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MYOZ2
Anti-MYOZ2 (GW22350F)
Mutations in MYOZ1 As Well As MYOZ2 Encoding the Calsarcins Are Not Associated with Idiopathic and Familial Dilated Cardiomyopathy
Discovery and Systematic Characterization of Risk Variants and Genes For
Cardiomyocyte-Specific Deletion of Orai1 Reveals Its Protective Role in Angiotensin-II-Induced Pathological Cardiac Remodeling
Genotype-Related Clinical Characteristics and Myocardial Fibrosis and Their Association with Prognosis in Hypertrophic Cardiomyopathy
PPP3CA Antibody (C-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap13757b
Table SI. Differentially Expressed Genes. Gene Logfc Aveexpr T Value
Review Article
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Calsarcin-2 Deficiency Increases Exercise Capacity in Mice Through Calcineurin/NFAT Activation
Hypertrophic Cardiomyopathy (Type 1–14)
Mono- and Bi-Allelic Protein Truncating Variants in Alpha-Actinin 2 Cause Cardiomyopathy Through Distinct Mechanisms
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
Exercise and the Cisd2 Prolongevity Gene: Two Promising Strategies to Delay the Aging of Skeletal Muscle
Supplementary Appendix
Myozenin-2 Recombinant Protein Cat
Evolutionarily Conserved Regulation of Embryonic Fast-Twitch Skeletal Muscle
Top View
Mutations in MYOZ1 As Well As MYOZ2 Encoding
Multi-Scale Analysis of Schizophrenia Risk Loci: Integrating Centenarian Genomes And
Genome-Wide Association Study Provides New Insights Into the Genetic Architecture and Pathogenesis of Heart Failure
Molecular Cloning and Characterization of Different Expression of MYOZ2 and MYOZ3 in Tianfu Goat
Association of Variation in ACTN3, MYOZ2 and MYOZ3 with Complex Quantitative
Science Inside – the National Genome Research Network
Platform Abstracts
Mutations in PDLIM5 Are Rare in Dilated Cardiomyopathy but Are Emerging As Potential Disease Modifiers
USING RNA-SEQ to CHARACTERIZE the BIOLOGICAL BASIS of VARIATION in FEED EFFICIENCY in BROILER CHICKENS by Nan Zhou a Thesis Su
(MYOZ2) (NM 016599) Human Tagged ORF Clone Lentiviral Particle Product Data
And Homozygous Loss-Of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
Human PPP3CA / Protein Phosphatase 2B Protein (His Tag)
Dilated Cardiomyopathy: New Variant in the Filamin-C Gene
Differential Expression of Calsarcin Genes in Orthognathic Surgery Patietns with Actn3 R577x Gene Deviations
Identification of MYOM2 As a Candidate Gene in Hypertrophic Cardiomyopathy and Tetralogy of Fallot and Its Functional Evaluation in the Drosophila Heart
Evidence for Association of Schizophrenia with Genetic Variation in the 8P21.3 Gene, PPP3CC, Encoding the Calcineurin Gamma Subunit
Expanded Panels Offer Limited Additional Sensitivity
Z-Disc Genes in Hypertrophic Cardiomyopathy