Weibin Zhou

发表

A Systematic Approach to Mapping Recessive Disease Genes in Individuals from Outbred Populations

Peter Nürnberg, Dominik Seelow, Shazia Ashraf, 2009, PLoS genetics.

Non-sense mutations in the dihydropyridine receptor beta1 gene, CACNB1, paralyze zebrafish relaxed mutants.

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2006, Cell calcium.

KANK deficiency leads to podocyte dysfunction and nephrotic syndrome.

Margaret Y. Nettleton, S. Levy, R. Lifton, 2015, The Journal of clinical investigation.

DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.

J. Kere, L. Pelletier, N. Sebire, 2015, American journal of human genetics.

Assaying autophagic activity in transgenic GFP-Lc3 and GFP-Gabarap zebrafish embryos

D. Klionsky, Weibin Zhou, Congcong He, 2009, Autophagy.

Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish.

F. Hildebrandt, Weibin Zhou, 2009, Gene expression patterns : GEP.

Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.

Johann M B Simbürger, P. Oefner, A. Hammers, 2018, Journal of the American Society of Nephrology : JASN.

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

S. Levy, C. Dang, R. Lewis, 2010, Nature Genetics.

Wnt5a Is Necessary for Normal Kidney Development in Zebrafish and Mice

Weibin Zhou, Soo‐Young Choi, J. Lipschutz, 2014, Nephron Experimental Nephrology.

Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing

F. Hildebrandt, M. Attanasio, Weibin Zhou, 2008, Human mutation.

Inducible podocyte injury and proteinuria in transgenic zebrafish.

F. Hildebrandt, Weibin Zhou, 2012, Journal of the American Society of Nephrology : JASN.

Transmembrane Sema4E Guides Branchiomotor Axons to Their Targets in Zebrafish

W. Shoji, J. Y. Kuwada, Weibin Zhou, 2003, The Journal of Neuroscience.

IFT46 plays an essential role in cilia development.

Cheol‐Hee Kim, H. Kiyonari, S. Aizawa, 2015, Developmental biology.

Mutations in EMP2 cause childhood-onset nephrotic syndrome.

S. Levy, T. Hurd, David S. Williams, 2014, American journal of human genetics.

Summary accordion , a zebrafish behavioral mutant , has a muscle relaxation defect due to a mutation in the ATPase Ca 2 + pump SERCA 1

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2004 .

Loss of Epithelial Membrane Protein 2 Aggravates Podocyte Injury via Upregulation of Caveolin-1.

F. Hildebrandt, Weibin Zhou, H. Gee, 2016, Journal of the American Society of Nephrology : JASN.

Myo1c is an unconventional myosin required for zebrafish glomerular development

M. Wagner, Weibin Zhou, L. Holzman, 2013, Kidney international.

Blood Flow Regulates Glomerular Capillary Formation in Zebrafish Pronephros

N. Mochizuki, Weibin Zhou, S. Fukuhara, 2022, Kidney360.

A possible zebrafish model of polycystic kidney disease: knockdown of wnt5a causes cysts in zebrafish kidneys.

Weibin Zhou, Soo‐Young Choi, J. Lipschutz, 2014, Journal of visualized experiments : JoVE.

Characterization of mesonephric development and regeneration using transgenic zebrafish.

C. Englert, F. Hildebrandt, Weibin Zhou, 2010, American journal of physiology. Renal physiology.

Characterization of Mesonephric Development and Regeneration Using

C. Englert, Weibin Zhou, F. Bollig, 2010 .

A zebrafish model of congenital nephrotic syndrome of the Finnish type

Weibin Zhou, J. He, mi-sun Lee, 2022, Frontiers in Cell and Developmental Biology.

Dosage-dependent role of Rac1 in podocyte injury.

Weibin Zhou, mi-sun Lee, Xiaoyang Wan, 2016, American journal of physiology. Renal physiology.

Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2007, Development.

RING finger protein 121 facilitates the degradation and membrane localization of voltage-gated sodium channels

J. Nakai, K. Kawakami, Hiromi Hirata, 2015, Proceedings of the National Academy of Sciences.

Alleviating experimental allergic eye disease by inhibiting pro-lymphangiogenic VEGFR3 signal.

Feng Zhang, Weibin Zhou, Ke-fang Liu, 2022, The ocular surface.

SARS-CoV-2 viral protein ORF3A injures renal tubules by interacting with TRIM59 to induce STAT3 activation

A. García-Sastre, Weibin Zhou, Kyung Lee, 2022, Molecular Therapy.

Molecular cloning and expression of two small leucine-rich proteoglycan (SLRP) genes, dspg3l and optcl, in zebrafish.

J. Y. Kuwada, Weibin Zhou, K. Shirabe, 2006, Gene expression patterns : GEP.

Prolonged podocyte depletion in larval zebrafish resembles mammalian focal and segmental glomerulosclerosis

Weibin Zhou, A. Blumenthal, K. Endlich, 2019, bioRxiv.

Analysis of the genomic architecture of a complex trait locus in hypertensive rat models links Tmem63c to kidney damage

A. Sporbert, Weibin Zhou, Emile de Heer, 2019, eLife.

Analysis of the genomic architecture of a complex trait locus in hypertensive rat 1 models links Tmem 63 c to kidney damage 2 3

Martina, A. Sporbert, Weibin Zhou, 2019 .

Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.

T. Abe, T. Hurd, G. Ghiggeri, 2013, Journal of the American Society of Nephrology : JASN.

Inside-out Ca2+ signalling prompted by STIM1 conformational switch

Shenyuan L. Zhang, A. Senes, Weibin Zhou, 2015, Nature Communications.

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.

M. Rosenfeld, S. Levy, H. Omran, 2013, American journal of human genetics.

Nephronophthisis-associated ciliopathies.

F. Hildebrandt, Weibin Zhou, 2007, Journal of the American Society of Nephrology : JASN.

Oncogenic Role of THOR, a Conserved Cancer/Testis Long Non-coding RNA

Huynh-Hoa Bui, Arul M. Chinnaiyan, Felix Y. Feng, 2017, Cell.

Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

Corinne Stoetzel, Richard A. Lewis, Colin A. Johnson, 2012, Cell.

Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy

Jeremy W. Linsley, Hiromi Hirata, M. Hauser, 2013, Nature Communications.

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

V. Pertegato, Y. Raphael, H. Prokisch, 2011, The Journal of clinical investigation.

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

H. Moch, S. Levy, T. Hurd, 2012, Nature Genetics.

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

S. Levy, T. Hurd, O. Gribouval, 2013, The Journal of clinical investigation.

Caspy, a Zebrafish Caspase, Activated by ASC Oligomerization Is Required for Pharyngeal Arch Development*

J. Postlethwait, J. Y. Kuwada, Weibin Zhou, 2003, The Journal of Biological Chemistry.

Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor beta-subunit.

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

S. Levy, N. Katsanis, T. Hurd, 2013, Kidney international.

ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption.

A. Paterson, H. Prokisch, S. Levy, 2013, The Journal of clinical investigation.

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy

Colin A. Johnson, T. Hurd, D. Milford, 2010, Journal of Medical Genetics.

Connexin 39.9 Protein Is Necessary for Coordinated Activation of Slow-twitch Muscle and Normal Behavior in Zebrafish*

K. Kawakami, Hiromi Hirata, J. Y. Kuwada, 2011, The Journal of Biological Chemistry.

accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2004, Development.

Explorer FAN 1 mutations cause karyomegalic interstitial nephritis , linking chronic kidney failure to defective DNA damage repair

H. Moch, S. Levy, T. Hurd, 2017 .

FAN 1 mutations cause karyomegalic interstitial nephritis , linking chronic kidney failure to defective DNA damage repair

Soliman, Agata, Kerstin, 2013 .

Zebrafish models of podocytopathies

Weibin Zhou, R. C. Boucher, 2014 .

A system for investigation of biological effects of diagnostic ultrasound on development of zebrafish embryos.

Douglas L. Miller, Weibin Zhou, 2013, Zebrafish.

Characterization of Mesonephric Development and Regeneration Using 2 Transgenic Zebrafish 3 4

C. Englert, F. Hildebrandt, Weibin Zhou, 2010 .

Nephronophthisis : A Frequent Genetic Cause of Kidney Failure in Children

F. Hildebrandt, Weibin Zhou, 2007 .

The zebrafish ennui behavioral mutation disrupts acetylcholine receptor localization and motor axon stability

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2008, Developmental neurobiology.

TRPM7 Is Required within Zebrafish Sensory Neurons for the Activation of Touch-Evoked Escape Behaviors

Jeremy W. Linsley, Hiromi Hirata, J. Y. Kuwada, 2011, The Journal of Neuroscience.

Evaluation of endogenous miRNA reference genes across different zebrafish strains, developmental stages and kidney disease models

G. Capasso, Weibin Zhou, K. Endlich, 2021, Scientific Reports.

Acute podocyte injury is not a stimulus for podocytes to migrate along the glomerular basement membrane in zebrafish larvae

Weibin Zhou, A. Blumenthal, K. Endlich, 2017, Scientific Reports.

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.

Bethan E. Hoskins, D. Seelow, H. Prokisch, 2010, The Journal of clinical investigation.

Nephrocystin-3 is required for ciliary function in zebrafish embryos.

F. Hildebrandt, M. Attanasio, Weibin Zhou, 2010, American journal of physiology. Renal physiology.

NaV1.6a is required for normal activation of motor circuits normally excited by tactile stimulation

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2010, Developmental neurobiology.

The retinitis pigmentosa protein RP2 interacts with polycystin 2 and regulates cilia-mediated vertebrate development.

Paul M. Jenkins, A. Swaroop, J. Martens, 2010, Human molecular genetics.

touché Is Required for Touch-Evoked Generator Potentials within Vertebrate Sensory Neurons

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2010, The Journal of Neuroscience.

ADCK 4 mutations promote steroid-resistant nephrotic syndrome through CoQ 10 biosynthesis disruption

A. Paterson, H. Prokisch, S. Levy, 2018 .

Identification and expression of voltage‐gated calcium channel β subunits in Zebrafish

Hiromi Hirata, J. Y. Kuwada, Weibin Zhou, 2008, Developmental dynamics : an official publication of the American Association of Anatomists.

MicroRNA-145 inhibits migration and invasion via inhibition of fascin 1 protein expression in non-small-cell lung cancer cells.

Weibin Zhou, Yingying Zhang, Haijun Wu, 2015, Molecular medicine reports.

Early Development in Zebrafish Maturation of Neuromuscular Transmission During

K. Kawakami, J. Y. Kuwada, P. Brehm, 2015 .

Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

Colin A. Johnson, S. Levy, Shaohui Wang, 2012, Cell.