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Muriel T Davisson

Showing results (31-40 of 40) with videos related to

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Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65DnLaura G Reinholdt, Yueming Ding, Griffith J Gilbert, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 5, 2012
Centralized mouse repositoriesLeah Rae Donahue, Martin Hrabe de Angelis, Michael Hagn, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
Nature Genetics|December 29, 2005
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic miceSandra L Gilbert, Li Zhang, Michele L Forster, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Molecular Vision|March 15, 2005
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)Ji-Jing Pang, Bo Chang, Norman L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2011
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouseCharlotte Lindfors, Ida A K Nilsson, Pablo M Garcia-Roves, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 2, 2008
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndromeSergey V Voronov, Samuel G Frere, Silvia Giovedi, et al.
Visual Neuroscience|April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesBo Chang, John R Heckenlively, Philippa R Bayley, et al.
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Showing results (31-40 of 40) with videos related to

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Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 29, 2011
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65DnLaura G Reinholdt, Yueming Ding, Griffith J Gilbert, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 5, 2012
Centralized mouse repositoriesLeah Rae Donahue, Martin Hrabe de Angelis, Michael Hagn, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 20, 2004
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in miceBettina Lorenz-Depiereux, Victoria E Guido, Kenneth R Johnson, et al.
Nature Genetics|December 29, 2005
Trak1 mutation disrupts GABA(A) receptor homeostasis in hypertonic miceSandra L Gilbert, Li Zhang, Michele L Forster, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 13, 2003
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisisLeah Rae Donahue, Bo Chang, Subburaman Mohan, et al.
Molecular Vision|March 15, 2005
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)Ji-Jing Pang, Bo Chang, Norman L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2011
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouseCharlotte Lindfors, Ida A K Nilsson, Pablo M Garcia-Roves, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 2, 2008
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndromeSergey V Voronov, Samuel G Frere, Silvia Giovedi, et al.
Visual Neuroscience|April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesBo Chang, John R Heckenlively, Philippa R Bayley, et al.
Pageof 4