A new case of 17p13.3p13.1 microduplication resulted from unbalanced translocation: clinical and molecular cytogenetic characterization

por Markova, Zhanna G., Minzhenkova, Marina E., Bessonova, Lyudmila A., Shilova, Nadezda V.
Publicado 2021

Previously Undescribed Gross HACE1 Deletions as a Cause of Autosomal Recessive Spastic Paraplegia

por Kovalskaia, Valeriia A., Zabnenkova, Victoriia V., Petukhova, Marina S., Markova, Zhanna G., Tabakov, Vyacheslav Yu., Ryzhkova, Oxana P.
Publicado 2022

Clinical Manifestations of Various Molecular Cytogenetic Variants of Eight Cases of “8p Inverted Duplication/Deletion Syndrome”

por Yurchenko, Darya A., Minzhenkova, Marina E., Dadali, Elena L., Markova, Zhanna G., Rudenskaya, Galina E., Matyushchenko, Galina N., Kanivets, Ilya V., Shilova, Nadezda V.
Publicado 2022

Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia–Alania, Case Series Report

por Vasilyeva, Tatyana A., Marakhonov, Andrey V., Tebieva, Inna S., Kadyshev, Vitaly V., Borovikov, Artem O., Markova, Zhanna G., Chukhrova, Alyona L., Ginter, Evgeny K., Kutsev, Sergey I., Zinchenko, Rena A.
Publicado 2023

A cookbook for DNase Hi-C

por Gridina, Maria, Mozheiko, Evgeniy, Valeev, Emil, Nazarenko, Ludmila P., Lopatkina, Maria E., Markova, Zhanna G., Yablonskaya, Maria I., Voinova, Viktoria Yu, Shilova, Nadezhda V., Lebedev, Igor N., Fishman, Veniamin
Publicado 2021

Trisomies Reorganize Human 3D Genome

por Zhegalova, Irina V., Vasiluev, Petr A., Flyamer, Ilya M., Shtompel, Anastasia S., Glazyrina, Eugene, Shilova, Nadezda, Minzhenkova, Marina, Markova, Zhanna, Petrova, Natalia V., Dashinimaev, Erdem B., Razin, Sergey V., Ulianov, Sergey V.
Publicado 2023

An Exposure to the Oxidized DNA Enhances Both Instability of Genome and Survival in Cancer Cells

por Kostyuk, Svetlana V., Konkova, Marina S., Ershova, Elizaveta S., Alekseeva, Anna J., Smirnova, Tatiana D., Stukalov, Sergey V., Kozhina, Ekaterina A., Shilova, Nadezda V., Zolotukhina, Tatiana V., Markova, Zhanna G., Izhevskaya, Vera L., Baranova, Ancha, Veiko, Natalia N.
Publicado 2013

A sporadic case of congenital aniridia caused by pericentric inversion inv(11)(p13q14) associated with a 977 kb deletion in the 11p13 region

por Vasilyeva, Tatyana A., Marakhonov, Andrey V., Minzhenkova, Marina E., Markova, Zhanna G., Petrova, Nika V., Sukhanova, Natella V., Koshkin, Philipp A., Pyankov, Denis V., Kanivets, Ilya V., Korostelev, Sergey A., Krynskaya, Irina A., Shilova, Nadezhda V., Kutsev, Sergey I., Kadyshev, Vitaly V., Zinchenko, Rena A.
Publicado 2020