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Chromosome 5

  • The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'

    The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'

  • Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases

    Cytogenetic and Molecular Delineation of the Smallest Commonly Deleted Region of Chromosome 5 in Malignant Myeloid Diseases

  • The Cytogenetics of Hematologic Neoplasms 1 5

    The Cytogenetics of Hematologic Neoplasms 1 5

  • Cri-Du-Chat Syndrome Diagnosed in a 21-Year-Old Woman by Means of Comparative Genomic Hybridization

    Cri-Du-Chat Syndrome Diagnosed in a 21-Year-Old Woman by Means of Comparative Genomic Hybridization

  • Allele-Specific Disparity in Breast Cancer Fatemeh Kaveh1, Hege Edvardsen1, Anne-Lise Børresen-Dale1,2, Vessela N Kristensen1,2,3* and Hiroko K Solvang1,4

    Allele-Specific Disparity in Breast Cancer Fatemeh Kaveh1, Hege Edvardsen1, Anne-Lise Børresen-Dale1,2, Vessela N Kristensen1,2,3* and Hiroko K Solvang1,4

  • Human Chromosome-Specific Cdna Libraries: New Tools for Gene Identification and Genome Annotation

    Human Chromosome-Specific Cdna Libraries: New Tools for Gene Identification and Genome Annotation

  • 5Q14.3 Deletions FTNW

    5Q14.3 Deletions FTNW

  • Deletions and Losses in Chromosomes 5 Or 7 in Adult Acute

    Deletions and Losses in Chromosomes 5 Or 7 in Adult Acute

  • Rare Allelic Forms of PRDM9 Associated with Childhood Leukemogenesis

    Rare Allelic Forms of PRDM9 Associated with Childhood Leukemogenesis

  • Ring Chromosome 5 with Dental Anomalies

    Ring Chromosome 5 with Dental Anomalies

  • The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'

    The Human Gene Encoding Phosphatidylinositol-3 Kinase Associated P85a Is at Chromosome Region 5Ql2-13'

  • Gain of Chromosome 4Qter and Loss of 5Pter: an Unusual Case with Features of Cri Du Chat Syndrome

    Gain of Chromosome 4Qter and Loss of 5Pter: an Unusual Case with Features of Cri Du Chat Syndrome

  • The Chicken Genome Has a Hybrid Centromere Model, Involving Either Long Arrays of Tandem Repeats on Some Chromosomes Or Relative

    The Chicken Genome Has a Hybrid Centromere Model, Involving Either Long Arrays of Tandem Repeats on Some Chromosomes Or Relative

  • Receptor Signaling Through Osteoclast-Associated Monocyte

    Receptor Signaling Through Osteoclast-Associated Monocyte

  • The Interleukin 3 Gene Is Located on Human Chromosome 5 and Is Deleted in Myeloid Leukemias with a Deletion of 5Q

    The Interleukin 3 Gene Is Located on Human Chromosome 5 and Is Deleted in Myeloid Leukemias with a Deletion of 5Q

  • GENE LIST ANTI-CORRELATED Systematic Common Description

    GENE LIST ANTI-CORRELATED Systematic Common Description

  • Mitochondrial Pseudogenes Suggest Repeated Inter-Species Hybridization in Hominid Evolution

    Mitochondrial Pseudogenes Suggest Repeated Inter-Species Hybridization in Hominid Evolution

  • Mapping Chromosome 5

    Mapping Chromosome 5

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  • Trisomy 5P Inverted Duplication & Deletion of 5Pftnp
  • Centromere-Mediated Chromosome Break Drives Karyotype Evolution in Closely Related 2 Malassezia Species
  • Inherited 5P Deletion Syndrome Due to Paternal Balanced Translocation: Phenotypic Heterogeneity Due to Duplication of 8Q and 12P
  • NDUFS6 Mutations Are a Novel Cause of Lethal Neonatal Mitochondrial Complex I Deficiency
  • Chromosome 5
  • Chromosome 5 Introduction the Size of Chromosome 5 (180 Mb) and The
  • Trisomy 5P: Duplications of 5P15
  • Genetics and Mitochondrial Abnormalities in Autism Spectrum Disorders: a Review
  • Centromere Deletion in Cryptococcus Deuterogattii Leads to Neocentromere Formation and Chromosome Fusions Klaas Schotanus, Joseph Heitman*
  • Condensin I Associates with Structural and Gene Regulatory Regions in Vertebrate Chromosomes
  • HHS Public Access Author Manuscript
  • Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
  • Centromere Repeats: Hidden Gems of the Genome
  • Gene Mapping and Medical Genetics Genetic Markers on Chromosome 7
  • Nuclear-Mitochondrial DNA Segments Resemble Paternally Inherited Mitochondrial DNA in Humans
  • Cancer-Associated Alteration of Pericentromeric Heterochromatin May Contribute to Chromosome Instability
  • Location of the Centromeres on the Linkage Maps of Maize'
  • Centromere Scission Drives Chromosome Shuffling and Reproductive Isolation


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