Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Inga S, Sakovich"'
Autor:
Tatiana P. Volodashchik, Ekaterina A. Polyakova, Taisia M. Mikhaleuskaya, Inga S. Sakovich, Aleksandra N. Kupchinskaya, Aliaxandr Ch. Dubrouski, Mikhail V. Belevtsev, Joseph F. Dasso, Dzmitry S. Varabyou, Luigi D. Notarangelo, Jolan E. Walter, Svetlana O. Sharapova
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Background and aimsThere is an increased risk of lymphomas in inborn errors of immunity (IEI); however, germline genetic testing is rarely used in oncological patients, even in those with early onset of cancer. Our study focuses on a child with a rec
Externí odkaz:
https://doaj.org/article/8c241992931f46a18da198fed8fd890f
Autor:
Anastasiia V. Bondarenko, Oksana R. Boyarchuk, Inga S. Sakovich, Ekaterina A. Polyakova, Alexander A. Migas, Aleksandra N. Kupchinskaya, Aleksandra Opalinska, Adam Reich, Liubov Volianska, Anna M. Hilfanova, Fedir I. Lapiy, Liudmyla I. Chernyshova, Alla P. Volokha, Dariia V. Zabara, Mikhail V. Belevtsev, Tatsiana V. Shman, Lyudmila V. Kukharenko, Mikhail V. Goltsev, Tatsiana G. Dubouskaya, Andrei Y. Hancharou, Weizhen Ji, Saquib Lakhani, Carrie L. Lucas, Olga V. Aleinikova, Svetlana O. Sharapova
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message Partial leukocyte adhesion deficiency type 1 (LAD‐1) deficiency is extremely rare condition with milder infectious manifestation and immune system imbalance leads to increased risks of autoinflammatory complications, such as py
Externí odkaz:
https://doaj.org/article/d7a1834289134a3d8c4a72fbb8c70136
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:
Laura Gámez-Díaz, Jessica Rojas, Yuliya Mareika, Olga Aleinikova, Bodo Grimbacher, Svetlana O. Sharapova, Taisiya M. Mikhaleuskaya, Irina E. Guryanova, Emma Haapaniemi, Alexandr A. Migas, Inga S. Sakovich
Publikováno v:
Journal of Clinical Immunology. 38:471-474
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::547182de41d581eb1fdecfb71ab139e5
https://doi.org/10.1007/s10875-018-0515-x
https://doi.org/10.1007/s10875-018-0515-x
Autor:
Svetlana O. Sharapova, Irina E. Guryanova, Alena V. Valochnik, Inga S. Sakovich, Olga Aleinikova
Publikováno v:
Immunogenetics. 70:613-617
Ataxia-telangiectasia (AT) is a rare neurodegenerative disease characterized by an early onset ataxia, oculocutaneous telangiectasia, immunodeficiency, recurrent infections, radio-sensitivity, and a predisposition to malignancy. We present the case o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6a35bd57a9459e5e5138d4bec43a93
https://doi.org/10.1007/s00251-018-1056-4
https://doi.org/10.1007/s00251-018-1056-4
Autor:
Svetlana O. Sharapova, Larysa Kostyuchenko, Gulsun Karasu, Oksana Malko, Amy P. Hsu, Vedat Uygun, Inga S. Sakovich, Anastasia Bondarenko, Alina Dulau-Florea, Olga Aleinikova, Thomas L. Leto, Agnes Donkó, Maria V. Stegantseva, Steven M. Holland, Emma Haapaniemi
Publikováno v:
Clinical immunology (Orlando, Fla.). 205
Here we describe a 10-year-old girl with combined immunodeficiency presenting as recurring chest infections, lung disease and herpetic skin infections. The patient experienced two hematopoietic stem cell transplantations and despite full chimerism, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52bcaa51e0cc138e5b6dd623ecd972ce
https://pubmed.ncbi.nlm.nih.gov/31071452
https://pubmed.ncbi.nlm.nih.gov/31071452
Autor:
Svetlana O. Sharapova, Christine M. Seroogy, Nurcicek Padem, Claudio Pignata, Jane Peake, Manish J. Butte, Marita Bosticardo, Anthony R. Hayward, Megan A. Cooper, Elena E. Perez, David A. Hill, Catherine M. Biggs, Nicholas L. Hartog, Jennifer Gebbia, Erwin W. Gelfand, Luigi D. Notarangelo, John W. Sleasman, Melissa E. Elder, Avinash Bhandoola, Cristina Corsino, Rosaria Prencipe, Jonathan S. Tam, Gary Kleiner, Jennifer Heimall, Lisa M. Bartnikas, Hana B. Niebur, Jennifer E. Cowan, Karin Chen, Jordan K. Abbott, Yasuhiro Yamazaki, Filiz O. Seeborg, Giuliana Giardino, Giulia Scalia, Irma Yemialyanava, Melanie A. Ruffner, Elena Crestani, Inga S. Sakovich
Publikováno v:
American journal of human genetics, vol 105, iss 3
FOXN1 is the master regulatory gene of thymic epithelium development. FOXN1 deficiency leads to thymic aplasia, alopecia, and nail dystrophy, accounting for the nude/severe combined immunodeficiency (nu/SCID) phenotype in humans and mice. We identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b34ef7c609d2a59e804ddf499b67fb74
http://hdl.handle.net/11588/758590
http://hdl.handle.net/11588/758590