Kendrick-Jones J - Search Results

1

The Emery-Dreifuss muscular dystrophy associated-protein emerin is phosphorylated on serine 49 by protein kinase A.

Roberts RC, Sutherland-Smith AJ, Wheeler MA, Jensen ON, Emerson LJ, Spiliotis II, Tate CG, Kendrick-Jones J, Ellis JA. Roberts RC, et al. FEBS J. 2006 Oct;273(19):4562-75. doi: 10.1111/j.1742-4658.2006.05464.x. FEBS J. 2006. PMID: 16972941 Free article.

2

The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.

Fairley EA, Riddell A, Ellis JA, Kendrick-Jones J. Fairley EA, et al. J Cell Sci. 2002 Jan 15;115(Pt 2):341-54. doi: 10.1242/jcs.115.2.341. J Cell Sci. 2002. PMID: 11839786

3

The Emery-Dreifuss muscular dystrophy phenotype arises from aberrant targeting and binding of emerin at the inner nuclear membrane.

Fairley EA, Kendrick-Jones J, Ellis JA. Fairley EA, et al. J Cell Sci. 1999 Aug;112 ( Pt 15):2571-82. doi: 10.1242/jcs.112.15.2571. J Cell Sci. 1999. PMID: 10393813

4

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. J Cell Sci. 1998 Mar;111 ( Pt 6):781-92. doi: 10.1242/jcs.111.6.781. J Cell Sci. 1998. PMID: 9472006

5

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. Hum Genet. 1999 Mar;104(3):262-8. doi: 10.1007/s004390050946. Hum Genet. 1999. PMID: 10323252

6

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

7

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. Neuromuscul Disord. 2000 Jan;10(1):24-30. doi: 10.1016/s0960-8966(99)00059-0. Neuromuscul Disord. 2000. PMID: 10677860

8

The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy.

Norwood FL, Sutherland-Smith AJ, Keep NH, Kendrick-Jones J. Norwood FL, et al. Structure. 2000 May 15;8(5):481-91. doi: 10.1016/s0969-2126(00)00132-5. Structure. 2000. PMID: 10801490 Free article.

9

Rab8-optineurin-myosin VI: analysis of interactions and functions in the secretory pathway.

Chibalina MV, Roberts RC, Arden SD, Kendrick-Jones J, Buss F. Chibalina MV, et al. Methods Enzymol. 2008;438:11-24. doi: 10.1016/S0076-6879(07)38002-6. Methods Enzymol. 2008. PMID: 18413238 Free PMC article.

10

An atomic model for actin binding by the CH domains and spectrin-repeat modules of utrophin and dystrophin.

Sutherland-Smith AJ, Moores CA, Norwood FL, Hatch V, Craig R, Kendrick-Jones J, Lehman W. Sutherland-Smith AJ, et al. J Mol Biol. 2003 May 23;329(1):15-33. doi: 10.1016/s0022-2836(03)00422-4. J Mol Biol. 2003. PMID: 12742015

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

183 results

Search Page

Filters