David S. Williams
David S. Williams
Dirección de correo verificada de ucla.edu
Citado por
Citado por
Axonopathy and transport deficits early in the pathogenesis of Alzheimer's disease
GB Stokin, C Lillo, TL Falzone, RG Brusch, E Rockenstein, SL Mount, ...
Science 307 (5713), 1282-1288, 2005
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
JA Sayer, EA Otto, JF O'Toole, G Nurnberg, MA Kennedy, C Becker, ...
Nature genetics 38 (6), 674-681, 2006
Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria
J Liu, C Lillo, PA Jonsson, CV Velde, CM Ward, TM Miller, ...
Neuron 43 (1), 5-17, 2004
Cadherin 23 is a component of the tip link in hair-cell stereocilia
J Siemens, C Lillo, RA Dumont, A Reynolds, DS Williams, PG Gillespie, ...
Nature 428 (6986), 950-955, 2004
Genetic evidence for selective transport of opsin and arrestin by kinesin-II in mammalian photoreceptors
JR Marszalek, X Liu, EA Roberts, D Chui, JD Marth, DS Williams, ...
Cell 102 (2), 175-187, 2000
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
EA Otto, B Loeys, H Khanna, J Hellemans, R Sudbrak, S Fan, U Muerb, ...
Nature genetics 37 (3), 282-288, 2005
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse
B Chang, H Khanna, N Hawes, D Jimeno, S He, C Lillo, SK Parapuram, ...
Human molecular genetics 15 (11), 1847-1857, 2006
Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy
EA Otto, TW Hurd, R Airik, M Chaki, W Zhou, C Stoetzel, SB Patil, S Levy, ...
Nature genetics 42 (10), 840-850, 2010
Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A
CH Xia, EA Roberts, LS Her, X Liu, DS Williams, DW Cleveland, ...
The Journal of cell biology 161 (1), 55-66, 2003
Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration.
K Arikawa, LL Molday, RS Molday, DS Williams
The Journal of cell biology 116 (3), 659-667, 1992
Myosin VIIa participates in opsin transport through the photoreceptor cilium
X Liu, IP Udovichenko, SDM Brown, KP Steel, DS Williams
Journal of Neuroscience 19 (15), 6267-6274, 1999
Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice
M Allocca, M Doria, M Petrillo, P Colella, M Garcia-Hoyos, D Gibbs, ...
The Journal of clinical investigation 118 (5), 1955-1964, 2008
Iron traffics in circulation bound to a siderocalin (Ngal)–catechol complex
G Bao, M Clifton, TM Hoette, K Mori, SX Deng, A Qiu, M Viltard, D Williams, ...
Nature chemical biology 6 (8), 602-609, 2010
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
S Ashraf, HY Gee, S Woerner, LX Xie, V Vega-Warner, S Lovric, H Fang, ...
The Journal of clinical investigation 123 (12), 5179-5189, 2013
Scara5 is a ferritin receptor mediating non-transferrin iron delivery
JY Li, N Paragas, RM Ned, A Qiu, M Viltard, T Leete, IR Drexler, X Chen, ...
Developmental cell 16 (1), 35-46, 2009
Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein
D Gibbs, J Kitamoto, DS Williams
Proceedings of the National Academy of Sciences 100 (11), 6481-6486, 2003
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Z Yang, Y Chen, C Lillo, J Chien, Z Yu, M Michaelides, M Klein, ...
The Journal of clinical investigation 118 (8), 2908-2916, 2008
Cone-like morphological, molecular, and electrophysiological features of the photoreceptors of the Nrl knockout mouse
LL Daniele, C Lillo, AL Lyubarsky, SS Nikonov, N Philp, AJ Mears, ...
Investigative ophthalmology & visual science 46 (6), 2156-2167, 2005
A naturally selected dimorphism within the HLA-B44 supertype alters class I structure, peptide repertoire, and T cell recognition
WA Macdonald, AW Purcell, NA Mifsud, LK Ely, DS Williams, L Chang, ...
The Journal of experimental medicine 198 (5), 679-691, 2003
Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells
X Liu, G Vansant, IP Udovichenko, U Wolfrum, DS Williams
Cell motility and the cytoskeleton 37 (3), 240-252, 1997
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
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