Jianfeng Xiao

Jianfeng Xiao

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Jianfeng Xiao

Jianfeng Xiao

Publications by authors named "Jianfeng Xiao"

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48Publications

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Gnal haploinsufficiency causes genomic instability and increased sensitivity to haloperidol.

Exp Neurol 2019 Aug 26;318:61-70. Epub 2019 Apr 26.

Department of Psychology, University of Memphis, Memphis, TN 38152, USA. Electronic address:

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http://dx.doi.org/10.1016/j.expneurol.2019.04.014DOI Listing
August 2019

Consequences of Cre-mediated deletion of Ciz1 exon 5 in mice.

FEBS Lett 2018 09 29;592(18):3101-3110. Epub 2018 Aug 29.

Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA.

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http://dx.doi.org/10.1002/1873-3468.13221DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6275157PMC
September 2018

Heterogeneous mutation pattern in tumor tissue and circulating tumor DNA warrants parallel NGS panel testing.

Mol Cancer 2018 08 28;17(1):131. Epub 2018 Aug 28.

State Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, University of Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.

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http://dx.doi.org/10.1186/s12943-018-0875-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114875PMC
August 2018

DNA damage and neurodegenerative phenotypes in aged Ciz1 null mice.

Neurobiol Aging 2018 02;62:180-190

Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01974580173035
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http://dx.doi.org/10.1016/j.neurobiolaging.2017.10.014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5877805PMC
February 2018

Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome.

Neurobiol Dis 2017 Feb 24;98:52-65. Epub 2016 Nov 24.

Department of Neurology, University of Tennessee Health Science Center, Memphis, TN 38163, USA; Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address:

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http://dx.doi.org/10.1016/j.nbd.2016.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5283163PMC
February 2017

Crystal structure of FabZ-ACP complex reveals a dynamic seesaw-like catalytic mechanism of dehydratase in fatty acid biosynthesis.

Cell Res 2016 Dec 22;26(12):1330-1344. Epub 2016 Nov 22.

Department of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

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http://dx.doi.org/10.1038/cr.2016.136DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5143422PMC
December 2016

Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.

Mov Disord 2016 11 10;31(11):1704-1710. Epub 2016 Sep 10.

Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

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http://dx.doi.org/10.1002/mds.26756DOI Listing
November 2016

Motor phenotypes and molecular networks associated with germline deficiency of Ciz1.

Exp Neurol 2016 09 7;283(Pt A):110-20. Epub 2016 May 7.

Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address:

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http://dx.doi.org/10.1016/j.expneurol.2016.05.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992595PMC
September 2016

A Genetic Algorithm Based Support Vector Machine Model for Blood-Brain Barrier Penetration Prediction.

Biomed Res Int 2015 4;2015:292683. Epub 2015 Oct 4.

Drug Discovery and Design Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 555 Zuchongzhi Road, Shanghai 201203, China.

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http://dx.doi.org/10.1155/2015/292683DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4609370PMC
August 2016

Clinical and genetic features of cervical dystonia in a large multicenter cohort.

Neurol Genet 2016 Jun 11;2(3):e69. Epub 2016 Apr 11.

Departments of Neurology and Anatomy & Neurobiology (M.S.L., S.R.V., J.X., M.M.T.), University of Tennessee Health Science Center, Memphis, TN; Department of Neurology (J.S.P., L.J.W.), Washington University School of Medicine, St. Louis, MO; Departments of Neurology (A.R.R.), Human Genetics, and Pediatrics (H.A.J.), School of Medicine, Emory University, Atlanta, GA; Department of Neurology (P.H.), Vanderbilt University, Nashville, TN; Department of Neurological Sciences (C.L.C.), Rush University, Chicago, IL; Institute of Neurogenetics (A.W., J. Junker), University of Lübeck, Germany; Department of Neurology (J. Jankovic), Baylor College of Medicine, Houston, TX; Department of Neurology (R.L.B.), University of Rochester, NY; Department of Neurology (S.G.R.), University of Maryland, Baltimore, MD; Department of Neurology (R.L.R.), University of Florida, Gainesville, FL; Department of Neurology (B.D.B.), University of Colorado Denver School of Medicine, Aurora, CO; Center of Excellence in Neuroscience (S.C.), University of Montreal, QC, Canada; Mirken Department of Neurology (L.S.), Mt. Sinai Beth Israel Medical Center, New York, NY; Booth Gardner Parkinson's Care Center (P.A.), Kirkland, WA; and Department of Neurology (N.P.S.), University of Alabama at Birmingham, AL.

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http://dx.doi.org/10.1212/NXG.0000000000000069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830199PMC
June 2016

Blepharospasm in a multiplex African-American pedigree.

J Neurol Sci 2016 Mar 2;362:299-303. Epub 2016 Feb 2.

Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2016.02.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779500PMC
March 2016

Homozygous p.D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism: further evidence of a fourth phenotype of PLA2G6-associated neurodegeneration.

Parkinsonism Relat Disord 2015 Apr 27;21(4):420-2. Epub 2015 Jan 27.

Department of Neurology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, 310009, PR China. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2015.01.012DOI Listing
April 2015

Phospho-Cdc25 correlates with activating G2/M checkpoint in mouse zygotes fertilized with hydrogen peroxide-treated mouse sperm.

Mol Cell Biochem 2014 Nov 11;396(1-2):41-8. Epub 2014 Jul 11.

Reproductive Center, The First Affiliated Hospital of Shantou University Medical College, Shantou University, Shantou, Guangdong, People's Republic of China,

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http://dx.doi.org/10.1007/s11010-014-2140-1DOI Listing
November 2014

Recent advances in the genetics of dystonia.

Curr Neurol Neurosci Rep 2014 Aug;14(8):462

Department of Neurology, University of Tennessee Health Science Center, 855 Monroe Avenue, Link Building Suite 415, Memphis, TN, 38163, USA,

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http://dx.doi.org/10.1007/s11910-014-0462-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886715PMC
August 2014

Zygotic G2/M cell cycle arrest induced by ATM/Chk1 activation and DNA repair in mouse embryos fertilized with hydrogen peroxide-treated epididymal mouse sperm.

PLoS One 2013 10;8(9):e73987. Epub 2013 Sep 10.

Reproductive Center, The First Affiliated Hospital of Shantou University Medical College, Shantou University, Shantou, Guangdong, People's Republic of China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0073987PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769350PMC
June 2014

Effectiveness of the antagonist/letrozole protocol for treating poor responders undergoing in vitro fertilization/intracytoplasmic sperm injection: a systematic review and meta-analysis.

Gynecol Endocrinol 2014 May 24;30(5):330-4. Epub 2014 Jan 24.

Reproductive Center, The First Affiliated Hospital of Shantou University Medical College, Shantou University , Shantou, Guangdong , People's Republic of China.

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http://dx.doi.org/10.3109/09513590.2013.875997DOI Listing
May 2014

Pathogenic variants in TUBB4A are not found in primary dystonia.

Neurology 2014 Apr 5;82(14):1227-30. Epub 2014 Mar 5.

From the Departments of Neurology and Anatomy & Neurobiology (S.R.V., J.X., M.S.L.), University of Tennessee Health Science Center, Memphis, TN; Bastian Voice Institute (R.W.B.), Downers Grove, IL; Clinic for Child Neurology and Psychiatry (D.M.), Medical Faculty University of Belgrade, Serbia; and New York Center for Voice and Swallowing Disorders (A.B.), NY.

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http://dx.doi.org/10.1212/WNL.0000000000000294DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001202PMC
April 2014

Role of Gα(olf) in familial and sporadic adult-onset primary dystonia.

Hum Mol Genet 2013 Jun 27;22(12):2510-9. Epub 2013 Feb 27.

Department of Neurology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1093/hmg/ddt102DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3658169PMC
June 2013

Effects of the insemination of hydrogen peroxide-treated epididymal mouse spermatozoa on γH2AX repair and embryo development.

PLoS One 2012 26;7(6):e38742. Epub 2012 Jun 26.

Reproductive Center, The First Affiliated Hospital of Shantou University Medical College, Shantou University, Shantou, Guangdong, People's Republic of China.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0038742PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3383764PMC
November 2012

Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia.

BMC Neurol 2012 Sep 18;12:93. Epub 2012 Sep 18.

Department of Neurology, Vanderbilt University, Nashville, TN, USA.

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http://dx.doi.org/10.1186/1471-2377-12-93DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460747PMC
September 2012

Genotype-phenotype correlations in THAP1 dystonia: molecular foundations and description of new cases.

Parkinsonism Relat Disord 2012 Jun 28;18(5):414-25. Epub 2012 Feb 28.

Department of Neurology, University of Tennessee Health Science Center, 855 Monroe Avenue, Link Building-Suite 415, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1016/j.parkreldis.2012.02.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358360PMC
June 2012

JPH3 repeat expansions cause a progressive akinetic-rigid syndrome with severe dementia and putaminal rim in a five-generation African-American family.

Neurogenetics 2012 May 25;13(2):133-40. Epub 2012 Mar 25.

Schilling Section of Clinical and Molecular Neurogenetics at the Department of Neurology, University of Lubeck, 23568 Lubeck, Germany.

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http://dx.doi.org/10.1007/s10048-012-0318-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370891PMC
May 2012

Mutations in CIZ1 cause adult onset primary cervical dystonia.

Ann Neurol 2012 Apr 23;71(4):458-69. Epub 2012 Mar 23.

Department of Neurology, University of Tennessee Health Science Center, Memphis, USA.

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http://dx.doi.org/10.1002/ana.23547DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334472PMC
April 2012

An African-American family with dystonia.

Parkinsonism Relat Disord 2011 Aug 20;17(7):547-50. Epub 2011 May 20.

Department of Neurology, Mayo Clinic, 4500 San Pablo Road, Jacksonville, FL 32224, USA.

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http://dx.doi.org/10.1016/j.parkreldis.2011.04.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137742PMC
August 2011

Potentiation of tumor necrosis factor-alpha-induced tumor cell apoptosis by a small molecule inhibitor for anti-apoptotic protein hPEBP4.

J Biol Chem 2010 Apr 22;285(16):12241-7. Epub 2010 Feb 22.

National Key Laboratory of Medical Immunology and Institute of Immunology, Second Military Medical University, Shanghai 200433, China.

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http://www.jbc.org/lookup/doi/10.1074/jbc.M110.111898
Publisher Site
http://dx.doi.org/10.1074/jbc.M110.111898DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852963PMC
April 2010

Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6.

Authors:
Jianfeng Xiao

Hum Genet 2010 Apr;127(4):469

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April 2010

Malonyl-CoA: acyl carrier protein transacylase from Helicobacter pylori: Crystal structure and its interaction with acyl carrier protein.

Protein Sci 2007 Jun;16(6):1184-92

Drug Discovery and Design Center, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.

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http://dx.doi.org/10.1110/ps.072757307DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206670PMC
June 2007

Murine central and peripheral nervous system transcriptomes: comparative gene expression.

Brain Res 2006 Aug 7;1107(1):24-41. Epub 2006 Jul 7.

University of Tennessee Health Science Center, Department of Neurology, and Center of Genomics and Bioinformatics, 855 Monroe Avenue, Link Building-Suite 415, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1016/j.brainres.2006.05.101DOI Listing
August 2006

Caytaxin deficiency causes generalized dystonia in rats.

Brain Res Mol Brain Res 2005 Nov 24;141(2):181-92. Epub 2005 Oct 24.

Department of Neurology, University of Tennessee Health Science Center, 855 Monroe Avenue, Link Building-Suite 415, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1016/j.molbrainres.2005.09.009DOI Listing
November 2005

Developmental expression of rat torsinA transcript and protein.

Brain Res Dev Brain Res 2004 Aug;152(1):47-60

Department of Neurology, University of Tennessee Health Science Center, 855 Monroe Avenue, Suite 415, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1016/j.devbrainres.2004.05.012DOI Listing
August 2004

Cloning, developmental regulation and neural localization of rat epsilon-sarcoglycan.

Brain Res Mol Brain Res 2003 Nov;119(2):132-43

Department of Neurology, University of Tennessee Health Science Center, 855 Monroe Avenue, Suite 415, Memphis, TN 38163, USA.

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http://dx.doi.org/10.1016/j.molbrainres.2003.09.004DOI Listing
November 2003

[Mutation analysis of neurofilament-light gene in Chinese Charcot-Marie-Tooth disease].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2003 Apr;20(2):169-70

Department of Neurology, National Key Laboratory of Medical Genetics, Central South University, Changsha, Hunan, 410008 P. R. China.

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April 2003

[The clinical and pathologic features of Charcot-Marie-Tooth disease].

Zhonghua Nei Ke Za Zhi 2002 Nov;41(11):736-8

Department of Neurology, Xiangya Hospital, the Central South University, Changsha 410008, China.

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November 2002

[A new mutation in the connexin 32 gene of a Chinese family with Charcot-Marie-Tooth disease associated with central conduction slowing].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2002 Oct;19(5):367-9

Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, 410008 P.R. China.

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October 2002