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Manir Ali

Showing results (1-10 of 80) with videos related to

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Methods in Molecular Medicine|November 7, 2007
Differential display reverse transcription-polymerase chain reaction to identify novel biomolecules in arthritis researchManir Ali, John D Isaacs
The British Journal of Ophthalmology|December 21, 2010
Familial pattern of Salzmann-type nodular corneal degeneration – a four generation series. Reply to Papanikolaou et alKamron Khan, Manir Ali, Chris Inglehearn
Molecular Vision|September 11, 2013
An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican villageCarlos Pantoja-Melendez, Manir Ali, Juan C Zenteno
Investigative Ophthalmology & Visual Science|January 19, 2013
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneDavid S M Burton, Manir Ali, Martin McKibbin
Experimental Eye Research|March 27, 2019
Matrix metalloproteinases in keratoconus - Too much of a good thing?Erica di Martino, Manir Ali, Chris F Inglehearn
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
Veterinary Ophthalmology|May 25, 2013
Spectral domain optical coherence tomography imaging of the posterior segment of the eye in the retinal dysplasia and degeneration chicken, an animal model of inherited retinal degenerationMartin McKibbin, Manir Ali, Chris Inglehearn, et al.
BMJ (Clinical Research Ed.)|November 8, 2013
Patterns of inheritance, not always easily visibleKamron N Khan, Manir Ali, James A Poulter, et al.
European Journal of Medical Genetics|February 25, 2006
Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansionKatherine Horsnell, Manir Ali, Saghira Malik, et al.
Molecular Diagnosis & Therapy|July 28, 2025
Long-Range PCR and Nanopore Sequencing Enables High-Throughput Detection of TCF4 Trinucleotide Repeat Expansions in Fuchs Endothelial Corneal DystrophyBushra Alayed, Salina Siddiqui, Seema Anand, et al.
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Methods in Molecular Medicine|November 7, 2007
Differential display reverse transcription-polymerase chain reaction to identify novel biomolecules in arthritis researchManir Ali, John D Isaacs
The British Journal of Ophthalmology|December 21, 2010
Familial pattern of Salzmann-type nodular corneal degeneration – a four generation series. Reply to Papanikolaou et alKamron Khan, Manir Ali, Chris Inglehearn
Molecular Vision|September 11, 2013
An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican villageCarlos Pantoja-Melendez, Manir Ali, Juan C Zenteno
Investigative Ophthalmology & Visual Science|January 19, 2013
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneDavid S M Burton, Manir Ali, Martin McKibbin
Experimental Eye Research|March 27, 2019
Matrix metalloproteinases in keratoconus - Too much of a good thing?Erica di Martino, Manir Ali, Chris F Inglehearn
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
Veterinary Ophthalmology|May 25, 2013
Spectral domain optical coherence tomography imaging of the posterior segment of the eye in the retinal dysplasia and degeneration chicken, an animal model of inherited retinal degenerationMartin McKibbin, Manir Ali, Chris Inglehearn, et al.
BMJ (Clinical Research Ed.)|November 8, 2013
Patterns of inheritance, not always easily visibleKamron N Khan, Manir Ali, James A Poulter, et al.
European Journal of Medical Genetics|February 25, 2006
Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansionKatherine Horsnell, Manir Ali, Saghira Malik, et al.
Molecular Diagnosis & Therapy|July 28, 2025
Long-Range PCR and Nanopore Sequencing Enables High-Throughput Detection of TCF4 Trinucleotide Repeat Expansions in Fuchs Endothelial Corneal DystrophyBushra Alayed, Salina Siddiqui, Seema Anand, et al.
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