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Kay Davies

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.

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Publications

TOP 3
Oliver Peter L; Davies Kay E
Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk.
Bitoun Emmanuelle; Davies Kay E
The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function.
Hoerder-Suabedissen Anna; Wang Wei Zhi; Lee Sheena; Davies Kay E; Goffinet André M; Rakic Sonja; Parnavelas John; Reim Kerstin; Nicolic Margareta; Paulsen Ole; Molnár Zoltán
Novel markers reveal subpopulations of subplate neurons in the murine cerebral cortex.

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All Publications

2009: Oliver Peter L; Davies Kay E
Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk.
Human molecular genetics 2009;18(23):4576-89.
2009: Bitoun Emmanuelle; Davies Kay E
The robotic mouse: understanding the role of AF4, a cofactor of transcriptional elongation and chromatin remodelling, in purkinje cell function.
Cerebellum (London, England) 2009;8(3):175-83.
2009: Hoerder-Suabedissen Anna; Wang Wei Zhi; Lee Sheena; Davies Kay E; Goffinet André M; Rakic Sonja; Parnavelas John; Reim Kerstin; Nicolic Margareta; Paulsen Ole; Molnár Zoltán
Novel markers reveal subpopulations of subplate neurons in the murine cerebral cortex.
Cerebral cortex (New York, N.Y. : 1991) 2009;19(8):1738-50.
2009: Goyenvalle Aurélie; Babbs Arran; van Ommen Gert-Jan B; Garcia Luis; Davies Kay E
Enhanced exon-skipping induced by U7 snRNA carrying a splicing silencer sequence: Promising tool for DMD therapy.
Molecular therapy : the journal of the American Society of Gene Therapy 2009;17(7):1234-40.
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.
2009: Becker Esther B E; Oliver Peter L; Glitsch Maike D; Banks Gareth T; Achilli Francesca; Hardy Andrea; Nolan Patrick M; Fisher Elizabeth M C; Davies Kay E
A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(16):6706-11.
2009: Kemp Matthew W; Edwards Ben; Burgess Matthew; Clarke W Thomas; Nicholson George; Parry David A D; Davies Kay E
Syncoilin isoform organization and differential expression in murine striated muscle.
Journal of structural biology 2009;165(3):196-203.
2008: Zhang Wen; ten Hove Michiel; Schneider Jürgen E; Stuckey Daniel J; Sebag-Montefiore Liam; Bia Britta L; Radda George K; Davies Kay E; Neubauer Stefan; Clarke Kieran
Abnormal cardiac morphology, function and energy metabolism in the dystrophic mdx mouse: an MRI and MRS study.
Journal of molecular and cellular cardiology 2008;45(6):754-60.
2008: Cauchi Ruben J; Davies Kay E; Liu Ji-Long
A motor function for the DEAD-box RNA helicase, Gemin3, in Drosophila.
PLoS genetics 2008;4(11):e1000265.
2008: Vernes Sonja C; Newbury Dianne F; Abrahams Brett S; Winchester Laura; Nicod Jérôme; Groszer Matthias; Alarcón Maricela; Oliver Peter L; Davies Kay E; Geschwind Daniel H; Monaco Anthony P; Fisher Simon E
A functional genetic link between distinct developmental language disorders.
The New England journal of medicine 2008;359(22):2337-45.
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: McCullagh Karl J A; Edwards Ben; Kemp Matthew W; Giles Laura C; Burgess Matthew; Davies Kay E
Analysis of skeletal muscle function in the C57BL6/SV129 syncoilin knockout mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2008;19(5):339-51.
2008: Talbot Kevin; Davies Kay E
Is good housekeeping the key to motor neuron survival?
Cell 2008;133(4):572-4.
2008: Gulston Melanie K; Rubtsov Denis V; Atherton Helen J; Clarke Kieran; Davies Kay E; Lilley Kathryn S; Griffin Julian L
A combined metabolomic and proteomic investigation of the effects of a failure to express dystrophin in the mouse heart.
Journal of proteome research 2008;7(5):2069-77.
2008: Baban Dilair; Davies Kay E
Microarray analysis of mdx mice expressing high levels of utrophin: therapeutic implications for dystrophin deficiency.
Neuromuscular disorders : NMD 2008;18(3):239-47.
2008: Johnson Reuben D; Oliver Peter L; Davies Kay E
SNARE proteins and schizophrenia: linking synaptic and neurodevelopmental hypotheses.
Acta biochimica Polonica 2008;55(4):619-28.
2007: Davies Kay E; Grounds Miranda D
Modified patient stem cells as prelude to autologous treatment of muscular dystrophy.
Cell stem cell 2007;1(6):595-6.
2007: Vernes Sonja C; Spiteri Elizabeth; Nicod Jérôme; Groszer Matthias; Taylor Jennifer M; Davies Kay E; Geschwind Daniel H; Fisher Simon E
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.
American journal of human genetics 2007;81(6):1232-50.
2007: McCullagh Karl J A; Edwards Ben; Poon Ellen; Lovering Richard M; Paulin Denise; Davies Kay E
Intermediate filament-like protein syncoilin in normal and myopathic striated muscle.
Neuromuscular disorders : NMD 2007;17(11-12):970-9.
2007: Oliver Peter L; Keays David A; Davies Kay E
Behavioural characterisation of the robotic mouse mutant.
Behavioural brain research 2007;181(2):239-47.
2007: Oliver Peter L; Bitoun Emmanuelle; Davies Kay E
Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(6-7):412-24.
2007: Jeans Alexander F; Oliver Peter L; Johnson Reuben; Capogna Marco; Vikman Jenny; Molnár Zoltán; Babbs Arran; Partridge Christopher J; Salehi Albert; Bengtsson Martin; Eliasson Lena; Rorsman Patrik; Davies Kay E
A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(7):2431-6.
2007: Keays David A; Tian Guoling; Poirier Karine; Huang Guo-Jen; Siebold Christian; Cleak James; Oliver Peter L; Fray Martin; Harvey Robert J; Molnár Zoltán; Piñon Maria C; Dear Neil; Valdar William; Brown Steve D M; Davies Kay E; Rawlins J Nicholas P; Cowan Nicholas J; Nolan Patrick; Chelly Jamel; Flint Jonathan
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.
Cell 2007;128(1):45-57.
2007: Bitoun Emmanuelle; Oliver Peter L; Davies Kay E
The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.
Human molecular genetics 2007;16(1):92-106.
2007: Kemp Matthew W; Davies Kay E
The role of intermediate filament proteins in the development of neurological disease.
Critical reviews in neurobiology 2007;19(1):1-27.
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.
2007: Mattei Elisabetta; Corbi Nicoletta; Di Certo Maria Grazia; Strimpakos Georgios; Severini Cinzia; Onori Annalisa; Desantis Agata; Libri Valentina; Buontempo Serena; Floridi Aristide; Fanciulli Maurizio; Baban Dilair; Davies Kay E; Passananti Claudio
Utrophin up-regulation by an artificial transcription factor in transgenic mice.
PloS one 2007;2(1):e774.
2006: Davies Kay E; Grounds Miranda D
Treating muscular dystrophy with stem cells?
Cell 2006;127(7):1304-6.
2006: Vernes Sonja C; Nicod Jérôme; Elahi Fanny M; Coventry Julie A; Kenny Niamh; Coupe Anne-Marie; Bird Louise E; Davies Kay E; Fisher Simon E
Functional genetic analysis of mutations implicated in a human speech and language disorder.
Human molecular genetics 2006;15(21):3154-67.
2006: Towers Paula R; Lescure Pascal; Baban Dilair; Malek Julie A; Duarte Jose; Jones Emma; Davies Kay E; Ségalat Laurent; Sattelle David B
Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18).
Genomics 2006;88(5):642-9.
2006: Davies Kay E; Nowak Kristen J
Molecular mechanisms of muscular dystrophies: old and new players.
Nature reviews. Molecular cell biology 2006;7(10):762-73.
2006: Wilding James R; Lygate Craig A; Davies Kay E; Neubauer Stefan; Clarke Kieran
MLP accumulation and remodelling in the infarcted rat heart.
European journal of heart failure : journal of the Working Group on Heart Failure of the European Society of Cardiology 2006;8(4):343-6.
2006: Jiang Yanyan; Oliver Peter; Davies Kay E; Platt Nick
Identification and characterization of murine SCARA5, a novel class A scavenger receptor that is expressed by populations of epithelial cells.
The Journal of biological chemistry 2006;281(17):11834-45.
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.
2005: Hirst R C; McCullagh K J A; Davies K E
Utrophin upregulation in Duchenne muscular dystrophy.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2005;24(3):209-16.
2005: Brown Susan C; Torelli Silvia; Ugo Isabella; De Biasia Floriana; Howman Emily V; Poon Ellen; Britton Joanna; Davies Kay E; Muntoni Francesco
Syncoilin upregulation in muscle of patients with neuromuscular disease.
Muscle & nerve 2005;32(6):715-25.
2005: Oliver Peter L; Davies Kay E
Analysis of human neurological disorders using mutagenesis in the mouse.
Clinical science (London, England : 1979) 2005;108(5):385-97.
2005: Wilding James R; Schneider Jürgen E; Sang A Elizabeth; Davies Kay E; Neubauer Stefan; Clarke Kieran
Dystrophin- and MLP-deficient mouse hearts: marked differences in morphology and function, but similar accumulation of cytoskeletal proteins.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(1):79-81.
2005: Nowak Kristen; McCullagh Karl; Poon Ellen; Davies Kay E
Muscular dystrophies related to the cytoskeleton/nuclear envelope.
Novartis Foundation symposium 2005;264():98-111; discussion 112-7, 227-30.
2004: Anderson Kirstie N; Baban Dilair; Oliver Peter L; Potter Allyson; Davies Kay E
Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit.
Neuromuscular disorders : NMD 2004;14(11):711-22.
2004: Oliver Peter L; Bitoun Emmanuelle; Clark Joanne; Jones Emma L; Davies Kay E
Mediation of Af4 protein function in the cerebellum by Siah proteins.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(41):14901-6.
2004: Nowak Kristen J; Davies Kay E
Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment.
EMBO reports 2004;5(9):872-6.
2004: Anderson Kirstie N; Potter Allyson C; Piccenna Loretta G; Quah Alvin K J; Davies Kay E; Cheema Surindar S
Isolation and culture of motor neurons from the newborn mouse spinal cord.
Brain research. Brain research protocols 2004;12(3):132-6.
2004: Weir Andrew P; Morgan Jennifer E; Davies Kay E
A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration.
Neuromuscular disorders : NMD 2004;14(1):19-23.
2003: Vargas J D; Herpers B; McKie A T; Gledhill S; McDonnell J; van den Heuvel M; Davies K E; Ponting C P
Stromal cell-derived receptor 2 and cytochrome b561 are functional ferric reductases.
Biochimica et biophysica acta 2003;1651(1-2):116-23.
2003: Anderson K; Potter A; Baban D; Davies K E
Protein expression changes in spinal muscular atrophy revealed with a novel antibody array technology.
Brain : a journal of neurology 2003;126(Pt 9):2052-64.
2003: Chan Yick Bun; Miguel-Aliaga Irene; Franks Chris; Thomas Natasha; Trülzsch Barbara; Sattelle David B; Davies Kay E; van den Heuvel Marcel
Neuromuscular defects in a Drosophila survival motor neuron gene mutant.
Human molecular genetics 2003;12(12):1367-76.
2003: Perkins Kelly J; Davies Kay E
Ets, Ap-1 and GATA factor families regulate the utrophin B promoter: potential regulatory mechanisms for endothelial-specific expression.
FEBS letters 2003;538(1-3):168-72.
2003: Isaacs Adrian M; Oliver Peter L; Jones Emma L; Jeans Alexander; Potter Allyson; Hovik Berit H; Nolan Patrick M; Vizor Lucie; Glenister Peter; Simon A Katharina; Gray Ian C; Spurr Nigel K; Brown Steve D M; Hunter A Jackie; Davies Kay E
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2003;23(5):1631-7.
2003: Howman Emily V; Sullivan Nicky; Poon Ellen P; Britton Joanna E; Hilton-Jones David; Davies Kay E
Syncoilin accumulation in two patients with desmin-related myopathy.
Neuromuscular disorders : NMD 2003;13(1):42-8.
2002: Squire S; Raymackers J M; Vandebrouck C; Potter A; Tinsley J; Fisher R; Gillis J M; Davies K E
Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system.
Human molecular genetics 2002;11(26):3333-44.
2002: Weir Andrew P; Burton Edward A; Harrod Graham; Davies Kay E
A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle.
The Journal of biological chemistry 2002;277(47):45285-90.
2002: Perkins Kelly J; Davies Kay E
The role of utrophin in the potential therapy of Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 2002;12 Suppl 1():S78-89.
2002: Isaacs Adrian M; Jeans Alexander; Oliver Peter L; Vizor Lucie; Brown Steve D M; Hunter A Jackie; Davies Kay E
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.
Molecular and cellular neurosciences 2002;21(1):114-25.
2002: Vargas J D; Culetto E; Ponting C P; Miguel-Aliaga I; Davies K E; Sattelle D B
Cloning and developmental expression analysis of ltd-1, the Caenorhabditis elegans homologue of the mouse kyphoscoliosis (ky) gene.
Mechanisms of development 2002;117(1-2):289-92.
2002: Blake Derek J; Weir Andrew; Newey Sarah E; Davies Kay E
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
Physiological reviews 2002;82(2):291-329.
2002: Poon Ellen; Howman Emily V; Newey Sarah E; Davies Kay E
Association of syncoilin and desmin: linking intermediate filament proteins to the dystrophin-associated protein complex.
The Journal of biological chemistry 2002;277(5):3433-9.
2002: Burton Edward A; Davies Kay E
Muscular dystrophy--reason for optimism?
Cell 2002;108(1):5-8.
2001: Perkins K J; Burton E A; Davies K E
The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: implications for therapeutic up-regulation in Duchenne muscular dystrophy.
Nucleic acids research 2001;29(23):4843-50.
2001: Fisher R; Tinsley J M; Phelps S R; Squire S E; Townsend E R; Martin J E; Davies K E
Non-toxic ubiquitous over-expression of utrophin in the mdx mouse.
Neuromuscular disorders : NMD 2001;11(8):713-21.
2001: Loh N Y; Nebenius-Oosthuizen D; Blake D J; Smith A J; Davies K E
Role of beta-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver.
Molecular and cellular biology 2001;21(21):7442-8.
2001: Culle M J; Walsh J M; Tinsle J M; Fisher R; Davies K E
Immunogold confirmation that utrophin is localized to the normal position of dystrophin in dystrophin-negative transgenic mouse muscle.
The Histochemical journal 2001;33(9-10):579-83.
2001: Talbot K; Davies K E
Spinal muscular atrophy.
Seminars in neurology 2001;21(2):189-97.
2001: Skordis L A; Dunckley M G; Burglen L; Campbell L; Talbot K; Patel S; Melki J; Davies K E; Dubowitz V; Muntoni F
Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA.
Human genetics 2001;108(4):356-7.
2001: Nakamura A; Harrod G V; Davies K E
Activation of calcineurin and stress activated protein kinase/p38-mitogen activated protein kinase in hearts of utrophin-dystrophin knockout mice.
Neuromuscular disorders : NMD 2001;11(3):251-9.
2001: Newey S E; Howman E V; Ponting C P; Benson M A; Nawrotzki R; Loh N Y; Davies K E; Blake D J
Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle.
The Journal of biological chemistry 2001;276(9):6645-55.
2001: Newey S E; Gramolini A O; Wu J; Holzfeind P; Jasmin B J; Davies K E; Blake D J
A novel mechanism for modulating synaptic gene expression: differential localization of alpha-dystrobrevin transcripts in skeletal muscle.
Molecular and cellular neurosciences 2001;17(1):127-40.
2000: Miguel-Aliaga I; Chan Y B; Davies K E; van den Heuvel M
Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila.
FEBS letters 2000;486(2):99-102.
2000: Hopkins J C; Bia B L; Crilley J G; Boehm E A; Sang A E; Tinsley J M; King L M; Radda G K; Davies K E; Clarke K
Muscular dystrophy: from gene to patient.
Magma (New York, N.Y.) 2000;11(1-2):7-9.
2000: Newey S E; Benson M A; Ponting C P; Davies K E; Blake D J
Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex.
Current biology : CB 2000;10(20):1295-8.
2000: Rafael J A; Nitta Y; Peters J; Davies K E
Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(9):725-8.
2000: Loh N Y; Newey S E; Davies K E; Blake D J
Assembly of multiple dystrobrevin-containing complexes in the kidney.
Journal of cell science 2000;113 ( Pt 15)():2715-24.
2000: Isaacs A M; Davies K E; Hunter A J; Nolan P M; Vizor L; Peters J; Gale D G; Kelsell D P; Latham I D; Chase J M; Fisher E M; Bouzyk M M; Potter A; Masih M; Walsh F S; Sims M A; Doncaster K E; Parsons C A; Martin J; Brown S D; Rastan S; Spurr N K; Gray I C
Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.
Human molecular genetics 2000;9(12):1865-71.
2000: Corbi N; Libri V; Fanciulli M; Tinsley J M; Davies K E; Passananti C
The artificial zinc finger coding gene 'Jazz' binds the utrophin promoter and activates transcription.
Gene therapy 2000;7(12):1076-83.
2000: Rafael J A; Townsend E R; Squire S E; Potter A C; Chamberlain J S; Davies K E
Dystrophin and utrophin influence fiber type composition and post-synaptic membrane structure.
Human molecular genetics 2000;9(9):1357-67.
2000: Rodrigues N R; Theodosiou A M; Nesbit M A; Campbell L; Tandle A T; Saranath D; Davies K E
Characterization of Ngef, a novel member of the Dbl family of genes expressed predominantly in the caudate nucleus.
Genomics 2000;65(1):53-61.
2000: Owen N; Doe C L; Mellor J; Davies K E
Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein.
Human molecular genetics 2000;9(5):675-84.
2000: Wakefield P M; Tinsley J M; Wood M J; Gilbert R; Karpati G; Davies K E
Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene.
Gene therapy 2000;7(3):201-4.
2000: Miller W J; Skinner J A; Foss G S; Davies K E
Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain.
The European journal of neuroscience 2000;12(1):381-4.
1999: Burton E A; Tinsley J M; Holzfeind P J; Rodrigues N R; Davies K E
A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(24):14025-30.
1999: Miguel-Aliaga I; Culetto E; Walker D S; Baylis H A; Sattelle D B; Davies K E
The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability.
Human molecular genetics 1999;8(12):2133-43.
1999: Bia B L; Cassidy P J; Young M E; Rafael J A; Leighton B; Davies K E; Radda G K; Clarke K
Decreased myocardial nNOS, increased iNOS and abnormal ECGs in mouse models of Duchenne muscular dystrophy.
Journal of molecular and cellular cardiology 1999;31(10):1857-62.
1999: Mohaghegh P; Rodrigues N R; Owen N; Ponting C P; Le T T; Burghes A H; Davies K E
Analysis of mutations in the tudor domain of the survival motor neuron protein SMN.
European journal of human genetics : EJHG 1999;7(5):519-25.
1999: Rafael J A; Trickett J I; Potter A C; Davies K E
Dystrophin and utrophin do not play crucial roles in nonmuscle tissues in mice.
Muscle & nerve 1999;22(4):517-9.
1999: Gramolini A O; Angus L M; Schaeffer L; Burton E A; Tinsley J M; Davies K E; Changeux J P; Jasmin B J
Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(6):3223-7.
1999: Holzfeind P J; Ambrose H J; Newey S E; Nawrotzki R A; Blake D J; Davies K E
Tissue-selective expression of alpha-dystrobrevin is determined by multiple promoters.
The Journal of biological chemistry 1999;274(10):6250-8.
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.
1998: Loh N Y; Ambrose H J; Guay-Woodford L M; DasGupta S; Nawrotzki R A; Blake D J; Davies K E
Genomic organization and refined mapping of the mouse beta-dystrobrevin gene.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(11):857-62.
1998: Nawrotzki R; Loh N Y; Ruegg M A; Davies K E; Blake D J
Characterisation of alpha-dystrobrevin in muscle.
Journal of cell science 1998;111 ( Pt 17)():2595-605.
1998: Goudemant J F; Deconinck N; Tinsley J M; Demeure R; Robert A; Davies K E; Gillis J M
Expression of truncated utrophin improves pH recovery in exercising muscles of dystrophic mdx mice: a 31P NMR study.
Neuromuscular disorders : NMD 1998;8(6):371-9.
1998: Deconinck N; Rafael J A; Beckers-Bleukx G; Kahn D; Deconinck A E; Davies K E; Gillis J M
Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse.
Neuromuscular disorders : NMD 1998;8(6):362-70.
1998: Campbell L; Daniels R J; Dubowitz V; Davies K E
Maternal mosaicism for a second mutational event in a type I spinal muscular atrophy family.
American journal of human genetics 1998;63(1):37-44.
1998: Porter J D; Rafael J A; Ragusa R J; Brueckner J K; Trickett J I; Davies K E
The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin.
Journal of cell science 1998;111 ( Pt 13)():1801-11.
1998: Rafael J A; Tinsley J M; Potter A C; Deconinck A E; Davies K E
Skeletal muscle-specific expression of a utrophin transgene rescues utrophin-dystrophin deficient mice.
Nature genetics 1998;19(1):79-82.
1998: Vater R; Young C; Anderson L V; Lindsay S; Blake D J; Davies K E; Zuellig R; Slater C R
Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction.
Molecular and cellular neurosciences 1998;10(5-6):229-42.
1998: Chakrabarti L; Bristulf J; Foss G S; Davies K E
Expression of the murine homologue of FMR2 in mouse brain and during development.
Human molecular genetics 1998;7(3):441-8.
1998: Gramolini A O; Burton E A; Tinsley J M; Ferns M J; Cartaud A; Cartaud J; Davies K E; Lunde J A; Jasmin B J
Muscle and neural isoforms of agrin increase utrophin expression in cultured myotubes via a transcriptional regulatory mechanism.
The Journal of biological chemistry 1998;273(2):736-43.
1998: Blake D J; Nawrotzki R; Loh N Y; Górecki D C; Davies K E
beta-dystrobrevin, a member of the dystrophin-related protein family.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(1):241-6.
1997: Davies K E
Challenges in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1997;7(8):482-6.
1997: Ritchie R J; Chakrabarti L; Knight S J; Harding R M; Davies K E
Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28.
American journal of medical genetics 1997;73(4):463-9.
1997: Deconinck A E; Rafael J A; Skinner J A; Brown S C; Potter A C; Metzinger L; Watt D J; Dickson J G; Tinsley J M; Davies K E
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy.
Cell 1997;90(4):717-27.
1997: Metzinger L; Blake D J; Squier M V; Anderson L V; Deconinck A E; Nawrotzki R; Hilton-Jones D; Davies K E
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
Human molecular genetics 1997;6(7):1185-91.
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: Chakrabarti L; Davies K E
Fragile X syndrome.
Current opinion in neurology 1997;10(2):142-7.
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: Gramolini A O; Dennis C L; Tinsley J M; Robertson G S; Cartaud J; Davies K E; Jasmin B J
Local transcriptional control of utrophin expression at the neuromuscular synapse.
The Journal of biological chemistry 1997;272(13):8117-20.
1997: Ambrose H J; Blake D J; Nawrotzki R A; Davies K E
Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene.
Genomics 1997;39(3):359-69.
1997: Deconinck A E; Potter A C; Tinsley J M; Wood S J; Vater R; Young C; Metzinger L; Vincent A; Slater C R; Davies K E
Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice.
The Journal of cell biology 1997;136(4):883-94.
1996: Tinsley J M; Potter A C; Phelps S R; Fisher R; Trickett J I; Davies K E
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene.
Nature 1996;384(6607):349-53.
1996: Nawrotzki R; Blake D J; Davies K E
The genetic basis of neuromuscular disorders.
Trends in genetics : TIG 1996;12(8):294-8.
1996: Morrison K E; Qureshi S J; Anderson S; Borrett J P; Theodosiou A; Rodrigues N; Blake D; Nesbit A; Davies K E; Porteous D J; Brookes A J
Novel transcribed sequences represented in the complex genomic region 5q13.
Biochimica et biophysica acta 1996;1308(2):97-102.
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: Pook M A; Thakrar R; Pottinger B; Harding B; Porteous D; van Heyningen V; Cowell J; Jones C; Povey S; Davies K E; Thakker R V
EagI and NotI linking clones from human chromosomes 11 and Xp.
Human genetics 1996;97(6):742-9.
1996: Theodosiou A M; Rodrigues N R; Nesbit M A; Ambrose H J; Paterson H; McLellan-Arnold E; Boyd Y; Leversha M A; Owen N; Blake D J; Ashworth A; Davies K E
A member of the MAP kinase phosphatase gene family in mouse containing a complex trinucleotide repeat in the coding region.
Human molecular genetics 1996;5(5):675-84.
1996: Knight S J; Ritchie R J; Chakrabarti L; Cross G; Taylor G R; Mueller R F; Hurst J; Paterson J; Yates J R; Dow D J; Davies K E
A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom.
American journal of human genetics 1996;58(5):906-13.
1996: Dennis C L; Tinsley J M; Deconinck A E; Davies K E
Molecular and functional analysis of the utrophin promoter.
Nucleic acids research 1996;24(9):1646-52.
1996: Rowe P S; Goulding J N; Francis F; Oudet C; Econs M J; Hanauer A; Lehrach H; Read A P; Mountford R C; Summerfield T; Weissenbach J; Fraser W; Drezner M K; Davies K E; O'Riordan J L
The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE).
Human genetics 1996;97(3):345-52.
1996: Blake D J; Nawrotzki R; Peters M F; Froehner S C; Davies K E
Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein.
The Journal of biological chemistry 1996;271(13):7802-10.
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.
1996: Chakrabarti L; Knight S J; Flannery A V; Davies K E
A candidate gene for mild mental handicap at the FRAXE fragile site.
Human molecular genetics 1996;5(2):275-82.
1996: Blake D J; Tinsley J M; Davies K E
Utrophin: a structural and functional comparison to dystrophin.
Brain pathology (Zurich, Switzerland) 1996;6(1):37-47.
1996: Ponting C P; Blake D J; Davies K E; Kendrick-Jones J; Winder S J
ZZ and TAZ: new putative zinc fingers in dystrophin and other proteins.
Trends in biochemical sciences 1996;21(1):11-13.
1996: Coleman M P; Ambrose H J; Carrel L; Németh A H; Willard H F; Davies K E
A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status.
Genomics 1996;31(1):135-8.
1995: Jasmin B J; Alameddine H; Lunde J A; Stetzkowski-Marden F; Collin H; Tinsley J M; Davies K E; Tomé F M; Parry D J; Cartaud J
Expression of utrophin and its mRNA in denervated mdx mouse muscle.
FEBS letters 1995;374(3):393-8.
1995: Winder S J; Hemmings L; Bolton S J; Maciver S K; Tinsley J M; Davies K E; Critchley D R; Kendrick-Jones J
Calmodulin regulation of utrophin actin binding.
Biochemical Society transactions 1995;23(3):397S.
1995: Davies K E; Tinsley J M; Blake D J
Molecular analysis of Duchenne muscular dystrophy: past, present, and future.
Annals of the New York Academy of Sciences 1995;758():287-96.
1995: Flannery A V; Hirst M C; Knight S J; Ritchie R J; Davies K E
The fragile X syndrome.
Biochimica et biophysica acta 1995;1271(2-3):293-303.
1995: Francis M J; Nesbit M A; Theodosiou A M; Rodrigues N R; Campbell L; Christodoulou Z; Qureshi S J; Porteous D J; Brookes A J; Davies K E
Mapping of retrotransposon sequences in the unstable region surrounding the spinal muscular atrophy locus in 5q13.
Genomics 1995;27(2):366-9.
1995: Blake D J; Tinsley J M; Davies K E; Knight A E; Winder S J; Kendrick-Jones J
Coiled-coil regions in the carboxy-terminal domains of dystrophin and related proteins: potentials for protein-protein interactions.
Trends in biochemical sciences 1995;20(4):133-5.
1995: Blake D J; Schofield J N; Zuellig R A; Górecki D C; Phelps S R; Barnard E A; Edwards Y H; Davies K E
G-utrophin, the autosomal homologue of dystrophin Dp116, is expressed in sensory ganglia and brain.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(9):3697-701.
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.
1995: Macpherson J N; Curtis G; Crolla J A; Dennis N; Migeon B; Grewal P K; Hirst M C; Davies K E; Jacobs P A
Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.
Journal of medical genetics 1995;32(3):236-9.
1995: Daniels R J; Campbell L; Rodrigues N R; Francis M J; Morrison K E; McLean M; MacKenzie A; Ignatius J; Dubowitz V; Davies K E
Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele.
Journal of medical genetics 1995;32(2):93-6.
1995: Black G C; Coleman M P; Chen Z Y; Nemeth A H; Davies K E; Craig I W
A bidirectional YAC walk from the Norrie disease (NDP) locus.
Genomics 1995;25(3):644-9.
1995: Brown C J; Miller A P; Carrel L; Rupert J L; Davies K E; Willard H F
The DXS423E gene in Xp11.21 escapes X chromosome inactivation.
Human molecular genetics 1995;4(2):251-5.
1995: Rocques P J; Clark J; Ball S; Crew J; Gill S; Christodoulou Z; Borts R H; Louis E J; Davies K E; Cooper C S
The human SB1.8 gene (DXS423E) encodes a putative chromosome segregation protein conserved in lower eukaryotes and prokaryotes.
Human molecular genetics 1995;4(2):243-9.
1995: Partridge T A; Davies K E
Myoblast-based gene therapies.
British medical bulletin 1995;51(1):123-37.
1995: Winder S J; Hemmings L; Maciver S K; Bolton S J; Tinsley J M; Davies K E; Critchley D R; Kendrick-Jones J
Utrophin actin binding domain: analysis of actin binding and cellular targeting.
Journal of cell science 1995;108 ( Pt 1)():63-71.
1995: Dubowitz V; Daniels R J; Davies K E
Olivopontocerebellar hypoplasia with anterior horn cell involvement (SMA) does not localize to chromosome 5q.
Neuromuscular disorders : NMD 1995;5(1):25-9.
1995: Slaney S F; Wilkie A O; Hirst M C; Charlton R; McKinley M; Pointon J; Christodoulou Z; Huson S M; Davies K E
DNA testing for fragile X syndrome in schools for learning difficulties.
Archives of disease in childhood 1995;72(1):33-7.
1994: Theodosiou A M; Morrison K E; Nesbit A M; Daniels R J; Campbell L; Francis M J; Christodoulou Z; Davies K E
Complex repetitive arrangements of gene sequence in the candidate region of the spinal muscular atrophy gene in 5q13.
American journal of human genetics 1994;55(6):1209-17.
1994: Ritchie R J; Knight S J; Hirst M C; Grewal P K; Bobrow M; Cross G S; Davies K E
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.
Human molecular genetics 1994;3(12):2115-21.
1994: Blair H J; Hirst M C; MacKinnon R; Davies K E; Boyd Y
Evaluation of human microdissection clones from the FRAXA region as tools for comparative mapping in the mouse: isolation of a conserved genomic clone close to FMR1.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(9):584-7.
1994: Hirst M C; Grewal P K; Davies K E
Precursor arrays for triplet repeat expansion at the fragile X locus.
Human molecular genetics 1994;3(9):1553-60.
1994: Tinsley J M; Blake D J; Zuellig R A; Davies K E
Increasing complexity of the dystrophin-associated protein complex.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(18):8307-13.
1994: Schofield J N; Blake D J; Simmons C; Morris G E; Tinsley J M; Davies K E; Edwards Y H
Apo-dystrophin-1 and apo-dystrophin-2, products of the Duchenne muscular dystrophy locus: expression during mouse embryogenesis and in cultured cell lines.
Human molecular genetics 1994;3(8):1309-16.
1994: Knight S J; Voelckel M A; Hirst M C; Flannery A V; Moncla A; Davies K E
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap.
American journal of human genetics 1994;55(1):81-6.
1994: Coleman M P; Németh A H; Campbell L; Raut C P; Weissenbach J; Davies K E
A 1.8-Mb YAC contig in Xp11.23: identification of CpG islands and physical mapping of CA repeats in a region of high gene density.
Genomics 1994;21(2):337-43.
1994: Rowe P S; Goulding J; Read A; Lehrach H; Francis F; Hanauer A; Oudet C; Biancalana V; Kooh S W; Davies K E
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2).
Human genetics 1994;93(3):291-4.
1993: Glass I A; Good P; Coleman M P; Fullwood P; Giles M G; Lindsay S; Nemeth A H; Davies K E; Willshaw H A; Fielder A
Genetic mapping of a cone and rod dysfunction (Aland Island eye disease) to the proximal short arm of the human X chromosome.
Journal of medical genetics 1993;30(12):1044-50.
1993: Pearce M; Blake D J; Tinsley J M; Byth B C; Campbell L; Monaco A P; Davies K E
The utrophin and dystrophin genes share similarities in genomic structure.
Human molecular genetics 1993;2(11):1765-72.
1993: Morrison K E; Daniels R J; Campbell L; McPherson J; Davies K E
Dinucleotide repeat polymorphism proximal to the spinal muscular atrophy region at D5S681.
Human molecular genetics 1993;2(10):1753.
1993: Tinsley J M; Davies K E
Utrophin: a potential replacement for dystrophin?
Neuromuscular disorders : NMD 1993;3(5-6):537-9.
1993: Hirst M C; Knight S J; Christodoulou Z; Grewal P K; Fryns J P; Davies K E
Origins of the fragile X syndrome mutation.
Journal of medical genetics 1993;30(8):647-50.
1993: Clerk A; Morris G E; Dubowitz V; Davies K E; Sewry C A
Dystrophin-related protein, utrophin, in normal and dystrophic human fetal skeletal muscle.
The Histochemical journal 1993;25(8):554-61.
1993: Rowe P S; Goulding J; Read A; Mountford R; Hanauer A; Oudet C; Whyte M P; Meier-Ewert S; Lehrach H; Davies K E
New markers for linkage analysis of X-linked hypophosphataemic rickets.
Human genetics 1993;91(6):571-5.
1993: Tinsley J M; Blake D J; Pearce M; Knight A E; Kendrick-Jones J; Davies K E
Dystrophin and related proteins.
Current opinion in genetics & development 1993;3(3):484-90.
1993: Thiselton D L; Kamakari S; Curtis A R; Coleman M P; Davies K E; Lindsay S; Bhattacharya S
Dinucleotide repeat polymorphism at the DXS556 locus.
Human molecular genetics 1993;2(5):613.
1993: Tinsley J M; Blake D J; Davies K E
Apo-dystrophin-3: a 2.2kb transcript from the DMD locus encoding the dystrophin glycoprotein binding site.
Human molecular genetics 1993;2(5):521-4.
1993: Passos-Bueno M R; Byth B C; Rosenberg S; Takata R I; Bakker E; Beggs A H; Pavanello R C; Vainzof M; Davies K E; Zatz M
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
American journal of medical genetics 1993;46(2):172-5.
1993: Hirst M C; Barnicoat A; Flynn G; Wang Q; Daker M; Buckle V J; Davies K E; Bobrow M
The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE.
Human molecular genetics 1993;2(2):197-200.
1993: Flynn G A; Hirst M C; Knight S J; Macpherson J N; Barber J C; Flannery A V; Davies K E; Buckle V J
Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.
Journal of medical genetics 1993;30(2):97-100.
1993: Love D R; Byth B C; Tinsley J M; Blake D J; Davies K E
Dystrophin and dystrophin-related proteins: a review of protein and RNA studies.
Neuromuscular disorders : NMD 1993;3(1):5-21.
1993: Németh A H; Hunter N; Coleman M P; Borts R H; Louis E J; Davies K E
Rescue of a single yeast artificial chromosome from a cotransformation event utilizing segregation at meiosis.
Genetic analysis, techniques and applications 1993;10(6):123-7.
1992: Suthers G K; Huson S M; Davies K E
Instability versus predictability: the molecular diagnosis of myotonic dystrophy.
Journal of medical genetics 1992;29(11):761-5.
1992: Nguyen T M; Le T T; Blake D J; Davies K E; Morris G E
Utrophin, the autosomal homologue of dystrophin, is widely-expressed and membrane-associated in cultured cell lines.
FEBS letters 1992;313(1):19-22.
1992: Hirst M C; Knight S J; Bell M V; Super M; Davies K E
The fragile X syndrome.
Clinical science (London, England : 1979) 1992;83(3):255-64.
1992: Rowe P S; Read A P; Mountford R; Benham F; Kruse T A; Camerino G; Davies K E; O'Riordan J L
Three DNA markers for hypophosphataemic rickets.
Human genetics 1992;89(5):539-42.
1992: Blake D J; Love D R; Tinsley J; Morris G E; Turley H; Gatter K; Dickson G; Edwards Y H; Davies K E
Characterization of a 4.8kb transcript from the Duchenne muscular dystrophy locus expressed in Schwannoma cells.
Human molecular genetics 1992;1(2):103-9.
1992: Laval S H; Blair H J; Hirst M C; Davies K E; Boyd Y
Mapping of FMR1, the gene implicated in fragile X-linked mental retardation, on the mouse X chromosome.
Genomics 1992;12(4):818-21.
1992: Wells D J; Wells K E; Walsh F S; Davies K E; Goldspink G; Love D R; Chan-Thomas P; Dunckley M G; Piper T; Dickson G
Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice.
Human molecular genetics 1992;1(1):35-40.
1992: Morrison K E; Daniels R J; Suthers G K; Flynn G A; Francis M J; Buckle V J; Davies K E
High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.
American journal of human genetics 1992;50(3):520-7.
1992: Lindsay S; Thiselton D L; Bateman J B; Ngo J T; Sparkes R S; Coleman M; Davies K E; Bhattacharya S S
Localisation of the gene for Norrie disease to between DXS7 and DXS426 on Xp.
Human genetics 1992;88(3):349-50.
1992: Dunckley M G; Love D R; Davies K E; Walsh F S; Morris G E; Dickson G
Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro.
FEBS letters 1992;296(2):128-34.
1992: Knight S J; Hirst M C; Davies K E
Molecular analysis of the fragile X syndrome.
Disease markers 1992;10(1):1-5.
1992: Hirst M C; Bassett J H; Roche A; Davies K E
Preparation of radiolabelled hybridization probes by STS labelling.
Trends in genetics : TIG 1992;8(1):6-7.
1992: Hirst M C; Knight S M; Nakahori Y; Roche A; Davies K E
Molecular analysis of the fragile X syndrome.
Journal of inherited metabolic disease 1992;15(4):532-8.
1992: Byth B C; Love D R; Murray J C; Davies K E
Localization of two new DNA markers on the linkage map of human chromosome 6q.
Cytogenetics and cell genetics 1992;60(3-4):216-8.
1991: Coleman M P; Murray J C; Willard H F; Nolan K F; Reid K B; Blake D J; Lindsay S; Bhattacharya S S; Wright A; Davies K E
Genetic and physical mapping around the properdin P gene.
Genomics 1991;11(4):991-6.
1991: Love D R; Flint T J; Genet S A; Middleton-Price H R; Davies K E
Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.
Journal of medical genetics 1991;28(12):860-4.
1991: Hirst M C; Nakahori Y; Knight S J; Schwartz C; Thibodeau S N; Roche A; Flint T J; Connor J M; Fryns J P; Davies K E
Genotype prediction in the fragile X syndrome.
Journal of medical genetics 1991;28(12):824-9.
1991: Dickson G; Love D R; Davies K E; Wells K E; Piper T A; Walsh F S
Human dystrophin gene transfer: production and expression of a functional recombinant DNA-based gene.
Human genetics 1991;88(1):53-8.
1991: Lafrenière R G; Brown C J; Powers V E; Carrel L; Davies K E; Barker D F; Willard H F
Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome.
Genomics 1991;11(2):352-63.
1991: Byth B C; Love D R; Passos-Bueno M R; Davies K E
A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q.
Nucleic acids research 1991;19(15):4310.
1991: Love D R; England S B; Speer A; Marsden R F; Bloomfield J F; Roche A L; Cross G S; Mountford R C; Smith T J; Davies K E
Sequences of junction fragments in the deletion-prone region of the dystrophin gene.
Genomics 1991;10(1):57-67.
1991: Love D R; Morris G E; Ellis J M; Fairbrother U; Marsden R F; Bloomfield J F; Edwards Y H; Slater C P; Parry D J; Davies K E
Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(8):3243-7.
1991: Passos-Bueno M R; Byth B; Love D; Terwilliger J; Ott J; Rapaport D; Vainzof M; Zatz M; Davies K E
Exclusion of the gene responsible for facioscapulohumeral muscular dystrophy (FSH) at 6q23-q27.
Journal of the neurological sciences 1991;102(2):206-8.
1991: Passos-Bueno M R; Terwilliger J; Ott J; Vainzof M; Love D R; Davies K E; Zatz M
Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.
American journal of medical genetics 1991;38(1):140-6.
1991: Davies K E; Thomas N H; Daniels R J; Dubowitz V
Molecular studies of spinal muscular atrophy.
Neuromuscular disorders : NMD 1991;1(2):83-5.
1990: Love D R; Flint T J; Marsden R F; Bloomfield J F; Daniels R J; Forrest S M; Gabrielli O; Giorgi P; Novelli G; Davies K E
Characterization of deletions in the dystrophin gene giving mild phenotypes.
American journal of medical genetics 1990;37(1):136-42.
1990: Love D R; Bloomfield J F; Kenwrick S J; Yates J R; Davies K E
Physical mapping distal to the DMD locus.
Genomics 1990;8(1):106-12.
1990: MacKinnon R N; Hirst M C; Bell M V; Watson J E; Claussen U; Ludecke H J; Senger G; Horsthemke B; Davies K E
Microdissection of the fragile X region.
American journal of human genetics 1990;47(2):181-6.
1990: Buckle V J; Guenet J L; Simon-Chazottes D; Love D R; Davies K E
Localisation of a dystrophin-related autosomal gene to 6q24 in man, and to mouse chromosome 10 in the region of the dystrophia muscularis (dy) locus.
Human genetics 1990;85(3):324-6.
1990: Passos-Bueno M R; Rapaport D; Love D; Flint T; Bortolini E R; Zatz M; Davies K E
Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.
Journal of medical genetics 1990;27(3):145-50.
1990: Nguyen thi Man; Cartwright A J; Morris G E; Love D R; Bloomfield J F; Davies K E
Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin.
FEBS letters 1990;262(2):237-40.
1990: England S B; Nicholson L V; Johnson M A; Forrest S M; Love D R; Zubrzycka-Gaarn E E; Bulman D E; Harris J B; Davies K E
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.
Nature 1990;343(6254):180-2.
1990: Speer A; Billwitz H; Huth A; Hanke R; Coutelle C; England S; Love D; Davies K E
Mapping and sequencing in two intron regions of the human dystrophin gene.
Biomedica biochimica acta 1990;49(4):K1-2.
1989: Bell M V; Bloomfield J; McKinley M; Patterson M N; Darlison M G; Barnard E A; Davies K E
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.
American journal of human genetics 1989;45(6):883-8.
1989: Winter R M; Davies K E; Bell M V; Huson S M; Patterson M N
MASA syndrome: further clinical delineation and chromosomal localisation.
Human genetics 1989;82(4):367-70.
1989: Love D R; Forrest S M; Smith T J; England S; Flint T; Davies K E; Speer A
Molecular analysis of Duchenne and Becker muscular dystrophies.
British medical bulletin 1989;45(3):659-80.
1989: Rosenthal A; Speer A; Billwitz H; Cross G S; Forrest S M; Davies K E
Two human cDNA molecules coding for the Duchenne muscular dystrophy (DMD) locus are highly homologous.
Nucleic acids research 1989;17(13):5391.
1989: Speer A; Rosenthal A; Billwitz H; Hanke R; Forrest S M; Love D; Davies K E; Coutelle C
DNA amplification of a further exon of Duchenne muscular dystrophy locus increase possibilities for deletion screening.
Nucleic acids research 1989;17(12):4892.
1989: Love D R; Hill D F; Dickson G; Spurr N K; Byth B C; Marsden R F; Walsh F S; Edwards Y H; Davies K E
An autosomal transcript in skeletal muscle with homology to dystrophin.
Nature 1989;339(6219):55-8.
1989: Hirst M C; Watson J E; Davies K E
The use of filter-bound DNA fragments as templates for radiolabelling by random priming.
Nucleic acids research 1989;17(7):2872.
1989: Bell M V; Patterson M N; Dorkins H R; Davies K E
Physical mapping of DXS134 close to the DXS52 locus.
Human genetics 1989;82(1):27-30.
1989: Love D R; Davies K E
Duchenne muscular dystrophy: the gene and the protein.
Molecular biology & medicine 1989;6(1):7-17.
1989: Speer A; Spiegler A W; Hanke R; Grade K; Giertler U; Schieck J; Forrest S; Davies K E; Neumann R; Bollmann R
Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
Journal of medical genetics 1989;26(1):1-5.
1989: Speer A; Davies K E; Hanke R; Grade K; Spiegler A W; Herrmann F H; Szibor R; Wulff K; Sommer D; Metzke H
[The molecular principles of Duchenne and Becker muscular dystrophy and their genetic diagnosis]
Zeitschrift für ärztliche Fortbildung 1989;83(3):117-20.
1988: Patterson M; Bell M; Kress W; Davies K E; Froster-Iskenius U
Linkage studies in a large fragile X family.
American journal of human genetics 1988;43(5):684-8.
1988: Read A P; Mountford R C; Forrest S M; Kenwrick S J; Davies K E; Harris R
Patterns of exon deletions in Duchenne and Becker muscular dystrophy.
Human genetics 1988;80(2):152-6.
1988: Froster-Iskenius U; Patterson M N; Bell M V; Bloomfield J; Davies K E
Molecular analysis of the fragile X syndrome.
The Quarterly journal of medicine 1988;68(258):755-63.
1988: Forrest S M; Smith T J; Cross G S; Kenwrick S J; England S; Flint T; Davies K E
Molecular analysis and diagnosis of Duchenne muscular dystrophy.
Journal of the Royal College of Physicians of London 1988;22(2):65-7.
1988: Davies K E; Patterson M N; Kenwrick S J; Bell M V; Sloan H R; Westman J A; Elsas L J; Mahan J
Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.
American journal of medical genetics 1988;29(3):557-64.
1988: Forrest S M; Cross G S; Flint T; Speer A; Robson K J; Davies K E
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
Genomics 1988;2(2):109-14.
1988: Kenwrick S J; Smith T J; England S; Collins F; Davies K E
Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.
Nucleic acids research 1988;16(4):1305-17.
1988: Davies K E; Kenwrick S J; Patterson M N; Smith T J; Forrest S M; Dorkins H R; Cross G S; England S B
Molecular analysis of muscular dystrophy.
Journal of muscle research and cell motility 1988;9(1):1-8.
1988: Davies K E; Smith T J; Bundey S; Read A P; Flint T; Bell M; Speer A
Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
Journal of medical genetics 1988;25(1):9-13.
1988: Rosenthal A; Speer A; Billwitz H; Cross G S; Forrest S M; Davies K E
Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene.
Biomedica biochimica acta 1988;47(2):K13-5.
1987: Smith T J; Forrest S M; Cross G S; Davies K E
Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.
Nucleic acids research 1987;15(23):9761-9.
1987: Patterson M; Schwartz C; Bell M; Sauer S; Hofker M; Trask B; van den Engh G; Davies K E
Physical mapping studies on the human X chromosome in the region Xq27-Xqter.
Genomics 1987;1(4):297-306.
1987: Forrest S M; Smith T J; Cross G S; Read A P; Thomas N S; Mountford R C; Harper P S; Geirsson R T; Davies K E
Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy.
Lancet 1987;2(8571):1294-7.
1987: Cross G S; Speer A; Rosenthal A; Forrest S M; Smith T J; Edwards Y; Flint T; Hill D; Davies K E
Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients.
The EMBO journal 1987;6(11):3277-83.
1987: Forrest S M; Cross G S; Speer A; Gardner-Medwin D; Burn J; Davies K E
Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
Nature 1987;329(6140):638-40.
1987: Smith T J; Wilson L; Kenwrick S J; Forrest S M; Speer A; Coutelle C; Davies K E
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
Nucleic acids research 1987;15(5):2167-74.
1986: Kunkel L M; Hejtmancik J F; Caskey C T; Speer A; Monaco A P; Middlesworth W; Colletti C A; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt S A; Bartlett R; Pericak-Vance M A; Roses A D; Thompson M W; Ray P N; Worton R G; Fischbeck K H; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan J C; Emery A; Dorkins H; McGlade S; Davies K E; Boehm C; Arveiler B; Lemaire C; Morgan G J; Denton M J; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox D E; Affara N A; Ferguson-Smith M A; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen G J; Pearson P L; Greenberg C R; Hamerton J L; Wrogemann K; Doherty R A; Polakowska R; Hyser C; Quirk S; Thomas N; Harper J F; Darras B T; Francke U
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Nature 1986;322(6074):73-7.
1986: Davies K E; Ball S P; Dorkins H R; Forrest S M; Kenwrick S J; King A W; Lavenir I J; McGlade S A; Patterson M N; Smith T J
Molecular analysis of human X-linked diseases.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():337-43.
1986: Davies K E; Ball S P; Dorkins H R; Forrest S M; Kenwrick S J; Patterson M N; Smith T J; Old J M; King A W; Thakker R V
Molecular analysis of X-linked diseases.
Annals of clinical research 1986;18(5-6):231-3.
1985: Davies K E; Speer A; Herrmann F; Spiegler A W; McGlade S; Hofker M H; Briand P; Hanke R; Schwartz M; Steinbicker V
Human X chromosome markers and Duchenne muscular dystrophy.
Nucleic acids research 1985;13(10):3419-26.
1985: Ball S P; Kenwrick S J; Davies K E
The molecular genetics of human monogenic diseases.
Biotechnology & genetic engineering reviews 1985;3():275-309.

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