000 01422 a2200421 4500
005 20250516134534.0
264 0 _c20130410
008 201304s 0 0 eng d
022 _a1460-2156
024 7 _a10.1093/brain/aws353
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDoddrell, Robin D S
245 0 0 _aLoss of SOX10 function contributes to the phenotype of human Merlin-null schwannoma cells.
_h[electronic resource]
260 _bBrain : a journal of neurology
_cFeb 2013
300 _a549-63 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAnimals
650 0 4 _aCells, Cultured
650 0 4 _aGene Knockdown Techniques
650 0 4 _aHumans
650 0 4 _aMice
650 0 4 _aMice, Transgenic
650 0 4 _aNeurilemmoma
_xgenetics
650 0 4 _aNeurofibromatosis 2
_xgenetics
650 0 4 _aNeurofibromin 2
_xdeficiency
650 0 4 _aPhenotype
650 0 4 _aSOXE Transcription Factors
_xdeficiency
700 1 _aDun, Xin-Peng
700 1 _aShivane, Aditya
700 1 _aFeltri, M Laura
700 1 _aWrabetz, Lawrence
700 1 _aWegner, Michael
700 1 _aSock, Elisabeth
700 1 _aHanemann, C Oliver
700 1 _aParkinson, David B
773 0 _tBrain : a journal of neurology
_gvol. 136
_gno. Pt 2
_gp. 549-63
856 4 0 _uhttps://doi.org/10.1093/brain/aws353
_zAvailable from publisher's website
999 _c22508015
_d22508015