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Paraplegin
Identification of the Drosophila Melanogaster Homolog of the Human Spastin Gene
Pathogenic Variants in the AFG3L2 Proteolytic Domain Cause SCA28
Life Without Paraplegin
Hereditary Spastic Paraparesis: a Review of New Developments
Emerging Roles of Mitochondrial Proteases in Neurodegeneration
Spastic Paraplegia Type 7
Hereditary Spastic Paraplegias
Hereditary Spastic Paraplegia: from Genes, Cells and Networks to Novel Pathways for Drug Discovery
Phd PROGRAM in TRANSLATIONAL and MOLECULAR MEDICINE DIMET Functional Analysis of M-AAA Homo- and Heterocomplexes: the Role of Mi
Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease
Axonal Degeneration in Paraplegin-Deficient Mice Is Associated with Abnormal Mitochondria and Impairment of Axonal Transport
Hereditary Spastic Paraplegias: Clinical Spectrum in Sudan, Further Deciphering of the Molecular Bases of Autosomal Recessive Forms and New Genes Emerging
Defects in Mitochondrial Axonal Transport and Membrane Potential Without Increased Reactive Oxygen Species Production in Adrosop
030626 Mitochondrial Respiratory-Chain Diseases
Loss of Paraplegin Drives Spasticity Rather Than Ataxia in a Cohort of 241 Patients with SPG7
Polyclonal Antibody to Paraplegin / SPG7 (Center) - Aff - Purified
Case Series of Autosomal Recessive Hereditary Spastic Paraparesis with Novel Mutation in SPG 7 Gene
In Silico Investigation of Traditional Chinese Medicine for Potential Lead Compounds As SPG7 Inhibitors Against Coronary Artery Disease
Top View
Mice Harbouring a SCA28 Patient Mutation in AFG3L2 Develop Late-Onset Ataxia Associated with Enhanced Mitochondrial Proteotoxicity T
Mitochondrial Ribosomal Proteins: Candidate Genes for Mitochondrial Disease James E
Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells
Spastic Paraplegia Type 7 Is Associated with Multiple Mitochondrial DNA Deletions
Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8Q
Prenatal Diagnosis of Hereditary Spastic Paraplegia{
Mice Harboring a SCA28 Patient Mutation in AFG3L2 Develop Late-Onset Ataxia Associated with Enhanced Mitochondrial Proteotoxicity
Unique Structural Features of the Mitochondrial AAA+ Protease AFG3L2 Reveal the Molecular Basis for Activity in Health and Disease
Differentiation of Hereditary Spastic Paraparesis from Primary Lateral Sclerosis in Sporadic Adult-Onset Upper Motor Neuron Syndromes
Loss of the Drosophila M-AAA Mitochondrial Protease Paraplegin Results in Mitochondrial Dysfunction, Shortened Lifespan, And
The Mitochondrial Protease AFG3L2 Is Essential for Axonal Development
Identification of Novel Compound Heterozygous
NMR Structure and MD Simulations of the AAA Protease Intermembrane Space Domain Indicates Peripheral Membrane Localization Within the Hexaoligomer ⇑ Theresa A
Haploinsufficiency of AFG3L2, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration
SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Clonal Expansion of Secondary Mitochondrial DNA Deletions Associated with Spinocerebellar Ataxia Type 28
Report Hereditary Spastic Paraplegia SPG13 Is Associated with a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60
SPG7 Gene SPG7, Paraplegin Matrix AAA Peptidase Subunit
Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells
M-AAA Proteases, Mitochondrial Calcium Homeostasis and Neurodegeneration