Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins

por KOSTAREVA, A., SJOBERG, G., GUDKOVA, A., SMOLINA, N., SEMERNIN, E., SHLYAKHTO, E., SEJERSEN, T.
Publicado 2011

Polymorphisms of β1-Adrenoreceptor Gene and Cardiovascular Complications in Patients with Thyrotoxicosis

por Babenko, A. Y., Grineva, E. N., Savitskaja, D. A., Kravchuk, E. N., Solncev, V. N., Kostareva, A. A.
Publicado 2014

A Randomised, Controlled Study of Different Glycaemic Targets during Gestational Diabetes Treatment: Effect on the Level of Adipokines in Cord Blood and ANGPTL4 Expression in Human...

por Popova, P., Vasilyeva, L., Tkachuck, A., Puzanov, M., Golovkin, A., Bolotko, Y., Pustozerov, E., Vasilyeva, E., Li, O., Zazerskaya, I., Dmitrieva, R., Kostareva, A., Grineva, E.
Publicado 2018

Desmin mutations impact the autophagy flux in C2C12 cell in mutation-specific manner

por Sukhareva, K. S., Smolina, N. A., Churkina, A. I., Kalugina, K. K., Zhuk, S. V., Khudiakov, A. A., Khodot, A. A., Faggian, G., Luciani, G. B., Sejersen, T., Kostareva, A. A.
Publicado 2023

Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood

por Muravyev, A., Vershinina, T., Tesner, P., Sjoberg, G., Fomicheva, Yu., Čajbiková, N. Novák, Kozyreva, A., Zhuk, S., Mamaeva, E., Tarnovskaya, S., Jornholt, J., Sokolnikova, P., Pervunina, T., Vasichkina, E., Sejersen, T., Kostareva, A.
Publicado 2022

Skeletal Muscle Resident Progenitor Cells Coexpress Mesenchymal and Myogenic Markers and Are Not Affected by Chronic Heart Failure-Induced Dysregulations

por Dmitrieva, R. I., Lelyavina, T. A., Komarova, M. Y., Galenko, V. L., Ivanova, O. A., Tikanova, P. A., Khromova, N. V., Golovkin, A. S., Bortsova, M. A., Sergushichev, A., Sitnikova, M. Yu., Kostareva, A. A.
Publicado 2019