Davies KE - Search Results

1

Sequences of junction fragments in the deletion-prone region of the dystrophin gene.

Love DR, England SB, Speer A, Marsden RF, Bloomfield JF, Roche AL, Cross GS, Mountford RC, Smith TJ, Davies KE. Love DR, et al. Among authors: davies ke. Genomics. 1991 May;10(1):57-67. doi: 10.1016/0888-7543(91)90484-v. Genomics. 1991. PMID: 2045110

2

Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.

Love DR, Flint TJ, Genet SA, Middleton-Price HR, Davies KE. Love DR, et al. Among authors: davies ke. J Med Genet. 1991 Dec;28(12):860-4. doi: 10.1136/jmg.28.12.860. J Med Genet. 1991. PMID: 1757963 Free PMC article.

3

Tissue distribution of the dystrophin-related gene product and expression in the mdx and dy mouse.

Love DR, Morris GE, Ellis JM, Fairbrother U, Marsden RF, Bloomfield JF, Edwards YH, Slater CP, Parry DJ, Davies KE. Love DR, et al. Among authors: davies ke. Proc Natl Acad Sci U S A. 1991 Apr 15;88(8):3243-7. doi: 10.1073/pnas.88.8.3243. Proc Natl Acad Sci U S A. 1991. PMID: 2014247 Free PMC article.

4

Physical mapping distal to the DMD locus.

Love DR, Bloomfield JF, Kenwrick SJ, Yates JR, Davies KE. Love DR, et al. Among authors: davies ke. Genomics. 1990 Sep;8(1):106-12. doi: 10.1016/0888-7543(90)90231-i. Genomics. 1990. PMID: 2081587

5

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.

Buckle VJ, Guenet JL, Simon-Chazottes D, Love DR, Davies KE. Buckle VJ, et al. Among authors: davies ke. Hum Genet. 1990 Aug;85(3):324-6. doi: 10.1007/BF00206755. Hum Genet. 1990. PMID: 2203673

6

Characterization of deletions in the dystrophin gene giving mild phenotypes.

Love DR, Flint TJ, Marsden RF, Bloomfield JF, Daniels RJ, Forrest SM, Gabrielli O, Giorgi P, Novelli G, Davies KE. Love DR, et al. Among authors: davies ke. Am J Med Genet. 1990 Sep;37(1):136-42. doi: 10.1002/ajmg.1320370132. Am J Med Genet. 1990. PMID: 2240031

7

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.

England SB, Nicholson LV, Johnson MA, Forrest SM, Love DR, Zubrzycka-Gaarn EE, Bulman DE, Harris JB, Davies KE. England SB, et al. Among authors: davies ke. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

8

An autosomal transcript in skeletal muscle with homology to dystrophin.

Love DR, Hill DF, Dickson G, Spurr NK, Byth BC, Marsden RF, Walsh FS, Edwards YH, Davies KE. Love DR, et al. Among authors: davies ke. Nature. 1989 May 4;339(6219):55-8. doi: 10.1038/339055a0. Nature. 1989. PMID: 2541343

9

Duchenne muscular dystrophy: the gene and the protein.

Love DR, Davies KE. Love DR, et al. Among authors: davies ke. Mol Biol Med. 1989 Feb;6(1):7-17. Mol Biol Med. 1989. PMID: 2666821 Review. No abstract available.

10

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Read AP, Thomas NS, Mountford RC, Harper PS, Geirsson RT, Davies KE. Forrest SM, et al. Among authors: davies ke. Lancet. 1987 Dec 5;2(8571):1294-7. doi: 10.1016/s0140-6736(87)91192-5. Lancet. 1987. PMID: 2890901

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