Sutherland-Smith AJ - Search Results

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 Free article.

2

DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.

Hamed S, Sutherland-Smith A, Gorospe J, Kendrick-Jones J, Hoffman E. Hamed S, et al. Clin Genet. 2005 Jul;68(1):69-79. doi: 10.1111/j.1399-0004.2005.00455.x. Clin Genet. 2005. PMID: 15952989

3

The crystal structure of methanogen McrD, a methyl-coenzyme M reductase-associated protein.

Sutherland-Smith AJ, Carbone V, Schofield LR, Cronin B, Duin EC, Ronimus RS. Sutherland-Smith AJ, et al. FEBS Open Bio. 2024 Aug;14(8):1222-1229. doi: 10.1002/2211-5463.13848. Epub 2024 Jun 14. FEBS Open Bio. 2024. PMID: 38877345 Free PMC article.

4

Structural characterisation of methanogen pseudomurein cell wall peptide ligases homologous to bacterial MurE/F murein peptide ligases.

Subedi BP, Schofield LR, Carbone V, Wolf M, Martin WF, Ronimus RS, Sutherland-Smith AJ. Subedi BP, et al. Among authors: sutherland smith aj. Microbiology (Reading). 2022 Sep;168(9). doi: 10.1099/mic.0.001235. Microbiology (Reading). 2022. PMID: 36178458 Free article.

5

Archaeal pseudomurein and bacterial murein cell wall biosynthesis share a common evolutionary ancestry.

Subedi BP, Martin WF, Carbone V, Duin EC, Cronin B, Sauter J, Schofield LR, Sutherland-Smith AJ, Ronimus RS. Subedi BP, et al. Among authors: sutherland smith aj. FEMS Microbes. 2021 Aug 24;2:xtab012. doi: 10.1093/femsmc/xtab012. eCollection 2021. FEMS Microbes. 2021. PMID: 37334239 Free PMC article.

6

Strigolactones regulate sepal senescence in Arabidopsis.

Xu X, Jibran R, Wang Y, Dong L, Flokova K, Esfandiari A, McLachlan ARG, Heiser A, Sutherland-Smith AJ, Brummell DA, Bouwmeester HJ, Dijkwel PP, Hunter DA. Xu X, et al. Among authors: sutherland smith aj. J Exp Bot. 2021 Jul 28;72(15):5462-5477. doi: 10.1093/jxb/erab199. J Exp Bot. 2021. PMID: 33970249

7

Covalent Functionalization of Bioengineered Polyhydroxyalkanoate Spheres Directed by Specific Protein-Protein Interactions.

Wong JX, Gonzalez-Miro M, Sutherland-Smith AJ, Rehm BHA. Wong JX, et al. Among authors: sutherland smith aj. Front Bioeng Biotechnol. 2020 Feb 6;8:44. doi: 10.3389/fbioe.2020.00044. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32117925 Free PMC article.

8

Structural determination of archaeal UDP-N-acetylglucosamine 4-epimerase from Methanobrevibacter ruminantium M1 in complex with the bacterial cell wall intermediate UDP-N-acetylmuramic acid.

Carbone V, Schofield LR, Sang C, Sutherland-Smith AJ, Ronimus RS. Carbone V, et al. Among authors: sutherland smith aj. Proteins. 2018 Dec;86(12):1306-1312. doi: 10.1002/prot.25606. Epub 2018 Oct 5. Proteins. 2018. PMID: 30242905

9

Mutations in MAP3K7 that Alter the Activity of the TAK1 Signaling Complex Cause Frontometaphyseal Dysplasia.

Wade EM, Daniel PB, Jenkins ZA, McInerney-Leo A, Leo P, Morgan T, Addor MC, Adès LC, Bertola D, Bohring A, Carter E, Cho TJ, Duba HC, Fletcher E, Kim CA, Krakow D, Morava E, Neuhann T, Superti-Furga A, Veenstra-Knol I, Wieczorek D, Wilson LC, Hennekam RC, Sutherland-Smith AJ, Strom TM, Wilkie AO, Brown MA, Duncan EL, Markie DM, Robertson SP. Wade EM, et al. Among authors: sutherland smith aj. Am J Hum Genet. 2016 Aug 4;99(2):392-406. doi: 10.1016/j.ajhg.2016.05.024. Epub 2016 Jul 15. Am J Hum Genet. 2016. PMID: 27426733 Free PMC article.

10

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.

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