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Matthew Carrigan
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Intravitreal delivery of AAV-NDI1 provides functional benefit in a murine model of Leber hereditary optic neuropathy
N Chadderton, A Palfi, S Millington-Ward, O Gobbo, N Overlack, ...
European Journal of Human Genetics 21 (1), 62-68, 2013
832013
Toward an elucidation of the molecular genetics of inherited retinal degenerations
GJ Farrar, M Carrigan, A Dockery, S Millington-Ward, A Palfi, ...
Human molecular genetics 26 (R1), R2-R11, 2017
792017
T-lex: a program for fast and accurate assessment of transposable element presence using next-generation sequencing data
AS Fiston-Lavier, M Carrigan, DA Petrov, J González
Nucleic acids research 39 (6), e36-e36, 2011
652011
Panel-based population next-generation sequencing for inherited retinal degenerations
M Carrigan, E Duignan, CPG Malone, K Stephenson, T Saad, ...
Scientific reports 6 (1), 33248, 2016
592016
Target 5000: target capture sequencing for inherited retinal degenerations
A Dockery, K Stephenson, D Keegan, N Wynne, G Silvestri, P Humphries, ...
Genes 8 (11), 304, 2017
472017
Insular Celtic population structure and genomic footprints of migration
RP Byrne, R Martiniano, LM Cassidy, M Carrigan, G Hellenthal, ...
PLoS Genetics 14 (1), e1007152, 2018
432018
Findings from a genotyping study of over 1000 people with inherited retinal disorders in Ireland
L Whelan, A Dockery, N Wynne, J Zhu, K Stephenson, G Silvestri, ...
Genes 11 (1), 105, 2020
392020
A novel homozygous truncating GNAT1 mutation implicated in retinal degeneration
M Carrigan, E Duignan, P Humphries, A Palfi, PF Kenna, GJ Farrar
British Journal of Ophthalmology 100 (4), 495-500, 2016
392016
microRNA regulatory circuits in a mouse model of inherited retinal degeneration
A Palfi, K Hokamp, SM Hauck, S Vencken, S Millington-Ward, ...
Scientific reports 6 (1), 31431, 2016
292016
Gene expression changes during retinal development and rod specification
FC Mansergh, M Carrigan, K Hokamp, GJ Farrar
Molecular vision 21, 61, 2015
132015
Novel 199 base pair NEFH promoter drives expression in retinal ganglion cells
S Millington-Ward, N Chadderton, M Berkeley, LK Finnegan, KS Hanlon, ...
Scientific Reports 10 (1), 16515, 2020
82020
Assessing cone photoreceptor structure in patients with mutations in the OPN1LW/OPN1MW gene array
EJ Patterson, M Kasilian, A Kalitzeos, CP Malone, M Carrigan, A Green, ...
Investigative Ophthalmology & Visual Science 58 (8), 1257-1257, 2017
72017
A novel FLVCR1 variant implicated in retinitis pigmentosa
A Dockery, M Carrigan, N Wynne, K Stephenson, D Keegan, PF Kenna, ...
Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 203-207, 2019
62019
Multimodal imaging in a pedigree of X-linked Retinoschisis with a novel RS1 variant
K Stephenson, A Dockery, N Wynne, M Carrigan, P Kenna, G Jane Farrar, ...
BMC Medical Genetics 19, 1-10, 2018
52018
AAV‐mediated gene therapy improving mitochondrial function provides benefit in age‐related macular degeneration models
S Millington‐Ward, N Chadderton, LK Finnegan, IJM Post, M Carrigan, ...
Clinical and Translational Medicine 12 (8), 2022
42022
Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction
N Chadderton, A Palfi, DM Maloney, M Carrigan, LK Finnegan, ...
Pharmaceutics 15 (2), 322, 2023
22023
RPE-Directed Gene Therapy Improves Mitochondrial Function in Murine Dry AMD Models
S Millington-Ward, N Chadderton, LK Finnegan, IJM Post, M Carrigan, ...
International Journal of Molecular Sciences 24 (4), 3847, 2023
12023
Variants of yeast NDI1 gene, and uses thereof in the treatment of disease associated with mitochondrial dysfunction
GJ Farrar, S Millington-Ward, N Chadderton, MA Carrigan, P Kenna
US Patent 10,220,102, 2019
12019
Amelioration of retinal mitochondrial dysfunction with AAV-ophNdi1
N Chadderton, A Palfi, DM Maloney, MA Carrigan, LK Finnegan, ...
HUMAN GENE THERAPY 33 (23-24), A90-A91, 2022
2022
AAV-delivered NDI1 improves mitochondrial function and provides benefit in AMD models
S Millington-Ward, N Chadderton, LK Finnegan, IJM Post, M Carrigan, ...
HUMAN GENE THERAPY 33 (23-24), A15-A16, 2022
2022
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