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DIP2A
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Genetic Analysis of Over One Million People Identifies 535 New Loci Associated with Blood 2 Pressure Traits
Loss of DIP2C in RKO Cells Stimulates Changes in DNA
Supplementary Materials
Genetic Variation As a Tool for Identifying Novel Transducers of Itch
Chromosome 21 Leading Edge Gene Set
Ohnologs in the Human Genome Are Dosage Balanced and Frequently Associated with Disease
Investigation of Common, Low-Frequency and Rare Genome-Wide Variation in Anorexia Nervosa
Peripheral Nerve Single-Cell Analysis Identifies Mesenchymal Ligands That Promote Axonal Growth
Investigating Contributions of Trisomy 21 in Down Syndrome to Alzheimer Disease Phenotypes in a Novel Mouse Cross
A Theoretical Molecular Network for Dyslexia
Estrogen's Impact on the Specialized Transcriptome, Brain, and Vocal
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Investigating the Genetic Basis of Reading and Language Skills
ARTICLE CGG-Repeat Expansion in the DIP2B Gene Is Associated with the Fragile Site FRA12A on Chromosome 12Q13.1
A Single Gene Expression Set Derived from Artificial
Systematic Characterization of Human 21St Chromosome Orthologs In
Fstl1/DIP2A/MGMT Signaling Pathway Plays Important Roles in Temozolomide Resistance in Glioblastoma
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Massively Parallel Sequencing Reveals the Complex Structure of an Irradiated Human Chromosome on a Mouse Background in the Tc1 Model of Down Syndrome
Analysis of Dip2b Expression in Adult Mouse Tissues Using the Lacz Reporter Gene
Transposon Insertional Mutagenesis in Mice Identifies Human Breast Cancer Susceptibility Genes and Signatures for Stratification
Biological Implications of Genetic Variations in Autism Spectrum Disorders from Genomics Studies Yue Zhang, Xuanshi Liu, Ruolan
Systematic Surveys of Iron Homeostasis Mechanisms Reveal Ferritin Superfamily and Nucleotide Surveillance Regulation to Be Modif
Genome-Wide Detection of Selective Signature in Chinese Holstein
Genetic Variations in Connection
Germline DNA Copy Number Variation in Familial and Early-Onset Breast
Neurogenetics of Developmental Dyslexia: from Genes to Behavior Through Brain Neuroimaging and Cognitive and Sensorial Mechanisms
WO 2014/100434 Al 26 June 2014 (26.06.2014) W P O P C T
Genetics of Developmental Dyslexia Thomas S
Rare and De Novo Variants in 827 Congenital Diaphragmatic Hernia Probands Implicate
De Novo and Rare Inherited Copy-Number Variations in the Hemiplegic Form of Cerebral Palsy
Supplementary Table 1. a Full List of Cancer Genes
Targeted Disruption of Mouse Dip2b Leads to Abnormal Lung Development and Prenatal Lethality