Zobrazeno 1 - 10
of 18
pro vyhledávání: '"FCGR3B Gene"'
Publikováno v:
Malaria Journal, Vol 19, Iss 1, Pp 1-12 (2020)
Abstract Background Malaria antigen-specific antibodies and polymorphisms in host receptors involved in antibody functionality have been associated with different outcomes of Plasmodium falciparum infections. Thus, to identify key prospective malaria
Externí odkaz:
https://doaj.org/article/3808326eb06b4782b17504170f29ace4
Publikováno v:
Malaria Journal, Vol 19, Iss 1, Pp 1-12 (2020)
Dwomoh, D, Adu, B, Dodoo, D, Theisen, M, Iddi, S & Gerds, T A 2020, ' Evaluating the predictive performance of malaria antibodies and FCGR3B gene polymorphisms on Plasmodium falciparum infection outcome : a prospective cohort study ', Malaria Journal, vol. 19, no. 1, 307 . https://doi.org/10.1186/s12936-020-03381-8
Malaria Journal
Dwomoh, D, Adu, B, Dodoo, D, Theisen, M, Iddi, S & Gerds, T A 2020, ' Evaluating the predictive performance of malaria antibodies and FCGR3B gene polymorphisms on Plasmodium falciparum infection outcome : a prospective cohort study ', Malaria Journal, vol. 19, no. 1, 307 . https://doi.org/10.1186/s12936-020-03381-8
Malaria Journal
Background Malaria antigen-specific antibodies and polymorphisms in host receptors involved in antibody functionality have been associated with different outcomes of Plasmodium falciparum infections. Thus, to identify key prospective malaria antigens
Akademický článek
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Publikováno v:
SSRN Electronic Journal.
Fcγ receptors (FcI³R) have been proposed to be involved in the pathogenesis of acute rejection (AR) after organ transplantation. However, the mechanisms by which FcγRIIIB mediate this process are still unclear. Previous studies suggested that the
Autor:
Suhani Almal, Harish Padh
Publikováno v:
International Journal of Immunogenetics. 42:26-30
Summary Amongst several human genome variations, copy number variations (CNVs) are considered as an important source of variability contributing to susceptibility to wide range of diseases. Although CNV is scattered for genes throughout the human gen
Autor:
Akemi K. Chiba, Neusa Pereira da Silva, Claudia Cristina Naufel Terzian, Viviani C. Santos, José Orlando Bordin
Publikováno v:
Transfusion. 52:629-634
BACKGROUND: The FCGR3B gene encoding the FcyRIIIb receptor for immunoglobulin G has three polymorphic forms known as HNA-1a, HNA-1b, and HNA-1c, encoded by the alleles FCGR3B*01, FCGR3B*02, and FCGR3B*03, respectively. It is not clear whether the inh
Publikováno v:
Genes & Immunity. 11:155-160
Copy number variation (CNV) in the human genome is an important determinant of susceptibility to autoimmune diseases. Many autoimmune diseases share similar clinical and pathogenic features. Thus, CNVs of genes involved in immunity may serve as share
Publikováno v:
Tissue Antigens. 60:64-70
The granulocyte antigens HNA-1a, -1b and -1c reside on the FcgammaIIIb receptor, which is exclusively expressed on neutrophils. They are involved in autoimmune and alloimmune neutropenias as well as in severe transfusion reactions. Recent family stud
Autor:
Richender Martijn, Renee Baak-Pablo, Toufik el Hajoui, Tahar van der Straaten, Henk-Jan Guchelaar
Publikováno v:
Pharmacogenetics and Genomics, 23(11), 631-635
Monoclonal antibodies, such as rituximab, trastuzumab, and cetuximab, mediate immune response by binding to Fcγ receptors. The frequently occurring Phe158Val variant of the FCGR3A gene has increased binding affinity and consequently may affect immun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a1a46440e12a39b1e2a2ae5ea01d66a
https://hdl.handle.net/1887/101380
https://hdl.handle.net/1887/101380
Autor:
Tony R. Merriman, Roger Hesselstrand, V. Fonollosa, Norberto Ortego-Centeno, Cushla McKinney, Javier Martin, Gabriela Riemekasten, P. Airo, J. C. A. Broen, M. J. H. Coenen, Madelon C. Vonk, Patricia Carreira, L. Beretta, R. Scorza, C. P. Simeon, Trdj Radstake, M. A. Gonzalez-Gay, N. Hunzelmann
Publikováno v:
Genes and Immunity, 13, 6, pp. 458-60
Genes and Immunity, 13, 458-60
Genes and Immunity, 13, 458-60
Contains fulltext : 107808.pdf (Publisher’s version ) (Closed access) There is increasing evidence that gene copy number (CN) variation influences clinical phenotype. The low-affinity Fc receptor 3B (FCGR3B) located in the FCGR gene cluster is a CN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a7103e0d8a1c416f91fcb335717347d
https://doi.org/10.1038/gene.2012.15
https://doi.org/10.1038/gene.2012.15