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Weihua Zeng, Ph.D. - Publications

Affiliations: 
2007 University of California, Irvine, Irvine, CA 
Area:
Genetics, Molecular Biology, Cell Biology
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16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Jiang S, Williams K, Kong X, Zeng W, Nguyen NV, Ma X, Tawil R, Yokomori K, Mortazavi A. Single-nucleus RNA-seq identifies divergent populations of FSHD2 myotube nuclei. Plos Genetics. 16: e1008754. PMID 32365093 DOI: 10.1371/Journal.Pgen.1008754  0.679
2017 Newkirk DA, Chen YY, Chien R, Zeng W, Biesinger J, Flowers E, Kawauchi S, Santos R, Calof AL, Lander AD, Xie X, Yokomori K. 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. PMID 28855971 DOI: 10.1186/S13148-017-0391-X  0.718
2017 Longabaugh WJR, Zeng W, Zhang JA, Hosokawa H, Jansen CS, Li L, Romero-Wolf M, Liu P, Kueh HY, Mortazavi A, Rothenberg EV. Bcl11b and combinatorial resolution of cell fate in the T-cell gene regulatory network. Proceedings of the National Academy of Sciences of the United States of America. 114: 5800-5807. PMID 28584128 DOI: 10.1073/Pnas.1610617114  0.402
2016 Zeng W, Jiang S, Kong X, El-Ali N, Ball AR, Ma CI, Hashimoto N, Yokomori K, Mortazavi A. Single-nucleus RNA-seq of differentiating human myoblasts reveals the extent of fate heterogeneity. Nucleic Acids Research. PMID 27566152 DOI: 10.1093/Nar/Gkw739  0.613
2014 Zeng W, Chen YY, Newkirk DA, Wu B, Balog J, Kong X, Ball AR, Zanotti S, Tawil R, Hashimoto N, Mortazavi A, van der Maarel SM, Yokomori K. 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. PMID 24838473 DOI: 10.1002/Humu.22593  0.71
2014 Kong X, Ball AR, Pham HX, Zeng W, Chen HY, Schmiesing JA, Kim JS, Berns M, Yokomori K. Distinct functions of human cohesin-SA1 and cohesin-SA2 in double-strand break repair. Molecular and Cellular Biology. 34: 685-98. PMID 24324008 DOI: 10.1128/Mcb.01503-13  0.664
2012 Wu N, Kong X, Ji Z, Zeng W, Potts PR, Yokomori K, Yu H. Scc1 sumoylation by Mms21 promotes sister chromatid recombination through counteracting Wapl. Genes & Development. 26: 1473-85. PMID 22751501 DOI: 10.1101/Gad.193615.112  0.695
2011 Chien R, Zeng W, Ball AR, Yokomori K. Cohesin: a critical chromatin organizer in mammalian gene regulation. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 89: 445-58. PMID 21851156 DOI: 10.1139/O11-039  0.775
2011 Chien R, Zeng W, Kawauchi S, Bender MA, Santos R, Gregson HC, Schmiesing JA, Newkirk DA, Kong X, Ball AR, Calof AL, Lander AD, Groudine MT, Yokomori K. Cohesin mediates chromatin interactions that regulate mammalian β-globin expression. The Journal of Biological Chemistry. 286: 17870-8. PMID 21454523 DOI: 10.1074/Jbc.M110.207365  0.657
2010 Zeng W, Ball AR, Yokomori K. HP1: heterochromatin binding proteins working the genome. Epigenetics. 5: 287-92. PMID 20421743 DOI: 10.4161/Epi.5.4.11683  0.697
2009 Zeng W, de Greef JC, Chen YY, Chien R, Kong X, Gregson HC, Winokur ST, Pyle A, Robertson KD, Schmiesing JA, Kimonis VE, Balog J, Frants RR, Ball AR, Lock LF, et al. 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. PMID 19593370 DOI: 10.1371/Journal.Pgen.1000559  0.743
2007 Murakawa Y, Sonoda E, Barber LJ, Zeng W, Yokomori K, Kimura H, Niimi A, Lehmann A, Zhao GY, Hochegger H, Boulton SJ, Takeda S. Inhibitors of the proteasome suppress homologous DNA recombination in mammalian cells. Cancer Research. 67: 8536-43. PMID 17875693 DOI: 10.1158/0008-5472.Can-07-1166  0.639
2007 Kim JS, Heale JT, Zeng W, Kong X, Krasieva TB, Ball AR, Yokomori K. In situ analysis of DNA damage response and repair using laser microirradiation. Methods in Cell Biology. 82: 377-407. PMID 17586265 DOI: 10.1016/S0091-679X(06)82013-3  0.705
2007 Saberi A, Hochegger H, Szuts D, Lan L, Yasui A, Sale JE, Taniguchi Y, Murakawa Y, Zeng W, Yokomori K, Helleday T, Teraoka H, Arakawa H, Buerstedde JM, Takeda S. RAD18 and poly(ADP-ribose) polymerase independently suppress the access of nonhomologous end joining to double-strand breaks and facilitate homologous recombination-mediated repair. Molecular and Cellular Biology. 27: 2562-71. PMID 17242200 DOI: 10.1128/Mcb.01243-06  0.666
2004 Chen G, Zeng W, Miyazato A, Billings E, Maciejewski JP, Kajigaya S, Sloand EM, Young NS. Distinctive gene expression profiles of CD34 cells from patients with myelodysplastic syndrome characterized by specific chromosomal abnormalities Blood. 104: 4210-4218. PMID 15315976 DOI: 10.1182/blood-2004-01-0103  0.358
2004 Zeng W, Chen G, Kajigaya S, Nunez O, Charrow A, Billings EM, Young NS. Gene expression profiling in CD34 cells to identify differences between aplastic anemia patients and healthy volunteers. Blood. 103: 325-32. PMID 14504100 DOI: 10.1182/blood-2003-02-0490  0.306
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