Elina Lemola

K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity

Nancy Mokbel, Biljana Ilkovski, Michaela Kreissl et al. · Brain · 2013 · 53 citations · Full text

Myofibre Calcium Sensitivity, Genetics, Pathology +19

Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in <i>TPM2</i>-related nemaline and cap myopathy

M. Marttila, Elina Lemola, William Wallefeld et al. · Biochemical Journal · 2011 · 52 citations · Full text

Muscle Function, Pathology, Cytoskeleton +27

Nebulin interactions with actin and tropomyosin are altered by disease-causing mutations

M. Marttila, Mubashir Hanif, Elina Lemola et al. · Skeletal Muscle · 2014 · 50 citations · Full text

Profiling of low molecular weight proteins in plasma from locally irradiated individuals

R Nylund, Elina Lemola, Sonja Hartwig et al. · Journal of Radiation Research · 2014 · 23 citations · Full text

Genome Instability, Dna Damage, Biochemistry +15