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199 related items for PubMed ID: 34628055
21. Inference on germline BAP1 mutations and asbestos exposure from the analysis of familial and sporadic mesothelioma in a high-risk area. Betti M, Casalone E, Ferrante D, Romanelli A, Grosso F, Guarrera S, Righi L, Vatrano S, Pelosi G, Libener R, Mirabelli D, Boldorini R, Casadio C, Papotti M, Matullo G, Magnani C, Dianzani I. Genes Chromosomes Cancer; 2015 Jan; 54(1):51-62. PubMed ID: 25231345 [Abstract] [Full Text] [Related]
22. Detecting germline BAP1 mutations in patients with peritoneal mesothelioma: benefits to patient and family members. Kittaneh M, Berkelhammer C. J Transl Med; 2018 Jul 13; 16(1):194. PubMed ID: 30001711 [Abstract] [Full Text] [Related]
23. Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma. Sneddon S, Leon JS, Dick IM, Cadby G, Olsen N, Brims F, Allcock RJ, Moses EK, Melton PE, de Klerk N, Musk AW, Robinson BW, Creaney J. Gene; 2015 May 25; 563(1):103-5. PubMed ID: 25796603 [Abstract] [Full Text] [Related]
24. Genomic profiling of multiple primary cancers including synchronous lung adenocarcinoma and bilateral malignant mesotheliomas: Identification of a novel BAP1 germline variant. Shinozaki-Ushiku A, Kohsaka S, Kage H, Oda K, Miyagawa K, Nakajima J, Aburatani H, Mano H, Ushiku T. Pathol Int; 2020 Oct 25; 70(10):775-780. PubMed ID: 32583627 [Abstract] [Full Text] [Related]
25. Mesothelioma patients with germline BAP1 mutations have 7-fold improved long-term survival. Baumann F, Flores E, Napolitano A, Kanodia S, Taioli E, Pass H, Yang H, Carbone M. Carcinogenesis; 2015 Jan 25; 36(1):76-81. PubMed ID: 25380601 [Abstract] [Full Text] [Related]
26. CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma. Betti M, Aspesi A, Biasi A, Casalone E, Ferrante D, Ogliara P, Gironi LC, Giorgione R, Farinelli P, Grosso F, Libener R, Rosato S, Turchetti D, Maffè A, Casadio C, Ascoli V, Dianzani C, Colombo E, Piccolini E, Pavesi M, Miccoli S, Mirabelli D, Bracco C, Righi L, Boldorini R, Papotti M, Matullo G, Magnani C, Pasini B, Dianzani I. Cancer Lett; 2016 Aug 10; 378(2):120-30. PubMed ID: 27181379 [Abstract] [Full Text] [Related]
27. Inactivation of Bap1 Cooperates with Losses of Nf2 and Cdkn2a to Drive the Development of Pleural Malignant Mesothelioma in Conditional Mouse Models. Kukuyan AM, Sementino E, Kadariya Y, Menges CW, Cheung M, Tan Y, Cai KQ, Slifker MJ, Peri S, Klein-Szanto AJ, Rauscher FJ, Testa JR. Cancer Res; 2019 Aug 15; 79(16):4113-4123. PubMed ID: 31151962 [Abstract] [Full Text] [Related]
30. An asbestos-exposed family with multiple cases of pleural malignant mesothelioma without inheritance of a predisposing BAP1 mutation. Cheung M, Kadariya Y, Pei J, Talarchek J, Facciolo F, Visca P, Righi L, Cozzi I, Testa JR, Ascoli V. Cancer Genet; 2015 Oct 15; 208(10):502-7. PubMed ID: 26364129 [Abstract] [Full Text] [Related]
34. Sensitivity to asbestos is increased in patients with mesothelioma and pathogenic germline variants in BAP1 or other DNA repair genes. Betti M, Aspesi A, Ferrante D, Sculco M, Righi L, Mirabelli D, Napoli F, Rondón-Lagos M, Casalone E, Vignolo Lutati F, Ogliara P, Bironzo P, Gironi CL, Savoia P, Maffè A, Ungari S, Grosso F, Libener R, Boldorini R, Valiante M, Pasini B, Matullo G, Scagliotti G, Magnani C, Dianzani I. Genes Chromosomes Cancer; 2018 Nov 15; 57(11):573-583. PubMed ID: 30338612 [Abstract] [Full Text] [Related]
36. Comparison of Germline versus Somatic BAP1 Mutations for Risk of Metastasis in Uveal Melanoma. Ewens KG, Lalonde E, Richards-Yutz J, Shields CL, Ganguly A. BMC Cancer; 2018 Nov 26; 18(1):1172. PubMed ID: 30477459 [Abstract] [Full Text] [Related]
37. Genotypic and Phenotypic Features of BAP1 Cancer Syndrome: A Report of 8 New Families and Review of Cases in the Literature. Haugh AM, Njauw CN, Bubley JA, Verzì AE, Zhang B, Kudalkar E, VandenBoom T, Walton K, Swick BL, Kumar R, Rana HQ, Cochrane S, McCormick SR, Shea CR, Tsao H, Gerami P. JAMA Dermatol; 2017 Oct 01; 153(10):999-1006. PubMed ID: 28793149 [Abstract] [Full Text] [Related]
38. Combined Genetic and Genealogic Studies Uncover a Large BAP1 Cancer Syndrome Kindred Tracing Back Nine Generations to a Common Ancestor from the 1700s. Carbone M, Flores EG, Emi M, Johnson TA, Tsunoda T, Behner D, Hoffman H, Hesdorffer M, Nasu M, Napolitano A, Powers A, Minaai M, Baumann F, Bryant-Greenwood P, Lauk O, Kirschner MB, Weder W, Opitz I, Pass HI, Gaudino G, Pastorino S, Yang H. PLoS Genet; 2015 Dec 01; 11(12):e1005633. PubMed ID: 26683624 [Abstract] [Full Text] [Related]
39. BAP1 missense mutation c.2054 A>T (p.E685V) completely disrupts normal splicing through creation of a novel 5' splice site in a human mesothelioma cell line. Morrison A, Chekaluk Y, Bacares R, Ladanyi M, Zhang L. PLoS One; 2015 Dec 01; 10(4):e0119224. PubMed ID: 25830670 [Abstract] [Full Text] [Related]
40. Well-differentiated papillary mesothelioma: clustering in a Portuguese family with a germline BAP1 mutation. Ribeiro C, Campelos S, Moura CS, Machado JC, Justino A, Parente B. Ann Oncol; 2013 Aug 01; 24(8):2147-50. PubMed ID: 23585512 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]