The lectin complement pathway serine proteases (MASPs) represent a possible crossroad between the coagulation and complement systems in thromboinflammation

Author:

Kozarcanin H.1,Lood C.2,Munthe-Fog L.3,Sandholm K.4,Hamad O. A.1,Bengtsson A. A.2,Skjoedt M.-O.3,Huber-Lang M.5,Garred P.3,Ekdahl K. N.14,Nilsson B.1

Affiliation:

1. Department of Immunology, Genetics and Pathology; Rudbeck Laboratory C5:3; Uppsala University; Uppsala Sweden

2. Section of Rheumatology; Department of Clinical Sciences Lund; Skåne University Hospital and Lund University; Lund Sweden

3. Laboratory of Molecular Medicine; Department of Clinical Immunology; Section 7631, Rigshospitalet; Faculty of Health and Medical Sciences; University of Copenhagen; Copenhagen Denmark

4. Linnaeus Center for Biomaterials Chemistry; Linnaeus University; Kalmar Sweden

5. Department of Traumatology, Hand, Plastic, Reconstructive Surgery; University Hospital of Ulm; Ulm Germany

Funder

Vetenskapsrådet

Seventh Framework Programme

Publisher

Wiley

Subject

Hematology

Reference39 articles.

1. The genetics of ficolins;Garred;J Innate Immun,2010

2. Mannose-binding lectin and its genetic variants;Garred;Genes Immun,2006

3. Mannose-binding lectin in innate immunity: past, present and future;Dommett;Tissue Antigens,2006

4. The role of ficolins in the lectin pathway of innate immunity;Endo;Int J Biochem Cell Biol,2011

5. The ficolins;Garred;J Innate Immun,2010

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