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Kevin Talbot

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Chemicals & Drugs

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Motor Neurons

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Physiology

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Publications

TOP 3
Talbot Kevin
Another gene for ALS: mutations in sporadic cases and the rare variant hypothesis.
Achilli Francesca; Bros-Facer Virginie; Williams Hazel P; Banks Gareth T; AlQatari Mona; Chia Ruth; Tucci Valter; Groves Michael; Nickols Carole D; Seburn Kevin L; Kendall Rachel; Cader Muhammed Z; Talbot Kevin; van Minnen Jan; Burgess Robert W; Brandner Sebastian; Martin Joanne E; Koltzenburg Martin; Greensmith Linda; Nolan Patrick M; Fisher Elizabeth M C
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
Turner Bradley J; Parkinson Nicholas J; Davies Kay E; Talbot Kevin
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.

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All Publications

2009: Talbot Kevin
Another gene for ALS: mutations in sporadic cases and the rare variant hypothesis.
Neurology 2009;73(15):1172-3.
2009: Achilli Francesca; Bros-Facer Virginie; Williams Hazel P; Banks Gareth T; AlQatari Mona; Chia Ruth; Tucci Valter; Groves Michael; Nickols Carole D; Seburn Kevin L; Kendall Rachel; Cader Muhammed Z; Talbot Kevin; van Minnen Jan; Burgess Robert W; Brandner Sebastian; Martin Joanne E; Koltzenburg Martin; Greensmith Linda; Nolan Patrick M; Fisher Elizabeth M C
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
Disease models & mechanisms 2009;2(7-8):359-73.
2009: Turner Bradley J; Parkinson Nicholas J; Davies Kay E; Talbot Kevin
Survival motor neuron deficiency enhances progression in an amyotrophic lateral sclerosis mouse model.
Neurobiology of disease 2009;34(3):511-7.
2008: Doran Graeme; Davies Kay E; Talbot Kevin
Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function.
Biochemical and biophysical research communications 2008;372(3):447-53.
2008: Talbot Kevin; Davies Kay E
Is good housekeeping the key to motor neuron survival?
Cell 2008;133(4):572-4.
2008: Turner Bradley J; Talbot Kevin
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.
Progress in neurobiology 2008;85(1):94-134.
2008: James P A; Rankin J; Talbot K
Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27).
Journal of neurology, neurosurgery, and psychiatry 2008;79(4):461-3.
2007: Schymick J C; Talbot K; Traynor B J
Genetics of sporadic amyotrophic lateral sclerosis.
Human molecular genetics 2007;16 Spec No. 2():R233-42.
2007: Cader Muhammed Z; Ren Jingshan; James Paul A; Bird Louise E; Talbot Kevin; Stammers David K
Crystal structure of human wildtype and S581L-mutant glycyl-tRNA synthetase, an enzyme underlying distal spinal muscular atrophy.
FEBS letters 2007;581(16):2959-64.
2007: Talbot Kevin
Neuromuscular disorders: therapeutic advances.
Lancet neurology 2007;6(1):18-9.
2007: Talbot Kevin; Davies Kay E
Chapter 7 Spinal muscular atrophies and hereditary motor neuropathies.
Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn 2007;82():141-53.
2006: James P A; Cader M Z; Muntoni F; Childs A-M; Crow Y J; Talbot K
Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene.
Neurology 2006;67(9):1710-2.
2006: James Paul A; Talbot Kevin
The molecular genetics of non-ALS motor neuron diseases.
Biochimica et biophysica acta 2006;1762(11-12):986-1000.
2006: Talbot Kevin; Ansorge Olaf
Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.
Human molecular genetics 2006;15 Spec No 2():R182-7.
2006: Ackerley Steven; James Paul A; Kalli Arran; French Sarah; Davies Kay E; Talbot Kevin
A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes.
Human molecular genetics 2006;15(2):347-54.
2004: Evgrafov Oleg V; Mersiyanova Irena; Irobi Joy; Van Den Bosch Ludo; Dierick Ines; Leung Conrad L; Schagina Olga; Verpoorten Nathalie; Van Impe Katrien; Fedotov Valeriy; Dadali Elena; Auer-Grumbach Michaela; Windpassinger Christian; Wagner Klaus; Mitrovic Zoran; Hilton-Jones David; Talbot Kevin; Martin Jean-Jacques; Vasserman Natalia; Tverskaya Svetlana; Polyakov Alexander; Liem Ronald K H; Gettemans Jan; Robberecht Wim; De Jonghe Peter; Timmerman Vincent
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy.
Nature genetics 2004;36(6):602-6.
2004: Irobi Joy; Van Impe Katrien; Seeman Pavel; Jordanova Albena; Dierick Ines; Verpoorten Nathalie; Michalik Andrej; De Vriendt Els; Jacobs An; Van Gerwen Veerle; Vennekens Krist'l; Mazanec Radim; Tournev Ivailo; Hilton-Jones David; Talbot Kevin; Kremensky Ivo; Van Den Bosch Ludo; Robberecht Wim; Van Vandekerckhove Joël; Van Broeckhoven Christine; Gettemans Jan; De Jonghe Peter; Timmerman Vincent
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy.
Nature genetics 2004;36(6):597-601.
2003: Anderson Kirstie; Talbot Kevin
Spinal muscular atrophies reveal motor neuron vulnerability to defects in ribonucleoprotein handling.
Current opinion in neurology 2003;16(5):595-9.
2003: Talbot K; Stradling J; Crosby J; Hilton-Jones D
Reduction in excess daytime sleepiness by modafinil in patients with myotonic dystrophy.
Neuromuscular disorders : NMD 2003;13(5):357-64.
2001: Talbot K; Davies K E
Spinal muscular atrophy.
Seminars in neurology 2001;21(2):189-97.
1998: Talbot K; Miguel-Aliaga I; Mohaghegh P; Ponting C P; Davies K E
Characterization of a gene encoding survival motor neuron (SMN)-related protein, a constituent of the spliceosome complex.
Human molecular genetics 1998;7(13):2149-56.
1997: Nesbit M A; Hodges M D; Campbell L; de Meulemeester T M; Alders M; Rodrigues N R; Talbot K; Theodosiou A M; Mannens M A; Nakamura Y; Little P F; Davies K E
Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.
Genomics 1997;42(2):284-94.
1997: Talbot K; Rodrigues N R; Ignatius J; Muntoni F; Davies K E
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype.
Neuromuscular disorders : NMD 1997;7(3):198-201.
1997: Talbot K; Ponting C P; Theodosiou A M; Rodrigues N R; Surtees R; Mountford R; Davies K E
Missense mutation clustering in the survival motor neuron gene: a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?
Human molecular genetics 1997;6(3):497-500.
1997: Talbot K
What's new in the molecular genetics of spinal muscular atrophy?
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1997;1(5-6):149-55.
1996: Talbot K; Rodrigues N; Bernert G; Bittner R; Davies K
Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy.
Journal of medical genetics 1996;33(12):1019-21.
1996: Rodrigues N R; Talbot K; Davies K E
Molecular genetics of autosomal recessive spinal muscular atrophy.
Molecular medicine (Cambridge, Mass.) 1996;2(4):400-4.
1996: Rodrigues N R; Owen N; Talbot K; Patel S; Muntoni F; Ignatius J; Dubowitz V; Davies K E
Gene deletions in spinal muscular atrophy.
Journal of medical genetics 1996;33(2):93-6.
1995: Rodrigues N R; Owen N; Talbot K; Ignatius J; Dubowitz V; Davies K E
Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.
Human molecular genetics 1995;4(4):631-4.

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