Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irina V. Naumchik"'
Autor:
Svetlana O. Sharapova, Olga E. Pashchenko, Anastasiia V. Bondarenko, Svetlana S. Vakhlyarskaya, Tatjana Prokofjeva, Alina S. Fedorova, Ihor Savchak, Yuliya Mareika, Timur T. Valiev, Alexander Popa, Irina A. Tuzankina, Elena V. Vlasova, Inga S. Sakovich, Ekaterina A. Polyakova, Natalia V. Rumiantseva, Irina V. Naumchik, Svetlana A. Kulyova, Svetlana N. Aleshkevich, Elena I. Golovataya, Nina V. Minakovskaya, Mikhail V. Belevtsev, Elena A. Latysheva, Tatiana V. Latysheva, Alexander G. Beznoshchenko, Hayane Akopyan, Halyna Makukh, Olena Kozlova, Dzmitry S. Varabyou, Mark Ballow, Mei-Sing Ong, Jolan E. Walter, Irina V. Kondratenko, Larysa V. Kostyuchenko, Olga V. Aleinikova
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
Nijmegen breakage syndrome (NBS) is a DNA repair disorder characterized by combined immunodeficiency and a high predisposition to lymphoid malignancies. The majority of NBS patients are identified with a homozygous five base pair deletion in the Nibr
Externí odkaz:
https://doaj.org/article/e6926b6147044ceab5e302498150276d
Autor:
Ihor Savchak, Irina A. Tuzankina, E.A. Latysheva, Halyna Makukh, Anastasiia Bondarenko, Mikhail Belevtsev, Inga S. Sakovich, Elena I. Golovataya, Svetlana A. Kulyova, Larysa Kostyuchenko, Jolan E. Walter, Alexander Popa, Dzmitry S. Varabyou, Natalia V. Rumiantseva, Mei-Sing Ong, Alexander G. Beznoshchenko, Svetlana S. Vakhlyarskaya, Mark Ballow, Ekaterina A. Polyakova, Olga E. Pashchenko, Olga Aleinikova, Yuliya Mareika, Svetlana Aleshkevich, Elena V. Vlasova, Olena Kozlova, Svetlana O. Sharapova, Irina V. Naumchik, Nina V. Minakovskaya, Hayane Akopyan, Timur T. Valiev, Alina Fedorova, Tatjana Prokofjeva, Tatiana V. Latysheva, Irina Kondratenko
Publikováno v:
Front. Immunol.
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2021)
Frontiers in Immunology
Frontiers in Immunology, Vol 11 (2021)
Nijmegen breakage syndrome (NBS) is a DNA repair disorder characterized by combined immunodeficiency and a high predisposition to lymphoid malignancies. The majority of NBS patients are identified with a homozygous five base pair deletion in the Nibr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ea6704d815be19bddc3bbc8a9ce8b98
https://www.frontiersin.org/articles/10.3389/fimmu.2020.602482/pdf
https://www.frontiersin.org/articles/10.3389/fimmu.2020.602482/pdf
Autor:
Svetlana O, Sharapova, Olga E, Pashchenko, Anastasiia V, Bondarenko, Svetlana S, Vakhlyarskaya, Tatjana, Prokofjeva, Alina S, Fedorova, Ihor, Savchak, Yuliya, Mareika, Timur T, Valiev, Alexander, Popa, Irina A, Tuzankina, Elena V, Vlasova, Inga S, Sakovich, Ekaterina A, Polyakova, Natalia V, Rumiantseva, Irina V, Naumchik, Svetlana A, Kulyova, Svetlana N, Aleshkevich, Elena I, Golovataya, Nina V, Minakovskaya, Mikhail V, Belevtsev, Elena A, Latysheva, Tatiana V, Latysheva, Alexander G, Beznoshchenko, Hayane, Akopyan, Halyna, Makukh, Olena, Kozlova, Dzmitry S, Varabyou, Mark, Ballow, Mei-Sing, Ong, Jolan E, Walter, Irina V, Kondratenko, Larysa V, Kostyuchenko, Olga V, Aleinikova
Publikováno v:
Frontiers in Immunology
Nijmegen breakage syndrome (NBS) is a DNA repair disorder characterized by combined immunodeficiency and a high predisposition to lymphoid malignancies. The majority of NBS patients are identified with a homozygous five base pair deletion in the Nibr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::07bb64b76511e1b8ee8669a35905644f
https://pubmed.ncbi.nlm.nih.gov/33488600
https://pubmed.ncbi.nlm.nih.gov/33488600
Autor:
Anna D, Polityko, Olga M, Khurs, Anna I, Kulpanovich, Konstantin A, Mosse, Angelica V, Solntsava, Natalia V, Rumyantseva, Irina V, Naumchik, Thomas, Liehr, Anja, Weise, Hasmik, Mkrtchyan
Publikováno v:
European journal of medical genetics. 52(4)
An unusual mosaic karyotype was detected in a 6-year-old female patient with clinical diagnosis of Turner syndrome (TS). Cytogenetic and molecular cytogenetic studies revealed besides a cell line with 45,X a second cell line where the short arm of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcb26d05f84fdae67c3d16e6406bfb8c
https://pubmed.ncbi.nlm.nih.gov/19375526
https://pubmed.ncbi.nlm.nih.gov/19375526