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GPR89B
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract
Noelia Díaz Blanco
Subterranean Mammals Show Convergent Regression in Ocular Genes and Enhancers, Along with Adaptation to Tunneling
Literature Mining Sustains and Enhances Knowledge Discovery from Omic Studies
Chromosomal Microarray Analysis in Turkish Patients with Unexplained Developmental Delay and Intellectual Developmental Disorders
Transcriptional Fates of Human-Specific Segmental Duplications in Brain
Evolution of Genetic and Genomic Features Unique to the Human Lineage
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Chromosomal Level Assembly and Population Sequencing of The
Evolutionary-Based Methods for Predicting Genotype-Phenotype Associations in the Mammalian Genome
Human-Specific NOTCH-Like Genes in a Region Linked to Neurodevelopmental Disorders Affect Cortical Neurogenesis
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Dissecting Molecular Genetic Mechanisms of 1Q21.1 CNV in Neuropsychiatric Disorders
The Evolution and Population Diversity of Human-Specific Segmental Duplications
The Presence of Two Rare Genomic Syndromes, 1Q21 Deletion And
Supplementary Information on Material and Methods
Cancer Sequence Service Data File Formats — Ii Table of Contents
Top View
Expanding the Phenotype of Reciprocal 1Q21.1 Deletions and Duplications: a Case Series Martina Busè1* , Helenia C
Standard Sequencing Service Data File Formats File Format V2.4 Software V2.4 December 2012
The Presence of Two Rare Genomic Syndromes, 1Q21 Deletion and Xq28 Duplication, Segregating Independently in a Family with Intellectual Disability
Primate Specific Retrotransposons, Svas, in the Evolution of Networks That Alter Brain Function
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
WO 2017/136709 A2 10 August 2017 (10.08.2017) P O P C T
Neuroscore: a Genome-Wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System
Identification of Key Genes Involved in Myocardial Infarction
Complex Genetics of Radial Ray Deficiencies: Screening of a Cohort of 54 Patients
Copy Number Variations in a Cohort of 420 Individuals with Neurodevelopmental Disorders from the South of Brazil
Importance and Usage of Chromosomal Microarray Analysis
Prevalence and Phenotypic Characterization of Rare Genetic Disorders Within Psychiatric Populations
Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder
Proteomic Profiling of Retinoblastoma-Derived Exosomes
Figure S1. RNA Quality Control Report. Neutrophils Were Stimulated with 1 Μg/Ml LTA. the Quality of Each Sample Was Examined Via the RIN Software
Human-Specific Genes, Cortical Progenitor Cells, and Microcephaly
Original Article SPOP Regulates the DNA Damage Response and Lung Adenocarcinoma Cell Response to Radiation