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BLOC1S1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
WO 2019/079361 Al 25 April 2019 (25.04.2019) W 1P O PCT
Supplementary Materials
Development of the Swimbladder Surfactant System and Biogenesis of Lysosome-Related Organelles Is Regulated by BLOS1 in Zebrafish
MUTED Antibody - C-Terminal Region (ARP63301 P050) Data Sheet
Towards the Identification of Causal Genes for Age-Related Macular
Genetic Analyses of Human Fetal Retinal Pigment Epithelium Gene Expression Suggest Ocular Disease Mechanisms
Inbred Mouse Strains Expression in Primary Immunocytes Across
BLOS2 Negatively Regulates Notch Signaling During Neural and Hematopoietic Stem And
Human BLOC1S2 / BLOS2 Protein (GST Tag)
Exploring the Human Genome with Functional Maps Curtis Huttenhower1,2,†, Erin M
A BLOC-1 Mutation Screen Reveals That PLDN Is Mutated in Hermansky-Pudlak Syndrome Type 9
Rabbit Anti-MUTED Antibody-SL19114R
Was Gathered from SMR Analysis at the Genome-Wide Significance Level
(12) Patent Application Publication (10) Pub. No.: US 2014/0018338A1 Chandran Et Al
Lethal Congenital Contractural Syndrome Type 2 (LCCS2) Is Caused by a Mutation in ERBB3 (Her3), a Modulator of the Phosphatidylinositol-3-Kinase/Akt Pathway
Figure S1. Endogenous MIR45
TFEB Links MYC Signaling to Epigenetic Control of Myeloid Differentiation and Acute Myeloid Leukemia
Top View
Unamplified Cap Analysis of Gene Expression on a Single-Molecule Sequencer
Coexpression Networks Based on Natural Variation in Human Gene Expression at Baseline and Under Stress
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Produktinformation
Exploring the Human Genome with Functional Maps
The Dystrobrevin-Binding Protein 1 Gene
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
TITLE Regulation of Mitophagy by the NSL Complex Underlies Genetic Risk
717298V2.Full.Pdf
Primepcr™Assay Validation Report
A New Drug Candidate for Glycogen Storage Disorders Enhances Glycogen Catabolism: Lessons From
Quantitative Proteomic and Genetic Analyses of the Schizophrenia
Recombinant Human PLDN Protein Catalog Number: ATGP1472
Amyotrophic Lateral Sclerosis (ALS) and Alzheimer's Disease (AD)