W. Pei

发表

Using Zebrafish to Study Human Deafness and Hearing Regeneration

S. Burgess, G. Varshney, W. Pei, 2016 .

Multiplexed CRISPR/Cas9 Targeting of Genes Implicated in Retinal Regeneration and Degeneration

J. Qian, S. Burgess, Lisha Xu, 2018, Front. Cell Dev. Biol..

A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3

M. Huizing, Y. Anikster, H. Dorward, 2010, Development.

Guided genetic screen to identify genes essential in the regeneration of hair cells and other tissues

Shuo Lin, Haigen Huang, S. Burgess, 2018, npj Regenerative Medicine.

A high-throughput functional genomics workflow based on CRISPR/Cas9-mediated targeted mutagenesis in zebrafish

S. Burgess, Lisha Xu, Zelin Chen, 2016, Nature Protocols.

Staphylococcus intermedius Produces a Functional agr Autoinducing Peptide Containing a Cyclic Lactone

Y. Benito, G. Lina, Rongde Qiu, 2005, Journal of bacteriology.

OPA3, mutated in 3-methylglutaconic aciduria type III, encodes two transcripts targeted primarily to mitochondria.

W. Gahl, M. Huizing, Y. Anikster, 2010, Molecular genetics and metabolism.

Suppressing STAT3 activity protects the endothelial barrier from VEGF-mediated vascular permeability

Luke H. Hoeppner, S. Burgess, D. Frank, 2020, bioRxiv.

Microinjection in Zebrafish for Genome Editing and Functional Studies.

S. Burgess, W. Pei, 2018, Methods in molecular biology.

A large-scale zebrafish gene knockout resource for the genome-wide study of gene function

Matteo Pellegrini, Bo Zhang, Suiyuan Zhang, 2013, Genome research.

A subset of SMN complex members have a specific role in tissue regeneration via ERBB pathway-mediated proliferation

J. Mullikin, G. Bouffard, Xiaobin Guan, 2020, npj Regenerative Medicine.

A subset of SMN complex members have a specific role in tissue regeneration via ERBB pathway-mediated proliferation

J. Mullikin, G. Bouffard, Xiaobin Guan, 2019, npj Regenerative Medicine.

Zrsr2 Is Essential for the Embryonic Development and Splicing of Minor Introns in RNA and Protein Processing Genes in Zebrafish

A. Elkahloun, Paul Liu, S. Burgess, 2022, International journal of molecular sciences.

Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors

W. C. Owen, M. Hafner, A. Šedivá, 2018, Annals of the rheumatic diseases.

High-throughput gene targeting and phenotyping in zebrafish using CRISPR/Cas9

Kevin Bishop, Lisha Xu, Anupam Prakash, 2015, Genome research.

Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds

W. Pavan, S. Burgess, Lisha Xu, 2018, Disease Models & Mechanisms.

Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease.

J. Mullikin, D. Kastner, W. Gahl, 2020, The New England journal of medicine.

Environmental and genetic modifiers of squint penetrance during zebrafish embryogenesis.

Matthew D Clark, Wuhong Pei, Benjamin Feldman, 2007, Developmental biology.

Extracellular HSP60 triggers tissue regeneration and wound healing by regulating inflammation and cell proliferation

R. Nussenblatt, Shuo Lin, Haigen Huang, 2016, npj Regenerative Medicine.

Early-onset stroke and vasculopathy associated with mutations in ADA2.

J. Mullikin, H. Kong, V. Pascual, 2014, The New England journal of medicine.

Splicing factor DHX15 affects tp53 and mdm2 expression via alternate splicing and promoter usage.

A. Prakash, S. Burgess, Zelin Chen, 2019, Human molecular genetics.

Identification of the Putative Staphylococcal AgrB Catalytic Residues Involving the Proteolytic Cleavage of AgrD to Generate Autoinducing Peptide*

Rongde Qiu, G. Ji, Linsheng Zhang, 2005, Journal of Biological Chemistry.

Redesign of a four-helix bundle protein by phage display coupled with proteolysis and structural characterization by NMR and X-ray crystallography.

Yawen Bai, Andrey V Kajava, Wuhong Pei, 2002, Journal of molecular biology.

Suppressing STAT3 activity protects the endothelial barrier from VEGF-mediated vascular permeability

Luke H. Hoeppner, S. Burgess, D. Frank, 2021, Disease models & mechanisms.

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly.

J. Belmont, J. Towbin, A. Baxevanis, 2009, Molecular genetics and metabolism.

An early requirement for maternal FoxH1 during zebrafish gastrulation.

H. Noushmehr, A. Elkahloun, B. Feldman, 2007, Developmental biology.

Guided genetic screen to identify genes essential in the regeneration of hair cells and other tissues

Shuo Lin, Haigen Huang, S. Burgess, 2018, npj Regenerative Medicine.

Novel degenerative and developmental defects in a zebrafish model of mucolipidosis type IV

S. Burgess, R. Puertollano, N. Raben, 2017, Human molecular genetics.

Loss of Mgat5a-mediated N-glycosylation stimulates regeneration in zebrafish

S. Burgess, M. Allende, Lisha Xu, 2016, Cell Regeneration.

Additive reductions in zebrafish PRPS1 activity result in a spectrum of deficiencies modeling several human PRPS1-associated diseases

K. Kindt, S. Burgess, Lisha Xu, 2016, Scientific Reports.

CRISPRz: a database of zebrafish validated sgRNAs

Tyra G. Wolfsberg, Shawn M. Burgess, Suiyuan Zhang, 2015, Nucleic Acids Res..

Relationship between the native-state hydrogen exchange and folding pathways of a four-helix bundle protein.

Yawen Bai, Wuhong Pei, Jiro Takei, 2002, Biochemistry.

Identification of common and unique modifiers of zebrafish midline bifurcation and cyclopia.

B. Feldman, W. Pei, 2009, Developmental biology.

Identi fi cation of common and unique modi fi ers of zebra fi sh midline bifurcation and cyclopia

B. Feldman, W. Pei, 2009 .