Tatiana O Gavrilina - JoVE Visualize

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Human Molecular Genetics|July 8, 2008

Embryonic motor axon development in the severe SMA mouseVicki L McGovern, Tatiana O Gavrilina, Christine E Beattie, et al.

Human Molecular Genetics|January 8, 2008

Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effectTatiana O Gavrilina, Vicki L McGovern, Eileen Workman, et al.

Human Molecular Genetics|February 11, 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 SMNThanh T Le, Lan T Pham, Matthew E R Butchbach, et al.

The Journal of Cell Biology|January 8, 2003

A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophyUmrao R Monani, Matthew T Pastore, Tatiana O Gavrilina, et al.

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Showing results (1-10 of 4) with videos related to

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Pageof 1

Human Molecular Genetics|July 8, 2008

Embryonic motor axon development in the severe SMA mouseVicki L McGovern, Tatiana O Gavrilina, Christine E Beattie, et al.

Human Molecular Genetics|January 8, 2008

Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effectTatiana O Gavrilina, Vicki L McGovern, Eileen Workman, et al.

Human Molecular Genetics|February 11, 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 SMNThanh T Le, Lan T Pham, Matthew E R Butchbach, et al.

The Journal of Cell Biology|January 8, 2003

A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophyUmrao R Monani, Matthew T Pastore, Tatiana O Gavrilina, et al.

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