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Dabing Zhang

Researcher at Shanghai Jiao Tong University

Publications -  393
Citations -  20270

Dabing Zhang is an academic researcher from Shanghai Jiao Tong University. The author has contributed to research in topics: Gene & Biology. The author has an hindex of 71, co-authored 352 publications receiving 15971 citations. Previous affiliations of Dabing Zhang include Ningxia University & Pennsylvania State University.

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Journal ArticleDOI

Transcript Profiling of MIKCc MADS-Box Genes Reveals Conserved and Novel Roles in Barley Inflorescence Development

TL;DR: For example, the authors showed that MIKCc MADS-box genes are generally expressed at key inflorescence developmental phases and across various floral organs in barley, as predicted by the ABCDE model.
Journal ArticleDOI

OsVIL2 Regulates Spikelet Development by Controlling Regulatory Genes in Oryza sativa.

TL;DR: It is reported that Oryza sativa VIN3-LIKE 2 (OsVIL2) induces flowering by mediating the trimethylation of Histone H3 on LFL1 chromatin and also plays crucial roles during spikelet development.
Book ChapterDOI

Generating Photoperiod-Sensitive Genic Male Sterile Rice Lines with CRISPR/Cas9.

TL;DR: A straightforward method for generating csa-based PGMS lines by using the CRISPR-Cas9 technology in rice is described.
Journal ArticleDOI

Inter-laboratory validation of visual loop-mediated isothermal amplification assays for GM contents screening.

TL;DR: A collaborative ring trial validation of three established visual LAMP assays targeting three common GM elements, namely CaMV 35S promoter, FMV35S promoter and NOS terminator, respectively, demonstrates that the three visual Lamp assays are sensitive and time-saving, with high application potential for on-spot testing and routine screening of GMOs.
Journal ArticleDOI

Expression and purification of the synthetic preS1 gene of Hepatitis B Virus with preferred Escherichia coli codon preference

TL;DR: The improved expression system could be used for practical, low-cost large-scale production of recombinant preS1 without refolding steps and Western blotting and indirect ELISA analysis demonstrate that the reactivity ofPreS1-specific antibody is comparable between the recombinant and commercialized preS 1 protein.