Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Angelica B W Boldt"'
Autor:
Emanuele Gustani Gustani-Buss, Carlos E Buss, Luciane R Cavalli, Carolina Panis, Felipe F Tuon, Joao P Telles, Franciele A C Follador, Guilherme W Wendt, Léia C Lucio, Lirane E D Ferreto, Isabela M de Oliveira, Emerson Carraro, Lualis E David, Andréa N C Simão, Angelica B W Boldt, Maria Luiza Petzl-Erler, Wilson A Silva, David L A Figueiredo
Publikováno v:
BMJ Open, Vol 12, Iss 10 (2022)
Objective The Brazilian state of Paraná has suffered from COVID-19 effects, understanding predictors of increased mortality in health system interventions prevent hospitalisation of patients. We selected the best models to evaluate the association o
Externí odkaz:
https://doaj.org/article/3fbac72eca93440383893fa57d7ca2df
Autor:
Paola Rosa Luz, Márcia I Miyazaki, Nelson Chiminacio Neto, Marcela C Padeski, Ana Cláudia M Barros, Angelica B W Boldt, Iara J Messias-Reason
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 10, Iss 1, p e0004257 (2016)
Chagas disease (CD) is caused by Trypanosoma cruzi, whose sugar moieties are recognized by mannan binding lectin (MBL), a soluble pattern-recognition molecule that activates the lectin pathway of complement. MBL levels and protein activity are affect
Externí odkaz:
https://doaj.org/article/af5be25f010e408ea69e2dec8f809c9a
Autor:
Isabela Goeldner, Thelma Skare, Angelica B W Boldt, Flavia R Nass, Iara J Messias-Reason, Shirley R Utiyama
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e90979 (2014)
BackgroundMannan-binding lectin-associated serine protease 2 (MASP-2) is a key protein of the lectin pathway of complement. MASP-2 levels have been associated with different polymorphisms within MASP2 gene as well as with the risk for inflammatory di
Externí odkaz:
https://doaj.org/article/1d5a3c09250d4b238d3fa5d93d0e5749
Autor:
Paola R Luz, Angelica B W Boldt, Caroline Grisbach, Jürgen F J Kun, Thirumalaisamy P Velavan, Iara J T Messias-Reason
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60237 (2013)
BackgroundL-ficolin (encoded by FCN2) binds to acetylated sugar moieties of many pathogens, including Trypanosoma cruzi, promoting their phagocytosis and lysis by the complement system.MethodsWe investigated L-ficolin levels in 160 T. cruzi infected
Externí odkaz:
https://doaj.org/article/7ba6002344eb4bd6a08b951ffdefa543
Autor:
Paola R Luz, Angelica B W Boldt, Caroline Grisbach, Jürgen F J Kun, Thirumalaisamy P Velavan, Iara J T Messias-Reason
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 4, p e60237 (2013)
PLoS ONE, Vol 8, Iss 4, p e60237 (2013)
BackgroundL-ficolin (encoded by FCN2) binds to acetylated sugar moieties of many pathogens, including Trypanosoma cruzi, promoting their phagocytosis and lysis by the complement system.MethodsWe investigated L-ficolin levels in 160 T. cruzi infected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3e53b36d6015a1ae599f92658c635998
https://pubmed.ncbi.nlm.nih.gov/23593180
https://pubmed.ncbi.nlm.nih.gov/23593180
Publikováno v:
Advances in clinical chemistry. 56
Due to its importance both in the clearance of pathogens that contribute as rheumatic etiological agents and in the disposal of apoptotic bodies and potential autoimmune initiators, deficiencies of the components of the lectin pathway of complement h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cc5d9e55f981a5c671156062dc912a49
https://pubmed.ncbi.nlm.nih.gov/22397030
https://pubmed.ncbi.nlm.nih.gov/22397030
Autor:
Yvonne, Kalmbach, Angelica B W, Boldt, Rolf, Fendel, Benjamin, Mordmüller, Peter G, Kremsner, Jürgen F J, Kun
Publikováno v:
European cytokine network. 17(3)
The outcome of a Plasmodium falciparum infection differs greatly between patients, ranging from an asymptomatic carrier status to the most severe characteristics influenced by activating and inhibiting immune factors. The inhibitory leukocyte immunog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::573050135e6538d63c73a09d03c24972
https://pubmed.ncbi.nlm.nih.gov/17194637
https://pubmed.ncbi.nlm.nih.gov/17194637