These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
415 related articles for article (PubMed ID: 20137775)
1. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. Schneppenheim R; Frühwald MC; Gesk S; Hasselblatt M; Jeibmann A; Kordes U; Kreuz M; Leuschner I; Martin Subero JI; Obser T; Oyen F; Vater I; Siebert R Am J Hum Genet; 2010 Feb; 86(2):279-84. PubMed ID: 20137775 [TBL] [Abstract][Full Text] [Related]
2. Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression. Hasselblatt M; Gesk S; Oyen F; Rossi S; Viscardi E; Giangaspero F; Giannini C; Judkins AR; Frühwald MC; Obser T; Schneppenheim R; Siebert R; Paulus W Am J Surg Pathol; 2011 Jun; 35(6):933-5. PubMed ID: 21566516 [TBL] [Abstract][Full Text] [Related]
4. Atypical teratoid/rhabdoid tumor with retained INI1 (SMARCB1) expression and loss of BRG1 (SMARCA4). Bookhout C; Bouldin TW; Ellison DW Neuropathology; 2018 Jun; 38(3):305-308. PubMed ID: 29271065 [TBL] [Abstract][Full Text] [Related]
5. Loss of BRG1 ( Saunders J; Ingley K; Wang XQ; Harvey M; Armstrong L; Ng T; Dunham C; Bush J Pediatr Dev Pathol; 2020; 23(2):132-138. PubMed ID: 31403913 [TBL] [Abstract][Full Text] [Related]
6. Genomic Alterations in Undifferentiated Malignant Tumors with Rhabdoid Phenotype and Loss of BRG1 Immunoexpression Identified by Fine Needle Aspirates. Mei L; Alikhan M; Mujacic I; Parilla M; Antic T Acta Cytol; 2019; 63(5):438-444. PubMed ID: 31230044 [TBL] [Abstract][Full Text] [Related]
7. Frequent co-inactivation of the SWI/SNF subunits SMARCB1, SMARCA2 and PBRM1 in malignant rhabdoid tumours. Rao Q; Xia QY; Wang ZY; Li L; Shen Q; Shi SS; Wang X; Liu B; Wang YF; Shi QL; Ma HH; Lu ZF; He Y; Zhang RS; Yu B; Zhou XJ Histopathology; 2015 Jul; 67(1):121-9. PubMed ID: 25496315 [TBL] [Abstract][Full Text] [Related]
8. SWI/SNF Complex-deficient Undifferentiated/Rhabdoid Carcinomas of the Gastrointestinal Tract: A Series of 13 Cases Highlighting Mutually Exclusive Loss of SMARCA4 and SMARCA2 and Frequent Co-inactivation of SMARCB1 and SMARCA2. Agaimy A; Daum O; Märkl B; Lichtmannegger I; Michal M; Hartmann A Am J Surg Pathol; 2016 Apr; 40(4):544-53. PubMed ID: 26551623 [TBL] [Abstract][Full Text] [Related]
9. Cancer Surveillance in Gorlin Syndrome and Rhabdoid Tumor Predisposition Syndrome. Foulkes WD; Kamihara J; Evans DGR; Brugières L; Bourdeaut F; Molenaar JJ; Walsh MF; Brodeur GM; Diller L Clin Cancer Res; 2017 Jun; 23(12):e62-e67. PubMed ID: 28620006 [TBL] [Abstract][Full Text] [Related]
11. Loss of expression of SMARCA4 (BRG1), SMARCA2 (BRM) and SMARCB1 (INI1) in undifferentiated carcinoma of the endometrium is not uncommon and is not always associated with rhabdoid morphology. Ramalingam P; Croce S; McCluggage WG Histopathology; 2017 Feb; 70(3):359-366. PubMed ID: 27656868 [TBL] [Abstract][Full Text] [Related]
12. Pattern of SMARCB1 (INI1) and SMARCA4 (BRG1) in poorly differentiated endometrioid adenocarcinoma of the uterus: analysis of a series with emphasis on a novel SMARCA4-deficient dedifferentiated rhabdoid variant. Strehl JD; Wachter DL; Fiedler J; Heimerl E; Beckmann MW; Hartmann A; Agaimy A Ann Diagn Pathol; 2015 Aug; 19(4):198-202. PubMed ID: 25920939 [TBL] [Abstract][Full Text] [Related]
13. Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases. Holdhof D; Johann PD; Spohn M; Bockmayr M; Safaei S; Joshi P; Masliah-Planchon J; Ho B; Andrianteranagna M; Bourdeaut F; Huang A; Kool M; Upadhyaya SA; Bendel AE; Indenbirken D; Foulkes WD; Bush JW; Creytens D; Kordes U; Frühwald MC; Hasselblatt M; Schüller U Acta Neuropathol; 2021 Feb; 141(2):291-301. PubMed ID: 33331994 [TBL] [Abstract][Full Text] [Related]
14. Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism. Gigante L; Paganini I; Frontali M; Ciabattoni S; Sangiuolo FC; Papi L Fam Cancer; 2016 Jan; 15(1):123-6. PubMed ID: 26342593 [TBL] [Abstract][Full Text] [Related]
15. Dual loss of the SWI/SNF complex ATPases SMARCA4/BRG1 and SMARCA2/BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type. Karnezis AN; Wang Y; Ramos P; Hendricks WP; Oliva E; D'Angelo E; Prat J; Nucci MR; Nielsen TO; Chow C; Leung S; Kommoss F; Kommoss S; Silva A; Ronnett BM; Rabban JT; Bowtell DD; Weissman BE; Trent JM; Gilks CB; Huntsman DG J Pathol; 2016 Feb; 238(3):389-400. PubMed ID: 26356327 [TBL] [Abstract][Full Text] [Related]
16. SMARCA4-deficient rhabdoid tumours show intermediate molecular features between SMARCB1-deficient rhabdoid tumours and small cell carcinomas of the ovary, hypercalcaemic type. Andrianteranagna M; Cyrta J; Masliah-Planchon J; Nemes K; Corsia A; Leruste A; Holdhof D; Kordes U; Orbach D; Corradini N; Entz-Werle N; Pierron G; Castex MP; Brouchet A; Weingertner N; Ranchère D; Fréneaux P; Delattre O; Bush J; Leary A; Frühwald MC; Schüller U; Servant N; Bourdeaut F J Pathol; 2021 Sep; 255(1):1-15. PubMed ID: 33999421 [TBL] [Abstract][Full Text] [Related]
18. Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back again. Witkowski L; Lalonde E; Zhang J; Albrecht S; Hamel N; Cavallone L; May ST; Nicholson JC; Coleman N; Murray MJ; Tauber PF; Huntsman DG; Schönberger S; Yandell D; Hasselblatt M; Tischkowitz MD; Majewski J; Foulkes WD J Pathol; 2013 Sep; 231(1):35-43. PubMed ID: 23775540 [TBL] [Abstract][Full Text] [Related]
19. Mechanisms by which SMARCB1 loss drives rhabdoid tumor growth. Kim KH; Roberts CW Cancer Genet; 2014 Sep; 207(9):365-72. PubMed ID: 24853101 [TBL] [Abstract][Full Text] [Related]