Defendi F, Leroy C, Epaulard O, Clavarino G, Vilotitch A, Le Marechal M
Front Immunol. 2021; 12:742446.
PMID: 34567008
PMC: 8461024.
DOI: 10.3389/fimmu.2021.742446.
Swierzko A, Cedzynski M
Front Immunol. 2020; 11:585243.
PMID: 33193407
PMC: 7609860.
DOI: 10.3389/fimmu.2020.585243.
Schaapman J, Amoros A, van der Reijden J, Laleman W, Zeuzem S, Banares R
Liver Int. 2020; 40(3):646-653.
PMID: 31991025
PMC: 7079071.
DOI: 10.1111/liv.14392.
Bodi J, Nsibu C, Longenge R, Aloni M, Akilimali P, Kayembe P
Malar J. 2020; 19(1):25.
PMID: 31941497
PMC: 6964107.
DOI: 10.1186/s12936-020-3100-8.
Polesello V, Segat L, Biasotto M, Ottaviani G, Gobbo M, Di Lenarda R
Genet Mol Biol. 2019; 42(1):9-14.
PMID: 30794720
PMC: 6428121.
DOI: 10.1590/1678-4685-GMB-2018-0015.
Association of Single-Nucleotide Polymorphisms of the with Atopic Dermatitis in Korean Patients.
Kim J, Lee S, Hahn H, Lee Y, Yu D, Kim J
Ann Dermatol. 2017; 29(5):571-577.
PMID: 28966513
PMC: 5597650.
DOI: 10.5021/ad.2017.29.5.571.
Phospholipase A2 Receptor-Related Membranous Nephropathy and Mannan-Binding Lectin Deficiency.
Bally S, Debiec H, Ponard D, Dijoud F, Rendu J, Faure J
J Am Soc Nephrol. 2016; 27(12):3539-3544.
PMID: 27153925
PMC: 5118485.
DOI: 10.1681/ASN.2015101155.
Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients.
Zachariah M, Al Zadjali S, Bashir W, Al Ambusaidi R, Misquith R, Wali Y
Mediterr J Hematol Infect Dis. 2016; 8(1):e2016013.
PMID: 26977272
PMC: 4771138.
DOI: 10.4084/MJHID.2016.013.
Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children.
Lundbo L, Sorensen H, Clausen L, Hollegaard M, Hougaard D, Konradsen H
Open Forum Infect Dis. 2015; 2(4):ofv127.
PMID: 26464842
PMC: 4602025.
DOI: 10.1093/ofid/ofv127.
Functional variations in MBL2 gene are associated with cutaneous leishmaniasis in the Amazonas state of Brazil.
de Araujo F, Mesquita T, da Silva L, de Almeida S, de S Vital W, Chrusciak-Talhari A
Genes Immun. 2015; 16(4):284-8.
PMID: 25764115
DOI: 10.1038/gene.2015.6.
Changes in the Expression and Distribution of Claudins, Increased Epithelial Apoptosis, and a Mannan-Binding Lectin-Associated Immune Response Lead to Barrier Dysfunction in Dextran Sodium Sulfate-Induced Rat Colitis.
Yuan B, Zhou S, Lu Y, Liu J, Jin X, Wan H
Gut Liver. 2015; 9(6):734-40.
PMID: 25717051
PMC: 4625702.
DOI: 10.5009/gnl14155.
The role of mannose-binding lectin in severe sepsis and septic shock.
De Pascale G, Cutuli S, Pennisi M, Antonelli M
Mediators Inflamm. 2013; 2013:625803.
PMID: 24223476
PMC: 3808714.
DOI: 10.1155/2013/625803.
Complement polymorphisms and cognitive dysfunction after carotid endarterectomy.
Heyer E, Kellner C, Malone H, Bruce S, Mergeche J, Ward J
J Neurosurg. 2013; 119(3):648-54.
PMID: 23662819
PMC: 3806214.
DOI: 10.3171/2013.4.JNS1368.
Mannose binding lectin deficiency: more than meets the eye.
Halbrich M, Ben-Shoshan M, McCusker C
Clin Med Insights Pediatr. 2013; 6:89-94.
PMID: 23641170
PMC: 3620812.
DOI: 10.4137/CMPed.S9860.
Genetic influences on cystic fibrosis lung disease severity.
Weiler C, Drumm M
Front Pharmacol. 2013; 4:40.
PMID: 23630497
PMC: 3632778.
DOI: 10.3389/fphar.2013.00040.
Complement activation and cardiac surgery: a novel target for improving outcomes.
Stahl G, Shernan S, Smith P, Levy J
Anesth Analg. 2012; 115(4):759-71.
PMID: 22798530
PMC: 3455120.
DOI: 10.1213/ANE.0b013e3182652b7d.
Complement genetics, deficiencies, and disease associations.
Mayilyan K
Protein Cell. 2012; 3(7):487-96.
PMID: 22773339
PMC: 4875391.
DOI: 10.1007/s13238-012-2924-6.
A novel mutation W388X underlying properdin deficiency in a Finnish family.
Helminen M, Seitsonen S, Jarva H, Meri S, Jarvela I
Scand J Immunol. 2012; 75(4):445-8.
PMID: 22229731
PMC: 3306489.
DOI: 10.1111/j.1365-3083.2012.02674.x.
Crosstalk between innate and adaptive immune responses to infectious bronchitis virus after vaccination and challenge of chickens varying in serum mannose-binding lectin concentrations.
Juul-Madsen H, Norup L, Jorgensen P, Handberg K, Wattrang E, Dalgaard T
Vaccine. 2011; 29(51):9499-507.
PMID: 22008821
PMC: 7115549.
DOI: 10.1016/j.vaccine.2011.10.016.
Structural gene variants in the porcine mannose-binding lectin 1 (MBL1) gene are associated with low serum MBL-A concentrations.
Juul-Madsen H, Kjaerup R, Toft C, Henryon M, Heegaard P, Berg P
Immunogenetics. 2011; 63(5):309-17.
PMID: 21274526
DOI: 10.1007/s00251-011-0512-1.