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ALG14
Bioinformatics Approach for the Identification of Fragile Regions On
The First Case of Congenital Myasthenic Syndrome Caused by A
Limb Girdle Myasthenia with Digenic RAPSN and a Novel Disease Gene AK9 Mutations
Associated with Low Dehydrodolichol Diphosphate Synthase (DHDDS) Activity S
Genetic Background of Ataxia in Children Younger Than 5 Years in Finland E444
Novel Exopolysaccharides Produced by Lactococcus Lactis Subsp
N-Glycan Chitobiose Core Biosynthesis by Agl24 Strengthens the Hypothesis of 2 an Archaeal Origin of the Eukaryal N-Glycosylation
Table S1 Genes with Coefficients of Variation (CV) Ratios (CVGHS/CVSD) in the Upper and Lower 10% of for Expression in Genetic Hypercalciuric Stone-Forming (GHS) And
A Sensitized Mutagenesis Screen in Factor V Leiden Mice Identifies Novel Thrombosis
Enrichment of in Vivo Transcription Data from Dietary Intervention
Alg13/Alg14 UDP-Glcnac Transferase
Small Chromosomal Regions Position Themselves Autonomously According to Their Chromatin Class
Investigating Developmental and Epileptic Encephalopathy Using Drosophila Melanogaster
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
The Role of Semen and Seminal Plasma in Inducing Large-Scale Genomic Changes in the Female Porcine Peri-Ovulatory Tract M
ONCOGENOMICS a Genome-Wide Study of the Repressive Effects of Estrogen Receptor Beta on Estrogen Receptor Alpha Signaling in Breast Cancer Cells
Alg14 (NM 024178) Mouse Tagged ORF Clone Product Data
Mouse Alg14 Conditional Knockout Project (CRISPR/Cas9)
Top View
High-Throughput Chronological Lifespan Screening of the Fission Yeast Deletion Library Using Barcode Sequencing
Deep Whole-Genome Sequencing of Multiple Proband Tissues and Parental Blood Reveals the Complex Genetic Etiology of Congenital Diaphragmatic Hernias
Primepcr™Assay Validation Report
Table S1. Complete List of Up- and Down-Regulated Genes in C1 Cells
Hippocampal Gene Expression Changes Underlying Stress Sensitization and Recovery
Membrane Topological Characterization of the Human Alg14 Protein
ALG13 Deficiency Associated with Increased Seizure Susceptibility
KIAA1109 Gene Mutation in Surviving Patients
Datasheet Blank Template
Choice of Transcripts and Software Has a Large Effect on Variant Annotation Mccarthy Et Al
EGL Test Description
Lineage-Specific Programming Target Genes Defines Potential for Th1
Supplementary Table 2: Genes Included in the Sorafenib Sensitivity Signature
Phenotypic Annotation of the Mouse X Chromosome
Small Chromosomal Regions Position Themselves Autonomously According to Their Chromatin Class
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
The 2021 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Supplementary Materials
Transcript-Level Annotation of Affymetrix Probesets Improves The
Genetic Screen Identifies Adaptive Aneuploidy As a Key Mediator of ER Stress Resistance in Yeast
Anti-ST6GAL1 Monoclonal Antibody, Clone LN-1 (CABT-52011MH) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Using Metabolic and Genetic Engineering to Develop Novel Cell Platforms for the Production of Recombinant Glycoproteins with Enhanced Pharmacokinetic Properties
Catalyzestheformationofthefirstlipid