Zhuojin Xu, Ph.D. - Publications

2010 Molecular, Cellular & Developmental Biology University of California, Santa Barbara, Santa Barbara, CA, United States 

22 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
2016 Liang D, Wang Y, Ji X, Hu H, Zhang J, Meng L, Lin Y, Ma D, Jiang T, Jiang H, Asan, Song L, Guo J, Hu P, Xu Z. Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations. Clinical Genetics. PMID 27491356 DOI: 10.1111/cge.12844  0.4
2016 Li L, Ma D, Sun Y, Zhang J, Wang Y, Jiang T, Xu Z. [Mutation screening and prenatal diagnosis of methylmalonic academia in a Chinese pedigree by Ion Torrent semiconductor sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 181-185. PMID 27060311 DOI: 10.3760/cma.j.issn.1003-9406.2016.02.012  0.4
2016 Wang Y, Lin Y, Luo C, Liang D, Ji X, Jiang T, Ma D, Xu Z. [Detection of TSC1/TSC2 gene mutations among patients with tuberous sclerosis complex by Ion Torrent semiconductor sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 33: 169-172. PMID 27060308 DOI: 10.3760/cma.j.issn.1003-9406.2016.02.009  0.4
2016 Ma D, Zhang J, Luo C, Lin Y, Ji X, Hu P, Xu Z. Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysis. Molecular Medicine Reports. PMID 26783197 DOI: 10.3892/mmr.2016.4769  0.4
2015 Zhang J, Ma D, Wang Y, Cao L, Wu Y, Qiao F, Liu A, Li L, Lin Y, Liu G, Liu C, Hu P, Xu Z. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect. Molecular Cytogenetics. 8: 100. PMID 26715944 DOI: 10.1186/s13039-015-0209-5  0.4
2015 Dong S, Dong S, Tian X, Xu Z, Ma D, Cui B, Ren N, Rittmann BE. Role of self-assembly coated Er(3+): YAlO3/TiO2 in intimate coupling of visible-light-responsive photocatalysis and biodegradation reactions. Journal of Hazardous Materials. 302: 386-394. PMID 26489913 DOI: 10.1016/j.jhazmat.2015.10.007  0.4
2015 Ji X, Liang D, Sun R, Liu C, Ma D, Wang Y, Hu P, Xu Z. Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing. Bmc Medical Genetics. 16: 57. PMID 26224010 DOI: 10.1186/s12881-015-0206-x  0.4
2015 Cheng J, Ma D, Wu Y, Luo C, Huang C, Hu P, Zhang J, Jiang T, Xu Z. Identification of one novel CHD7 mutation in a patient from China with atypical CHARGE syndrome. Gene. PMID 26187070 DOI: 10.1016/j.gene.2015.07.042  0.4
2015 Zhou D, Xu Z, Dong S, Huo M, Dong S, Tian X, Cui B, Xiong H, Li T, Ma D. Intimate Coupling of Photocatalysis and Biodegradation for Degrading Phenol Using Different Light Types: Visible Light vs UV Light. Environmental Science & Technology. PMID 26076382 DOI: 10.1021/acs.est.5b00989  0.4
2015 Sun Y, Jiang T, Ma D, Yang G, Yang B, Wang Y, Xu Z. [Detection of pathogenic mutations for methylmalonic acidemia using new-generation semiconductor targeted sequencing]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 32: 56-9. PMID 25636100 DOI: 10.3760/cma.j.issn.1003-9406.2015.01.012  0.4
2015 Hu P, Meng L, Ma D, Qiao F, Wang Y, Zhou J, Yi L, Xu Z. A novel 11p13 microdeletion encompassing PAX6 in a Chinese Han family with aniridia, ptosis and mental retardation. Molecular Cytogenetics. 8: 3. PMID 25628759 DOI: 10.1186/s13039-015-0110-2  0.4
2014 Kim MR, Xu Z, Chen G, Ma D. Semiconductor and metallic core-shell nanostructures: synthesis and applications in solar cells and catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11256-75. PMID 25044334 DOI: 10.1002/chem.201402277  0.4
2014 Wang Y, Zhang J, Qin L, Meng L, Jiang T, Ma D, Hui W, Hu P, Xu Z. [Single nueleotide polymorphism array detection of Xq28 duplication in a child with mental retardation]. Zhonghua Er Ke Za Zhi. Chinese Journal of Pediatrics. 52: 227-8. PMID 24824396  0.4
2014 Ma D, Ge H, Li X, Jiang T, Chen F, Zhang Y, Hu P, Chen S, Zhang J, Ji X, Xu X, Jiang H, Chen M, Wang W, Xu Z. Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing. Gene. 544: 252-8. PMID 24768736 DOI: 10.1016/j.gene.2014.04.055  0.4
2014 Zhang J, Hu P, Luo C, Ji Q, Zhou J, Liu A, Ma D, Xu Z. [Application of multiplex ligation-dependent probe amplification for rapid detection of aneuploidies and structural chromosomal abnormalities in prenatal diagnosis]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 31: 11-5. PMID 24510553 DOI: 10.3760/cma.j.issn.1003-9406.2014.01.003  0.4
2014 Ma D, Chen Y, Sun Y, Yang B, Cheng J, Huang M, Zhang J, Zhang J, Hu P, Lin Y, Jiang T, Xu Z. Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency. Clinical Biochemistry. 47: 455-63. PMID 24503005 DOI: 10.1016/j.clinbiochem.2014.01.019  0.4
2011 Hu P, Ji X, Yang C, Zhang J, Lin Y, Cheng J, Ma D, Cao L, Yi L, Xu Z. 22q11.2 microduplication in a family with recurrent fetal congenital heart disease. European Journal of Medical Genetics. 54: e433-6. PMID 21473936 DOI: 10.1016/j.ejmg.2011.03.009  0.4
2011 Xiong Y, Zhou SF, Zhou R, Yang D, Xu ZF, Lou YT, Guo QS, Hu R, Peng T, Ma D, Li XT. Alternations of maternal and cord plasma hemostasis in preeclampsia before and after delivery. Hypertension in Pregnancy. 30: 347-58. PMID 21174589 DOI: 10.3109/10641950903572274  0.4
2010 Xu Z, Xia B, Gong Q, Bailey J, Groves B, Radeke M, Wood SA, Szumlinski KK, Ma D. Identification of a deubiquitinating enzyme as a novel AGS3-interacting protein. Plos One. 5: e9725. PMID 20305814 DOI: 10.1371/journal.pone.0009725  0.4
2009 Xu Z, Gong Q, Xia B, Groves B, Zimmermann M, Mugler C, Mu D, Matsumoto B, Seaman M, Ma D. A role of histone H3 lysine 4 methyltransferase components in endosomal trafficking. The Journal of Cell Biology. 186: 343-53. PMID 19651892 DOI: 10.1083/jcb.200902146  0.4
2007 Groves B, Gong Q, Xu Z, Huntsman C, Nguyen C, Li D, Ma D. A specific role of AGS3 in the surface expression of plasma membrane proteins. Proceedings of the National Academy of Sciences of the United States of America. 104: 18103-8. PMID 17991770 DOI: 10.1073/pnas.0709282104  0.4
2007 Gong Q, Weide M, Huntsman C, Xu Z, Jan LY, Ma D. Identification and characterization of a new class of trafficking motifs for controlling clathrin-independent internalization and recycling. The Journal of Biological Chemistry. 282: 13087-97. PMID 17331948 DOI: 10.1074/jbc.M700767200  0.4
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