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POMT1
Broad and Thematic Remodeling of the Surface Glycoproteome on Isogenic
Congenital Disorders of Glycosylation from a Neurological Perspective
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
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
B3GALNT2 Is a Gene Associated with Congenital Muscular Dystrophy with Brain Malformations
Influenza-Specific Effector Memory B Cells Predict Long-Lived Antibody Responses to Vaccination in Humans
Glycan Metabolism a Validated Grna Library for CRISPR/Cas9
SI Correction
Discovery of an O-Mannosylation Pathway Selectively Serving Cadherins and Protocadherins
Discovery of a Nucleocytoplasmic O-Mannose Glycoproteome in Yeast
POMT1 Modulates the Severe Congenital Muscular Dystrophy Phenotype Associated with POMT1 Nonsense Mutations
Supplemental Figures 04 12 2017
SUPPLEMENTARY MATERIALS and METHODS PBMC Transcriptomics
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Top View
Congenital Disorders of Glycosylation
Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging
Targeted Genes and Methodology Details for Congenital Disorders of Glycosylation Gene Panel
The Glucuronyltransferase B4GAT1 Is Required for Initiation of LARGE
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Congenital Disorders of Glycosylation Gene Panel, Varies
Molecular Characterization of Protein O-Linked Mannose Β-1, 2-N
Immunity Resolution of Inflammation and Airway Diversity in Expression with Critical Roles in Macrophage Populations Reveals
SUPPLEMENTARY APPENDIX Targetable Driver Mutations in Multicentric Reticulohistiocytosis
A Systems Based Framework to Computationally Predict Putative Transcription Factors and Signaling Pathways Regulating Glycan
Supplemental Information
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
Congenital Disorders of Glycosylation (CDG)
Newborndxtm Advanced Sequencing Evaluation Disorders List
Cardiomyopathy in Patients with POMT1-Related Congenital and Limb-Girdle Muscular Dystrophy
POMT1 Gene Protein O-Mannosyltransferase 1
Functional Roles of Fucosylated and O-Glycosylated Cadherins During