Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

29 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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
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
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
Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders.
Clark AR, Sawyer GM, Robertson SP, Sutherland-Smith AJ. Clark AR, et al. Hum Mol Genet. 2009 Dec 15;18(24):4791-800. doi: 10.1093/hmg/ddp442. Epub 2009 Sep 22. Hum Mol Genet. 2009. PMID: 19773341
Disease-associated substitutions in the filamin B actin binding domain confer enhanced actin binding affinity in the absence of major structural disturbance: Insights from the crystal structures of filamin B actin binding domains.
Sawyer GM, Clark AR, Robertson SP, Sutherland-Smith AJ. Sawyer GM, et al. J Mol Biol. 2009 Jul 31;390(5):1030-47. doi: 10.1016/j.jmb.2009.06.009. Epub 2009 Jun 6. J Mol Biol. 2009. PMID: 19505475
Crystal structure of the filamin N-terminal region reveals a hinge between the actin binding and first repeat domains.
Sawyer GM, Sutherland-Smith AJ. Sawyer GM, et al. J Mol Biol. 2012 Dec 14;424(5):240-7. doi: 10.1016/j.jmb.2012.09.016. Epub 2012 Oct 2. J Mol Biol. 2012. PMID: 23036857
The crystal structures of dystrophin and utrophin spectrin repeats: implications for domain boundaries.
Muthu M, Richardson KA, Sutherland-Smith AJ. Muthu M, et al. PLoS One. 2012;7(7):e40066. doi: 10.1371/journal.pone.0040066. Epub 2012 Jul 20. PLoS One. 2012. PMID: 22911693 Free PMC article.
An open or closed case for the conformation of calponin homology domains on F-actin?
Lehman W, Craig R, Kendrick-Jones J, Sutherland-Smith AJ. Lehman W, et al. J Muscle Res Cell Motil. 2004;25(4-5):351-8. doi: 10.1007/s10974-004-0690-7. J Muscle Res Cell Motil. 2004. PMID: 15548864 Review.
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid.
Laue K, Pogoda HM, Daniel PB, van Haeringen A, Alanay Y, von Ameln S, Rachwalski M, Morgan T, Gray MJ, Breuning MH, Sawyer GM, Sutherland-Smith AJ, Nikkels PG, Kubisch C, Bloch W, Wollnik B, Hammerschmidt M, Robertson SP. Laue K, et al. Am J Hum Genet. 2011 Nov 11;89(5):595-606. doi: 10.1016/j.ajhg.2011.09.015. Epub 2011 Oct 20. Am J Hum Genet. 2011. PMID: 22019272 Free PMC article.
Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley-Bixler syndromes.
Morton JE, Frentz S, Morgan T, Sutherland-Smith AJ, Robertson SP. Morton JE, et al. Among authors: sutherland smith aj. Am J Med Genet A. 2016 Oct;170(10):2706-10. doi: 10.1002/ajmg.a.37804. Epub 2016 Jul 13. Am J Med Genet A. 2016. PMID: 27410456 Review.
29 results
Jump to page