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POMT2
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Novel Cardiovascular Findings in Association with a POMT2
Congenital Disorders of Glycosylation from a Neurological Perspective
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Molecular Diagnostic Requisition
Viruses Like Sugars: How to Assess Glycan Involvement in Viral Attachment
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Prenatal Testing Requisition Form
Myo-Glyco Disease Biology: Genetic Myopathies Caused by Abnormal Glycan Synthesis and Degradation
WO 2017/054086 Al 6 April 2017 (06.04.2017) P O P C T
Glycomic and Transcriptomic Response of GSC11 Glioblastoma Stem Cells to STAT3 Phosphorylation Inhibition and Serum- Induced Differentiation
Congenital Muscular Dystrophy
SI Correction
Epilepsy Next-Generation Sequencing Guide
Supplemental Figures 04 12 2017
Muscular Dystrophy with Ribitol- Phosphate Deficiency: a Novel Post-Translational Mechanism in Dystroglycanopathy
Genetic Testing for Neuromuscular Disorders
A Novel POMT2 Mutation Causes Mild Congenital Muscular Dystrophy with Normal Brain MRI
Top View
Congenital Disorders of Glycosylation Precision Panel Overview
POMT2 Gene Protein O-Mannosyltransferase 2
Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome Only) Vol
Supplementary Table S1. Distributions of Characteristics of CM Patients in MDACC and NHS/HPFS Datasets Parameter Frequency MFT H
Targeted Genes and Methodology Details for Congenital Disorders of Glycosylation Gene Panel
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Congenital Disorders of Glycosylation Gene Panel, Varies
Impact of MLL5 Expression on Decitabine Efficacy and DNA Methylation in Acute Myeloid Leukemia
Genomic Unity® Prenatal Analysis
Somatic Mutations
Name Gene Symbol Hypertrophic /LVH Dilated/LV Systolic
Targeted-Sequencing Gene Panels Used by Each Hospital Huashan
Demonstration of Mammalian Protein O-Mannosyltransferase Activity: Coexpression of POMT1 and POMT2 Required for Enzymatic Activity
Broad and Thematic Remodeling of the Surfaceome and Glycoproteome On
Diagnostic Genetic Testing Requisition
Discovery of an O-Mannosylation Pathway Selectively Serving Cadherins and Protocadherins
Congenital Disorders of Glycosylation (CDG)
Newborndxtm Advanced Sequencing Evaluation Disorders List