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E M Stone

Showing results (131-140 of 174) with videos related to

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Human Molecular Genetics|January 1, 1997
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.
Carcinogenesis|February 5, 1998
DNA damage in breast epithelial cells: detection by the single-cell gel (comet) assay and induction by human mammary lipid extractsF L Martin, S Venitt, P L Carmichael, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Human Molecular Genetics|August 1, 1995
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.
Eye (London, England)|August 16, 2008
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic waveletsT S Aleman, B L Lam, A V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Experimental Eye Research|May 5, 2007
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)B Bakall, R A Radu, J B Stanton, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Pageof 18

Showing results (131-140 of 174) with videos related to

Sort By:
Pageof 18
Human Molecular Genetics|January 1, 1997
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysisV C Sheffield, M E Pierpont, D Nishimura, et al.
Carcinogenesis|February 5, 1998
DNA damage in breast epithelial cells: detection by the single-cell gel (comet) assay and induction by human mammary lipid extractsF L Martin, S Venitt, P L Carmichael, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 28, 2000
Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindnessJ P Van Hooser, T S Aleman, Y G He, et al.
Human Molecular Genetics|August 1, 1995
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.
Eye (London, England)|August 16, 2008
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic waveletsT S Aleman, B L Lam, A V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Experimental Eye Research|May 5, 2007
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2)B Bakall, R A Radu, J B Stanton, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Pageof 18