Top View
- An Allosteric Network in Spastin Couples Multiple Activities Required for Microtubule Severing
- Spastin Couples Microtubule Severing to Membrane Traffic in Completion of Cytokinesis and Secretion
- Recessive REEP1 Mutation Is Associated with Congenital Axonal Neuropathy and Diaphragmatic Palsy
- The Microtubule Skeleton and the Evolution of Neuronal Complexity in Vertebrates
- Spectrum of SPG4 Mutations in a Large Collection of North American Families with Hereditary Spastic Paraplegia
- Gene: Association with Multiple Sclerosis in Two Avected Siblings and Epilepsy in Other Avected Family Members
- A Patient-Derived Stem Cell Model of Hereditary Spastic Paraplegia with SPAST Mutations
- Uniprot: the Universal Protein Knowledgebase the Uniprot Consortium1,2,3,4,*
- SPAST Gene Spastin
- Patient-Derived Stem Cell Models in SPAST HSP: Disease Modelling and Drug Discovery
- Spastin (SPAST) (NM 014946) Human Untagged Clone Product Data
- Spastin Antibody [Clone Sp 3G11-1] (V8093)
- ENTREZ GENE ID Logfc Aveexpr Adj.P.Val
- Automated Splicing Mutation Analysis by Information Theory
- Modelling Hereditary Spastic Paraplegias Using Human Pluripotent Stem Cells Kyle Denton University of Connecticut - Storrs, [email protected]
- Mental Deficiency in Three Families with SPG4 Spastic Paraplegia
- Autosomal Dominant (AD) Pure Spastic Paraplegia (HSP) Linked to Locus
- Hereditary Spastic Paraplegia: Clinical Genetic Study of 15 Families
- The 15Q11.2 BP1-BP2 Microdeletion
- Loss of Drosophila Melanogaster P21-Activated Kinase 3 Suppresses Defects in Synapse Structure and Function Caused by Spastin Mutations
- Datasheet: 8350-1010 Product Details
- Innate Immune Activity Is Detected Prior to Seroconversion in Children
- Ejhg2008147.Pdf
- Modulation of Myotilin and Fylamin C in Various Muscle Diseases: a Microarray Analysis
- University of Florida Thesis Or Dissertation Formatting
- Clinical and Genetic Heterogeneity in Hereditary Spastic Paraplegias: from SPG1 to SPG72 and Still Counting Stephan Klebe, Giovanni Stevanin, Christel Depienne
- Spastin Recovery in Hereditary Spastic Paraplegia by Preventing Neddylation-Dependent Degradation
- 2021 Pathology & Lab CPT Updates
- Overlapping Molecular Pathological Themes Link Charcot–Marie–Tooth Neuropathies and Hereditary Spastic Paraplegias
- Cellular Pathways of Hereditary Spastic Paraplegia*
- Cytoskeletal Rearrangement During Developmental Motor Axon Remodeling
- Spastin Recovery in Hereditary Spastic Paraplegia by Preventing Neddylation-Dependent Degradation
- The Clinical Spectrum of Inherited Diseases Involved in the Synthesis and Remodeling of Complex Lipids. a Tentative Overview
- Hereditary Spastic Paraplegia Proteins REEP1, Spastin, and Atlastin-1 Coordinate Microtubule Interactions with the Tubular ER Network
- Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms
- Mutation Analysis of the Spastin Gene (SPG4) in Patients with Hereditary
- Spastin (SPAST) (NM 014946) Human Recombinant Protein Product Data
- Anti-Spastin Antibody (Clone 2F5) Mouse Anti Human Monoclonal Antibody Catalog # ALS17683