Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ruslan Abasov"'
Autor:
Anna Khoreva, MD, Kirill R. Butov, MD, Elena I. Nikolaeva, MD, Alexey Martyanov, PhD, Elena Kulakovskaya, MD, Dmitry Pershin, MD, Maxim Alexenko, MD, Maria Kurnikova, MD, Ruslan Abasov, MD, Elena Raykina, PhD, Dmitry Abramov, MD, Kristina Arnaudova, PhD, Yulia Rodina, PhD, Natalia Trubina, MD, Yulia Skvortsova, PhD, Dmitry Balashov, PhD, Anastasia Sveshnikova, PhD, Alexey Maschan, PhD, Galina Novichkova, PhD, Mikhail Panteleev, PhD, Anna Shcherbina, PhD
Publikováno v:
Journal of Allergy and Clinical Immunology: Global, Vol 3, Iss 1, Pp 100172- (2024)
Background: To date, fewer than 20 patients have been identified as having germline biallelic mutations in the coronin-1A gene (CORO1A) and its protein with clinical features of combined immunodeficiency characterized by T-cell lymphopenia ranging fr
Externí odkaz:
https://doaj.org/article/cdcf224730d14bf088b654de844c66a1
Autor:
Yaroslav Menchits, Tatiana Salimova, Alexander Komkov, Dmitry Abramov, Tatiana Konyukhova, Ruslan Abasov, Elena Raykina, Albert Itov, Marina Gaskova, Aleksandra Borkovskaia, Anna Kazakova, Olga Soldatkina, Svetlana Kashpor, Alexandra Semchenkova, Alexander Popov, Galina Novichkova, Yulia Olshanskaya, Alexey Maschan, Elena Zerkalenkova
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 19, p 14451 (2023)
Simultaneous multilineage hematologic malignancies are uncommon and associated with poorer prognosis than single-lineage leukemia or lymphoma. Here, we describe a concomitant malignant neoplasm in a 4-year-old boy. The child presented with massive ly
Externí odkaz:
https://doaj.org/article/59ab0ba0858f4b1681e7e63c4f1a9c36
Autor:
Yury A. Barbitoff, Ruslan Abasov, Varvara E. Tvorogova, Andrey S. Glotov, Alexander V. Predeus
Publikováno v:
BMC Genomics, Vol 23, Iss 1, Pp 1-17 (2022)
Abstract Background Accurate variant detection in the coding regions of the human genome is a key requirement for molecular diagnostics of Mendelian disorders. Efficiency of variant discovery from next-generation sequencing (NGS) data depends on mult
Externí odkaz:
https://doaj.org/article/e14da3cefc3c451384b518989335e414
Autor:
Ksenia Sinichenkova, Ludmila Yasko, Dmitry Akhaladze, Anton Petrushin, Dmitry Konovalov, Ruslan Abasov, Yulia Mareeva, Olga Melekhina, Natalia Usman, Alexander Karachunsky, Galina Novichkova, Dmitry Litvinov, Alexander Druy
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
IntroductionIn this report we firstly describe undifferentiated embryonal sarcoma of the liver (UESL) in a patient with neurofibromatosis type 1 (NF1), fatally complicated by synchronous malignant peripheral nerve sheath tumor (MPNST) with a highly a
Externí odkaz:
https://doaj.org/article/e9cb42b7641e4110a20e9e35056dd48c
Autor:
Alexandra Semchenkova, Ekaterina Mikhailova, Alexander Komkov, Marina Gaskova, Ruslan Abasov, Evgenii Matveev, Marat Kazanov, Ilgar Mamedov, Anna Shmitko, Vera Belova, Anna Miroshnichenkova, Olga Illarionova, Yulia Olshanskaya, Grigory Tsaur, Tatiana Verzhbitskaya, Natalia Ponomareva, Gleb Bronin, Konstantin Kondratchik, Larisa Fechina, Yulia Diakonova, Liudmila Vavilova, Natalia Myakova, Galina Novichkova, Alexey Maschan, Michael Maschan, Elena Zerkalenkova, Alexander Popov
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 4019 (2022)
We report incidence and deep molecular characteristics of lineage switch in 182 pediatric patients affected by B-cell precursor acute lymphoblastic leukemia (BCP-ALL), who were treated with blinatumomab. We documented six cases of lineage switch that
Externí odkaz:
https://doaj.org/article/f4082722d4c145ceb68d465b8fc7583a
Autor:
Gennady V. Ponomarev, Bulat Fatykhov, Vladimir A. Nazarov, Ruslan Abasov, Evgeny Shvarov, Nina-Vicky Landik, Alexandra A. Denisova, Almira A. Chervova, Mikhail S. Gelfand, Marat D. Kazanov
Publikováno v:
iScience. 25(7)
While somatic mutations are known to be enriched in genome regions with non-canonical DNA secondary structure, the impact of particular mutagens still needs to be elucidated. Here, we demonstrate that in human cancers, the APOBEC mutagenesis is not e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76d4e66d1515ec2561bb836a53041ca7
https://pubmed.ncbi.nlm.nih.gov/35754742
https://pubmed.ncbi.nlm.nih.gov/35754742
Autor:
Nina-Vicky Landik, Ruslan Abasov, Mikhail S. Gelfand, Bulat Fatykhov, Alexandra A. Denisova, Almira Chervova, Gennady V. Ponomarev, Vladimir A. Nazarov, Evgeny Shvarov, Marat D. Kazanov
While somatic mutations are known to be enriched in genome regions with non-canonical DNA secondary structure, the impact of particular mutagens still needs to be elucidated. Here, we demonstrate that in human cancers, the APOBEC mutagenesis is not e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f8164a32bc0d6de8c3cf3e842d7161e
https://doi.org/10.1101/2021.10.12.464135
https://doi.org/10.1101/2021.10.12.464135
