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YIPF5
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Fine Mapping of the Hereditary Haemorrhagic Telangiectasia (HHT)3 Locus on Chromosome 5 Excludes VE-Cadherin-2, Sprouty4 And
Variation in Protein Coding Genes Identifies Information
Unique Networks: a Method to Identify Disease-Specific Regulatory Networks from Microarray Data
Genomic Diagnostics Within a Medically Underserved Population: Efficacy and Implications
High-Resolution Gene Maps of Horse Chromosomes 14 and 21: Additional Insights Into Evolution and Rearrangements of HSA5 Homologs in Mammals
Integrative Systems Biology Applied to Toxicology
Characterization of Five Transmembrane Proteins: with Focus on the Tweety, Sideroflexin, and YIP1 Domain Families
(12) United States Patent (10) Patent No.: US 9,057,109 B2 Chang (45) Date of Patent: Jun
Mood, Stress and Longevity: Convergence on ANK3
The Changing Chromatome As a Driver of Disease: a Panoramic View from Different Methodologies
Predict AID Targeting in Non-Ig Genes Multiple Transcription Factor
A Network Inference Approach to Understanding Musculoskeletal
Genetic Markers in Celiac Disease
FMN Reduces Amyloid-β Toxicity in Yeast by Regulating Redox Status
1 a Thorough RNA-Seq Characterization of The
YIPF5 Mutations Cause Neonatal Diabetes and Microcephaly Through Endoplasmic Reticulum Stress
Complex Karyotype with Cryptic FUS Gene Rearrangement and Deletion of NR3C1 and VPREB1 Genes in Childhood B‑Cell Acute Lymphoblastic Leukemia: a Case Report
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Evolution of Resistance in Vitro Reveals Mechanisms of Artemisinin Activity in Toxoplasma Gondii
Effects of Inhibitors of FGFR3 on Gene Transcription
HBV DNA Integration and Clonal Hepatocyte Expansion in Chronic Hepatitis B Patients Considered Immune Tolerant
YIPF5 Mutations Cause Neonatal Diabetes and Microcephaly: Progress for Precision Medicine and Mechanistic Understanding
Corticolimbic Transcriptome Changes Are State-Dependent and Region-Specific in a Rodent Model of Depression and of Antidepressant Reversal
Two Contrasting Classes of Nucleolus-Associated Domains in Mouse Fibroblast Heterochromatin
Is a Novel Cellular Binding Partner of the Papillomavirus E5 Proteins
Global Analyses of Chromosome 17 and 18 Genes of Lung Telocytes
Detecting Gene Modules Differentially Expressed in Multiple Human Brain
Network-Based Identification and Prioritization of Key Regulators of Coronary Artery Disease Loci
Microscopy-Based High-Content Analyses Identify Novel Chromosome Instability Genes
Microrna Binding Microrna Binding Probe Set Entrez Gene Gene
Quantitative Proteome Pro Ling of Respiratory
Whiston, E., Wise, H
Table I: Incubation of Primary Human Endothelial Cells with IFN-Γ Results in a Significant Increase in the Transcription of 215 Genes
Supplemental Table 2: UC Vs. NL Gene List Gene Name Symbol
Inhibition of TFG Function Causes Hereditary Axon Degeneration by Impairing Endoplasmic Reticulum Structure
YIPF5 Mutations Cause Neonatal Diabetes and Microcephaly: Progress for Precision Medicine and Mechanistic Understanding