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5. Expression of SMARCB1 (INI1) mutations in familial schwannomatosis. Smith MJ; Walker JA; Shen Y; Stemmer-Rachamimov A; Gusella JF; Plotkin SR Hum Mol Genet; 2012 Dec; 21(24):5239-45. PubMed ID: 22949514 [TBL] [Abstract][Full Text] [Related]
6. Germline mutation of INI1/SMARCB1 in familial schwannomatosis. Hulsebos TJ; Plomp AS; Wolterman RA; Robanus-Maandag EC; Baas F; Wesseling P Am J Hum Genet; 2007 Apr; 80(4):805-10. PubMed ID: 17357086 [TBL] [Abstract][Full Text] [Related]
7. Immunohistochemical analysis supports a role for INI1/SMARCB1 in hereditary forms of schwannomas, but not in solitary, sporadic schwannomas. Patil S; Perry A; Maccollin M; Dong S; Betensky RA; Yeh TH; Gutmann DH; Stemmer-Rachamimov AO Brain Pathol; 2008 Oct; 18(4):517-9. PubMed ID: 18422762 [TBL] [Abstract][Full Text] [Related]
8. Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation. Bacci C; Sestini R; Provenzano A; Paganini I; Mancini I; Porfirio B; Vivarelli R; Genuardi M; Papi L Neurogenetics; 2010 Feb; 11(1):73-80. PubMed ID: 19582488 [TBL] [Abstract][Full Text] [Related]
9. Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri. van den Munckhof P; Christiaans I; Kenter SB; Baas F; Hulsebos TJ Neurogenetics; 2012 Feb; 13(1):1-7. PubMed ID: 22038540 [TBL] [Abstract][Full Text] [Related]
10. Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis. Hadfield KD; Newman WG; Bowers NL; Wallace A; Bolger C; Colley A; McCann E; Trump D; Prescott T; Evans DG J Med Genet; 2008 Jun; 45(6):332-9. PubMed ID: 18285426 [TBL] [Abstract][Full Text] [Related]
11. [Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis: an evolving paradigm]. Dereure O Ann Dermatol Venereol; 2009 Mar; 136(3):296-7. PubMed ID: 19328320 [No Abstract] [Full Text] [Related]
13. Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas. Sestini R; Bacci C; Provenzano A; Genuardi M; Papi L Hum Mutat; 2008 Feb; 29(2):227-31. PubMed ID: 18072270 [TBL] [Abstract][Full Text] [Related]
14. Identification of a novel germline SMARCB1 nonsense mutation in a family manifesting both schwannomatosis and unilateral vestibular schwannoma. Wu J; Kong M; Bi Q J Neurooncol; 2015 Nov; 125(2):439-41. PubMed ID: 26342709 [No Abstract] [Full Text] [Related]
15. A germline missense mutation in COQ6 is associated with susceptibility to familial schwannomatosis. Zhang K; Lin JW; Wang J; Wu X; Gao H; Hsieh YC; Hwu P; Liu YR; Su L; Chiou HY; Wang D; Yuan YC; Whang-Peng J; Chiu WT; Yen Y Genet Med; 2014 Oct; 16(10):787-92. PubMed ID: 24763291 [TBL] [Abstract][Full Text] [Related]
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17. Broadening the spectrum of SMARCB1-associated malignant tumors: a case of uterine leiomyosarcoma in a patient with schwannomatosis. Paganini I; Sestini R; Cacciatore M; Capone GL; Candita L; Paolello C; Sbaraglia M; Dei Tos AP; Rossi S; Papi L Hum Pathol; 2015 Aug; 46(8):1226-31. PubMed ID: 26001331 [TBL] [Abstract][Full Text] [Related]
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19. Premature termination of SMARCB1 translation may be followed by reinitiation in schwannomatosis-associated schwannomas, but results in absence of SMARCB1 expression in rhabdoid tumors. Hulsebos TJ; Kenter S; Verhagen WI; Baas F; Flucke U; Wesseling P Acta Neuropathol; 2014 Sep; 128(3):439-48. PubMed ID: 24740647 [TBL] [Abstract][Full Text] [Related]
20. Multiple schwannomatosis caused by the recently described INI1 gene--molecular pathology, and implications for prognosis. Brennan PM; Barlow A; Geraghty A; Summers D; Fitzpatrick MM Br J Neurosurg; 2011 Jun; 25(3):330-2. PubMed ID: 20854059 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]