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Manir Ali

Showing results (21-30 of 80) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2010
Genotype-phenotype correlation for leber congenital amaurosis in Northern PakistanMartin McKibbin, Manir Ali, Moin D Mohamed, et al.
Molecular Vision|November 4, 2008
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degenerationManir Ali, Vedam Lakshmi Ramprasad, Nagasamy Soumittra, et al.
Biophysical Journal|June 25, 2013
An x-ray scattering study into the structural basis of corneal refractive function in an avian modelSiân R Morgan, Erin P Dooley, Paul M Hocking, et al.
Investigative Ophthalmology & Visual Science|November 6, 2010
The influence of lamellar orientation on corneal material behavior: biomechanical and structural changes in an avian corneal disorderCraig Boote, Ahmed Elsheikh, Wael Kassem, et al.
Journal of Structural Biology|March 5, 2009
Ultrastructural changes in the retinopathy, globe enlarged (rge) chick corneaCraig Boote, Sally Hayes, Robert D Young, et al.
Human Mutation|November 5, 2011
Identification of autosomal recessive disease loci using out-bred nuclear familiesIan M Carr, Christine P Diggle, Nader Touqan, et al.
Investigative Ophthalmology & Visual Science|December 14, 2011
Profiling retinal biochemistry in the MPDZ mutant retinal dysplasia and degeneration chick: a model of human RP and LCAJames R Beattie, Sorcha Finnegan, Ross W Hamilton, et al.
Molecular Vision|June 13, 2022
Novel homozygous mutations in the transcription factor <i>NRL</i> cause non-syndromic retinitis pigmentosaMohammed E El-Asrag, Marta Corton, Martin McKibbin, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategiesBenjamin McClinton, Laura A Crinnion, Martin McKibbin, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 13, 2010
Genotype-phenotype correlation for leber congenital amaurosis in Northern PakistanMartin McKibbin, Manir Ali, Moin D Mohamed, et al.
Molecular Vision|November 4, 2008
A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degenerationManir Ali, Vedam Lakshmi Ramprasad, Nagasamy Soumittra, et al.
Biophysical Journal|June 25, 2013
An x-ray scattering study into the structural basis of corneal refractive function in an avian modelSiân R Morgan, Erin P Dooley, Paul M Hocking, et al.
Investigative Ophthalmology & Visual Science|November 6, 2010
The influence of lamellar orientation on corneal material behavior: biomechanical and structural changes in an avian corneal disorderCraig Boote, Ahmed Elsheikh, Wael Kassem, et al.
Journal of Structural Biology|March 5, 2009
Ultrastructural changes in the retinopathy, globe enlarged (rge) chick corneaCraig Boote, Sally Hayes, Robert D Young, et al.
Human Mutation|November 5, 2011
Identification of autosomal recessive disease loci using out-bred nuclear familiesIan M Carr, Christine P Diggle, Nader Touqan, et al.
Investigative Ophthalmology & Visual Science|December 14, 2011
Profiling retinal biochemistry in the MPDZ mutant retinal dysplasia and degeneration chick: a model of human RP and LCAJames R Beattie, Sorcha Finnegan, Ross W Hamilton, et al.
Molecular Vision|June 13, 2022
Novel homozygous mutations in the transcription factor <i>NRL</i> cause non-syndromic retinitis pigmentosaMohammed E El-Asrag, Marta Corton, Martin McKibbin, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategiesBenjamin McClinton, Laura A Crinnion, Martin McKibbin, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Pageof 8