1996 - Member of the Royal Irish Academy
Peter Humphries mainly investigates Retinitis pigmentosa, Genetics, Gene, Rhodopsin and Retinal. His research in Retinitis pigmentosa intersects with topics in Retinal degeneration, Night vision, Congenital stationary night blindness and Point mutation. His Rhodopsin study integrates concerns from other disciplines, such as Molecular biology, Mutant, Electroretinography and Novel mutation.
His Retinal research includes themes of Retinopathy, Retina and Cell biology. His research integrates issues of Biophysics, Homeostasis and Anatomy in his study of Retina. In his research, Transgene is intimately related to Opsin, which falls under the overarching field of Cell biology.
The scientist’s investigation covers issues in Genetics, Retinitis pigmentosa, Gene, Cell biology and Molecular biology. In his work, Mutant, Genetically modified mouse and Transgene is strongly intertwined with Rhodopsin, which is a subfield of Retinitis pigmentosa. His Gene course of study focuses on Nucleic acid and Effector.
The various areas that Peter Humphries examines in his Cell biology study include Retina, Retinal, Knockout mouse and Gene expression. His Retinal research includes themes of Macular degeneration and Pathology. His biological study deals with issues like DNA, which deal with fields such as Recombinant DNA.
Peter Humphries spends much of his time researching Retina, Retinal, Cell biology, Retinal degeneration and Retinitis pigmentosa. The Retina study combines topics in areas such as Genetic enhancement and Pathology. The study incorporates disciplines such as Cell type and Bioinformatics in addition to Retinal.
His studies in Cell biology integrate themes in fields like Programmed cell death, Transgene and Blood-retina barrier. Peter Humphries interconnects Degeneration, Rhodopsin and Knockout mouse in the investigation of issues within Retinal degeneration. His Retinitis pigmentosa study deals with the bigger picture of Genetics.
Peter Humphries mainly focuses on Genetics, Retinitis pigmentosa, Retina, Tight junction and Retinal. His research in Retinal degeneration, Mutation and Gene are components of Genetics. His Retinitis pigmentosa study incorporates themes from Disease and DNA sequencing.
His Retina study combines topics in areas such as Transgene, Recombinant DNA, Real-time polymerase chain reaction, Green fluorescent protein and Flow cytometry. His work deals with themes such as Cognition, Homeostasis and Small interfering RNA, which intersect with Tight junction. His Retinal study combines topics from a wide range of disciplines, such as Inflammasome, Notch signaling pathway and Transplantation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Genetic Reactivation of Cone Photoreceptors Restores Visual Responses in Retinitis Pigmentosa
Volker Busskamp;Jens Duebel;David Balya;Mathias Fradot;Mathias Fradot;Mathias Fradot.
Science (2010)
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
Humphries Mm;Rancourt D;Farrar Gj;Kenna P;Kenna P.
Nature Genetics (1997)
A three-base-pair deletion in the peripherin– RDS gene in one form of retinitis pigmentosa
Farrar Gj;Kenna P;Jordan Sa;Kumar-Singh R.
Nature (1991)
NLRP3 has a protective role in age-related macular degeneration through the induction of IL-18 by drusen components
Sarah L. Doyle;Matthew Campbell;Ema Ozaki;Robert G. Salomon.
Nature Medicine (2012)
Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3
Peter McWilliam;G.Jane Farrar;Paul Kenna;Daniel G. Bradley.
Genomics (1989)
On the genetics of retinitis pigmentosa and on mutation-independent approaches to therapeutic intervention
G. Jane Farrar;Paul F. Kenna;Peter Humphries.
The EMBO Journal (2002)
On the molecular genetics of retinitis pigmentosa
P Humphries;P Kenna;GJ Farrar.
Science (1992)
New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis.
Mathias W. Seeliger;Christian Grimm;Fredrik Ståhlberg;Fredrik Ståhlberg;Christoph Friedburg.
Nature Genetics (2001)
The Blood-Retina Barrier
Matthew Campbell;Peter Humphries.
Advances in Experimental Medicine and Biology (2013)
Evaluation of mixed chimerism by in vitro amplification of dinucleotide repeat sequences using the polymerase chain reaction
M Lawler;P Humphries;SR McCann.
Blood (1991)
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