Generation and Characterization of a genetic zebrafish model of SMA carrying the human SMN2gene

[1] Lefebvre S(1995)Identification and characterization of a spinal muscular atrophy-determining gene Cell 80 155-165

[2] Burglen L(2000)A mouse model for spinal muscular atrophy Nat Genet 24 66-70

[3] Reboullet S(2000)The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy Hum Mol Genet 9 333-339

[4] Clermont O(2002)Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2 Genet Med 4 20-26

[5] Burlet P(1999)A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2 Hum Mol Genet 8 1177-1183

[6] Viollet L(1999)A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy Proc Natl Acad Sci USA 96 6307-6311

[7] Benichou B(2005)SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN Hum Mol Genet 14 845-857

[8] Cruaud C(2009)Regulation of SMN protein stability Mol Cell Biol 29 1107-1115

[9] Millasseau P(2001)SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens Hum Genet 108 255-266

[10] Zeviani M(2003)A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy J Cell Biol 160 41-52

[1] Lefebvre S(1995)Identification and characterization of a spinal muscular atrophy-determining gene Cell 80 155-165

[2] Burglen L(2000)A mouse model for spinal muscular atrophy Nat Genet 24 66-70

[3] Reboullet S(2000)The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy Hum Mol Genet 9 333-339

[4] Clermont O(2002)Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2 Genet Med 4 20-26

[5] Burlet P(1999)A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2 Hum Mol Genet 8 1177-1183

[6] Viollet L(1999)A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy Proc Natl Acad Sci USA 96 6307-6311

[7] Benichou B(2005)SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN Hum Mol Genet 14 845-857

[8] Cruaud C(2009)Regulation of SMN protein stability Mol Cell Biol 29 1107-1115

[9] Millasseau P(2001)SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens Hum Genet 108 255-266

[10] Zeviani M(2003)A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy J Cell Biol 160 41-52