Williams DS - Search Results

1

Elevated PGC-1α activity sustains mitochondrial biogenesis and muscle function without extending survival in a mouse model of inherited ALS.

Da Cruz S, Parone PA, Lopes VS, Lillo C, McAlonis-Downes M, Lee SK, Vetto AP, Petrosyan S, Marsala M, Murphy AN, Williams DS, Spiegelman BM, Cleveland DW. Da Cruz S, et al. Among authors: williams ds. Cell Metab. 2012 May 2;15(5):778-86. doi: 10.1016/j.cmet.2012.03.019. Cell Metab. 2012. PMID: 22560226 Free PMC article.

2

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

Liu J, Lillo C, Jonsson PA, Vande Velde C, Ward CM, Miller TM, Subramaniam JR, Rothstein JD, Marklund S, Andersen PM, Brännström T, Gredal O, Wong PC, Williams DS, Cleveland DW. Liu J, et al. Among authors: williams ds. Neuron. 2004 Jul 8;43(1):5-17. doi: 10.1016/j.neuron.2004.06.016. Neuron. 2004. PMID: 15233913 Free article.

3

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.

Xia CH, Roberts EA, Her LS, Liu X, Williams DS, Cleveland DW, Goldstein LS. Xia CH, et al. Among authors: williams ds. J Cell Biol. 2003 Apr 14;161(1):55-66. doi: 10.1083/jcb.200301026. Epub 2003 Apr 7. J Cell Biol. 2003. PMID: 12682084 Free PMC article.

4

Microtubule motors transport phagosomes in the RPE, and lack of KLC1 leads to AMD-like pathogenesis.

Jiang M, Esteve-Rudd J, Lopes VS, Diemer T, Lillo C, Rump A, Williams DS. Jiang M, et al. Among authors: williams ds. J Cell Biol. 2015 Aug 17;210(4):595-611. doi: 10.1083/jcb.201410112. Epub 2015 Aug 10. J Cell Biol. 2015. PMID: 26261180 Free PMC article.

5

Roles and interactions of usher 1 proteins in the outer retina.

Lillo C, Kitamoto J, Williams DS. Lillo C, et al. Among authors: williams ds. Adv Exp Med Biol. 2006;572:341-8. doi: 10.1007/0-387-32442-9_48. Adv Exp Med Biol. 2006. PMID: 17249594

6

Axonal stress kinase activation and tau misbehavior induced by kinesin-1 transport defects.

Falzone TL, Stokin GB, Lillo C, Rodrigues EM, Westerman EL, Williams DS, Goldstein LS. Falzone TL, et al. Among authors: williams ds. J Neurosci. 2009 May 6;29(18):5758-67. doi: 10.1523/JNEUROSCI.0780-09.2009. J Neurosci. 2009. PMID: 19420244 Free PMC article.

7

The many different cellular functions of MYO7A in the retina.

Williams DS, Lopes VS. Williams DS, et al. Biochem Soc Trans. 2011 Oct;39(5):1207-10. doi: 10.1042/BST0391207. Biochem Soc Trans. 2011. PMID: 21936790 Free PMC article. Review.

8

Gene therapy strategies for Usher syndrome type 1B.

Williams DS, Lopes VS. Williams DS, et al. Adv Exp Med Biol. 2012;723:235-42. doi: 10.1007/978-1-4614-0631-0_31. Adv Exp Med Biol. 2012. PMID: 22183338 Review. No abstract available.

9

Gene Therapy for the Retinal Degeneration of Usher Syndrome Caused by Mutations in MYO7A.

Lopes VS, Williams DS. Lopes VS, et al. Among authors: williams ds. Cold Spring Harb Perspect Med. 2015 Jan 20;5(6):a017319. doi: 10.1101/cshperspect.a017319. Cold Spring Harb Perspect Med. 2015. PMID: 25605753 Free PMC article. Review.

10

Dysfunction of heterotrimeric kinesin-2 in rod photoreceptor cells and the role of opsin mislocalization in rapid cell death.

Lopes VS, Jimeno D, Khanobdee K, Song X, Chen B, Nusinowitz S, Williams DS. Lopes VS, et al. Among authors: williams ds. Mol Biol Cell. 2010 Dec;21(23):4076-88. doi: 10.1091/mbc.E10-08-0715. Epub 2010 Oct 6. Mol Biol Cell. 2010. PMID: 20926680 Free PMC article.

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