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COG1
Genetic and Genomic Analysis of Hyperlipidemia, Obesity and Diabetes Using (C57BL/6J × TALLYHO/Jngj) F2 Mice
Large-Scale Rnai Screening Uncovers New Therapeutic Targets in the Human Parasite
Open Data for Differential Network Analysis in Glioma
(Siberian Roe Deer and Grey Brocket Deer) Unravelled by Chromosome-Specific DNA Sequencing Alexey I
Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content
Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content
Simpintlists Package
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome
University of Groningen Fatal Outcome Due to Deficiency of Subunit 6
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
(Siberian Roe Deer and Grey Brocket Deer) Unravelled by Chromosome- Specific DNA Sequencing Alexey I
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
S41467-019-13965-X.Pdf
NIH Public Access Author Manuscript Mol Cell
Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
Conserved Oligomeric Golgi Complex Subunit 1 Deficiency Reveals a Previously Uncharacterized Congenital Disorder of Glycosylation Type II
Supplemental Information File
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Golgi Function and Dysfunction in the First COG4- Deficient CDG Type II Patient
Identification of Novel Fusion Genes with 28S Ribosomal DNA in Hematologic Malignancies
Copy Number Variation of Tddof Controls Solid-Stemmed Architecture in Wheat
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Conserved Oligomeric Golgi Complex Subunit 1 Deficiency Reveals a Previously Uncharacterized Congenital Disorder of Glycosylation Type II
Comparative Analyses of the Conserved Oligomeric Golgi (COG) Complex in Vertebrates BMC Evolutionary Biology 2010, 10:212
'Deficiency in COG5 Causes a Moderate Form of Congenital
Break-Seq Reveals Hydroxyurea-Induced Chromosome Fragility As a Result of Unscheduled Conflict Between DNA Replication and Transcription
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Genome-Wide Binding Analysis of the Tomato Transcription Factor Sldof1 Reveals Its Regulatory Impacts on Fruit Ripening
Autosomal Recessive Variants in Intellectual Disability and Autism Spectrum Disorder
CELL STRUCTURE and FUNCTION Advance Publication by J-STAGE Doi:10.1247/Csf.18014 Title: Detailed Analysis of the Interaction O
Clinical and Genetic Characterization of Patients with Pierre Robin Sequence and Spinal Disease: Review of the Literature and Novel Terminal 10Q Deletion
Congenital Disorders of Glycosylation: an Update on Defects Affecting the Biosynthesis of Dolichol-Linked Oligosaccharides
Anti-COG4 (SAB4200568)
Genome-Wide in Silico Identification and Comparative Analysis of Dof Gene Family in Brassica Napus
Evolutionary Genomics Suggests That Chev Is an Additional Adaptor for Accommodating Specific Chemoreceptors Within the Chemotaxis Signaling Complex
U2AF1 Mutations Alter Splice Site Recognition in Hematological Malignancies