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Manir Ali

Showing results (11-20 of 80) with videos related to

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Molecular Vision|January 14, 2010
Proteomic profiling of the retinal dysplasia and degeneration chick retinaSorcha Finnegan, Joanne Robson, Paul M Hocking, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 23, 2023
Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants: Lessons Learned From the ABCA4 LocusBenjamin McClinton, Christopher M Watson, Laura A Crinnion, et al.
The British Journal of Ophthalmology|May 12, 2011
CFH, VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degenerationMartin McKibbin, Manir Ali, Shveta Bansal, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Mutation in the guanine nucleotide-binding protein beta-3 causes retinal degeneration and embryonic mortality in chickensHemanth Tummala, Manir Ali, Paul Getty, et al.
Brain and Behavior|May 20, 2017
The effect of <i>COMT Val158Met</i> and <i>DRD2 C957T</i> polymorphisms on executive function and the impact of early life stressKristel Klaus, Kevin Butler, Simon J Durrant, et al.
Journal of Structural Biology|October 16, 2007
Collagen organization in the chicken cornea and structural alterations in the retinopathy, globe enlarged (rge) phenotype--an X-ray diffraction studyCraig Boote, Sally Hayes, Simon Jones, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Molecular Vision|April 9, 2026
Exploring the molecular basis of microphthalmia and anophthalmia: Insights from an Egyptian cohortGehad Elmakkawy, Amira Nabil, Karim Nabil, et al.
Human Genetics|April 21, 2015
A missense variant in CST3 exerts a recessive effect on susceptibility to age-related macular degeneration resembling its association with Alzheimer's diseaseJoe M Butler, Umar Sharif, Manir Ali, et al.
Plos One|September 3, 2011
The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickensHemanth Tummala, Stewart Fleming, Paul M Hocking, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Molecular Vision|January 14, 2010
Proteomic profiling of the retinal dysplasia and degeneration chick retinaSorcha Finnegan, Joanne Robson, Paul M Hocking, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|April 23, 2023
Haplotyping Using Long-Range PCR and Nanopore Sequencing to Phase Variants: Lessons Learned From the ABCA4 LocusBenjamin McClinton, Christopher M Watson, Laura A Crinnion, et al.
The British Journal of Ophthalmology|May 12, 2011
CFH, VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degenerationMartin McKibbin, Manir Ali, Shveta Bansal, et al.
Investigative Ophthalmology & Visual Science|October 27, 2006
Mutation in the guanine nucleotide-binding protein beta-3 causes retinal degeneration and embryonic mortality in chickensHemanth Tummala, Manir Ali, Paul Getty, et al.
Brain and Behavior|May 20, 2017
The effect of <i>COMT Val158Met</i> and <i>DRD2 C957T</i> polymorphisms on executive function and the impact of early life stressKristel Klaus, Kevin Butler, Simon J Durrant, et al.
Journal of Structural Biology|October 16, 2007
Collagen organization in the chicken cornea and structural alterations in the retinopathy, globe enlarged (rge) phenotype--an X-ray diffraction studyCraig Boote, Sally Hayes, Simon Jones, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Molecular Vision|April 9, 2026
Exploring the molecular basis of microphthalmia and anophthalmia: Insights from an Egyptian cohortGehad Elmakkawy, Amira Nabil, Karim Nabil, et al.
Human Genetics|April 21, 2015
A missense variant in CST3 exerts a recessive effect on susceptibility to age-related macular degeneration resembling its association with Alzheimer's diseaseJoe M Butler, Umar Sharif, Manir Ali, et al.
Plos One|September 3, 2011
The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickensHemanth Tummala, Stewart Fleming, Paul M Hocking, et al.
Pageof 8