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E M Stone

Showing results (71-80 of 174) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|September 12, 2000
Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutationK T Oh, R G Weleber, A Lotery, et al.
Brain Research. Molecular Brain Research|May 13, 1999
Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brainR E Swiderski, L Ying, M D Cassell, et al.
Human Molecular Genetics|January 1, 1995
Novel frameshift mutations in the procollagen 2 gene (COL2A1) associated with Stickler syndrome (hereditary arthro-ophthalmopathy)D M Brown, K Vandenburgh, A E Kimura, et al.
Biochemistry|March 29, 1983
Cloning and sequencing of a deoxyribonucleic acid copy of glyceraldehyde-3-phosphate dehydrogenase messenger ribonucleic acid isolated from chicken muscleA Dugaiczyk, J A Haron, E M Stone, et al.
Ophthalmology|January 1, 1990
The pathology of posterior amorphous corneal dystrophyA T Johnson, R Folberg, M P Vrabec, et al.
Genes, Chromosomes & Cancer|March 10, 2001
TCL1 is activated by chromosomal rearrangement or by hypomethylationM R Yuille, A Condie, E M Stone, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Human Molecular Genetics|May 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Gene|November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)N B Haider, C Searby, E Galperin, et al.
Pageof 18

Showing results (71-80 of 174) with videos related to

Sort By:
Pageof 18
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 12, 2000
Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutationK T Oh, R G Weleber, A Lotery, et al.
Brain Research. Molecular Brain Research|May 13, 1999
Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brainR E Swiderski, L Ying, M D Cassell, et al.
Human Molecular Genetics|January 1, 1995
Novel frameshift mutations in the procollagen 2 gene (COL2A1) associated with Stickler syndrome (hereditary arthro-ophthalmopathy)D M Brown, K Vandenburgh, A E Kimura, et al.
Biochemistry|March 29, 1983
Cloning and sequencing of a deoxyribonucleic acid copy of glyceraldehyde-3-phosphate dehydrogenase messenger ribonucleic acid isolated from chicken muscleA Dugaiczyk, J A Haron, E M Stone, et al.
Ophthalmology|January 1, 1990
The pathology of posterior amorphous corneal dystrophyA T Johnson, R Folberg, M P Vrabec, et al.
Genes, Chromosomes & Cancer|March 10, 2001
TCL1 is activated by chromosomal rearrangement or by hypomethylationM R Yuille, A Condie, E M Stone, et al.
Investigative Ophthalmology & Visual Science|December 1, 2001
Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cellsA R Shepard, N Jacobson, J H Fingert, et al.
Human Molecular Genetics|May 1, 1993
A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the foveaB E Nichols, A V Drack, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 1, 1994
Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6qE M Stone, B E Nichols, A E Kimura, et al.
Gene|November 24, 1999
Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1)N B Haider, C Searby, E Galperin, et al.
Pageof 18