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Publications by Thomas Z. Armel

Mutations at the Same Amino Acid in Myosin That Cause Either Skeletal or Cardiac Myopathy Have Distinct Molecular Phenotypes

Journal of Molecular and Cellular Cardiology

Cardiovascular Medicine

Molecular Biology

English

Related publications

Different Amino Acid Substitutions at the Same Position in Rhodopsin Lead to Distinct Phenotypes

Investigative Ophthalmology and Visual Science

Molecular Neuroscience

Sensory Systems

English

Expression of Myosin Storage Myopathy Mutations in Drosophila Disrupts Skeletal and Cardiac Muscle Structure and Function

Biophysical Journal

English

Mutations in the LHX3 Gene Cause Dysregulation of Pituitary and Neural Target Genes That Reflect Patient Phenotypes

English

The Amino-Acid Composition of Rabbit Myosin

Biochemical Journal

English

Do Bilateral Pleural Effusions Always Have the Same Cause?

European Journal of Case Reports in Internal Medicine

Internal Medicine

English

Partial and Complete SPINK1 Deficiency Cause Distinct Pancreatic Phenotypes

English

Skeletal Myopathy in a Family With Lamin a/C Cardiac Disease

Cardiovascular Diagnosis and Therapy

Cardiovascular Medicine

English

Molecular Pathology of Familial Hypertrophic Cardiomyopathy Caused by Mutations in the Cardiac Myosin Binding Protein C Gene.

Journal of Medical Genetics

English

Protein Structure-Function Relationship at Work: Learning From Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin T

Frontiers in Physiology

English