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- Enrichment of Phosphorylated Tau (Thr181) and Functionally Interacting Molecules in Chronic Traumatic Encephalopathy Brain-Derived Extracellular Vesicles
- Novel Somatic and Germline Mutations in Cancer Candidate Genes in Glioblastoma, Melanoma, and Pancreatic Carcinoma
- Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
- Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
- Integrated Transcriptomic and Neuroimaging Brain Model Decodes Biological Mechanisms in Aging and Alzheimer's Disease
- S41467-019-13144-Y.Pdf
- Review Article the Role of Nonerythroid Spectrin II in Cancer
- Supplementary Table S1
- Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
- AXL Confers Cell Migration and Invasion by Hijacking a PEAK1-Regulated Focal Adhesion Protein Network
- Supplementary Materials
- Proteomic Study Revealed Cellular Assembly and Lipid Metabolism
- DSF Conference June 2016
- Figure S1. GO and KEGG Pathways, Protein Domains and Cluster Analysis of Crotonylated Proteins in Immunoglobulin a Nephropathy
- Exome Sequencing Identifies a Mutation in The
- Evidence for Compromised Brain Metabolism and Oxidative Stress
- Proteome Profile of Peripheral Myelin in Healthy Mice and in a Neuropathy
- Exome Sequencing Identifies a Mutation in The
- Development and Validation of a Protein-Based Risk Score for Cardiovascular Outcomes Among Patients with Stable Coronary Heart Disease
- Nonsense Mutations in Alpha-II Spectrin in Three Families
- Regulation of Cardiac Conduction and Arrhythmias by Ankyrin/Spectrin-Based Macromolecular Complexes
- Comprehensive Genetic Test Menu
- The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
- The 2021 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
- Tauopathy in the Appswe/PS1ΔE9 Mouse Model of Familial Alzheimer's Disease
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- LY75 Ablation Mediates Mesenchymal-Epithelial Transition (MET)
- Gain-Of-Function Cardiomyopathic Mutations in RBM20 Rewire Splicing Regulation and Re-Distribute Ribonucleoprotein Granules Within Processing Bodies
- Human Periprostatic Adipose Tissue
- Pathogenic SPTBN1 Variants Cause a Novel Autosomal Dominant Neurodevelopmental Syndrome
- 1 Defining New Mechanistic Roles for Αii Spectrin in Cardiac Function And
- Large-Scale Informatic Analysis to Algorithmically Identify Blood Biomarkers of Neurological Damage
- SPTAN1 Expression Predicts Treatment and Survival Outcomes in Colorectal Cancer
- Lung Cancer Cell-Derived Secretome Mediates Paraneoplastic Inflammation and Fibrosis in Kidney in Mice
- Genomic Unity® Neurology Analysis
- Agrin Has a Pathological Role in the Progression of Oral Cancer
- Increased Muscleblind Levels by Chloroquine Treatment Improve Myotonic Dystrophy Type 1 Phenotypes in in Vitro and in Vivo Models
- West Syndrome, Pontocerebellar Hypoplasia, and Hypomyelination in a 6-Month-Old Boy
- Na,K-Atpase and Spectrin Skeleton in Myofibers
- SPTAN1 Encephalopathy: Distinct Phenotypes and Genotypes
- The Extracellular Bone Marrow Microenvironment – a Proteomic Comparison of Constitutive Protein Release by in Vitro Cultured Osteoblasts and Mesenchymal Stem Cells