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ALG9
Broad and Thematic Remodeling of the Surface Glycoproteome on Isogenic
Yeast Genome Gazetteer P35-65
Congenital Disorders of Glycosylation from a Neurological Perspective
Supplemental Material Placed on This Supplemental Material Which Has Been Supplied by the Author(S) J Med Genet
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Molecular Diagnostic Requisition
Prenatal Testing Requisition Form
Overview Gene List Target Scan Vs DIANA Group a Group B Group A
Gillessen-Kaesbach–Nishimura Skeletal Dysplasia Due to Pathogenic Variants in ALG9
CDG-Ih) (ALG8 Deficiency
N-Glycosylation Processing Pathways Across Kingdoms Cheng-Yu Chung, Natalia I
Identification of Genomic Targets of Krüppel-Like Factor 9 in Mouse Hippocampal
Ordered Assembly of the Asymmetrically Branched Lipid
Structural and Biochemical Insights Into Biosynthesis and Degradation of and Degradation Into Insights Biosynthesis and Biochemical Structural
Multiplexed Surrogate Analysis of Glycotransferase Activity in Whole Biospecimens † † ‡ Chad R
Glycobiology of the Epithelial to Mesenchymal Transition
Supplemental Data
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Top View
Supplementary Figure S1 A
BMC Molecular Biology Biomed Central
MOL #82305 TITLE PAGE Title: Induced CYP3A4 Expression In
Skeletal and Bone Mineral Density Features, Genetic Profile In
Loss of α2-6 Sialylation Promotes the Transformation Of
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
SWATH-MS Glycoproteomics Reveals Consequences of Defects in the Glycosylation Machinery*□S
ALG9-CDG New Clinical Case and Review of the Literature
Online Supporting Information S2: Proteins in Each Negative Pathway
Name Gene Symbol Hypertrophic /LVH Dilated/LV Systolic
ALG9 Mutation Carriers Develop Kidney and Liver Cysts
Broad and Thematic Remodeling of the Surfaceome and Glycoproteome On
S41467-019-09752-3.Pdf
Report Identification and Functional Analysis of a Defect in the Human
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Blueprint Genetics Comprehensive Metabolism Panel
Key Genes Associated with Diabetes Mellitus and Hepatocellular Carcinoma T ⁎ ⁎ Gao-Min Liu , Hua-Dong Zeng, Cai-Yun Zhang, Ji-Wei Xu
Further Delineation of the ALG9-CDG Phenotype
Diseases of Glycosylation Beyond Classical Congenital Disorders of Glycosylation
Metabolske Sykdommer V02
Investigating the Pathway of Asparagine-Linked Glycoprotein Biosynthesis
EGL Test Description
Transcriptomics Identified a Critical Role for Th2 Cell-Intrinsic Mir-155 In
Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity Without Compromising Cisplatin Anticancer Properties
1 Reference Sequence Number Gene Symbol Alleles Chromosomal
Stepwise Assembly of the Lipid-Linked Oligosaccharide in The
Glycosyltransferase Genes That Cause Monogenic Congenital
Source: State: 12.06.2018 ORPHA68367 10507
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
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
The Role of N-Linked Glycosylation in Drosophila
Genomic Unity® Neurology Analysis
Differential Expression of Glycosyltransferases Identified Through Comprehensive Pan-Cancer Analysis
Extreme Calorie Restriction and Energy Source Starvation in Saccharomyces Cerevisiae Represent Distinct Physiological States