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VPS33B
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Clathrin-Dependent Mechanisms Modulate the Subcellular Distribution of Class C Vps/HOPS Tether Subunits in Polarized and Nonpolarized Cells Stephanie A
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Identifying Potential Binding Partners of VPS16B and VPS33B in Mammalian Cells
The Role of SNAP29 During Epidermal Differentiation
Cldn19 Clic2 Clmp Cln3
CORVET, CHEVI and HOPS – Multisubunit Tethers of the Endo
Arthrogryposis and Congenital Myasthenic Syndrome Precision Panel
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
A Mutation in SNAP29, Coding for a SNARE Protein
Supplemental Solier
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
VPS33B and VIPAR Are Essential for Epidermal Lamellar Body Biogenesis
The Endosome Is a Master Regulator of Plasma Membrane Collagen Fibril Assembly
Identification of Human Myometrial Target Genes of the C-Jun NH2
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses by a Synthetic TLR3 Ligand Mitigates
Vacuolar Protein Sorting 33B Is a Tumor Suppressor In
Lipid Rafts and Caveolae in the Terminal Differentiation of Epidermal Keratinocytes Truus Roelandt1, Diane Roseeuw1, Christina Giddelo1 and Jean-Pierre Hachem*,1,2
Top View
Clinical Exome Gene Panels List V2
Mutations in VPS33B, Encoding a Regulator of SNARE- Dependent Membrane Fusion, Cause Arthrogryposis–Renal Dysfunction–Cholestasis (ARC) Syndrome
Structural Basis of Vps33a Recruitment to the Human HOPS Complex by Vps16
(LY6E) Provides Robust Tumor Killing in a Wi
The Anti-Apoptosis Ubiquitin E3 Ligase XIAP Promotes Autophagosome- Lysosome Fusion During Autophagy
Insulin's Discovery
Hvps41 and VAMP7 Function in Direct TGN to Late Endosome Transport of Lysosomal Membrane Proteins
Identification and Characterization of the Interaction Between VPS33B and Snares
Newborndxtm Advanced Sequencing Evaluation Disorders List
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
A Link Between Intrahepatic Cholestasis and Genetic Variations in Intracellular Trafficking Regulators
A Novel Mutation of Gene Associated with Incomplete Arthrogryposis
Sec22b Determines Weibel-Palade Body Length by Controlling
Table SI. Targets of Berberine. Gene Symbol Gene Name ABL1 ABO
RNA-Sequencing Identifies Dysregulation of the Human Pancreatic Islet Transcriptome
STAT Autism and Intellectual Disability Panel
Identification of Genes and Signaling Pathways Associated with Arthrogryposis‑Renal Dysfunction‑Cholestasis Syndrome Using Weighted Correlation Network Analysis
Characterization of VPS33B and VPS16B in Megakaryocyte and Platelet Α-Granule Biogenesis