Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Meningioma and SMARCB1[original query] |
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SMARCB1 mutations are not a common cause of multiple meningiomas. Journal of medical genetics 2010 Aug 47 (8): 567-8. Hadfield K D, Smith M J, Trump D, Newman W G, Evans D |
Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young Adults. JAMA neurology 2017 8 74 (9): 1123-1129. Pathmanaban Omar N, Sadler Katherine V, Kamaly-Asl Ian D, King Andrew T, Rutherford Scott A, Hammerbeck-Ward Charlotte, McCabe Martin G, Kilday John-Paul, Beetz Christian, Poplawski Nicola K, Evans D Gareth, Smith Miriam |
Germline variants in SMARCB1 and other members of the BAF chromatin-remodeling complex across human disease entities: a meta-analysis. European journal of human genetics : EJHG 2018 5 26 (8): 1083-1093. Holsten Till, Bens Susanne, Oyen Florian, Nemes Karolina, Hasselblatt Martin, Kordes Uwe, Siebert Reiner, Frühwald Michael C, Schneppenheim Reinhard, Schüller Ulri |
Loss of SMARCB1/INI1 Immunoexpression in Chordoid Meningiomas. Neurology India 0 67 (6): 1492-1497. Malgulwar Prit B, Kakkar Aanchal, Sharma Mehar C, Ghosh Ranajoy, Pathak Pankaj, Sarkar Chitra, Suri Vaishali, Singh Manmohan, Kale Shashank S, Faruq Mohamm |
SWI/SNF chromatin remodeling complex alterations in meningioma. Journal of cancer research and clinical oncology 2021 Mar . Gill Corey M, Loewenstern Joshua, Rutland John W, Arib Hanane, Pain Margaret, Umphlett Melissa, Kinoshita Yayoi, McBride Russell B, Bederson Joshua, Donovan Michael, Sebra Robert, Fowkes Mary, Shrivastava Raj |
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