Molecular basis and genetics of hypohidrotic ectodermal dysplasias

por Kovalskaia, V.A., Cherevatova, T.B., Polyakov, A.V., Ryzhkova, O.P.
Publicado 2023

Mutational Spectrum of Spast (Spg4) and Atl1 (Spg3a) Genes In Russian Patients With Hereditary Spastic Paraplegia

por Kadnikova, V. A., Rudenskaya, G. E., Stepanova, A. A., Sermyagina, I. G., Ryzhkova, O. P.
Publicado 2019

A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy

por Chausova, P. A., Ryzhkova, O. P., Rudenskaya, G. E., Chernykh, V. B., Shchagina, O. A., Polyakov, A. V.
Publicado 2021

Influence of human peripheral blood samples preprocessing on the quality of Hi-C libraries

por Gridina, M.M., Vesna, E., Minzhenkova, M.E., Shilova, N.V., Ryzhkova, O.P., Nazarenko, L.P., Belyaeva, E.O., Lebedev, I.N., Fishman, V.S.
Publicado 2023

KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families

por Rudenskaya, G. E., Kadnikova, V. A., Ryzhkova, O. P., Bessonova, L. A., Dadali, E. L., Guseva, D. S., Markova, T. V., Khmelkova, D. N., Polyakov, A. V.
Publicado 2020