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Torsin A
Candidate Chromosome 1 Disease Susceptibility Genes for Sjogren's Syndrome Xerostomia Are Narrowed by Novel NOD.B10 Congenic Mice P
Human Social Genomics in the Multi-Ethnic Study of Atherosclerosis
The Genetics of Primary Dystonias and Related Disorders
TOR1A Gene Torsin Family 1 Member A
Using Zebrafish As a Model System for Dyt1 Dystonia
Transcriptional Regulators Are Upregulated in the Substantia Nigra
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
Whole Exome Sequencing Identifies Novel DYT1 Dystonia- 2 Associated Genome Variants As Potential Disease Modifiers 3 4 Chih-Fen Hu1*, G
WIRING of PRESYNAPTIC INHIBITORY CIRCUITRY in the MOUSE SPINAL CORD a Dissertation Presented to the Faculty of the Weill Cornell
Genetics of Movement Disorders and Ataxia *
The TOR1A (DYT1) Gene Family and Its Role in Early Onset Torsion Dystonia Laurie J
Commentary Mitochondria and Dystonia: the Movement Disorder
Novel 9Q34.11 Gene Deletions Encompassing Combinations of Four Mendelian Disease Genes: STXBP1, SPTAN1, ENG, and TOR1A
Identification of Genes Modulated in Rheumatoid Arthritis Using
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Invertebrate Models of Dystonia
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Cellular Distribution of Torsin a and Torsin B in Normal Human Brain
Top View
The Pathogenic Human Torsin a in Drosophila Activates the Unfolded
The 2018 Version of the Gene Table of Monogenic Neuromuscular Disorders (Nuclear Genome) Gisèle Bonne, Francois Rivier, Dalil Hamroun
PDF Datasheet
DYT1 Dystonia Patient-Derived Fibroblasts Have Increased Deformability and Susceptibility to Damage by Mechanical Forces
Lineage-Specific Programming Target Genes Defines Potential for Th1
DYT1 Dystonia Patient-Derived Fibroblasts Have Increased Deformability and Susceptibility to Damage by Mechanical Forces
Function of Torsin AAA+ Atpases in Pseudorabies Virus Nuclear Egress
Sirna Screen Identifies QPCT As a Druggable Target For
Suppementary Table 9. Predicted Targets of Hsa-Mir-181A by Targetscan 6.2
Genetics of Dystonia
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
LULL1 Retargets Torsina to the Nuclear Envelope Revealing an Activity That Is Impaired by the DYT1 Dystonia Mutation Abigail B
Cellular Distribution of Torsin a and Torsin B in Normal Human Brain
PTCH1 Pathway Network Model in Diffuse-Type Gastric Cancer And
Supplementary Table 1. a Full List of Cancer Genes
Whole Exome Sequencing Identifies Novel DYT1 Dystonia-Associated
Reviews Risk Factor Genes in Patients with Dystonia: a Comprehensive Review