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STAC3
Investigation of Functional Genes at Homologous Loci Identified Based
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Mining Public Toxicogenomic Data Reveals Insights and Challenges in Delineating Liver Steatosis Adverse Outcome Pathways
The Genomic and Clinical Landscape of Fetal Akinesia
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Stac3 Is a Component of the Excitation&Ndash
High Motivation for Exercise Is Associated with Altered Chromatin Regulators of Monoamine Receptor Gene Expression in the Striatum of Selectively Bred Mice
Investigating the Effect of Chronic Activation of AMP-Activated Protein
Hypermethylation of Human DNA: Fine-Tuning Transcription Associated with Development
Supplementary Material Localizing Regions in the Genome
STAC3 Variants Cause a Congenital Myopathy with Distinctive Dysmorphic Features and Malignant Hyperthermia Susceptibility
The Diagnostic Workup in Children with Arthrogryposis Multiplex Congenita: Description of Practices Through a Monocentric Cohort
Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
UI Health Care Letterhead Template
Downloaded Chip-Seq Data with Non-Synchronized Myoblasts Did Not Show a Specific Increase Or
Evolutionarily Conserved Regulation of Embryonic Fast-Twitch Skeletal Muscle
1 Imipramine Treatment and Resiliency Exhibit Similar
Gene Ontology Analysis of Arthrogryposis (Multiple Congenital Contractures)
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Degenerative and Regenerative Pathways Underlying Duchenne Muscular Dystrophy Revealed by Single-Nucleus RNA Sequencing
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Mouse Stac3 Conditional Knockout Project (CRISPR/Cas9)
Genetic Variants Underlying Cognitive Ability Gosso, M.F
STAC3 Gene SH3 and Cysteine Rich Domain 3
STAC3 Polyclonal Antibody
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun