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- DNA Methylation Variations in Familial Female and Male Breast Cancer
- Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
- Blueprint Genetics Charcot-Marie-Tooth Neuropathy
- Next Generation Sequencing (NGS)
- Oxa-Induced Model of Chronic Atopic Dermatitis. Data from Two
- TITLE: Characterization of Neuronal Synaptopodin Reveals a Myosin V-Dependent Mechanism of Synaptopodin Clustering at the Post-Synaptic Sites
- Proteomic Signatures Corresponding to the SS18/SSX Fusion Gene in Synovial Sarcoma
- Neurofilaments As Biomarkers in Neurological Disorders
- Systematic Mutation Analysis in Rare Colorectal Cancer Presenting
- Altered CSNK1E, FABP4 and NEFH Protein Levels in the Dorsolateral Prefrontal Cortex in Schizophrenia
- High-Throughput Genetic Testing in ALS: the Challenging Path of Variant Classification Considering the ACMG Guidelines
- Myelin Proteomics: Molecular Anatomy of an Insulating Sheath
- (12) Patent Application Publication (10) Pub. No.: US 2014/0163118A1 Giuliani Et Al
- Induction of Therapeutic Tissue Tolerance Foxp3 Expression Is
- The 2018 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome) Gisèle Bonne, Francois Rivier, Dalil Hamroun
- Proteome Profile of Peripheral Myelin in Healthy Mice and in a Neuropathy
- Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
- Molecular Classification of Amyotrophic Lateral Sclerosis by Unsupervised Clustering of Gene Expression in Motor Cortex
- Gene Expression Profiling and Functional Studies of Astrocytes in SOD1-Related Amyotrophic Lateral Sclerosis
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- Review Neurofilament Proteins in Neurodegenerative Diseases
- 1 Cryptic Amyloidogenic Elements in the 3`-‐UTR of Neurofilament Genes
- Post Translational Modifications of Milk Proteins in Geographically Diverse
- 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
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- 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
- Supplemental Table III Differentially Regulated Transcripts Between Knockout and Wild-Type Mtecs for Two-Fold Change in Expressi
- Genomic Unity® Neurology Analysis
- NEGATIVE: No Clinically Significant Variants Detected
- Neurofilament Proteins in Brain Diseases