Altered retinal microRNA expression profile in a mouse model of retinitis pigmentosa (2007)
Loscher, Carol J, Hokamp, Karsten, Kenna, Paul F, Ivens, Alasdair C, Humphries, Peter, Palfi, Arpad, ...
Abstract Background The role played by microRNAs (miRs) as common regulators in physiologic processes such as development and various disease states was recently highlighted. Retinitis pigmentosa...
Conceptualising the worker-client relationship in social work practice (2000)
Typescript (photocopy) Bibliography: leaves 112-119.
Farrar, G.Jane, Kenna, Paul F., Humphries, Peter
Retinitis pigmentosa (RP), the group of hereditary conditions involving death of retinal photoreceptors, represents the most prevalent cause of visual handicap among working populations in developed...
Dinucleotide repeat polymorphism at the T cell receptor δ locus (TCRD)
Jordan, Siobhan A., McWilliam, Peter, O'Briain, D.S., Humphries, Peter
Humphries, Peter, McConnell, David J., Gordon, Robert L.
A rapid procedure involving DNA–cellulose chromatography followed either by sedimentation in a high-salt glycerol gradient or by gel filtration is described for the complete purification of...
Hamosh, Ada, King, Terri M., Rosenstein, Beryl J., Corey, Mary, Levison, Henry, Durie, Peter, ...
The glycine-to-aspartic acid missense mutation at codon 551 (G551D), which is within the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator (CFTR), is the third...
Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families
Inglehearn, Chris F., Lester, Douglas H., Bashir, Rumaisa, Atif, Uzma, Keen, T. Jeffrey, Sertedaki, Amalia, ...
Autosomal dominant retinitis pigmentosa (adRP) has shown linkage to the chromosome 3q marker C17 (D3S47) in two large adRP pedigrees known as TCDM1 and adRP3. On the basis of this evidence the...
Farrar, G.Jane, Kenna, Paul F., Humphries, Peter
Retinitis pigmentosa (RP), the group of hereditary conditions involving death of retinal photoreceptors, represents the most prevalent cause of visual handicap among working populations in developed...
Dinucleotide repeat polymorphism at the T cell receptor δ locus (TCRD)
Jordan, Siobhan A., McWilliam, Peter, O'Briain, D.S., Humphries, Peter
Humphries, Peter, McConnell, David J., Gordon, Robert L.
A rapid procedure involving DNA–cellulose chromatography followed either by sedimentation in a high-salt glycerol gradient or by gel filtration is described for the complete purification of...
Hamosh, Ada, King, Terri M., Rosenstein, Beryl J., Corey, Mary, Levison, Henry, Durie, Peter, ...
The glycine-to-aspartic acid missense mutation at codon 551 (G551D), which is within the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator (CFTR), is the third...
Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families
Inglehearn, Chris F., Lester, Douglas H., Bashir, Rumaisa, Atif, Uzma, Keen, T. Jeffrey, Sertedaki, Amalia, ...
Autosomal dominant retinitis pigmentosa (adRP) has shown linkage to the chromosome 3q marker C17 (D3S47) in two large adRP pedigrees known as TCDM1 and adRP3. On the basis of this evidence the...
Altered retinal microRNA expression profile in a mouse model of retinitis pigmentosa
Loscher, Carol J, Hokamp, Karsten, Kenna, Paul F, Ivens, Alasdair C, Humphries, Peter, Palfi, Arpad, ...
MicroRNA expression profiling showed that the retina of mice carrying a rhodopsin mutation that leads to retinitis pigmentosa have notably different microRNA profiles from wildtype mice; further in...