Zhou Weibin
Title
Cited by
Cited by
Year
Nephronophthisis-associated ciliopathies
F Hildebrandt, W Zhou
Journal of the American Society of Nephrology 18 (6), 1855-1871, 2007
3912007
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
3542011
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
3412010
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
3352012
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
2902013
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
2102012
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
2092013
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
1762013
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 (1), 1-11, 2013
1732013
A systematic approach to mapping recessive disease genes in individuals from outbred populations
F Hildebrandt, SF Heeringa, F Rüschendorf, M Attanasio, G Nürnberg, ...
PLoS Genet 5 (1), e1000353, 2009
1732009
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
1642015
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
1632009
Oncogenic role of THOR, a conserved cancer/testis long non-coding RNA
Y Hosono, YS Niknafs, JR Prensner, MK Iyer, SM Dhanasekaran, ...
Cell 171 (7), 1559-1572. e20, 2017
1482017
Inside-out Ca 2+ 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 (1), 1-14, 2015
1462015
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
1402011
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
1342009
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
1242010
Inducible podocyte injury and proteinuria in transgenic zebrafish
W Zhou, F Hildebrandt
Journal of the American Society of Nephrology 23 (6), 1039-1047, 2012
1232012
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
1182010
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
1122007
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