Weibin Zhou

Weibin Zhou

Department of Pediatrics, University of Michigan

Affiliated withUniversity of Michigan

Research Area

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JoVE Journal Publications

ArticleTotal : 1
Year
A Possible Zebrafish Model of Polycystic Kidney Disease: Knockdown of <em>wnt5a</em> Causes Cysts in Zebrafish Kidneys
Publication title

Cited by 15

2014

Other Publications

Article
Year
Caspy, a zebrafish caspase, activated by ASC oligomerization is required for pharyngeal arch development.

The Journal of biological chemistry| PubMed ID: 12464617

2003
Transmembrane sema4E guides branchiomotor axons to their targets in zebrafish.

The Journal of neuroscience : the official journal of the Society for Neuroscience| PubMed ID: 12764107

2003
2004
Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor beta-subunit.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 15928085

2005
2005
The ROC analysis for different time points during oral glucose tolerance test.

Diabetes research and clinical practice| PubMed ID: 16288818

2006
2006
2006
2006
2006
Assessing 1-h plasma glucose and shape of the glucose curve during oral glucose tolerance test.

European journal of endocrinology / European Federation of Endocrine Societies| PubMed ID: 16793967

2006
Nephronophthisis-associated ciliopathies.

Journal of the American Society of Nephrology : JASN| PubMed ID: 17513324

2007
2007
2007
2008
2008
2008
Identification and expression of voltage-gated calcium channel beta subunits in Zebrafish.

Developmental dynamics : an official publication of the American Association of Anatomists| PubMed ID: 19035348

2008
2009
2009
Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish.

Gene expression patterns : GEP| PubMed ID: 19332147

2009
Integrity of N- and C-termini is important for E. coli Hsp31 chaperone activity.

Protein science : a publication of the Protein Society| PubMed ID: 19517531

2009
2010
Single-pot biofabrication of zinc sulfide immuno-quantum dots.

Journal of the American Chemical Society| PubMed ID: 20218715

2010
2010
Nephrocystin-3 is required for ciliary function in zebrafish embryos.

American journal of physiology. Renal physiology| PubMed ID: 20462968

2010
touché Is required for touch-evoked generator potentials within vertebrate sensory neurons.

The Journal of neuroscience : the official journal of the Society for Neuroscience| PubMed ID: 20631165

2010
2010
Characterization of mesonephric development and regeneration using transgenic zebrafish.

American journal of physiology. Renal physiology| PubMed ID: 20810610

2010
2010
2011
2011
TRPM7 is required within zebrafish sensory neurons for the activation of touch-evoked escape behaviors.

The Journal of neuroscience : the official journal of the Society for Neuroscience| PubMed ID: 21832193

2011
2011
2012
2012
2012
Inducible podocyte injury and proteinuria in transgenic zebrafish.

Journal of the American Society of Nephrology : JASN| PubMed ID: 22440901

2012
2012
2012
Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.

Journal of the American Society of Nephrology : JASN| PubMed ID: 23661805

2013
2013
2013
2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

The Journal of clinical investigation| PubMed ID: 23867502

2013
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.

American journal of human genetics| PubMed ID: 23891469

2013
2014
2013
2014
Mutations in EMP2 cause childhood-onset nephrotic syndrome.

American journal of human genetics| PubMed ID: 24814193

2014
2014
2014
Wnt5a Is Necessary for Normal Kidney Development in Zebrafish and Mice.

Nephron. Experimental nephrology| PubMed ID: 25412793

2014