A Genetic Analysis of the α-Glycerophosphate Oxidase Locus in Drosophila Melanogaster

Por Davis, M. B., MacIntyre, R. J.
Publicado em 1988

Familial polyposis coli: growth characteristics of karyotypically variable cultured fibroblasts, response to epidermal growth factor and the tumour promoter 12-0-tetradecanoyl phor...

Por Rider, S H, Mazzullo, H A, Davis, M B, Delhanty, J D
Publicado em 1986

Sequence of the superoxide dismutase 1 (SOD 1) gene in familial Parkinson's disease.

Por Bandmann, O, Davis, M B, Marsden, C D, Harding, A E
Publicado em 1995

Transposable element insertions respecify alternative exon splicing in three Drosophila myosin heavy chain mutants.

Por Davis, M B, Dietz, J, Standiford, D M, Emerson, C P
Publicado em 1998

Positive and negative intronic regulatory elements control muscle-specific alternative exon splicing of Drosophila myosin heavy chain transcripts.

Por Standiford, D M, Sun, W T, Davis, M B, Emerson, C P
Publicado em 2001

Splice-Junction Elements and Intronic Sequences Regulate Alternative Splicing of the Drosophila Myosin Heavy Chain Gene Transcript

Por Standiford, D. M., Davis, M. B., Sun, W., Emerson-Jr., C. P.
Publicado em 1997

Prenatal diagnosis of mitochondrial DNA8993 T----G disease.

Por Harding, A E, Holt, I J, Sweeney, M G, Brockington, M, Davis, M B
Publicado em 1992

Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

Por Planté-Bordeneuve, V, Davis, M B, Maraganore, D M, Marsden, C D, Harding, A E
Publicado em 1994

Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Por Sweeney, M G, Davis, M B, Lashwood, A, Brockington, M, Toscano, A, Harding, A E
Publicado em 1992

Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.

Por Chalmers, R. M., Davis, M. B., Sweeney, M. G., Wood, N. W., Harding, A. E.
Publicado em 1996

Presymptomatic detection or exclusion of prion protein gene defects in families with inherited prion diseases.

Por Collinge, J, Poulter, M, Davis, M B, Baraitser, M, Owen, F, Crow, T J, Harding, A E
Publicado em 1991

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Por Worth, P F, Giunti, P, Gardner-Thorpe, C, Dixon, P H, Davis, M B, Wood, N W
Publicado em 1999

Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families.

Por Cachon-Gonzalez, M B, Delhanty, J D, Burn, J, Tsioupra, K, Davis, M B, Attwood, J, Chapman, P
Publicado em 1991

Loss of heterozygosity for DNA polymorphisms mapping to chromosomes 10 and 17 and prognosis in patients with gliomas.

Por Jones, C E, Davis, M B, Darling, J L, Geddes, J F, Thomas, D G, Harding, A E
Publicado em 1995

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

Por Matthews, E., Portaro, S., Ke, Q., Sud, R., Haworth, A., Davis, M.B., Griggs, R.C., Hanna, M.G.
Publicado em 2011

Transthyretin gene mutations in British and French patients with amyloid neuropathy.

Por Bhatia, K, Reilly, M, Adams, D, Davis, M B, Hawkes, C H, Thomas, P K, Said, G, Harding, A E
Publicado em 1993

Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.

Por Jarman, P R, Wood, N W, Davis, M T, Davis, P V, Bhatia, K P, Marsden, C D, Davis, M B
Publicado em 1997

Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence

Por Rath, P P, Jenkins, S, Michaelides, M, Smith, A, Sweeney, M G, Davis, M B, Fitzke, F W, Bird, A C
Publicado em 2008

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

Por Matthews, E, Labrum, R, Sweeney, M G., Sud, R, Haworth, A, Chinnery, P F., Meola, G, Schorge, S, Kullmann, D M., Davis, M B., Hanna, M G.
Publicado em 2009

Episodic ataxia and hemiplegia caused by the 8993T→C mitochondrial DNA mutation

Por Craig, K, Elliott, H R, Keers, S M, Lambert, C, Pyle, A, Graves, T D, Woodward, C, Sweeney, M G, Davis, M B, Hanna, M G, Chinnery, P F
Publicado em 2007