Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Inna S. Tebieva"'
Autor:
Sofya A. Ionova, Aysylu F. Murtazina, Andrey A. Marakhonov, Olga A. Shchagina, Nina V. Ryadninskaya, Inna S. Tebieva, Vitaly V. Kadyshev, Artem O. Borovikov, Evgeny K. Ginter, Sergey I. Kutsev, Rena A. Zinchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 17, p 9734 (2024)
Myotonic dystrophy type 1 (DM1) is a multisystem disorder with progressive myopathy and myotonia. The clinical study was conducted in the Republic of North Ossetia-Alania (RNOA), and in it 39 individuals from 17 unrelated families were identified wit
Externí odkaz:
https://doaj.org/article/86166c8852db4680a725410044d44bda
Autor:
Inna S. Tebieva, Polina V. Mishakova, Yulia V. Gabisova, Alana V. Khokhova, Tamara G. Kaloeva, Andrey V. Marakhonov, Olga A. Shchagina, Alexander V. Polyakov, Evgeny K. Ginter, Sergey I. Kutsev, Rena A. Zinchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 9, p 4598 (2024)
This study, conducted in the Republic of North Ossetia-Alania (RNOA), aimed to explore the genetic landscape of hyperphenylalaninemia (HPA) and phenylketonuria (PKU) in the Ossetian population using data from newborn screening (NBS). Through comprehe
Externí odkaz:
https://doaj.org/article/934068c12947485a86366cc8dab6da1d
Autor:
Tatyana A. Vasilyeva, Andrey V. Marakhonov, Inna S. Tebieva, Vitaly V. Kadyshev, Artem O. Borovikov, Zhanna G. Markova, Alyona L. Chukhrova, Evgeny K. Ginter, Sergey I. Kutsev, Rena A. Zinchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4515 (2023)
North Caucasus has always been a residence of a lot of different authentic ethnic groups speaking different languages and still living their traditional lifestyle. The diversity appeared to be reflected in the accumulation of different mutations caus
Externí odkaz:
https://doaj.org/article/60755cec364b4c109c627263acc1ad30
Autor:
Sofya A. Ionova, Aysylu F. Murtazina, Inna S. Tebieva, Zalina K. Getoeva, Elena L. Dadali, Polina A. Chausova, Olga A. Shchagina, Andrey V. Marakhonov, Sergey I. Kutsev, Rena A. Zinchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12127 (2022)
Here, we described three affected boys from two unrelated families of Ossetian-Digor origin from the Republic of North Ossetia-Alania who were admitted to the Research Centre for Medical Genetics with unspecified muscular dystrophy. High-throughput s
Externí odkaz:
https://doaj.org/article/0c533f3bbdee4c7a8f2a398ceb394191