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Chromosome 17
Searching the Genomes of Inbred Mouse Strains for Incompatibilities That Reproductively Isolate Their Wild Relatives
Laboratory Testing for Her2 Status in Breast Cancer
Duplications of 17P FTNW
An In-Depth Analysis of the HER2 Amplicon and Chromosome 17
BRCA1 and BRCA2 Genes and Their Relationship to Breast and Ovarian Cancer
The Genomic Landscape of Centromeres in Cancers Anjan K
Understanding the Genetics of FTD a Guide for Patients and Their Families Acknowledgements
17P13.3 Microdeletions
Chromosome 17
Loss of Heterozygosity on Chromosomes 11 and 17 Are Markers of Recurrence in TCC of the Bladder
The Mitotic Tensegrity Guardian Tau Protects Mammary Epithelia from Katanin-Like1-Induced Aneuploidy
Dark Matter of Primate Genomes: Satellite DNA Repeats and Their Evolutionary Dynamics
Translocation and Amplification of an X-Chromosome DNA Repeat in Inbred Strains of Mice
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
Receptor Signaling Through Osteoclast-Associated Monocyte
GENE LIST ANTI-CORRELATED Systematic Common Description
Mitotic Checkpoints and Chromosome Instability Are Strong Predictors of Clinical Outcome in Gastrointestinal Stromal Tumors
Functional Analysis of Mutations of Murine Chromosome 17 with the Use of Tertiary Trisomy
Top View
Spatial Separation of Xist RNA and Polycomb Proteins Revealed by Superresolution Microscopy
A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation Between Mouse and Human
Mapping of Human Chromosomal Regions Related to Neoplasia: Evidence from Chromosomes 1 and 17 (Gene Mapping/Virus Interaction/Hematologic Disorders) JANET D
A Homozygous Splicing Mutation in ELAC2 Suggests Phenotypic Variability Including Intellectual Disability with Minimal Cardiac Involvement Nadia A
1 NOVEL INSIGHTS from CLINICAL PRACTICE Ring Chromosome 17
Translocations Involving the Short Arm of Chromosome 17 in Chronic B-Lymphoid Disorders
Centromere Protein B Assembles Human Centromeric A-Satellite DNA
Centromeres Under Pressure: Evolutionary Innovation in Conflict with Conserved Function
Identification of Overlapping DNA-Binding and Centromere
Microdeletions of 17P13.1 and 17P13.2
Keeping It Complicated: Mitochondrial Genome Plasticity Across Diplonemids Received: 30 June 2017 Matus Valach 1, Sandrine Moreira 1,10, Steve Hofmann2, Peter F
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Autism and Genes, in English
Uniparental Propagation of Mitochondrial DNA in Mouse-Human Cell Hybrids
17 Chromosome Chapter
An Overview on the Phylogeny of Aerobic Metabolism and the Preponderance of Mitochondrial Functions in Evolution Denis Rousseau*
Histocompatibility Complex
Fusion Transcripts of Adjacent Genes: New Insights Into the World of Human Complex Transcripts in Cancer
Cytogenetics Lecture 1: Introduction to Clinical Cytogenetics
Microdeletion Syndromes, Balanced Translocations, and Gene Mapping
Construction of a Genetic Map Ofhuman Chromosome 17 by Use Of
HER2-Positive Breast Carcinomas with Co-Amplification Or Gain of Chromosome 17 Centromere Locus: Report of Three Cases and an Impact on HER2 Testing
Ring Chromosome 17 Epilepsy May Resemble That of Ring Chromosome 20 Syndrome
Chromosome Translocation
17Q12 Microduplications
Humcfs: a Database of Fragile Sites in Human Chromosomes
Patterns of Expression of Chromosome 17 Genes in Primary Cultures of Normal Ovarian Surface Epithelia and Epithelial Ovarian Cancer Cell Lines
Co-Amplification of the HER2 Gene and Chromosome 17 Centromere: A
Human Cytogenetics Case Report Yet Unreported Heteromorphic Variant
Supplementary Table 1. a Full List of Cancer Genes
A Variant Chromosome 17 in a Mother with Repeated Abortions and a 46,XY/47,XXY Klinefelter Son