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E M Stone

Showing results (41-50 of 174) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1994
Ocular findings associated with a Cys39Arg mutation in the Norrie disease geneK M Joos, A E Kimura, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Mutagenesis|March 17, 2000
Pathways of heterocyclic amine activation in the breast: DNA adducts of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) formed by peroxidases and in human mammary epithelial cells and fibroblastsJ A Williams, E M Stone, B C Millar, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1992
Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosaG A Fishman, E M Stone, V C Sheffield, et al.
Genomics|May 1, 1993
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutionsV C Sheffield, J S Beck, A E Kwitek, et al.
Eye (London, England)|October 8, 2016
Structural and molecular changes in the aging choroid: implications for age-related macular degenerationK R Chirco, E H Sohn, E M Stone, et al.
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Complete sequence of the chicken glyceraldehyde-3-phosphate dehydrogenase geneE M Stone, K N Rothblum, M C Alevy, et al.
Pageof 18

Showing results (41-50 of 174) with videos related to

Sort By:
Pageof 18
Archives of Ophthalmology (Chicago, Ill. : 1960)|December 1, 1994
Ocular findings associated with a Cys39Arg mutation in the Norrie disease geneK M Joos, A E Kimura, K Vandenburgh, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Mutagenesis|March 17, 2000
Pathways of heterocyclic amine activation in the breast: DNA adducts of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) formed by peroxidases and in human mammary epithelial cells and fibroblastsJ A Williams, E M Stone, B C Millar, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1992
Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosaG A Fishman, E M Stone, V C Sheffield, et al.
Genomics|May 1, 1993
The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutionsV C Sheffield, J S Beck, A E Kwitek, et al.
Eye (London, England)|October 8, 2016
Structural and molecular changes in the aging choroid: implications for age-related macular degenerationK R Chirco, E H Sohn, E M Stone, et al.
Nature Genetics|July 1, 1992
Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13E M Stone, B E Nichols, L M Streb, et al.
American Journal of Human Genetics|August 1, 1996
An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindredsD A Scott, R Carmi, K Elbedour, et al.
American Journal of Human Genetics|October 1, 1991
Identification of novel rhodopsin mutations associated with retinitis pigmentosa by GC-clamped denaturing gradient gel electrophoresisV C Sheffield, G A Fishman, J S Beck, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Complete sequence of the chicken glyceraldehyde-3-phosphate dehydrogenase geneE M Stone, K N Rothblum, M C Alevy, et al.
Pageof 18