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Chris F Inglehearn

Showing results (1-10 of 138) with videos related to

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Experimental Eye Research|March 27, 2019
Matrix metalloproteinases in keratoconus - Too much of a good thing?Erica di Martino, Manir Ali, Chris F Inglehearn
European Journal of Human Genetics : EJHG|December 2, 2005
Comment on 'cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy'Helen M Bottomley, Louise M Downey, Chris F Inglehearn, et al.
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|January 1, 2010
Molecular confirmation of the causes of inherited visual impairment in Northern PakistanMehreen Adhi, Yasmin Rashid, Syed Hussain Jafri, et al.
Investigative Ophthalmology & Visual Science|June 17, 2008
Decreased levels of the RNA splicing factor Prpf3 in mice and zebrafish do not cause photoreceptor degenerationJohn J Graziotto, Chris F Inglehearn, Michael A Pack, 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.
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.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 15, 2022
Unlocking the potential of the UK 100,000 Genomes Project-lessons learned from analysis of the "Congenital Malformations caused by Ciliopathies" cohortSunayna Best, Chris F Inglehearn, Christopher M Watson, et al.
Molecular Vision|January 14, 2010
Proteomic profiling of the retinal dysplasia and degeneration chick retinaSorcha Finnegan, Joanne Robson, Paul M Hocking, et al.
Experimental Cell Research|October 12, 2004
PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factorHiroshi Maita, Hirotake Kitaura, T Jeffrey Keen, et al.
Pageof 14

Showing results (1-10 of 138) with videos related to

Sort By:
Pageof 14
Experimental Eye Research|March 27, 2019
Matrix metalloproteinases in keratoconus - Too much of a good thing?Erica di Martino, Manir Ali, Chris F Inglehearn
European Journal of Human Genetics : EJHG|December 2, 2005
Comment on 'cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy'Helen M Bottomley, Louise M Downey, Chris F Inglehearn, et al.
The British Journal of Ophthalmology|January 19, 2011
Changing the status quo biasKamron N Khan, Manir Ali, Carmel Toomes, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|January 1, 2010
Molecular confirmation of the causes of inherited visual impairment in Northern PakistanMehreen Adhi, Yasmin Rashid, Syed Hussain Jafri, et al.
Investigative Ophthalmology & Visual Science|June 17, 2008
Decreased levels of the RNA splicing factor Prpf3 in mice and zebrafish do not cause photoreceptor degenerationJohn J Graziotto, Chris F Inglehearn, Michael A Pack, 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.
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.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 15, 2022
Unlocking the potential of the UK 100,000 Genomes Project-lessons learned from analysis of the "Congenital Malformations caused by Ciliopathies" cohortSunayna Best, Chris F Inglehearn, Christopher M Watson, et al.
Molecular Vision|January 14, 2010
Proteomic profiling of the retinal dysplasia and degeneration chick retinaSorcha Finnegan, Joanne Robson, Paul M Hocking, et al.
Experimental Cell Research|October 12, 2004
PAP-1, the mutated gene underlying the RP9 form of dominant retinitis pigmentosa, is a splicing factorHiroshi Maita, Hirotake Kitaura, T Jeffrey Keen, et al.
Pageof 14