England S - Search Results

1

Molecular analysis and diagnosis of Duchenne muscular dystrophy.

Forrest SM, Smith TJ, Cross GS, Kenwrick SJ, England S, Flint T, Davies KE. Forrest SM, et al. Among authors: england s. J R Coll Physicians Lond. 1988 Apr;22(2):65-7. J R Coll Physicians Lond. 1988. PMID: 3294388 Free PMC article. Review. No abstract available.

2

Localisation of the endpoints of deletions in the 5' region of the Duchenne gene using a sequence isolated by chromosome jumping.

Kenwrick SJ, Smith TJ, England S, Collins F, Davies KE. Kenwrick SJ, et al. Among authors: england s. Nucleic Acids Res. 1988 Feb 25;16(4):1305-17. doi: 10.1093/nar/16.4.1305. Nucleic Acids Res. 1988. PMID: 3347492 Free PMC article.

3

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. Nature. 1990 Jan 11;343(6254):180-2. doi: 10.1038/343180a0. Nature. 1990. PMID: 2404210

4

Molecular analysis of muscular dystrophy.

Davies KE, Kenwrick SJ, Patterson MN, Smith TJ, Forrest SM, Dorkins HR, Cross GS, England SB. Davies KE, et al. Among authors: england sb. J Muscle Res Cell Motil. 1988 Feb;9(1):1-8. doi: 10.1007/BF01682143. J Muscle Res Cell Motil. 1988. PMID: 3292577 Review.

5

Molecular analysis of Duchenne and Becker muscular dystrophies.

Love DR, Forrest SM, Smith TJ, England S, Flint T, Davies KE, Speer A. Love DR, et al. Among authors: england s. Br Med Bull. 1989 Jul;45(3):659-80. doi: 10.1093/oxfordjournals.bmb.a072351. Br Med Bull. 1989. PMID: 2688822 Review.

6

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: england sb. Genomics. 1991 May;10(1):57-67. doi: 10.1016/0888-7543(91)90484-v. Genomics. 1991. PMID: 2045110

7

Mapping and sequencing in two intron regions of the human dystrophin gene.

Speer A, Billwitz H, Huth A, Hanke R, Coutelle C, England S, Love D, Davies KE. Speer A, et al. Among authors: england s. Biomed Biochim Acta. 1990;49(4):K1-2. Biomed Biochim Acta. 1990. PMID: 2206126 No abstract available.

8

Cough capacity in patients with muscular dystrophy.

Szeinberg A, Tabachnik E, Rashed N, McLaughlin FJ, England S, Bryan CA, Levison H. Szeinberg A, et al. Among authors: england s. Chest. 1988 Dec;94(6):1232-5. doi: 10.1378/chest.94.6.1232. Chest. 1988. PMID: 3191765

9

The tetrodotoxin-resistant sodium channel SNS has a specialized function in pain pathways.

Akopian AN, Souslova V, England S, Okuse K, Ogata N, Ure J, Smith A, Kerr BJ, McMahon SB, Boyce S, Hill R, Stanfa LC, Dickenson AH, Wood JN. Akopian AN, et al. Among authors: england s. Nat Neurosci. 1999 Jun;2(6):541-8. doi: 10.1038/9195. Nat Neurosci. 1999. PMID: 10448219

10

Localization of 24 cosmid clones on the human Y chromosome.

Nagafuchi S, Nakahori Y, Nakamura Y, England SB, Tamura T, Numabe H, Nakagome Y. Nagafuchi S, et al. Among authors: england sb. Jpn J Hum Genet. 1992 Dec;37(4):307-10. doi: 10.1007/BF01883322. Jpn J Hum Genet. 1992. PMID: 1297451

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

337 results

Search Page

Filters