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ALG8
Congenital Disorders of Glycosylation from a Neurological Perspective
Biomedical Applications of Bacteria-Derived Polymers
Viruses Like Sugars: How to Assess Glycan Involvement in Viral Attachment
Prenatal Testing Requisition Form
F04b57ca351b0dc3389ebe992c
Metabolic Enzyme Expression Highlights a Key Role for MTHFD2 and the Mitochondrial Folate Pathway in Cancer
Genome-Wide Investigation of Cellular Functions for Trna Nucleus
CDG-Ih) (ALG8 Deficiency
N-Glycosylation Processing Pathways Across Kingdoms Cheng-Yu Chung, Natalia I
Cloning of the ALG8 Locus
Clinical, Molecular, and Immune Analysis of Dabrafenib-Trametinib
Structural and Biochemical Insights Into Biosynthesis and Degradation of and Degradation Into Insights Biosynthesis and Biochemical Structural
SI Correction
Multiplexed Surrogate Analysis of Glycotransferase Activity in Whole Biospecimens † † ‡ Chad R
Wide Clinical Spectrum in ALG8-CDG: Clues from Molecular findings Suggest an Explanation for a Milder Phenotype in the first-Described Patient
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Supplemental Figure 1. Infection Efficacy, Cytoxicity and Decrease in Barrier Integrity of HIBCPP Cells Following Infection with MOI 20 of E-30
Top View
Supplemental Figures 04 12 2017
Enabling Tools for Toxoplasma Glycobiology 02Sept2018
Supplementary Figure S1 A
Clinical Application of a Phenotype-Based NGS Panel for Differential Diagnosis of Inherited Kidney Disease and the Beyond
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
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Congenital Disorders of Glycosylation Gene Panel, Varies
Hereditary Disorders of Carbohydrate Metabolism
Name Gene Symbol Hypertrophic /LVH Dilated/LV Systolic
ALG9 Mutation Carriers Develop Kidney and Liver Cysts
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Congenital Disorders of Glycosylation (CDG)
Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Blueprint Genetics Comprehensive Metabolism Panel
Further Delineation of the ALG9-CDG Phenotype
Diseases of Glycosylation Beyond Classical Congenital Disorders of Glycosylation
Quantitative Analysis of the Mitochondrial Proteome in Human Ovarian Carcinomas
Metabolske Sykdommer V02
Common Variants in Mendelian Kidney Disorder Genes and Their Association with Renal Function And
Investigating the Pathway of Asparagine-Linked Glycoprotein Biosynthesis
EGL Test Description
From Glycosylation Disorders Back to Glycosylation: What Have We Learned?
Carbohydrates and Glycosylation* Patricia M
Glycosyltransferase Genes That Cause Monogenic Congenital
Source: State: 12.06.2018 ORPHA68367 10507
ALG8-CDG: Novel Patients and Review of the Literature
Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
Individual Genome Sequence Gene List (By Disease)
Download Gene List
Hereditary Hypertrophic Cardiomyopathy in Children and Young Adults—The Value of Reevaluating and Expanding Gene Panel Analyses
Expression Pattern and Biological Significance of the Lncrna ST3GAL6-AS1 in Multiple Myeloma
Genomic Unity® Neurology Analysis