DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» SHC2
SHC2
An Investigation Into the Genetic Architecture of Multiple System Atrophy and Familial Parkinson's Disease
Reconstruction and Analysis of Gene Networks of Human
Multiple System Atrophy: Genetic Or Epigenetic?
Comparative Transcriptome Profiling of the Human and Mouse Dorsal Root Ganglia: an RNA-Seq-Based Resource for Pain and Sensory Neuroscience Research
Comparative Transcriptome Profiling of the Human and Mouse Dorsal Root
Strong Synaptic Transmission Impact by Copy Number Variations in Schizophrenia
RAS/MAPK Pathway Genes 210 200 RAS Genes - Total No 190 180 Linked to ID (Strong, Monogenic 170 Cause) 160 Linked to ID (Mild) 150
The Pdx1 Bound Swi/Snf Chromatin Remodeling Complex Regulates Pancreatic Progenitor Cell Proliferation and Mature Islet Β Cell
Deep Transcriptomic Analysis of Black Rockfish (Sebastes Schlegelii)
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Transcriptome Profiling Reveals the Complexity of Pirfenidone Effects in IPF
(NF1) As a Breast Cancer Driver
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Visual Signs and Symptoms of Multiple System Atrophy (Msa)
Diverse Transcriptional Regulation and Functional Effects Revealed by CRISPR/Cas9-Directed Epigenetic Editing
Data-Driven and Knowledge-Driven Computational Models of Angiogenesis in Application to Peripheral Arterial Disease
Somatic Mutations and T-Cell Clonality in Patients with Immunodeficiency
Mouse Shc2 Conditional Knockout Project (CRISPR/Cas9)
Top View
Biomedical Informatics
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Copy Number Loss of (Src Homology 2 Domain Containing)-Transforming
Transcriptomic Comparison of Human and Mouse Brain Microvessels Hannah W
Shc2 (NM 001024539) Mouse Tagged ORF Clone Product Data
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Unraveling the Molecular Mechanism Underlying ALS-Linked Astrocyte
Anti-SHC2 (C-Terminal) Polyclonal Antibody (CPBT- 66656GH) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
The Neurogenomics View of Neurological Diseases
Identification of Balanced Chromosomal
(SHC2) (NM 012435) Human Tagged ORF Clone Product Data
Chromosome 19P13.3 Microdeletions
Ii Binding Specificity of SH2 Domains Revealed by a Combinatorial