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MYL3
Identification of the Binding Partners for Hspb2 and Cryab Reveals
Genetic Mutations and Mechanisms in Dilated Cardiomyopathy
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Novel Pathogenic Variants in Filamin C Identified in Pediatric Restrictive Cardiomyopathy
MYL3 Monoclonal ANTIBODY Catalog Number:66286-1-Ig
Illuminating the Divergent Role of Filamin C Mutations in Human Cardiomyopathy
Transcriptomic Uniqueness and Commonality of the Ion Channels and Transporters in the Four Heart Chambers Sanda Iacobas1, Bogdan Amuzescu2 & Dumitru A
Autosomal Recessive Cardiomyopathy and Sudden Cardiac Death Associated with Variants in MYL3
Hypertrophic Cardiomyopathy- Associated Mutations in Genes That Encode Calcium-Handling Proteins
SETD3 Is an Actin Histidine Methyltransferase That Prevents Primary Dystocia
Genetic Cardiomyopathies: the Lesson Learned from Hipscs
DIPPER, a Spatiotemporal Proteomics Atlas of Human Intervertebral Discs
Supplementary Table 2
In Vitro Generation of Functional Murine Heart Organoids Via FGF4
Perturbation of the Titin/MURF1 Signaling Complex Is Associated With
A Pilot Study on Searching for Peri-Nuclear Neun-Positive Cells
Transcriptomic Causal Networks Identified Patterns of Differential Gene Regulation in Human Brain from Schizophrenia Cases Versus Controls
The Use of Genetic Analyses and Functional Assays for the Interpretation of Rare Variants in Pediatric Heart Disease
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Genetic Testing Medical Policy – Genetics
Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients with Familial Hypertrophic Cardiomyopathy
The Role of Sarcomere Gene Mutations in Patients with Idiopathic Dilated Cardiomyopathy
Identifying Cardiac Actinin Interactomes Reveals Sarcomere Crosstalk with RNA-Binding Proteins
Mutations in Filamin C Cause a New Form of Familial Hypertrophic
Systematic Analysis of the Regulatory and Essential Myosin Light Chain Genes: Genetic Variants and Mutations in Hypertrophic Cardiomyopathy
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Hypertrophic Cardiomyopathy (Type 1–14)
Clinical Considerations for a Family with Dilated Cardiomyopathy, Sudden Cardiac Death, and a Novel TTN Frameshift Mutation
Inguinal Ring RNA Sequencing Reveals Downregulation of Muscular Genes Related to Scrotal Hernia in Pigs
Electronic Letter Myosin Light Chain Mutations in Familial Hypertrophic Cardiomyopathy
A Proteomic View of Isoproterenol
Differential Expression of Innate and Adaptive Immune Genes in the Survivors of Three Gibel Carp Gynogenetic Clones After Herpes
Cardiac Next-Generation Sequencing Panels
Analysis of 51 Proposed Hypertrophic Cardiomyopathy Genes from Genome Sequencing Data in Sarcomere Negative Cases Has Negligible Diagnostic Yield
Mutation P.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Implications for Genetic Testing and Counselling J Ingles, a Doolan, C Chiu, J Seidman, C Seidman, C Semsarian
Transcriptome Profiling Analysis of Muscle Tissue Reveals