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N L Hawes

Showing results (11-20 of 29) with videos related to

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Investigative Ophthalmology & Visual Science|July 7, 1999
Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient miceS Ikeda, N L Hawes, B Chang, et al.
Molecular Vision|September 24, 1999
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypesN 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 17R 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 11p15J 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 mouseB 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 lipofuscinosisB 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 neovascularizationR S Smith, N L Hawes, S D Kuhlmann, et al.
Visual Neuroscience|December 8, 2005
Mouse models of ocular diseasesB 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 cataractR S Smith, N L Hawes, B Chang, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Investigative Ophthalmology & Visual Science|July 7, 1999
Severe ocular abnormalities in C57BL/6 but not in 129/Sv p53-deficient miceS Ikeda, N L Hawes, B Chang, et al.
Molecular Vision|September 24, 1999
Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypesN 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 17R 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 11p15J 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 mouseB 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 lipofuscinosisB 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 neovascularizationR S Smith, N L Hawes, S D Kuhlmann, et al.
Visual Neuroscience|December 8, 2005
Mouse models of ocular diseasesB 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 cataractR S Smith, N L Hawes, B Chang, et al.
Pageof 3