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Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome.
McDonell LM, Mirzaa GM, Alcantara D, Schwartzentruber J, Carter MT, Lee LJ, Clericuzio CL, Graham JM Jr, Morris-Rosendahl DJ, Polster T, Acsadi G, Townshend S, Williams S, Halbert A, Isidor B, David A, Smyser CD, Paciorkowski AR, Willing M, Woulfe J, Das S, Beaulieu CL, Marcadier J; FORGE Canada Consortium; Geraghty MT, Frey BJ, Majewski J, Bulman DE, Dobyns WB, O'Driscoll M, Boycott KM. McDonell LM, et al. Among authors: woulfe j. Nat Genet. 2013 May;45(5):556-62. doi: 10.1038/ng.2602. Epub 2013 Mar 31. Nat Genet. 2013. PMID: 23542699 Free PMC article.
Lipofuscin and aging: a matter of toxic waste.
Gray DA, Woulfe J. Gray DA, et al. Among authors: woulfe j. Sci Aging Knowledge Environ. 2005 Feb 2;2005(5):re1. doi: 10.1126/sageke.2005.5.re1. Sci Aging Knowledge Environ. 2005. PMID: 15689603 Review.
A complex of C9ORF72 and p62 uses arginine methylation to eliminate stress granules by autophagy.
Chitiprolu M, Jagow C, Tremblay V, Bondy-Chorney E, Paris G, Savard A, Palidwor G, Barry FA, Zinman L, Keith J, Rogaeva E, Robertson J, Lavallée-Adam M, Woulfe J, Couture JF, Côté J, Gibbings D. Chitiprolu M, et al. Among authors: woulfe j. Nat Commun. 2018 Jul 18;9(1):2794. doi: 10.1038/s41467-018-05273-7. Nat Commun. 2018. PMID: 30022074 Free PMC article.
Role of Cdk5-mediated phosphorylation of Prx2 in MPTP toxicity and Parkinson's disease.
Qu D, Rashidian J, Mount MP, Aleyasin H, Parsanejad M, Lira A, Haque E, Zhang Y, Callaghan S, Daigle M, Rousseaux MW, Slack RS, Albert PR, Vincent I, Woulfe JM, Park DS. Qu D, et al. Among authors: woulfe jm. Neuron. 2007 Jul 5;55(1):37-52. doi: 10.1016/j.neuron.2007.05.033. Neuron. 2007. PMID: 17610816 Free article.
152 results