Zobrazeno 1 - 10
of 104
pro vyhledávání: '"β2GPI"'
Autor:
Sara Garcinuño, Antonio Lalueza, Francisco Javier Gil-Etayo, Raquel Diaz-Simón, Ignacio Lizasoain, Ana Moraga, Blanca Diaz-Benito, Laura Naranjo, Oscar Cabrera-Marante, Daniel Enrique Pleguezuelo, Maria Ruiz-Ruigomez, Blanca Ayuso, Estibaliz Arrieta, Dolores Folgueira, Estela Paz-Artal, Cecilia Cueto, Carlos Lumbreras, Antonio Serrano, Manuel Serrano
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/abe914cddb964ed39a80c0dad3441af6
Autor:
Sara Garcinuño, Antonio Lalueza, Francisco Javier Gil-Etayo, Raquel Díaz-Simón, Ignacio Lizasoain, Ana Moraga, Blanca Diaz-Benito, Laura Naranjo, Oscar Cabrera-Marante, Daniel Enrique Pleguezuelo, Maria Ruiz-Ruigomez, Blanca Ayuso, Estibaliz Arrieta, Dolores Folgueira, Estela Paz-Artal, Cecilia Cueto, Carlos Lumbreras, Antonio Serrano, Manuel Serrano
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionInfluenza virus infection can cause a range of clinical symptoms, including respiratory failure (RF) and even death. The mechanisms responsible for the most severe forms of the disease are not yet well understood. The objective is to asse
Externí odkaz:
https://doaj.org/article/a11bb4784f4e45ccaa37f9348df97030
Autor:
Claudia Grossi, Nagaja Capitani, Marisa Benagiano, Cosima Tatiana Baldari, Chiara Della Bella, Paolo Macor, Francesco Tedesco, Maria Orietta Borghi, Norma Maugeri, Mario Milco D’Elios, Pier Luigi Meroni
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
Antiphospholipid syndrome (APS) is a systemic autoimmune disorder characterized by recurrent vascular thrombosis and miscarriages in the absence of known causes. Antibodies against phospholipid-binding proteins (aPL) are pathogenic players in both cl
Externí odkaz:
https://doaj.org/article/9f15eca05e6845d489f4edd9b0b9ff04
Autor:
Chun-Yu Lin, Chun-Ching Chiu, Ju Cheng, Chia-Yun Lin, Ya-Fang Shi, Chun-Chou Tsai, Bor-Show Tzang, Tsai-Ching Hsu
Publikováno v:
Virulence, Vol 9, Iss 1, Pp 208-216 (2018)
Mounting evidence suggests a connection between human parvovirus B19 (B19) and autoimmune diseases, and especially an association between the B19-VP1 unique region (VP1u) and anti-phospholipid syndrome (APS). However, little is known about the antige
Externí odkaz:
https://doaj.org/article/c89a305ed72746b5b6c2f810420eaf60
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Stojanović, Maja
Publikováno v:
Универзитет у Београду
Uvod: Takajaši arteritis (TA) je idiopatska, zapaljenska bolest hroničnog toka, koja se karakteriše granulomatoznim zapaljenjem aorte i njenih grana. Određeni genetički faktori mogu imati značaja u nastanku TA. Sekundarni antifosfolipidni sindr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=nardusnacion::9bef0d3c04064bd73c729672fd10cd2d
https://nardus.mpn.gov.rs/handle/123456789/21057
https://nardus.mpn.gov.rs/handle/123456789/21057
Autor:
Roberta Misasi, Agostina Longo, Serena Recalchi, Daniela Caissutti, Gloria Riitano, Valeria Manganelli, Tina Garofalo, Maurizio Sorice, Antonella Capozzi
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 21, p 8411 (2020)
Antiphospholipid Syndrome (APS) is an autoimmune disease characterized by arterial and/or venous thrombosis and/or pregnancy morbidity, associated with circulating antiphospholipid antibodies (aPL). In some cases, patients with a clinical profile ind
Externí odkaz:
https://doaj.org/article/f58b63d386ca4a4da1af385c0e825266
Autor:
Anna Gries, Ruth Prassl, Satoshi Fukuoka, Manfred Rössle, Yani Kaconis, Lena Heinbockel, Thomas Gutsmann, Klaus Brandenburg
Publikováno v:
FEBS Open Bio, Vol 4, Iss C, Pp 432-440 (2014)
There are several human serum proteins for which no clear role is yet known. Among these is the abundant serum protein beta2-glycoprotein-I (β2GPI), which is known to bind to negatively charged phospholipids as well as to bacterial lipopolysaccharid
Externí odkaz:
https://doaj.org/article/4c98b3d9ad404a9dbb8e35e297c66aa6
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Serena Recalchi, Agostina Longo, Tina Garofalo, Roberta Misasi, Valeria Manganelli, Antonella Capozzi, Maurizio Sorice, Daniela Caissutti, Gloria Riitano
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 8411, p 8411 (2020)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Antiphospholipid Syndrome (APS) is an autoimmune disease characterized by arterial and/or venous thrombosis and/or pregnancy morbidity, associated with circulating antiphospholipid antibodies (aPL). In some cases, patients with a clinical profile ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22ded83973e0305afe222bd446583124
https://www.mdpi.com/1422-0067/21/21/8411
https://www.mdpi.com/1422-0067/21/21/8411