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Author Details

Xiao-Ning Chen
College of Geographic and Environmental Science, Northwest Normal University
1991
83
38
PMIDPaper TitleJournal TitlePublished Year
33314840[Characteristics and driving forces of wetland landscape pattern evolution of the city belt along the Yellow River in Ningxia, China].Ying Yong Sheng Tai Xue Bao2020
26575889[Clinical and pathological characteristics and prognosis of children with histiocytic necrotizing lymphadenitis].Zhongguo Dang Dai Er Ke Za Zhi2015
21130848Distribution of retinoic acid receptor-α immunoreactivity in the human hypothalamus.Neuroscience2011
21664419Stress and glucocorticoids regulated corticotropin releasing factor in rat prefrontal cortex.Mol Cell Endocrinol2011
20659790Chronic all-trans retinoic acid administration induced hyperactivity of HPA axis and behavioral changes in young rats.Eur Neuropsychopharmacol2010
19282872William's syndrome: gene expression is related to parental origin and regional coordinate control.J Hum Genet2009
19597142The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies.Proc Natl Acad Sci U S A2009
19596122The involvement of retinoic acid receptor-alpha in corticotropin-releasing hormone gene expression and affective disorders.Biol Psychiatry2009
19356693Distribution of acid-sensing ion channel 3 in the rat hypothalamus.Neuroscience2009
19205026Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays.Am J Med Genet A2009
18597742Estrogen receptor-alpha and -beta regulate the human corticotropin-releasing hormone gene through similar pathways.Brain Res2008
16418593Deletion of chromosome 21 disturbs human brain morphogenesis.Genet Med2006
15952108Detection of chromosome aberrations in Chinese children with autism using G-banding and BAC FISH.Zhonghua Yi Xue Yi Chuan Xue Za Zhi2005
15020820BAC mapping using fluorescence in situ hybridization.Methods Mol Biol2004
12865760Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.Genet Med2003
12909340The 200-kb segmental duplication on human chromosome 21 originates from a pericentromeric dissemination involving human chromosomes 2, 18 and 13.Gene2003
12697057Refined physical map of the human PAX2/HOX11/NFKB2 cancer gene region at 10q24 and relocalization of the HPV6AI1 viral integration site to 14q13.3-q21.1.BMC Genomics2003
12051741Mammalian DSCAMs: roles in the development of the spinal cord, cortex, and cerebellum?Biochem Biophys Res Commun2002
12397812BAC resource for molecular cytogenetics.Methods Mol Biol2002
11977162Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.Am J Med Genet2002
11576731Towards a full karyotype screening of interphase cells: 'FISH and chip' technology.Mol Cell Endocrinol2001
11280950Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel.Genet Med2001
11280955Down syndrome congenital heart disease: a narrowed region and a candidate gene.Genet Med2001
11237021Integration of cytogenetic landmarks into the draft sequence of the human genome.Nature2001
11237014A physical map of the human genome.Nature2001
11353394A triple color FISH technique for mouse chromosome identification.Mamm Genome2001
11304567Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.Lab Invest2001
11283799Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans.Am J Hum Genet2001
11015462Partial tetrasomy 21 in a male infant.J Med Genet2000
10861662Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).Am J Med Genet2000
10953236VI. Genome structure and cognitive map of Williams syndrome.J Cogn Neurosci2000
10938284The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity.J Biol Chem2000
10523528Human genome anatomy: BACs integrating the genetic and cytogenetic maps for bridging genome and biomedicine.Genome Res1999
10405324A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24.Biochem Biophys Res Commun1999
10438519Involvement of protein kinase Cepsilon (PKCepsilon) in thyroid cell death. A truncated chimeric PKCepsilon cloned from a thyroid cancer cell line protects thyroid cells from apoptosis.J Biol Chem1999
10330132Mouse molecular cytogenetic resource: 157 BACs link the chromosomal and genetic maps.Genome Res1999
10191094Localization of a human nucleoporin 155 gene (NUP155) to the 5p13 region and cloning of its cDNA.Genomics1999
10636446FISH analysis of terminal deletions in patients diagnosed with cri-du-chat syndrome.Clin Genet1999
9683604From amplification to gene in thyroid cancer: a high-resolution mapped bacterial-artificial-chromosome resource for cancer chromosome aberrations guides gene discovery after comparative genome hybridization.Am J Hum Genet1998
9426258DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system.Hum Mol Genet1998
10072586Assignment of the GOV (Glioblastoma overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization.Cytogenet Cell Genet1998
9675132JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.Biochem Biophys Res Commun1998
9344663The structure and chromosome location of the human chondroadherin gene (CHAD).Genomics1997
9169140Molecular characterization of human neogenin, a DCC-related protein, and the mapping of its gene (NEO1) to chromosomal position 15q22.3-q23.Genomics1997
9110173Cloning, characterization, and copy number of the murine survival motor neuron gene: homolog of the spinal muscular atrophy-determining gene.Genome Res1997
9143497BAC and PAC contigs covering 3.5 Mb of the Down syndrome congenital heart disease region between D21S55 and MX1 on chromosome 21.Genomics1997
9325053A high-resolution PAC and BAC map of the SCA2 region.Genomics1997
8661061Chromosomal localization of murine and human oligodendrocyte-specific protein genes.Genomics1996
8954791The gene organization, chromosome location, and expression of a 55-kDa matrix protein (PRELP) of human articular cartilage.Genomics1996
8896555Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.Nat Genet1996
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Collaborators

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Co-authored papers 72
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RIKEN Center for Brain Science
Co-authored papers 5
University of Wisconsin-Madison
Co-authored papers 3
Amgen Inc.
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Co-authored papers 2
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Co-authored papers 2
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Co-authored papers 2
University of North Carolina at Chapel Hill
Co-authored papers 2
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Genomics Institute, University of California Santa Cruz
Co-authored papers 2
Center for Genetics, Children's Hospital Oakland Research Institute
Co-authored papers 2
Knight Cancer Institute, Oregon Health and Science University
Co-authored papers 2
Institut Francois Jacob, CNRS, Universite Paris-Saclay
Co-authored papers 2
Los Alamos National Laboratory
Co-authored papers 1
Co-authored papers 1
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Co-authored papers 1
University of British Columbia
Co-authored papers 1
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Baylor College of Medicine
Co-authored papers 1
Center for Cancer Research, National Cancer Institute
Co-authored papers 1
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NIH and National Human Genome Research Institute
Co-authored papers 1
University of Michigan ann arbor
Co-authored papers 1