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ATOX1
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Calcium-Dependent Copper Redistributions in Neuronal Cells Revealed by a Fluorescent Copper Sensor and X-Ray Fluorescence Microscopy
Current Biomedical Use of Copper Chelation Therapy
Ncomms4301.Pdf
Essential Trace Elements in Human Health: a Physician's View
Supplementary Material and Methods
And Copper Homeostatic Mechanisms in Brain Contributes to the Pathogenesis of Neurodegenerative Disorders
Effect of Dietary Copper Deficiency on Iron Metabolism in the Pregnant
ATOX1 (NM 004045) Human Untagged Clone Product Data
Transcriptomic and Functional Analysis of Aβ1-42 Oligomer-Stimulated
The Bioinorganic Periodic Table
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Supplementary Table S1. Relative Change in Proteins Associated with Heme Biosynthesis and Degradation
Conserved Residues Modulate Copper Release in Human Copper Chaperone Atox1
Expanding the Metallomics Toolbox: Development Of
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Abnormal Copper Homeostasis: Mechanisms and Roles in Neurodegeneration
Interaction Between the Anticancer Drug Cisplatin and the Copper Chaperone Atox1 in Human Melanoma Cells
Top View
Structure and Chemistry of the Copper Chaperone Proteins Amy C Rosenzweig* and Thomas V O’Halloran†
Targeting the Copper Transport System to Improve Treatment Efficacies of Platinum-Containing Drugs in Cancer Chemotherapy
Wilson's Disease: Facing the Challenge of Diagnosing a Rare
Unresolved Questions in Human Copper Pump Mechanisms
Cloning and Expression of the Two Isoforms of Copper Atpase in a Fish
Cellular Dynamics of Transition Metal Exchange on Proteins: a Challenge but a Bonanza for Coordination Chemistry
ATP7B Variant Penetrance Explains Differences Between Genetic And
Making Sense of Microarray Data to Classify Cancer
The Role of Copper Chaperone Atox1 in Coupling Redox Homeostasis to Intracellular Copper Distribution
Genetic Factors Characterising the Clinical Course of Wilson's Disease
Genetic Variant Nutritional Assessment Genetic Variants That
AMTC Hypothesis
Bioinorganic Chemistry of Alzheimers Disease
Mechanism of Copper Transport at the Blood–Cerebrospinal fluid Barrier: Influence of Iron Deficiency in an in Vitro Model
Study of Serum Copper and Iron in Children with Chronic Liver Diseases
Single-Cell Tracking Demonstrates Copper Chaperone Atox1 to Be Required for Breast Cancer Cell Migration
Bioinorganic Chemistry: a Short Course
Effect of Dietary Copper Deficiency on Iron Metabolism in the Pregnant
Single-Molecule Dynamics and Mechanisms of Metalloregulators and Metallochaperones † ‡ § Peng Chen,* Aaron M
Human Glutaredoxin-1 Can Transfer Copper to Isolated Metal Binding Domains of the P1B-Type Atpase, ATP7B Shadi Maghool1, Sharon La Fontaine2,3, Blaine R
High Genetic Carrier Frequency of Wilson's Disease in France
Special Reports and Reviews
Structural and Functional Studies of ATP7B, the Copper(I)-Transporting P-Type Atpase Implicated in Wilson Disease
Effects of the Loss of Atox1 on the Cellular Pharmacology of Cisplatin
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
Systems Approach to Metal- Based Pharmacology Isolda Romero-Canelón and Peter J
Gutself: Interindividual Variability in the Processing of Dietary Compounds by the Human Gastrointestinal Tract
Intersection of Iron and Copper Metabolism in the Mammalian Intestine and Liver
Gene Interactions in Ageing and Inflammatory Age-Related Diseases
Iron-Heme-Bach1 Axis Is Involved in Erythroblast Adaptation to Iron Deficiency
Liver As a Key Organ in the Supply, Storage, and Excretion of Copper1– 4