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Ataxin 10
Design of a Bioactive Small Molecule That Targets R(AUUCU) Repeats in Spinocerebellar Ataxia 10
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Differentially Expressed on Collagen Networks 1, 2, 10 © 2000-2009 Ingenuity Systems, Inc. All Rights Reserved. Symbol Entrez
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Autosomal Dominant Cerebellar Ataxia Type I: a Review of the Phenotypic and Genotypic Characteristics
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A Master Autoantigen-Ome Links Alternative Splicing, Female Predilection, and COVID-19 to Autoimmune Diseases
50 Clinical Neurogenetics Brent L
Molecular Evidence for Mitochondrial Dysfunction in Bipolar Disorder
Genetic Variation and Functional Analysis of the Cardiomedin Gene
Sheet1 Page 1 Gene Symbol Gene Description Entrez Gene ID
An Autoantigen-Ome from HS-Sultan B-Lymphoblasts Offers a Molecular Map for Investigating Autoimmune Sequelae of COVID-19
Intrinsic Disorder in Proteins with Pathogenic Repeat Expansions
A Master Autoantigen-Ome Links Alternative Splicing, Female Predilection, and COVID-19 to Autoimmune Diseases
Molecular Genetic Characterization of Ataxic Movement Disorders in Mouse and Human
1 Supplementary Material Figure S1. Volcano Plot of Differentially
A Transcriptional Signature of Postmitotic Maintenance in Neural Tissues
Motor Performances of Spontaneous and Genetically Modified Mutants with Cerebellar Atrophy
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Repeats Are Associated with Aberrant Replication at the ATX10 Locus and R
Multi-Scale Systems Genomics Analysis Predicts Pathways, Cell Types and Drug Targets Involved in Normative Human Cognition Varia
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Systematic Genome-Wide Screening and Prediction of Micrornas in EBOV During the 2014 Ebolavirus Outbreak
Gene Expression Profiling Predicts Response to Temozolomide in Malignant Gliomas
Modeling Microcephaly Caused by Inactivation of the Minor
Ataxic Disorders
Ataxic Disorders
Spinocerebellar Ataxias
Systematic Interaction Mapping Reveals Novel Modifiers of Neurodegenerative Disease Processes
Aurora B-Dependent Phosphorylation of Ataxin-10 Promotes The
22Q13.2Q13.32 Genomic Regions Associated with Severity of Speech Delay, Developmental Delay, and Physical Features in Phelan–Mcdermid Syndrome