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MYH3
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Communication Pathways in Human Nonmuscle Myosin-2C 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Authors: 25 Krishna Chinthalapudia,B,C,1, Sarah M
Microrna Regulatory Pathways in the Control of the Actin–Myosin Cytoskeleton
A Curated Gene List for Reporting Results of Newborn Genomic Sequencing
Full Disclosure Forms
Premyogenic Progenitors Derived from Human Pluripotent Stem Cells
Chemical Agent and Antibodies B-Raf Inhibitor RAF265
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Download from the GEO Database (Accession Number GSE123879)
Role of 5' UTR MYH3 Variant in Distal Arthrogryposis
Alteration of Gene Expression in Mice After Glaucoma Filtration Surgery
Skeletal Muscle in Aged Mice Reveals Extensive Transformation of Muscle
The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: a Case Series on 12 Children
Transcriptional Profiling Reveals Extraordinary Diversity Among
Regulation of Motor Axon Innervation at the Neuromuscular Junction By
Blueprint Genetics Arthrogryposes Panel
Developmental MYH3 Myopathy Associated with Expression of Mutant Protein and Reduced Expression Levels of Embryonic Myhc
Embryonic Myosin Heavy-Chain Mutations Cause Distal Arthrogryposis and Developmental Myosin Myopathy That Persists Postnatally
Top View
Myosin Heavy Chain-Embryonic Regulates Skeletal Muscle
First Korean Family with a Mutation in Tpm2associated with Sheldon-Hall
Microrna Deep Sequencing in Two Adult Stem Cell Populations
Identification of a Novel Pathogenic Mutation of the MYH3 Gene in A
Transcriptomic Profile of Primary Culture of Skeletal Muscle Cells
Protein-Altering MYH3 Variants Are Associated with a Spectrum of Phenotypes Extending to Spondylocarpotarsal Synostosis Syndrome
MYH3 Antibody Cat
Uva-DARE (Digital Academic Repository)
MYH3 (F1.652): Sc-53091
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
UC Davis UC Davis Previously Published Works
Acute Recurrent Rhabdomyolysis in a Chinese Boy
MYH1/2/3 (N3.36): Sc-53092
Evaluation of Valid Reference Genes During Stimulation with Static Magnetic Fields in Human Myoblast Cultures
A Missense Mutation in MYH1 Is Associated with Susceptibility to Immune-Mediated Myositis in Quarter Horses Carrie J
MYH3 Gene Myosin Heavy Chain 3
Supplementary Information
Molecular Regulation of High Muscle Mass in Developing Blonde D'aquitaine Cattle Fetuses