Zhou Weibin
Zhou Weibin
Dirección de correo verificada de duke.edu - Página principal
Citado por
Citado por
Nephronophthisis-associated ciliopathies
F Hildebrandt, W Zhou
Journal of the American Society of Nephrology 18 (6), 1855-1871, 2007
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ...
The Journal of clinical investigation 121 (5), 2013-2024, 2011
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
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
M Chaki, R Airik, AK Ghosh, RH Giles, R Chen, GG Slaats, H Wang, ...
Cell 150 (3), 533-548, 2012
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, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
HY Gee, P Saisawat, S Ashraf, TW Hurd, V Vega-Warner, H Fang, ...
The Journal of clinical investigation 123 (8), 3243-3253, 2013
FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair
W Zhou, EA Otto, A Cluckey, R Airik, TW Hurd, M Chaki, K Diaz, FP Lach, ...
Nature genetics 44 (8), 910-915, 2012
A systematic approach to mapping recessive disease genes in individuals from outbred populations
F Hildebrandt, SF Heeringa, F Rüschendorf, M Attanasio, G Nürnberg, ...
PLoS genetics 5 (1), e1000353, 2009
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6
MA Zariwala, HY Gee, M Kurkowiak, DA Al-Mutairi, MW Leigh, TW Hurd, ...
The American Journal of Human Genetics 93 (2), 336-345, 2013
Stac3 is a component of the excitation–contraction coupling machinery and mutated in Native American myopathy
EJ Horstick, JW Linsley, JJ Dowling, MA Hauser, KK McDonald, ...
Nature communications 4, 2013
KANK deficiency leads to podocyte dysfunction and nephrotic syndrome.
HY Gee, F Zhang, S Ashraf, S Kohl, CE Sadowski, V Vega-Warner, ...
The Journal of clinical investigation 125 (6), 2375-2384, 2015
Assaying autophagic activity in transgenic GFP-Lc3 and GFP-Gabarap zebrafish embryos
C He, CR Bartholomew, W Zhou, DJ Klionsky
Autophagy 5 (4), 520-526, 2009
Inside-out Ca2+ signalling prompted by STIM1 conformational switch
G Ma, M Wei, L He, C Liu, B Wu, SL Zhang, J Jing, X Liang, A Senes, ...
Nature communications 6, 2015
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
EA Otto, G Ramaswami, S Janssen, M Chaki, SJ Allen, W Zhou, R Airik, ...
Journal of Medical Genetics 48 (2), 105-116, 2011
Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11)
EA Otto, K Tory, M Attanasio, W Zhou, M Chaki, Y Paruchuri, EL Wise, ...
Journal of medical genetics 46 (10), 663-670, 2009
Characterization of mesonephric development and regeneration using transgenic zebrafish
W Zhou, RC Boucher, F Bollig, C Englert, F Hildebrandt
American Journal of Physiology-Renal Physiology 299 (5), F1040-F1047, 2010
Inducible podocyte injury and proteinuria in transgenic zebrafish
W Zhou, F Hildebrandt
Journal of the American Society of Nephrology 23 (6), 1039-1047, 2012
Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
JF O’Toole, Y Liu, EE Davis, CJ Westlake, M Attanasio, EA Otto, D Seelow, ...
The Journal of clinical investigation 120 (3), 791-802, 2010
Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease
H Hirata, T Watanabe, J Hatakeyama, SM Sprague, L Saint-Amant, ...
Development 134 (15), 2771-2781, 2007
Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor β-subunit
H Hirata, L Saint-Amant, GB Downes, WW Cui, W Zhou, M Granato, ...
Proceedings of the National Academy of Sciences of the United States of …, 2005
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Artículos 1–20