Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Immunoglobulin Heavy Chain Variable Region"'
Autor:
Cristiana Rodrigues, Paula Laranjeira, Aryane Pinho, Isabel Silva, Sandra Silva, Margarida Coucelo, Ana Catarina Oliveira, Ana Teresa Simões, Inês Damásio, Helena Matos Silva, Mafalda Urbano, Ana Bela Sarmento-Ribeiro, Catarina Geraldes, M. Rosário Domingues, Julia Almeida, Ignacio Criado, Alberto Orfao, Artur Paiva
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionIn monoclonal B cell lymphocytosis (MBL) and chronic lymphocytic leukemia (CLL), the expansion of malignant B cells disrupts the normal homeostasis and interactions between B cells and T cells, leading to immune dysregulation. CD20+ T cel
Externí odkaz:
https://doaj.org/article/ef2fa18731824c91b219d5f3ebc98310
Autor:
María Del Mar Sánchez Suárez, Alicia Martín Roldán, Carolina Alarcón-Payer, Miguel Ángel Rodríguez-Gil, Jaime Eduardo Poquet-Jornet, José Manuel Puerta Puerta, Alberto Jiménez Morales
Publikováno v:
Pharmaceutics, Vol 16, Iss 1, p 55 (2023)
Chronic lymphocytic leukemia is a lymphoproliferative disorder marked by the expansion of monoclonal, mature CD5+CD23+ B cells in peripheral blood, secondary lymphoid tissues, and bone marrow. The disease exhibits significant heterogeneity, with nume
Externí odkaz:
https://doaj.org/article/9ab1ed293fd0427ea1d38c761853b905
Autor:
Ke Shi, Qian Sun, Chun Qiao, Huayuan Zhu, Li Wang, Jiazhu Wu, Lili Wang, Jianxin Fu, Ken H. Young, Lei Fan, Yi Xia, Wei Xu, Jianyong Li
Publikováno v:
Cancer Medicine, Vol 9, Iss 3, Pp 999-1007 (2020)
Abstract Immunoglobulin heavy chain variable region (IGHV) mutational status has been an important prognostic factor for chronic lymphocytic leukemia (CLL) for decades. Patients with unmutated IGHV (≥98% identity to the germline sequence) have infe
Externí odkaz:
https://doaj.org/article/748ea71550bf4daf8d0eb725645e4b4e
Akademický článek
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Autor:
Valērija Gorbačova
Biomedicīna Dzīvās dabas zinātnes Biomedicine Natural Sciences Pētījums tika veikts, lai izpētītu hipotēzi, ka Epšteina-Barra vīrusa (EBV) infekcija varētu būt saistīta ar agresīvu augsta riska hroniskas limfoleikozes (HLL) formu, ar n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10002::34bbf286976e4c99ea644dbf6b80fe6f
https://dspace.rsu.lv/jspui/handle/123456789/13944
https://dspace.rsu.lv/jspui/handle/123456789/13944
Autor:
Masahide Yazaki, Fuyuki Kametani, Yoshiki Sekijima, Nagaaki Katoh, Tsuneaki Yoshinaga, Keiichi Higuchi, Mayuko Nakagawa
Publikováno v:
Pathology International. 71:245-254
It is difficult to diagnose immunoglobulin heavy chain amyloidosis (AH amyloidosis) without proteomic analysis due to no useful diagnostic antibodies. The aim of this study was to develop diagnostic antibodies available to immunohistochemistry and im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfa1f59d00ea6741b665ffd8e0d3fdb7
https://doi.org/10.1111/pin.13081
https://doi.org/10.1111/pin.13081
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Wei Xu, Hua-Yuan Zhu, Li Wang, Jianxin Fu, Ke Shi, Lili Wang, Ken H. Young, Yi Xia, Jia-Zhu Wu, Jianyong Li, Qian Sun, Lei Fan, C. Qiao
Publikováno v:
Cancer Medicine, Vol 9, Iss 3, Pp 999-1007 (2020)
Cancer Medicine
Cancer Medicine
Immunoglobulin heavy chain variable region (IGHV) mutational status has been an important prognostic factor for chronic lymphocytic leukemia (CLL) for decades. Patients with unmutated IGHV (≥98% identity to the germline sequence) have inferior prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae5db05b33cfecd45c569547da254e79
https://doaj.org/article/748ea71550bf4daf8d0eb725645e4b4e
https://doaj.org/article/748ea71550bf4daf8d0eb725645e4b4e
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1991 Jul 01. 88(13), 5640-5644.
Externí odkaz:
https://www.jstor.org/stable/2357234
Publikováno v:
British Journal of Haematology. 192
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::483c05eca2d85213efe28c801d8b9b16
https://doi.org/10.1111/bjh.17257
https://doi.org/10.1111/bjh.17257