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MYOT
The Role of Z-Disc Proteins in Myopathy and Cardiomyopathy
Myosin Binding Protein H-Like (MYBPHL): a Promising Biomarker
Multisystem Myotilinopathy, Including Myopathy and Left Ventricular Noncompaction, Due to the MYOT Variant C.179C>T
The Limb-Girdle Muscular Dystrophies and the Dystrophinopathies Review Article
Characterization of the Dysferlin Protein and Its Binding Partners Reveals Rational Design for Therapeutic Strategies for the Treatment of Dysferlinopathies
Myotilin (MYOT) Mouse Monoclonal Antibody [Clone ID: OTI8A7] Product Data
Exome Sequencing Identifies a Novel TTN Mutation in a Family
MYOT Polyclonal Antibody
The Histopathological Features of Muscular Dystrophies
Skeletal Muscle in Aged Mice Reveals Extensive Transformation of Muscle
MYOT Gene Myotilin
ISPD Mutations Account for a Small Proportion of Italian Limb Girdle Muscular Dystrophy Cases
MYOT Antibody (Center) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap17231c
RNA SEQ Analysis Indicates That the AE3 Cl-/HCO3
University of Nevada, Reno INVESTIGATION of the ROLE for TERMINAL SCHWANN CELLS in NEUROMUSCULAR JUNCTION DEVELOPMENT and DISEAS
Protein Aggregate Myopathies
Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
MYOT Antibody Cat
Top View
Autophagy: from Membrane Movement to Nuclear Regulation
Muscle Biopsy Essential Diagnostic Advice for Pathologists Ana Cotta1* , Elmano Carvalho2, Antonio Lopes Da-Cunha-Júnior3, Jaquelin Valicek2, Monica M
MRC Centre for Neuromuscular Diseases PI Publications 2008 – Present
New Names for Limb Girdle Muscular Dystrophies
Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype
Classification of Myopathy
MYOT Polyclonal Antibody Catalog Number:10731-1-AP 4 Publications
The Human Cardiac and Skeletal Muscle Proteomes Defined by Transcriptomics and Antibody-Based Profiling Lindskog Et Al
Studies Into the Structure and Function of Various Domains of Obscurin and Titin Rachel A
Supplementary Data
MYOT Antibody
Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients
Gene Therapy for Muscular Dystrophy
Use of Whole-Exome Sequencing for Diagnosis of Limb-Girdle Muscular Dystrophy: Outcomes and Lessons Learned
Volker Straub Advances in the Limb-Girdle Muscular Dystrophies
Fibroblast Growth Factor 2-Mediated Cardioprotection: the Kinase Mediators and Downstream Targets of FGF2-Induced Protection from Ischemia and Reperfusion Injury
1 SUPPLEMENTARY FILES Mutations in TRIM63 Cause an Autosomal
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