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The EMBO Journal
|
February 28, 2002
On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
G Jane Farrar, Paul F Kenna, Peter Humphries
Trends in Genetics : TIG
|
June 13, 2013
Mitochondrial disorders: aetiologies, models systems, and candidate therapies
G Jane Farrar, Naomi Chadderton, Paul F Kenna, et al.
Neuro-Ophthalmology (Aeolus Press)
|
May 16, 2022
The Natural History of Leber's Hereditary Optic Neuropathy in an Irish Population and Assessment for Prognostic Biomarkers
Kirk A J Stephenson, Joseph McAndrew, Paul F Kenna, et al.
BMJ Open Ophthalmology
|
March 12, 2024
Peripapillary retinal nerve fibre layer thinning, perfusion changes and optic neuropathy in carriers of Leber hereditary optic neuropathy-associated mitochondrial variants
Clare Quigley, Kirk A J Stephenson, Paul F Kenna, et al.
Journal of Dermatological Science
|
December 7, 2007
Reference gene selection for real-time rtPCR in human epidermal keratinocytes
Danny Allen, Eleanor Winters, Paul F Kenna, et al.
Investigative Ophthalmology & Visual Science
|
March 18, 2008
Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram
Alison L Reynolds, Michael Danciger, G Jane Farrar, et al.
Investigative Ophthalmology & Visual Science
|
October 31, 2002
Sensitivity of photoreceptor-derived cell line (661W) to baculoviral p35, Z-VAD.FMK, and Fas-associated death domain
Gearóid Tuohy, Sophia Millington-Ward, Paul F Kenna, et al.
The British Journal of Ophthalmology
|
October 17, 2015
A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration
Matthew Carrigan, Emma Duignan, Pete Humphries, et al.
European Journal of Human Genetics : EJHG
|
February 27, 2014
Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy
Fiona C Mansergh, Naomi Chadderton, Paul F Kenna, et al.
Advances in Experimental Medicine and Biology
|
December 30, 2019
A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa
Adrian Dockery, Matthew Carrigan, Niamh Wynne, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
The EMBO Journal
|
February 28, 2002
On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
G Jane Farrar, Paul F Kenna, Peter Humphries
Trends in Genetics : TIG
|
June 13, 2013
Mitochondrial disorders: aetiologies, models systems, and candidate therapies
G Jane Farrar, Naomi Chadderton, Paul F Kenna, et al.
Neuro-Ophthalmology (Aeolus Press)
|
May 16, 2022
The Natural History of Leber's Hereditary Optic Neuropathy in an Irish Population and Assessment for Prognostic Biomarkers
Kirk A J Stephenson, Joseph McAndrew, Paul F Kenna, et al.
BMJ Open Ophthalmology
|
March 12, 2024
Peripapillary retinal nerve fibre layer thinning, perfusion changes and optic neuropathy in carriers of Leber hereditary optic neuropathy-associated mitochondrial variants
Clare Quigley, Kirk A J Stephenson, Paul F Kenna, et al.
Journal of Dermatological Science
|
December 7, 2007
Reference gene selection for real-time rtPCR in human epidermal keratinocytes
Danny Allen, Eleanor Winters, Paul F Kenna, et al.
Investigative Ophthalmology & Visual Science
|
March 18, 2008
Influence of a quantitative trait locus on mouse chromosome 19 to the light-adapted electroretinogram
Alison L Reynolds, Michael Danciger, G Jane Farrar, et al.
Investigative Ophthalmology & Visual Science
|
October 31, 2002
Sensitivity of photoreceptor-derived cell line (661W) to baculoviral p35, Z-VAD.FMK, and Fas-associated death domain
Gearóid Tuohy, Sophia Millington-Ward, Paul F Kenna, et al.
The British Journal of Ophthalmology
|
October 17, 2015
A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration
Matthew Carrigan, Emma Duignan, Pete Humphries, et al.
European Journal of Human Genetics : EJHG
|
February 27, 2014
Cell therapy using retinal progenitor cells shows therapeutic effect in a chemically-induced rotenone mouse model of Leber hereditary optic neuropathy
Fiona C Mansergh, Naomi Chadderton, Paul F Kenna, et al.
Advances in Experimental Medicine and Biology
|
December 30, 2019
A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa
Adrian Dockery, Matthew Carrigan, Niamh Wynne, et al.
Page
of 7