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HIRIP3
Identifying Developing Interneurons As a Potential Target for Multiple Genetic 3 Autism Risk Factors in Human and Rodent Forebrain
Autism Multiplex Family with 16P11.2P12.2 Microduplication Syndrome in Monozygotic Twins and Distal 16P11.2 Deletion in Their Brother
Endoglin Protein Interactome Profiling Identifies TRIM21 and Galectin-3 As
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Association of Gene Ontology Categories with Decay Rate for Hepg2 Experiments These Tables Show Details for All Gene Ontology Categories
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Oas1b-Dependent Immune Transcriptional Profiles of West Nile
Associated 16P11.2 Deletion in Drosophila Melanogaster
WO 2012/174282 A2 20 December 2012 (20.12.2012) P O P C T
A Rare Duplication on Chromosome 16P11.2 Is Identified in Patients with Psychosis in Alzheimer’S Disease
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
Oschz1 Acts As a Histone Chaperone in Modulating Chromatin
A High Throughput, Functional Screen of Human Body Mass Index GWAS Loci Using Tissue-Specific Rnai Drosophila Melanogaster Crosses Thomas J
Connecting Myelin-Related and Synaptic Dysfunction In
The Genetic Program of Pancreatic Beta-Cell Replication in Vivo
Identification and Characterization of HIRIP3 As a Novel Histone H2A Chaperone Maria Ignatyeva
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
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A Cell Type-Specific Expression Signature Predicts Haploinsufficient Autism-Susceptibility Genes
Three Case Reports of Patients Indicating the Diversity of Molecular
Connecting Myelin-Related and Synaptic Dysfunction in Schizophrenia with SNP-Rich Gene Expression Hubs
Genome-Wide Analysis of Promoter Methylation Associated with Gene Expression Profile in Pancreatic Adenocarcinoma
Genomic Imbalances Detected by Array-CGH in Patients with Syndromal Ocular Developmental Anomalies
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Evolutionary Turnover of Mammalian Transcription Start Sites
(12) Patent Application Publication (10) Pub. No.: US 2009/0203014 A1 WU Et Al
Neuroscore: a Genome-Wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System
TBX6, LHX1 and Copy Number Variations in the Complex Genetics of Müllerian Aplasia
Copy-Number Variant Analysis of Classic Heterotaxy Highlights the Importance of Body Patterning Pathways
Product Description SALSA® MLPA® Probemix P297-D1 Microdeletion Syndromes-2 to Be Used with the MLPA General Protocol
From Obesity Genetics to the Future of Personalized Obesity Therapy Julia S
Prediction of Future Metastasis and Molecular Characterization of Head and Neck Squamous-Cell Carcinoma Based on Transcriptome and Genome Analysis Bymicroarrays
Transcriptional Profiling of Type 1 Diabetes Genes on Chromosome 21 in a Rat Beta-Cell Line and Human Pancreatic Islets
Engineering Microdeletions and Microduplications by Targeting
Submicroscopic Aberrations of Chromosome 16 in Prenatal Diagnosis