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TNNT3
RESEARCH ARTICLE Body Weight-Dependent Troponin T Alternative Splicing Is Evolutionarily Conserved from Insects to Mammals and I
TNNT3 Rabbit Pab
Snapshot: the Splicing Regulatory Machinery Mathieu Gabut, Sidharth Chaudhry, and Benjamin J
NICU Gene List Generator.Xlsx
A Missense Mutation in the RSRSP Stretch of Rbm20 Causes Dilated
Key Genes Regulating Skeletal Muscle Development and Growth in Farm Animals
Troponin Variants in Congenital Myopathies: How They Affect Skeletal Muscle Mechanics
Cldn19 Clic2 Clmp Cln3
S1 Table Protein
Full Disclosure Forms
Identification of Tumor Mutation Burden-Related Hub Genes and the Underlying Mechanism in Melanoma
First Profiling of Lysine Crotonylation of Myofilament Proteins and Ribosomal
TNNT3 Related Distal Arthrogryposis Type 2B in Hong Kong
The Use of Genetic Analyses and Functional Assays for the Interpretation of Rare Variants in Pediatric Heart Disease
Transcriptional Profiling Reveals Extraordinary Diversity Among
Quantitative Proteome Profiling of Dystrophic Dog Skeletal Muscle
Gene Expression Profiling in the Developing Secondary Palate in The
Sarcomeric Gene Variants and Their Role with Left Ventricular Dysfunction in Background of Coronary Artery Disease
Top View
Integrated Bioinformatics Analysis Reveals Novel Key Biomarkers and Potential Candidate Small Molecule Drugs in Gestational Diabetes Mellitus
Identifying Dynamic Protein and RNA Proximity Interaction Networks of Actinin Reveals RNA
Four Parameters Increase the Sensitivity and Specificity of The
Up-Regulated Genes
Aberrant Alternative Splicing in Skeletal Muscle Of
Gene Expression Profile in Similar Tissues Using Transcriptome Sequencing Data of Whole-Body Horse Skeletal Muscle
Supplementary Table 2
Significant Genes List
Genome-Wide Association Studies in the Japanese Population Identify Seven Novel Loci for Type 2 Diabetes
HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3
Thermoneutrality Induces Skeletal Muscle Myopathy Via Brown Adipose Tissue in an IRF4- and Myostatin-Dependent Manner
Loss of Prox1 in Striated Muscle Causes Slow to Fast Skeletal Muscle Fiber Conversion and Dilated Cardiomyopathy
University of Groningen Matters of the Heart: Genetic and Molecular
Identification and Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis
Adipose Liver Muscle Brain
Extreme Enrichment of VNTR-Associated Polymorphicity In
And Homozygous Loss-Of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
Troponin T1 (TNNT1) Mouse Monoclonal Antibody [Clone ID: TT-98] Product Data