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MYPN
The Role of Z-Disc Proteins in Myopathy and Cardiomyopathy
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Effect of Nebulin Variants on Nebulin-Actin Interaction
MYC Acts Via the PTEN Tumor Suppressor to Elicit Autoregulation and Genome-Wide Gene Repression by Activation of the Ezh2 Methyltransferase
Novel Trigenic CACNA1C/DES/MYPN Mutations in a Family of Hypertrophic Cardiomyopathy with Early Repolarization and Short QT Synd
Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach
Myopalladin Gene Polymorphism Is Associated with Rabbit Meat Quality Traits
Changes in Gene Methylation Patterns in Neonatal Murine Hearts
Setd1 Histone 3 Lysine 4 Methyltransferase Complex Components in Epigenetic Regulation
(B6;129.Cg-Gt(ROSA)26Sor Tm20(CAG-Ctgf-GFP)Jsd) Were Crossed with Female Foxd1cre/+ Heterozygote Mice 1, and Experimental Mice Were Selected As Foxd1cre/+; Rs26cig/+
UC Davis UC Davis Previously Published Works
Targeted Next-Generation Sequencing of Candidate Genes Reveals Novel Mutations in Patients with Dilated Cardiomyopathy
Identifying Cardiac Actinin Interactomes Reveals Sarcomere Crosstalk with RNA-Binding Proteins
Identification and Functional Characterization of Novel Genes Implicated in Congenital Myopathies Xavière Lornage
MYPN Rabbit Pab
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Abstracts from the 50Th European Society of Human Genetics Conference: Oral Presentations
Nemaline Myopathy with Dilated Cardiomyopathy and Severe Heart Failure: a Case Report
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Genetic Variants and Pathways Implicated in a Pediatric Inflammatory Bowel Disease Cohort
Network-Based Stratification of Tumor Mutations
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication ARUP Test Code 2010183 Cardiomyopathy/Arrhythmia Panel Specimen Whole Blood
Inherited Cardiovascular Diseases and Sudden Cardiac Death to Provide an Exhaustive Study of Genes
Cardiac Ankyrin Repeat Protein Gene (ANKRD1) Mutations in Hypertrophic Cardiomyopathy
Supplementary Appendix
Evolutionarily Conserved Regulation of Embryonic Fast-Twitch Skeletal Muscle
World Journal of Cardiology
1Μm–20Μm) in the ARPE19 and RF/6A Cells Measured by the MTS Method
Cardiac Next-Generation Sequencing Panels
PDF Output of CLIC (Clustering by Inferred Co-Expression)
Testing of Therapies in a Novel Nebulin Nemaline Myopathy Model Demonstrate a Lack of Efficacy Tamar E
Mutation P.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
Nemaline Rod/Cap Myopathy Due to Novel Homozygous Mypnmutations
Identification of Atrial Fibrillation-Associated Genes
Nebulin Nemaline Myopathy Recapitulated in a Compound Heterozygous Mouse Model with Both a Missense and a Nonsense Mutation in Neb Jenni M
1 KLF2 and KLF4 Control Endothelial Identity and Vascular Integrity
The Role of Myopalladin in Muscle Function and Disease