Deletion of smn-1 , the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan

By Briese Michael   Esmaeili Behrooz   Fraboulet Sandrine   Burt Emma C.   Christodoulou Stefanos   Towers Paula R.   Davies Kay E.   Sattelle David B.  

Human Molecular Genetics, Vol. 18, Iss. 1, 2009-01 ,pp. : 97-104

Oxford University Press

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The Caenorhabditis elegans homolog of FGD1, the human Cdc42 GEF gene responsible for faciogenital dysplasia, is critical for excretory cell morphogenesis

By Gao Jingtong  

Human Molecular Genetics, Vol. 10, Iss. 26, 2001-12 ,pp. : 3049-3062

Oxford University Press

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The human centromeric survival motor neuron gene ( SMN2 ) rescues embryonic lethality in Smn –/– mice and results in a mouse with spinal muscular atrophy

By Monani Umrao R.  

Human Molecular Genetics, Vol. 9, Iss. 3, 2000-02 ,pp. : 333-339

Oxford University Press

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The role of the SMN gene in proximal spinal muscular atrophy

By Melki J.  

Human Molecular Genetics, Vol. 7, Iss. 10, 1998-10 ,pp. : 1531-1536

Oxford University Press

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A novel Caenorhabditis elegans allele, smn-1(cb131) , mimicking a mild form of spinal muscular atrophy, provides a convenient drug screening platform highlighting new and pre-approved compounds

By Sleigh James N.   Buckingham Steven D.   Esmaeili Behrooz   Viswanathan Mohan   Cuppen Edwin   Westlund Bethany M.   Sattelle David B.  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 245-260

Oxford University Press

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