Association of MBL2 Exon 1 Polymorphisms With Multibacillary Leprosy-Reference-Cited by-同舟云学术

Association of MBL2 Exon 1 Polymorphisms With Multibacillary Leprosy

Published:2020-09-03 Issue: Volume:11 Page:
ISSN:1664-3224
Container-title:Frontiers in Immunology
language:
Short-container-title:Front. Immunol.

Author:

Tiyo Bruna Tiaki,Vendramini Evelyn Castillo Lima,de Souza Victor Hugo,Colli Cristiane Maria,Alves Hugo Vicentin,Sell Ana Maria,Zucoloto Sylmara Bessani Paixão,Visentainer Jeane Eliete Laguila

Publisher

Frontiers Media SA

Subject

Immunology,Immunology and Allergy

Reference30 articles.

1. Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein;Madsen;J Immunol.,1995

2. The role of mannose-binding lectin in health and disease;Turner;Mol Immunol.,2003

3. Mannan-binding lectin and its role in innate immunity;Kilpatrick;Transfus Med.,2002

4. Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China;Zhang;Hum Genet.,2013

5. Mannose-binding lectin: biologic characteristics and role in the susceptibility to infections and ischemia-reperfusion related injury in critically Ill neonates;Auriti;J Immunol Res.,2017

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Leprosy: treatment, prevention, immune response and gene function;Frontiers in Immunology;2024-02-19

2. Mannose-binding lectin gene polymorphism in psoriasis and vitiligo: an observational study and computational analysis;Frontiers in Medicine;2024-02-09

3. MBL2 gene variants and susceptibility to meningitis in Egyptian patients;Gene;2023-07

4. Ficolin‐3 and MASP‐2 gene variants in Siberian arctic populations: Summarized evidence of selective pressure for the high frequency of lectin complement pathway deficiency;Scandinavian Journal of Immunology;2023-01-10

5. MBL2 polymorphism may be a protective factor of autoimmune thyroid disease susceptibility;Molecular Genetics and Genomics;2022-11-01