spiegler syndrome. Kacerovská D, Szép Z, Kolláriková L, Vaneček T, Michal M, Daniš D, Kazakov D. Cesk Patol; 2013 Apr; 49(2):89-92. PubMed ID: 23641715 [Abstract] [Full Text] [Related]
26. Brooke-Spiegler syndrome presenting multiple concurrent cutaneous and parotid gland neoplasms: cytologic findings on fine-needle sample and description of a novel mutation of the CYLD gene. Malzone MG, Campanile AC, Losito NS, Longo F, Perri F, Caponigro F, Schiavone C, Ionna F, Maiello F, Martinuzzi C, Nasti S, Botti G, Fulciniti F. Diagn Cytopathol; 2015 Aug; 43(8):654-8. PubMed ID: 25995191 [Abstract] [Full Text] [Related]
28. Morphologic diversity of malignant neoplasms arising in preexisting spiradenoma, cylindroma, and spiradenocylindroma based on the study of 24 cases, sporadic or occurring in the setting of Brooke-Spiegler syndrome. Kazakov DV, Zelger B, Rütten A, Vazmitel M, Spagnolo DV, Kacerovska D, Vanecek T, Grossmann P, Sima R, Grayson W, Calonje E, Koren J, Mukensnabl P, Danis D, Michal M. Am J Surg Pathol; 2009 May; 33(5):705-19. PubMed ID: 19194280 [Abstract] [Full Text] [Related]
30. CYLD GeneticTesting for Brooke-Spiegler Syndrome, Familial Cylindromatosis and Multiple Familial Trichoepitheliomas. Dubois A, Wilson V, Bourn D, Rajan N. PLoS Curr; 2015 Feb 19; 7():. PubMed ID: 25737804 [Abstract] [Full Text] [Related]
31. Overexpression of MYB drives proliferation of CYLD-defective cylindroma cells. Rajan N, Andersson MK, Sinclair N, Fehr A, Hodgson K, Lord CJ, Kazakov DV, Vanecek T, Ashworth A, Stenman G. J Pathol; 2016 Jun 19; 239(2):197-205. PubMed ID: 26969893 [Abstract] [Full Text] [Related]
35. A novel large deletion of the CYLD gene causes CYLD cutaneous syndrome in a Chinese family. Zhu R, Xu J, Shen J, Li W, Tan F, Li C, Wei Z, Liu Y, Bai Y. Mol Genet Genomic Med; 2020 Oct 19; 8(10):e1441. PubMed ID: 32783365 [Abstract] [Full Text] [Related]
36. Multiple trichoepitheliomas--a novel mutation in the CYLD gene. Amaro C, Freitas I, Lamarão P, Afonso A, Skrzypczak M, Heinritz W. J Eur Acad Dermatol Venereol; 2010 Jul 19; 24(7):844-6. PubMed ID: 19929939 [Abstract] [Full Text] [Related]