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A Swaroop

Showing results (81-90 of 96) with videos related to

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Human Molecular Genetics|August 1, 1994
Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6A Swaroop, T L Yang-Feng, W Liu, et al.
Human Molecular Genetics|June 1, 1994
Dinucleotide repeat polymorphism at the DXS977 locusD Yan, D Wong, K Zheng, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Nature Genetics|April 7, 1999
A mutation in NRL is associated with autosomal dominant retinitis pigmentosaD A Bessant, A M Payne, K P Mitton, et al.
Bioorganic Chemistry|November 20, 2020
Design, synthesis and drug resistance reversal potential of novel curcumin mimics Van D: Synergy potential of curcumin mimicsGaurav Raj Dwivedi, Sadiya Khwaja, Arvind Singh Negi, et al.
Human Molecular Genetics|March 13, 2009
Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndromeW S Layman, D P McEwen, L A Beyer, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Human Mutation|February 17, 2001
Five novel RPGR mutations in families with X-linked retinitis pigmentosaM Guevara-Fujita, S Fahrner, K Buraczynska, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Pageof 10

Showing results (81-90 of 96) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|August 1, 1994
Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6A Swaroop, T L Yang-Feng, W Liu, et al.
Human Molecular Genetics|June 1, 1994
Dinucleotide repeat polymorphism at the DXS977 locusD Yan, D Wong, K Zheng, et al.
American Journal of Human Genetics|September 6, 2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15A J Mears, S Hiriyanna, R Vervoort, et al.
Nature Genetics|April 7, 1999
A mutation in NRL is associated with autosomal dominant retinitis pigmentosaD A Bessant, A M Payne, K P Mitton, et al.
Bioorganic Chemistry|November 20, 2020
Design, synthesis and drug resistance reversal potential of novel curcumin mimics Van D: Synergy potential of curcumin mimicsGaurav Raj Dwivedi, Sadiya Khwaja, Arvind Singh Negi, et al.
Human Molecular Genetics|March 13, 2009
Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndromeW S Layman, D P McEwen, L A Beyer, et al.
Human Molecular Genetics|April 3, 2010
Transcriptome analysis and molecular signature of human retinal pigment epitheliumN V Strunnikova, A Maminishkis, J J Barb, et al.
American Journal of Human Genetics|July 1, 1996
A recombination outside the BB deletion refines the location of the X linked retinitis pigmentosa locus RP3R Fujita, E Bingham, P Forsythe, et al.
Human Mutation|February 17, 2001
Five novel RPGR mutations in families with X-linked retinitis pigmentosaM Guevara-Fujita, S Fahrner, K Buraczynska, et al.
Neuron|January 14, 1998
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degenerationP K Swain, S Chen, Q L Wang, et al.
Pageof 10