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AFG3L2
18P Deletions FTNW
A Novel AFG3L2 Mutation in a German Family with Young Onset, Slow
Atpase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy
Phd DIMET Functional Analysis of AFG3L2 Mutations Causing
AFG3L2 Polyclonal Antibody Catalog # AP74280
Detection of Novel 3L Untranslated Region Extensions
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
Instability in NAD Metabolism Leads to Impaired Cardiac Mitochondrial
Introduction to Metascape.Org What Data to Gather
Early Onset and Slow Progression of SCA28, a Rare Dominant Ataxia in a Large Four-Generation Family with a Novel AFG3L2 Mutation
Full Text (PDF)
Structure and Evolution of N-Domains in AAA Metalloproteases
Global Proteome of Lonp1+/- Mouse Embryonal Fibroblasts Reveals Impact on Respiratory Chain, but No Interdependence Between Eral1 and Mitoribosomes
Mitochondrial Protein Quality Control in Cancer
A Novel Mutation of AFG3L2 Might Cause Dominant Optic Atrophy in Patients with Mild Intellectual Disability
S41467-019-13965-X.Pdf
Investigating the Influence of Mtdna and Nuclear Encoded Mitochondrial Variants on High Intensity Interval Training Outcomes
Mice Harboring a SCA28 Patient Mutation in AFG3L2 Develop Late-Onset Ataxia Associated with Enhanced Mitochondrial Proteotoxicity
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Missense Mutations in the Afg3l2 Proteolytic Domain
AFG3L2 Antibody (R32419)
Unique Structural Features of the Mitochondrial AAA+ Protease AFG3L2 Reveal the Molecular Basis for Activity in Health and Disease
AFG3L2 (NM 006796) Human Untagged Clone Product Data
Mice Harbouring a SCA28 Patient Mutation in AFG3L2 Develop Late-Onset Ataxia Associated with Enhanced Mitochondrial Proteotoxicity
Long Noncoding Rnas Are Rarely Translated in Two Human Cell Lines
Genetic Targeting in Cerebellar Purkinje Cells: an Update
The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development
NMR Structure and MD Simulations of the AAA Protease Intermembrane Space Domain Indicates Peripheral Membrane Localization Within the Hexaoligomer ⇑ Theresa A
A Review of 18P Deletions
Genetic Targeting in Cerebellar Purkinje Cells: an Update
Mitochondrial Stress Response Triggered by Defects in Protein Synthesis Quality Control
Haploinsufficiency of AFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration
Genome-Wide Crispri Screening Identifies OCIAD1 As a Prohibitin
Genome-Wide Expression Profiling and Functional Characterization Of
Investigating the Influence of Mtdna and Nuclear Encoded Mitochondrial
M-AAA Proteases, Mitochondrial Calcium Homeostasis and Neurodegeneration