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Serum Albumin OS=Homo Sapiens
Supplementary Figure S4
Excluded Test List – As of 08/01/2016
Antigen-Specific Memory CD4 T Cells Coordinated Changes in DNA
SUPPLEMENTARY MATERIAL Effect of Next
Transcriptional Recapitulation and Subversion Of
The Wnt Receptor FZD1 Mediates Chemoresistance in Neuroblastoma Through Activation of the Wnt/B-Catenin Pathway
Tissue-Specific Conditional CCM2 Knockout Mice Establish The
1 SUPPLEMENTAL DATA Figure S1. Poly I:C Induces IFN-Β Expression
Skippy Reference: Variants That Create Ectopic Splice Sites (Hg18)
Vast Human-Specific Delay in Cortical Ontogenesis Associated With
Supplemental Solier
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
GENE LIST ANTI-CORRELATED Systematic Common Description
Rap1 and Its Effector KRIT1/CCM1 Regulate -Catenin Signaling
Molecular Genetic Approaches to Disease of Neural Development Mohamad Bydon Yale University
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Top View
Update on Mapping the Landscape of Genetic Tests for Non-Cancer
After a Review of the Current Available Literature, CGS Administrators Has Determined That Testing for the Following Genes/Gene
KRIT1, a Gene Mutated in Cerebral Cavernous Malformation, Encodes a Microtubule- Associated Protein
Two Rare AKAP9 Variants Are Associated with Alzheimer's Disease in African Americans
Augmenting and Accelerating Drug Discovery Using Artificial Intelligence Christopher C
KRIT1 Gene KRIT1, Ankyrin Repeat Containing
Functional Genomics of Krit1, the Gene Mutated in Cerebral Cavernous Malformation Maxwell Laurans Yale University
Table S-1 Mpkccd Transcriptome
Supplementary Table S4
RNA Editing Signatures Predict Response to Immunotherapies in Melanoma Patients
TEST REQUISITION FORM with TARGETED VARIANT TESTING Please Print Clearly and Provide All Requested Information
Differential Preventive Activity of Sulindac and Atorvastatin in Apc+
NDPK) Proteins
POSITIVE RESULT Likely Pathogenic Variant Identified
Spectrum and Expression Analysis of KRIT1 Mutations in 121 Consecutive and Unrelated Patients with Cerebral Cavernous Malformations
Neurodevelopment Next-Generation Sequencing Panels
Neuron, Volume 62 Supplemental Data Functional and Evolutionary
Table S1 All Prioritized Candidate Genes in L4 Drgs from Toppgene
Lineage-Specific Programming Target Genes Defines Potential for Th1
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In
SNP Discovery in Candidate Adaptive Genes Using Exon Capture in a Free-Ranging Alpine Ungulate
Athena Diagnostics International Neurology Test Requisition (April
A Universal Scaling Law for Atomic Diffusion in Condensed Matter Initial
Supplementary Data
Top Ten Discoveries of the Year: Neurovascular Disease
Comprehensive Genetic Test Menu
Chebulic Acid Prevents Methylglyoxal-Induced Mitochondrial Dysfunction in INS-1 Pancreatic Β-Cells
Supplementary File 2B Revised
Cellular Dynamics of KRIT1 : Implications for the Pathogenesis of Cerebral Cavernous Malformations Nduka M
Inbred Mouse Strains Expression in Primary Immunocytes Across
I. Supplemental Methods A. Lipid Analysis B. Proteomics C. Gene Reporter (Luciferase) Assays D
Lineage-Specific Programming Target Genes Defines Potential for Th1
Dermatology Gene Panel
In Systemic Sclerosis, a Unique Long Non Coding RNA Regulates Genes
A Genetic Map of the Response to DNA Damage in Human Cells
Therapeutic Manipulation of IKBKAP Mis-Splicing with a Small Molecule to Cure Familial Dysautonomia
Overview of Genes Derived from Possum Database in the Category and Subcategories of Skin Vascular Changes (N=139)
Genomic Unity® Neurology Analysis
The Function of the Heg-CCM Pathway in Zebrafish Heart Development
Mutations in a Mechanosensitive Channel Enable Intravascular Metaststic Cell Survival Paul William Furlow
Supplemental Material