Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice

By Turner Bradley J.   Ackerley Steven   Davies Kay E.   Talbot Kevin  

Human Molecular Genetics, Vol. 19, Iss. 5, 2010-03 ,pp. : 815-824

Oxford University Press

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Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy

By Homma Sachiko   Beermann Mary Lou   Miller Jeffrey Boone  

Human Molecular Genetics, Vol. 20, Iss. 13, 2011-07 ,pp. : 2662-2672

Oxford University Press

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Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas

By Welander Jenny   Larsson Catharina   Bäckdahl Martin   Hareni Niyaz   Sivlér Tobias   Brauckhoff Michael   Söderkvist Peter   Gimm Oliver  

Human Molecular Genetics, Vol. 21, Iss. 26, 2012-12 ,pp. : 5406-5416

Oxford University Press

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The CMT4B disease-causing phosphatases Mtmr2 and Mtmr13 localize to the Schwann cell cytoplasm and endomembrane compartments, where they depend upon each other to achieve wild-type levels of protein expression

By Ng Aubree A.   Logan Anne M.   Schmidt Eric J.   Robinson Fred L.  

Human Molecular Genetics, Vol. 22, Iss. 8, 2013-04 ,pp. : 1493-1506

Oxford University Press

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Somatic Mutation Processes at a Muman Minisatellite

By Jeffreys Alec J.   Neumann Rita  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 129-136

Oxford University Press

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