Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Anastasiia Danishevich"'
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, 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:
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:
Maria Makarova, Marina Nemtsova, Anastasiia Danishevich, Denis Chernevskiy, Maxim Belenikin, Anastasiia Krinitsina, Elena Baranova, Olesya Sagaydak, Maria Vorontsova, Igor Khatkov, Lyudmila Zhukova, Natalia Bodunova, Sergey Nikolaev, Mariya Byakhova, Anna Semenova, Vsevolod Galkin, Saida Gadzhieva
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 9; Pages: 7940
More than 275 million people in the world are carriers of a heterozygous mutation of the CFTR gene, associated with cystic fibrosis, the most common autosomal recessive disease among Caucasians. Some recent studies assessed the association between ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e72fe5628b5c0f63bd6fb7a87c2f4c1