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Vision Research
|
July 4, 2006
Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function
S Nusinowitz, W H Ridder, J J Pang, et al.
Visual Neuroscience
|
December 8, 2005
Mouse models of ocular diseases
B Chang, N L Hawes, R E Hurd, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 1, 1997
Light reduction and the electroretinogram of preterm infants
K A Kennedy, M A Ipson, D G Birch, et al.
Infection Control and Hospital Epidemiology
|
June 1, 1999
Control of transmission of vancomycin-resistant Enterococcus faecium in a long-term-care facility
M Armstrong-Evans, M Litt, M A McArthur, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 6, 2000
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice
J E Sligh, S E Levy, K G Waymire, 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.
BMC Genetics
|
November 28, 2001
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure
B Chang, R S Smith, M Peters, et al.
Human Molecular Genetics
|
December 23, 1999
Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene
S Ikeda, N Shiva, A Ikeda, 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 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Vision Research
|
July 4, 2006
Cortical visual function in the rd12 mouse model of Leber Congenital Amarousis (LCA) after gene replacement therapy to restore retinal function
S Nusinowitz, W H Ridder, J J Pang, et al.
Visual Neuroscience
|
December 8, 2005
Mouse models of ocular diseases
B Chang, N L Hawes, R E Hurd, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|
May 1, 1997
Light reduction and the electroretinogram of preterm infants
K A Kennedy, M A Ipson, D G Birch, et al.
Infection Control and Hospital Epidemiology
|
June 1, 1999
Control of transmission of vancomycin-resistant Enterococcus faecium in a long-term-care facility
M Armstrong-Evans, M Litt, M A McArthur, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 6, 2000
Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice
J E Sligh, S E Levy, K G Waymire, 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.
BMC Genetics
|
November 28, 2001
Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure
B Chang, R S Smith, M Peters, et al.
Human Molecular Genetics
|
December 23, 1999
Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene
S Ikeda, N Shiva, A Ikeda, 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 3