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The Journal of Clinical Investigation
|
April 1, 1989
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency
E H Birkenmeier, M T Davisson, W G Beamer, et al.
Nature Genetics
|
April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
B Chang, R S Smith, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1993
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta
S D Chipman, H O Sweet, D J McBride, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18
A J Griffith, G L Radice, D L Burgess, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens
N L Hawes, B Chang, G S Hageman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report on the committee on comparative mapping
P A Lalley, S J O'Brien, N Créau-Goldberg, et al.
Genome Research
|
December 16, 2000
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
R Chrast, H S Scott, M P Papasavvas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
N B Akhmedov, N I Piriev, B Chang, et al.
Vision Research
|
February 3, 2007
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene
B Chang, N L Hawes, M T Pardue, et al.
Page
of 14
Search research articles
Search
Showing results (131-140 of 139) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 139 results.
The Journal of Clinical Investigation
|
April 1, 1989
Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency
E H Birkenmeier, M T Davisson, W G Beamer, et al.
Nature Genetics
|
April 7, 1999
Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice
B Chang, R S Smith, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1993
Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta
S D Chipman, H O Sweet, D J McBride, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18
A J Griffith, G L Radice, D L Burgess, et al.
Investigative Ophthalmology & Visual Science
|
September 1, 2000
Retinal degeneration 6 (rd6): a new mouse model for human retinitis punctata albescens
N L Hawes, B Chang, G S Hageman, et al.
Cytogenetics and Cell Genetics
|
January 1, 1987
Report on the committee on comparative mapping
P A Lalley, S J O'Brien, N Créau-Goldberg, et al.
Genome Research
|
December 16, 2000
The mouse brain transcriptome by SAGE: differences in gene expression between P30 brains of the partial trisomy 16 mouse model of Down syndrome (Ts65Dn) and normals
R Chrast, H S Scott, M P Papasavvas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 11, 2000
A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse
N B Akhmedov, N I Piriev, B Chang, et al.
Vision Research
|
February 3, 2007
Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene
B Chang, N L Hawes, M T Pardue, et al.
Page
of 14