Yates JR - Search Results

1

Genotype-phenotype analysis in X-linked Emery-Dreifuss muscular dystrophy and identification of a missense mutation associated with a milder phenotype.

Yates JR, Bagshaw J, Aksmanovic VM, Coomber E, McMahon R, Whittaker JL, Morrison PJ, Kendrick-Jones J, Ellis JA. Yates JR, et al. Neuromuscul Disord. 1999 May;9(3):159-65. Neuromuscul Disord. 1999. PMID: 10382909

2

Aberrant intracellular targeting and cell cycle-dependent phosphorylation of emerin contribute to the Emery-Dreifuss muscular dystrophy phenotype.

Ellis JA, Craxton M, Yates JR, Kendrick-Jones J. Ellis JA, et al. Among authors: yates jr. J Cell Sci. 1998 Mar;111 ( Pt 6):781-92. doi: 10.1242/jcs.111.6.781. J Cell Sci. 1998. PMID: 9472006

3

Changes at P183 of emerin weaken its protein-protein interactions resulting in X-linked Emery-Dreifuss muscular dystrophy.

Ellis JA, Yates JR, Kendrick-Jones J, Brown CA. Ellis JA, et al. Among authors: yates jr. Hum Genet. 1999 Mar;104(3):262-8. doi: 10.1007/s004390050946. Hum Genet. 1999. PMID: 10323252

4

Two distal mutations in the gene encoding emerin have profoundly different effects on emerin protein expression.

Ellis JA, Brown CA, Tilley LD, Kendrick-Jones J, Spence JE, Yates JR. Ellis JA, et al. Among authors: yates jr. Neuromuscul Disord. 2000 Jan;10(1):24-30. doi: 10.1016/s0960-8966(99)00059-0. Neuromuscul Disord. 2000. PMID: 10677860

5

The Emery-Dreifuss Muscular Dystrophy Mutation Database.

Yates JR, Wehnert M. Yates JR, et al. Neuromuscul Disord. 1999 May;9(3):199. Neuromuscul Disord. 1999. PMID: 10382916 No abstract available.

6

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease.

Bione S, Small K, Aksmanovic VM, D'Urso M, Ciccodicola A, Merlini L, Morandi L, Kress W, Yates JR, Warren ST, et al. Bione S, et al. Among authors: yates jr. Hum Mol Genet. 1995 Oct;4(10):1859-63. doi: 10.1093/hmg/4.10.1859. Hum Mol Genet. 1995. PMID: 8595407

7

A protein truncation test for Emery-Dreifuss muscular dystrophy (EMD): detection of N-terminal truncating mutations.

de Koning Gans PA, Ginjaar I, Bakker E, Yates JR, den Dunnen JT. de Koning Gans PA, et al. Among authors: yates jr. Neuromuscul Disord. 1999 Jun;9(4):247-50. doi: 10.1016/s0960-8966(98)00128-x. Neuromuscul Disord. 1999. PMID: 10399752

8

European workshop on Emery-Dreifuss muscular dystrophy 1991.

Yates JR. Yates JR. Neuromuscul Disord. 1991;1(6):393-6. doi: 10.1016/0960-8966(91)90002-a. Neuromuscul Disord. 1991. PMID: 1822351 No abstract available.

9

43rd ENMC International Workshop on Emery-Dreifuss Muscular Dystrophy, 22 June 1996, Naarden, The Netherlands.

Yates JR. Yates JR. Neuromuscul Disord. 1997 Jan;7(1):67-9. doi: 10.1016/s0960-8966(96)00403-8. Neuromuscul Disord. 1997. PMID: 9132143 No abstract available.

10

Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Zhang Y, McMahon R, Charles SJ, Green JS, Moore AT, Barton DE, Yates JR. Zhang Y, et al. Among authors: yates jr. J Med Genet. 1993 Nov;30(11):923-5. doi: 10.1136/jmg.30.11.923. J Med Genet. 1993. PMID: 8301646 Free PMC article.

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