Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1)

By Grohmann Katja  

Human Molecular Genetics, Vol. 13, Iss. 18, 2004-09 ,pp. : 2031-2042

Oxford University Press

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A novel mouse model with impaired dynein/dynactin function develops amyotrophic lateral sclerosis (ALS)-like features in motor neurons and improves lifespan in SOD1-ALS mice

By Teuling Eva   van Dis Vera   Wulf Phebe S.   Haasdijk Elize D.   Akhmanova Anna   Hoogenraad Casper C.   Jaarsma Dick  

Human Molecular Genetics, Vol. 17, Iss. 18, 2008-09 ,pp. : 2849-2862

Oxford University Press

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Restoration of SMN to Emx-1 expressing cortical neurons is not sufficient to provide benefit to a severe mouse model of Spinal Muscular Atrophy

By Taylor Alexander   Glascock Jacqueline   Rose Ferrill   Lutz Cathleen   Lorson Christian  

Transgenic Research, Vol. 22, Iss. 5, 2013-10 ,pp. : 1029-1036

Springer Publishing Company

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Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

By Murray Lyndsay M.   Comley Laura H.   Thomson Derek   Parkinson Nick   Talbot Kevin   Gillingwater Thomas H.  

Human Molecular Genetics, Vol. 17, Iss. 7, 2008-04 ,pp. : 949-962

Oxford University Press

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The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal -actin mRNA translocation in spinal motor neurons

By Glinka Michael   Herrmann Thomas   Funk Natalja   Havlicek Steven   Rossoll Wilfried   Winkler Christoph   Sendtner Michael  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1951-1966

Oxford University Press

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