Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Airat Bilyalov"'
Autor:
Alina Bilyalova, Airat Bilyalov, Nikita Filatov, Elena Shagimardanova, Andrey Kiyasov, Maria Vorontsova, Oleg Gusev
Publikováno v:
Laboratory Animal Research, Vol 40, Iss 1, Pp 1-11 (2024)
Abstract The study of adrenal disorders is a key component of scientific research, driven by the complex innervation, unique structure, and essential functions of the adrenal glands. This review explores the use of non-traditional animal models for s
Externí odkaz:
https://doaj.org/article/95da2d6437c7406c8fe39bbc6e080996
Autor:
Alina Bilyalova, Elena Shagimardanova, Airat Bilyalov, Marina Zaripova, Leyla Shigapova, Guzel Gazizova, Pavel Mazin, Bukina Tatiana, Oleg Gusev
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
Tay-Sachs disease (TSD) is a rare genetic disorder with diverse clinical manifestations, often leading to underdiagnosis due to symptom similarities with other neurological conditions. In this study, we aimed to identify the genetic mutations underly
Externí odkaz:
https://doaj.org/article/17f82b761ae244f797dd3a8257f9f58d
Autor:
Anastasiia Danishevich, Anzhelika Chegodar, Natalia Bodunova, Fedor Konovalov, Maria Nefedova, Natalya Kremneva, Nizhat Kurbanov, Airat Bilyalov, Sergey Nikolaev, Igor Khatkov, Galina Dudina
Publikováno v:
Life, Vol 14, Iss 5, p 637 (2024)
Myelodysplastic syndrome (MDS) is a clonal disease derived from hematopoietic stem cells, characterized by ineffective hematopoiesis (resulting in peripheral blood cytopenia) and an increased risk of transformation into acute myeloid leukemia. MDS is
Externí odkaz:
https://doaj.org/article/141509cf58024103bd58f1d1160d66c6
Autor:
Angelina Titova, Sergey Nikolaev, Airat Bilyalov, Nikita Filatov, Sergei Brovkin, Dmitrii Shestakov, Igor Khatkov, Ekaterina Pismennaya, Vyacheslav Bondarev, Margarita Antyuxina, Elena Shagimardanova, Natalia Bodunova, Oleg Gusev
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 9, p 4985 (2024)
The extraocular muscles (EOMs) possess unique characteristics that set them apart from other skeletal muscles. These muscles, responsible for eye movements, exhibit remarkable resistance to various muscular dystrophies and aging, presenting a signifi
Externí odkaz:
https://doaj.org/article/dcfb52c6fba44f4ca2e797ee2cdba9d4
Autor:
Airat Bilyalov, Sergey Nikolaev, Anastasiia Danishevich, Igor Khatkov, Komron Makhmudov, Zhainagul Isakova, Nurbek Bakirov, Ernis Omurbaev, Alena Osipova, Ramaldan Ramaldanov, Elena Shagimardanova, Andrey Kiyasov, Oleg Gusev, Natalia Bodunova
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 8, Pp 6383-6394 (2023)
Gastric cancer is a major challenge in modern oncology due to its high detection rate and prevalence. While sporadic cases make up the majority of gastric cancer, hereditary gastric cancer is caused by germline mutations in several genes linked to di
Externí odkaz:
https://doaj.org/article/1009827571844f7f91be537b15ce0a10
Autor:
Anastasiia Danishevich, Airat Bilyalov, Sergey Nikolaev, Nodirbec Khalikov, Daria Isaeva, Yuliya Levina, Maria Makarova, Marina Nemtsova, Denis Chernevskiy, Olesya Sagaydak, Elena Baranova, Maria Vorontsova, Mariya Byakhova, Anna Semenova, Vsevolod Galkin, Igor Khatkov, Saida Gadzhieva, Natalia Bodunova
Publikováno v:
Biomedicines, Vol 11, Iss 12, p 3343 (2023)
Malignant neoplasms, including pancreatic cancer and melanoma, are major global health challenges. This study investigates melanoma pancreatic syndrome, a rare hereditary tumor syndrome associated with CDKN2A gene mutations. CDKN2A mutations contribu
Externí odkaz:
https://doaj.org/article/b39a07ce5d0847f2b2d949d1348c5726
Autor:
Airat Bilyalov, Sergey Nikolaev, Leila Shigapova, Igor Khatkov, Anastasia Danishevich, Ludmila Zhukova, Sergei Smolin, Marina Titova, Tatyana Lisica, Natalia Bodunova, Elena Shagimardanova, Oleg Gusev
Publikováno v:
Biology, Vol 11, Iss 10, p 1461 (2022)
Background: Approximately 5–10% of all cancers are associated with hereditary cancer predisposition syndromes (HCPS). Early identification of HCPS is facilitated by widespread use of next-generation sequencing (NGS) and brings significant benefits
Externí odkaz:
https://doaj.org/article/c83237aaf0b448f1b4dfad5be63a497a
Autor:
Natalia Bodunova, Maria Vorontsova, Igor Khatkov, Elena Baranova, Svetlana Bykova, Daniil Degterev, Maria Litvinova, Airat Bilyalov, Maria Makarova, Olesya Sagaydak, Anastasia Danishevich
Publikováno v:
Diagnostics, Vol 12, Iss 8, p 1887 (2022)
Introduction: Vulto-van Silfhout-de Vries Syndrome (VSVS; OMIM#615828) is a rare hereditary disease associated with impaired intellectual development and speech, delayed psychomotor development, and behavioral anomalies, including autistic behavioral
Externí odkaz:
https://doaj.org/article/1aca38c801c248f380c386a6db7248ab
Autor:
Vera Polyakova, Natalia Bodunova, Konstantin Rumyantsev, Igor Khatkov, Dmitry Bordin, Airat Bilyalov, Philipp Sviridov, Tatiana Yanova
Publikováno v:
BioNanoScience. 13:322-329
Autor:
Natalia Bodunova, Anna Akopova, Andrey Karmadonov, Olga Mikheeva, Airat Bilyalov, Galina Dudina, Konstantin Lesko, Evgeniy Kharlamenkov, Maria Litvinova
Publikováno v:
BioNanoScience. 12:302-306