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Actinin alpha 2
Anti-ACTN2 Monoclonal Antibody, Clone FQ3630Z (DCABH-9438) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Genetic Cardiomyopathies: the Lesson Learned from Hipscs
Final Draft Masterthesis Gabbin
Induction of Therapeutic Tissue Tolerance Foxp3 Expression Is
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Program in Human Neutrophils Fails To
Advanced Evolution of Pathogenesis Concepts in Cardiomyopathies
ALLEN Human Brain Atlas
Detecting Disease Genes Based on Semi-Supervised Learning and Protein–Protein
1 SUPPLEMENTARY TABLES Table S1. Membrane, Cytoskeletal, And
Advancing Molecular Diagnostics in Sudden Unexplained Deaths
Somatic Mutations
Supplemental Material
Genetics and Molecular Pathogenesis of Non-Ischemic Cardiomyopathies”
Exome Sequencing Identifies a Mutation in The
MOMA Heart Panel V4 (2018-08-15), 102 Genes
The Molecular Mechanisms of Testosterone Depletion During Skeletal Myogenesis Connor Geraghty Honors Thesis College of Arts
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Yield of Rare Variants Detected by Targeted Next-Generation Sequencing in a Cohort of Romanian Index Patients with Hypertrophic Cardiomyopathy
Anti-Sarcomeric Actinin Alpha 2 / ACTN2 Monoclonal Antibody(Clone: ACTN2/3291)
Actinin Alpha 2 Antibody / Sarcomeric Alpha Actinin / ACTN2 [Clone ACTN2/3295] (V8189)
Actinin Alpha 2 (ACTN2) Organism: Mus Musculus (Mouse) Instruction Manual
Exome Sequencing Identifies a Mutation in The
Development of a Label‒Free Nanolc/Ms/Ms Assay for Monitoring the Changes in the Proteomic Landscape of Thrombin‒Activated Human Platelets
Structural Characterization of Two Different F- Actin Cross-Linking Proteins by Electron Microscopy Cheri M
PDF-Document
Table S7. List of Differentially Expressed Genes That Were
Gene Protein Inheritance Disease Association ACTC1 Actin, Alpha, Cardiac Muscle AD CHD, DCM, HCM, LVNC
Legends of Supplementary Figure
The Mutations Associated with Dilated Cardiomyopathy
Responsive Nuclear Proteins in Collecting Duct Cells
Causes and Consequences of Dilated Cardiomyopathy
Supplementary Table S2. in Vitro and in Vivo Growth Analyses
Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome 1