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Sacsin
Environmental Influences on Endothelial Gene Expression
A Reduction in Drp1-Mediated Fission Compromises
Product Description P441-A2 SACS-V01
1 Mutational Heterogeneity in Cancer Akash Kumar a Dissertation
Population Genetics of the Coral Acropora Millepora: Towards a Genomic Predictor of Bleaching
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
Hereditary Spastic Paraplegias: Clinical Spectrum in Sudan, Further Deciphering of the Molecular Bases of Autosomal Recessive Forms and New Genes Emerging
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
393LN V 393P 344SQ V 393P Probe Set Entrez Gene
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
The Cellular Phenotype of the Neurodegenerative Disease Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Distinct Transcriptomes Define Rostral and Caudal 5Ht Neurons
Gadus Morhua) Spleen Transcriptome Response to Intraperitoneal Viral Mimic Injection Tiago S Hori*, a Kurt Gamperl, Marije Booman, Gordon W Nash and Matthew L Rise
The Ataxia Protein Sacsin Is a Functional Co-Chaperone That Protects Against Polyglutamine-Expanded Ataxin-1
Gadus Morhua) Spleen Transcriptome Response to Intraperitoneal Viral Mimic Injection
New Practical Definitions for the Diagnosis of Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay
The Unusual Structure of the Ubiquitin-Like Domain of the Protein
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Sacsin Cotranslational Degradation Causes Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
Sacsin (SACS) (NM 014363) Human Tagged ORF Clone – RC219094 | Origene
Development and Application of Liquid Chromatography and Mass Spectrometry Platforms to Cancer Samples
Anti-Sacsin Antibody (ARG59300)
Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy
Supplementary Table S1 One Hundred Twenty-Six Genes Composing Our Prognostic Index
SACS Gene Sacsin Molecular Chaperone
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Neuromuscular Diseases Due to Chaperone Mutations: a Review and Some New Results
Structure Determination and Biochemical Characterization of Novel Human Ubiquitin-Like Domains
Seascape Genomics Reveals Candidate Molecular Targets of Heat
Supplementary Table 1. a Full List of Cancer Genes