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Chromosome 19

  • (APOCI, -C2, and -E and LDLR) and the Genes C3, PEPD, and GPI (Whole-Arm Translocation/Somatic Cell Hybrids/Genomic Clones/Gene Family/Atherosclerosis) A

    (APOCI, -C2, and -E and LDLR) and the Genes C3, PEPD, and GPI (Whole-Arm Translocation/Somatic Cell Hybrids/Genomic Clones/Gene Family/Atherosclerosis) A

  • Human Chromosome‐Specific Aneuploidy Is Influenced by DNA

    Human Chromosome‐Specific Aneuploidy Is Influenced by DNA

  • Alzheimer's Disease Genetics Fact Sheet

    Alzheimer's Disease Genetics Fact Sheet

  • The Cytogenetics of Hematologic Neoplasms 1 5

    The Cytogenetics of Hematologic Neoplasms 1 5

  • Stem Cells® Original Article

    Stem Cells® Original Article

  • Definition of the Landscape of Promoter DNA Hypomethylation in Liver Cancer

    Definition of the Landscape of Promoter DNA Hypomethylation in Liver Cancer

  • Variation in Chromosome 19

    Variation in Chromosome 19

  • Rapid Molecular Assays to Study Human Centromere Genomics

    Rapid Molecular Assays to Study Human Centromere Genomics

  • Mitochondrial DNA and Genetic Disease

    Mitochondrial DNA and Genetic Disease

  • 1 SUPPLEMENTARY RESULTS Hypomethylated Promoters Are

    1 SUPPLEMENTARY RESULTS Hypomethylated Promoters Are

  • 19P13.13 Microdeletions

    19P13.13 Microdeletions

  • Receptor Signaling Through Osteoclast-Associated Monocyte

    Receptor Signaling Through Osteoclast-Associated Monocyte

  • Chicken Skeletal Muscle-Associated Macroarray for Gene Discovery

    Chicken Skeletal Muscle-Associated Macroarray for Gene Discovery

  • Chromosome 19

    Chromosome 19

  • Is Mitochondrial DNA Depletion Involved in Alzheimer's Disease?

    Is Mitochondrial DNA Depletion Involved in Alzheimer's Disease?

  • Chromosome 19 Annotations with Disease Speciation: a First Report from the Global Research Consortium † ‡ ‡ † § § Carol L

    Chromosome 19 Annotations with Disease Speciation: a First Report from the Global Research Consortium † ‡ ‡ † § § Carol L

  • Analysis of Human Mutations in the Supernumerary Subunits of Complex I

    Analysis of Human Mutations in the Supernumerary Subunits of Complex I

  • Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21

    Extreme Reduction of Chromosome-Specific Α-Satellite Array Is Unusually Common in Human Chromosome 21

Top View
  • Chromosome Translocation in Three Cases of Human Malignant Melanoma1
  • ORIGINAL ARTICLE Hyperdiploid Karyotypes in Acute Myeloid
  • Mitochondrial Ribosomal Proteins: Candidate Genes for Mitochondrial Disease James E
  • Transcriptome Characterization of Human Mammary Cell Lines Expressing Different Levels of ERBB2 by Serial Analysis of Gene Expression
  • Chromosome Translocation in Three Cases of Human Malignant Melanoma1
  • Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
  • Effects of Inhibitors of FGFR3 on Gene Transcription
  • Chromosome 19 Introduction the Genetic Size of Chromosome 19 Is
  • Novel Recurrent Structural Chromosomal Aberrations in Primary Bladder Cancer
  • Mosaic Supernumerary Ring Chromosome 19 J Med Genet: First Published As 10.1136/Jmg.35.10.836 on 1 October 1998
  • Loss of Heterozygosity on Chromosome 10 Is More Extensive in Primary (De Novo) Than in Secondary Glioblastomas Hironori Fujisawa, Rui M
  • Bennett 1965; Ford
  • Gene Mapping and Chromosome 19
  • Genetic Markers on Chromosome 19P and Prenatal Diagnosis of HLA Class II-Deficient Combined Immunodeficiency
  • Supplementary Table S1. Statistically Significant Degs (Adj.P
  • 1209177A.Pdf
  • Supplementary Table 1. a Full List of Cancer Genes
  • Chromosome 19P13.3 Microdeletions


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