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Spectrin repeat
Nesprins: from the Nuclear Envelope and Beyond
Current Understanding of the Role of Cytoskeletal Cross-Linkers in the Onset and Development of Cardiomyopathies
SCIENCE CHINA Spectrin: Structure, Function and Disease
Mesoscale Dynamics of Spectrin and Acto-Myosin Shape Membrane 2 Territories During Mechanoresponse
Actinin Rod Reveals an Extensive Torsional Twist
Structure and Function of a Spectrin-Like Regulator of Bacterial Cytokinesis
Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism
The Spectrin Superfamily
Molecular Extensibility of Mini-Dystrophins and a Dystrophin Rod Construct
Review Article the Role of Nonerythroid Spectrin II in Cancer
2111396504.Pdf
Membrane Domains Based on Ankyrin and Spectrin Associated with Cell–Cell Interactions
Molecular Characterization and Evolution of Α-Actinin: from Protozoa to Vertebrates
Large-Scale Modelling of the Divergent Spectrin Repeats in Nesprins: Giant Modular Proteins
Structure and Function of a Spectrin-Like Regulator of Bacterial Cytokinesis
Βii Spectrin (SPTBN1): Biological Function and Clinical Potential In
A New Twist to Coiled Coil. Elisabeth Le Rumeur, Jean-François Hubert, Steve Winder
Mechanical Behavior of Axonal Actin, Spectrin, and Their Periodic Structure: a Brief
Top View
Cytoskeletal Giants with Characteristics of Both Spectrin and Plakin Families
Regulation of Cardiac Conduction and Arrhythmias by Ankyrin/Spectrin-Based Macromolecular Complexes
Structural Characterization of Two Different F- Actin Cross-Linking Proteins by Electron Microscopy Cheri M
Characterization of the Interactions of Α-Catenin with Α-Actinin and Β- Catenin/Plakoglobin
Β-III-Spectrin Spinocerebellar Ataxia Type 5 Mutation Reveals a Dominant
Spectrin in the Secretory Pathway 2333 2334 M
Pathogenic SPTBN1 Variants Cause a Novel Autosomal Dominant Neurodevelopmental Syndrome
Heterozygous Missense Variants of SPTBN2 Are a Frequent Cause of Congenital Cerebellar Ataxia
Role of Spectrin Mutations in Spinocerebellar Ataxia Type 5 (SCA5)