Weihua Zeng, Ph.D.

Affiliations: 
2007 University of California, Irvine, Irvine, CA 
Area:
Genetics, Molecular Biology, Cell Biology
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"Weihua Zeng"
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Parents

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Kyoko Yokomori grad student 2007 UC Irvine
 (Identification of cohesin binding sites in the mammalian genome: An interplay between cohesin and histone modification in gene regulation.)
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Publications

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Jiang S, Williams K, Kong X, et al. (2020) Single-nucleus RNA-seq identifies divergent populations of FSHD2 myotube nuclei. Plos Genetics. 16: e1008754
Newkirk DA, Chen YY, Chien R, et al. (2017) The effect of Nipped-B-like (Nipbl) haploinsufficiency on genome-wide cohesin binding and target gene expression: modeling Cornelia de Lange syndrome. Clinical Epigenetics. 9: 89
Zeng W, Jiang S, Kong X, et al. (2016) Single-nucleus RNA-seq of differentiating human myoblasts reveals the extent of fate heterogeneity. Nucleic Acids Research
Zeng W, Chen YY, Newkirk DA, et al. (2014) Genetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologs. Human Mutation. 35: 998-1010
Kong X, Ball AR, Pham HX, et al. (2014) Distinct functions of human cohesin-SA1 and cohesin-SA2 in double-strand break repair. Molecular and Cellular Biology. 34: 685-98
Wu N, Kong X, Ji Z, et al. (2012) Scc1 sumoylation by Mms21 promotes sister chromatid recombination through counteracting Wapl. Genes & Development. 26: 1473-85
Chien R, Zeng W, Ball AR, et al. (2011) Cohesin: a critical chromatin organizer in mammalian gene regulation. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 89: 445-58
Chien R, Zeng W, Kawauchi S, et al. (2011) Cohesin mediates chromatin interactions that regulate mammalian β-globin expression. The Journal of Biological Chemistry. 286: 17870-8
Zeng W, Ball AR, Yokomori K. (2010) HP1: heterochromatin binding proteins working the genome. Epigenetics. 5: 287-92
Zeng W, de Greef JC, Chen YY, et al. (2009) Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD). Plos Genetics. 5: e1000559
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