scholarly journals Quantitative Characterization of the Activation Steps of Mannan-binding Lectin (MBL)-associated Serine Proteases (MASPs) Points to the Central Role of MASP-1 in the Initiation of the Complement Lectin Pathway

2013 ◽  
Vol 288 (13) ◽  
pp. 8922-8934 ◽  
Author(s):  
Márton Megyeri ◽  
Veronika Harmat ◽  
Balázs Major ◽  
Ádám Végh ◽  
Júlia Balczer ◽  
...  
2014 ◽  
Vol 109 ◽  
pp. S168
Author(s):  
Azza Karrar ◽  
Siddharth Hariharan ◽  
Khatera Malik ◽  
Zheng Li ◽  
Munkhzul Otgonsuren ◽  
...  

2007 ◽  
Vol 178 (9) ◽  
pp. 5710-5716 ◽  
Author(s):  
Florence Teillet ◽  
Monique Lacroix ◽  
Steffen Thiel ◽  
Dietmar Weilguny ◽  
Teit Agger ◽  
...  

2002 ◽  
Vol 169 (10) ◽  
pp. 5735-5743 ◽  
Author(s):  
Sandor Cseh ◽  
Loanys Vera ◽  
Misao Matsushita ◽  
Teizo Fujita ◽  
Gérard J. Arlaud ◽  
...  

Structure ◽  
2017 ◽  
Vol 25 (2) ◽  
pp. 364-375 ◽  
Author(s):  
Ruodan Nan ◽  
Christopher M. Furze ◽  
David W. Wright ◽  
Jayesh Gor ◽  
Russell Wallis ◽  
...  

2000 ◽  
Vol 48 (2) ◽  
pp. 457-463 ◽  
Author(s):  
Julio Escribano ◽  
Angela Rubio ◽  
Manuel Alvarez-Ortí ◽  
Antonio Molina ◽  
José A. Fernández

2011 ◽  
Vol 48 (14) ◽  
pp. 1668-1669
Author(s):  
J. Dobó ◽  
M. Megyeri ◽  
K. Szilágyi ◽  
V. Harmat ◽  
P. Závodszky ◽  
...  

2008 ◽  
Vol 36 (6) ◽  
pp. 1461-1466 ◽  
Author(s):  
Peter Garred

MBL (mannose-binding lectin) is primarily a liver-derived collagen-like serum protein. It binds sugar structures on micro-organisms and on dying host cells and is one of the four known mediators that initiate activation of the complement system via the lectin pathway. Common variant alleles situated both in promoter and structural regions of the human MBL gene (MBL2) influence the stability and the serum concentration of the protein. Epidemiological studies have suggested that genetically determined variations in MBL serum concentrations influence the susceptibility to and the course of different types of infectious, autoimmune, neoplastic, metabolic and cardiovascular diseases, but this is still a subject under discussion. The fact that these genetic variations are very frequent, indicates a dual role of MBL. This overview summarizes the current molecular understanding of human MBL2 genetics.


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