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ALG12
The Diversity of Dolichol-Linked Precursors to Asn-Linked Glycans Likely Results from Secondary Loss of Sets of Glycosyltransferases
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Congenital Disorders of Glycosylation from a Neurological Perspective
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
CDG and Immune Response: from Bedside to Bench and Back Authors
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
CDG-Ih) (ALG8 Deficiency
N-Glycosylation Processing Pathways Across Kingdoms Cheng-Yu Chung, Natalia I
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
Diagnosis of ALG12-CDG by Exome Sequencing in a Case of Severe Skeletal Dysplasia
Supplemental Figures 04 12 2017
Blueprint Genetics Congenital Disorders of Glycosylation Panel
Skeletal and Bone Mineral Density Features, Genetic Profile In
Understanding the Transcriptional Landscape of Chinese Hamster
Top View
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
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
SWATH-MS Glycoproteomics Reveals Consequences of Defects in the Glycosylation Machinery*□S
ALG9-CDG New Clinical Case and Review of the Literature
LOSS of INVERSIN CONTRIBUTES to RENAL CYSTIC DISEASE THROUGH ALTERED CELLULAR PROCESSES and DECREASED SODIUM TRANSPORT in RENAL EPITHELIAL CELLS by Nalini H
Cardiac Next-Generation Sequencing Panels
Generate Metabolic Map Poster
Name Gene Symbol Hypertrophic /LVH Dilated/LV Systolic
ALG12 Gene ALG12, Alpha-1,6-Mannosyltransferase
Congenital Disorders of Glycosylation: an Update on Defects Affecting the Biosynthesis of Dolichol-Linked Oligosaccharides
S41467-019-09752-3.Pdf
Congenital Disorders of Glycosylation (CDG)
ALG12 Mannosyltransferase Defect in Congenital Disorder of Glycosylation Type Lg
Newborndxtm Advanced Sequencing Evaluation Disorders List
Blueprint Genetics Comprehensive Metabolism Panel
Diseases of Glycosylation Beyond Classical Congenital Disorders of Glycosylation
Metabolske Sykdommer V02
Investigating the Pathway of Asparagine-Linked Glycoprotein Biosynthesis
EGL Test Description
Suppl Table V
Glycosyltransferase Genes That Cause Monogenic Congenital
Source: State: 12.06.2018 ORPHA68367 10507
ALG12-Congenital Disorder of Glycosylation
ALG8-CDG: Novel Patients and Review of the Literature
Abnormal Glycosylation of Red Cell Membrane Band 3 in the Congenital Disorder of Glycosylation Ig
Yeast Protein Release During Fermentation and Aging in a Model Wine
Individual Genome Sequence Gene List (By Disease)
Insights Into Transcriptome Profiles Associated with Wooden Breast
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 Glycosylation Design Space for Recombinant Lysosomal Replacement Enzymes Produced in CHO Cells