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Chromosome 12
12Q Deletions FTNW
Investigation of Differentially Expressed Genes in Nasopharyngeal Carcinoma by Integrated Bioinformatics Analysis
Chromosomes 8, 12, and 17 Copy Number in Astler-Coller Stage C Colon Cancer in Relation to Proliferative Activity and DNA Ploidy1
Pallister-Killian Syndrome Groups Worldwide Who Are Studying the Different Aspects of This Syndrome
Centromere Repositioning Causes Inversion of Meiosis and Generates a Reproductive Barrier
Receptor Signaling Through Osteoclast-Associated Monocyte
Chicken Skeletal Muscle-Associated Macroarray for Gene Discovery
Supplementary Table 3. Genes Specifically Regulated by Zol (Non-Significant for Fluva)
Chromosome 12 Introduction the Genetic Length of Chromosome 12 Is ~132 Mb. It Is ~4–4.5% of the Total Human Genome, Approximat
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Is Mitochondrial DNA Depletion Involved in Alzheimer's Disease?
Novel and Highly Recurrent Chromosomal Alterations in Se´Zary Syndrome
Delineation of C12orf65-Related Phenotypes: a Genotype&Ndash
Not Para-, Not Peri-, but Centric Inversion of Chromosome 12
Translocations Involving the Short Arm of Chromosome 17 in Chronic B-Lymphoid Disorders
Supplementary Materials and Methods
Chromosome 12 Breakpoints Are Cytogenetically Different in Benign and Malignant Lipogenic Tumors
Chromosome 12, Frequently Deleted in Human Pancreatic Cancer, May Encode a Tumor-Suppressor Gene That Suppresses Angiogenesis
Top View
ETV6 Is the Target of Chromosome 12P Deletions in T(12;21) Childhood Acute Lymphocytic Leukemia
CENP-A-Chromatin in Health and Cancer
Chromosome 12
Linkage Analyses of Murine Immunoglobulinheavy Chain and Serum Prealbumin Genes Establish Their Location on Chromosome 12 Proxim
Chromosomal Instability in Chromosome Band 12P13
Paternal Uniparental Disomy of Chromosome 14 and Unique Exchange of Chromosome 7 in Cases of Spontaneous Abortion
A C-Terminal Nonsense Mutation Links PTPRQ with Autosomal-Dominant Hearing Loss, DFNA73
Chromosome 12
Pallister-Killian Mosaic Syndrome
Duplications of 12P
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Identification of Potential and Novel Target Genes in Pituitary Prolactinoma by Bioinformatics Analysis
Impaired CENP-E Function Renders Large Chromosomes More Vulnerable to Congression Failure
An Overview on the Phylogeny of Aerobic Metabolism and the Preponderance of Mitochondrial Functions in Evolution Denis Rousseau*
A Genomic Region Associated with Protection Against Severe COVID-19 Is Inherited from Neandertals
Dynamic Changes in the Copy Number of Pluripotency and Cell Proliferation Genes in Human Escs and Ipscs During Reprogramming and Time in Culture
E-One Mapping and Medical Genetics
Demonstration of the Genuine Iso-12P Character of the Standard Marker
(12) United States Patent (10) Patent No.: US 8,637.240 B2 Tian Et Al
In-Depth Sequence Analysis of the Tomato Chromosome 12 Centromeric Region: Identification of a Large CAA Block and Characterization of Pericentromere Retrotranposons
Non-Mosaic Partial Duplication 12P in a Patient with Dysmorphic Characteristics and Developmental Delay
CENPC (NM 001812) Human Tagged ORF Clone Product Data
Regional Mapping of the Phenylalanine Hydroxylase Gene and the Phenylketonuria Locus in the Human Genome
REVIEW Neocentromeres: New Insights Into Centromere Structure, Disease Development, and Karyotype Evolution
Identification of Potential and Novel Target Genes in Pituitary Prolactinoma by Bioinformatics Analysis
Title the Evolutionary Life Cycle of the Resilient Centromere