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SMARCE1 deficiency generates a targetable mSWI/SNF dependency in clear cell meningioma.
St Pierre R, Collings CK, Samé Guerra DD, Widmer CJ, Bolonduro O, Mashtalir N, Sankar A, Liang Y, Bi WL, Gerkes EH, Ramesh V, Qi J, Smith MJ, Meredith DM, Kadoch C. St Pierre R, et al. Among authors: smith mj. Nat Genet. 2022 Jun;54(6):861-873. doi: 10.1038/s41588-022-01077-0. Epub 2022 Jun 9. Nat Genet. 2022. PMID: 35681054
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset.
Smith MJ, Higgs JE, Bowers NL, Halliday D, Paterson J, Gillespie J, Huson SM, Freeman SR, Lloyd S, Rutherford SA, King AT, Wallace AJ, Ramsden RT, Evans DG. Smith MJ, et al. J Med Genet. 2011 Apr;48(4):261-5. doi: 10.1136/jmg.2010.085241. Epub 2011 Jan 28. J Med Genet. 2011. PMID: 21278391
Germline and somatic mutations in meningiomas.
Smith MJ. Smith MJ. Cancer Genet. 2015 Apr;208(4):107-14. doi: 10.1016/j.cancergen.2015.02.003. Epub 2015 Feb 19. Cancer Genet. 2015. PMID: 25857641 Review.
SMARCE1 mutations in pediatric clear cell meningioma: case report.
Evans LT, Van Hoff J, Hickey WF, Smith MJ, Evans DG, Newman WG, Bauer DF. Evans LT, et al. Among authors: smith mj. J Neurosurg Pediatr. 2015 Sep;16(3):296-300. doi: 10.3171/2015.3.PEDS14417. Epub 2015 Jun 26. J Neurosurg Pediatr. 2015. PMID: 26114992
Pain correlates with germline mutation in schwannomatosis.
Jordan JT, Smith MJ, Walker JA, Erdin S, Talkowski ME, Merker VL, Ramesh V, Cai W, Harris GJ, Bredella MA, Seijo M, Suuberg A, Gusella JF, Plotkin SR. Jordan JT, et al. Among authors: smith mj. Medicine (Baltimore). 2018 Feb;97(5):e9717. doi: 10.1097/MD.0000000000009717. Medicine (Baltimore). 2018. PMID: 29384852 Free PMC article.
1,744 results