Search research articles
Contact Us
Filters
Showing results (11-20 of 29) with videos related to
Page
of 3
Sort By:
Investigative Ophthalmology & Visual Science
|
July 7, 1999
Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice
S Ikeda, N L Hawes, B Chang, et al.
Molecular Vision
|
September 24, 1999
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes
N L Hawes, R S Smith, B Chang, et al.
Genomics
|
August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)
B Chang, N L Hawes, R S Smith, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 29, 1999
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17
R S Smith, K R Johnson, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
J R Heckenlively, B Chang, L C Erway, et al.
Molecular Vision
|
September 24, 1999
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse
B Chang, N L Hawes, T H Roderick, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1994
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis
B Chang, R T Bronson, N L Hawes, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1996
Corn1: a mouse model for corneal surface disease and neovascularization
R S Smith, N L Hawes, S D Kuhlmann, et al.
Visual Neuroscience
|
December 8, 2005
Mouse models of ocular diseases
B Chang, N L Hawes, R E Hurd, et al.
Genomics
|
March 8, 2000
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract
R S Smith, N L Hawes, B Chang, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Investigative Ophthalmology & Visual Science
|
July 7, 1999
Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient mice
S Ikeda, N L Hawes, B Chang, et al.
Molecular Vision
|
September 24, 1999
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes
N L Hawes, R S Smith, B Chang, et al.
Genomics
|
August 15, 1996
Chromosomal localization of a new mouse lens opacity gene (lop18)
B Chang, N L Hawes, R S Smith, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 29, 1999
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17
R S Smith, K R Johnson, N L Hawes, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 21, 1995
Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15
J R Heckenlively, B Chang, L C Erway, et al.
Molecular Vision
|
September 24, 1999
Identification of a missense mutation in the alphaA-crystallin gene of the lop18 mouse
B Chang, N L Hawes, T H Roderick, et al.
Investigative Ophthalmology & Visual Science
|
March 1, 1994
Retinal degeneration in motor neuron degeneration: a mouse model of ceroid lipofuscinosis
B Chang, R T Bronson, N L Hawes, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1996
Corn1: a mouse model for corneal surface disease and neovascularization
R S Smith, N L Hawes, S D Kuhlmann, et al.
Visual Neuroscience
|
December 8, 2005
Mouse models of ocular diseases
B Chang, N L Hawes, R E Hurd, et al.
Genomics
|
March 8, 2000
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract
R S Smith, N L Hawes, B Chang, et al.
Page
of 3