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DPM2
Congenital Disorders of Glycosylation from a Neurological Perspective
Dystroglycanopathies; Natural History and Clinical Observations
Novel Driver Strength Index Highlights Important Cancer Genes in TCGA Pancanatlas Patients
Original Communication Genomic and Expression Array Profiling of Chromosome 20Q Amplicon in Human Colon Cancer Cells
More Than 1,001 Problems with Protein Domain Databases: Transmembrane Regions, Signal Peptides and the Issue of Sequence Homology
TIBS-Revised Eichler and Imperiali-2017-Withfigs
B3GALNT2 Is a Gene Associated with Congenital Muscular Dystrophy with Brain Malformations
Anti-DPM1 Antibody (ARG64722)
A New Intronic Mutation in the DPM1 Gene Is Associated with a Milder Form of CDG Ie in Two French Siblings
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Genome-Wide Gene Expression Profiling of Randall's Plaques In
146823088.Pdf
Dystroglycan: Extracellular Matrix Receptor That Links to Cytoskeleton 153
DPM2 (NM 003863) Human Tagged ORF Clone Lentiviral Particle Product Data
Health and Population Effects of Rare Gene Knockouts in Adult Humans with Related Parents
De Novo Mutations in the Gene Encoding STXBP1 (MUNC18-1) Cause Early Infantile Epileptic Encephalopathy
Dolichol Phosphate Mannose Synthase (DPM1) Mutations Define Congenital Disorder of Glycosylation Ie (CDG-Ie)
Requirement of Protein Kinase Type I for Camp- Mediated Up-Regulation of Lipid-Linked Oligosaccharide for Asparagine-Linked Protein Glycosylation
Top View
A Bioinformatic Pipeline to Prioritise Small Open Reading Frames Identifies Candidate Secreted Small Proteins
Ubiquitination/Proteasome Pathways Specialized in Cellular Stress
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
UNIVERSITY of CALIFORNIA, IRVINE Genomics
Type of the Paper (Article
Modeling Gene Regulation from Paired Expression and Chromatin Accessibility Data
RNA-Seq Reveals Genetic Differences in African American and European American Prostate Cancer James P
Identification of Genetic Elements in Metabolism by High-Throughput Mouse Phenotyping ARTICLE
The Role of Glycosylphosphatidylinositol Biosynthesis and Remodeling in Neural
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
The JAX Synteny Browser for Mouse-Human Comparative Genomics
I. Supplemental Methods A. Lipid Analysis B. Proteomics C. Gene Reporter (Luciferase) Assays D
About Numerous Genes Involved in Glycosylation of One Single Glycoprotein
Description of Strs in Trinucleotide-Repeat Diseases
Comprehensive Characterization of the Transcriptional Signaling of Human Parturition Through Integrative Analysis of Myometrial Tissues and Cell Lines