Mannose-Binding Lectin 2 (MBL2) combined genotypes deficiency is associated with susceptibility for Oral Lichen Planus
Author:
Affiliation:
1. Institute for Maternal and Child Health, Italy
2. Division of Oral Medicine and Pathology, Italy; University of Trieste, Italy
3. University of Trieste, Italy
4. Institute for Maternal and Child Health, Italy; University of Trieste, Italy
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v42n1/1415-4757-GMB-1678-4685-GMB-2018-0015.pdf
Reference28 articles.
1. Association of interleukin (IL)18 and IL10 gene polymorphisms with oral lichen planus risk; A case-control study;Abdel Hay R;J Dermatol Sci,2016
2. Association of genetic polymorphisms in interferon-gamma, interleukin-6 and transforming growth factor-beta1 gene with oral lichen planus susceptibility;Al-Mohaya MA;BMC Oral Health,2016
3. Human mannose-binding protein gene is regulated by interleukins, dexamethasone and heat shock;Arai T;Q J Med,1993
4. Phenotypic variability and therapeutic implications of Candida species in patients with oral lichen planus;Arora S;Biotech Histochem,2016
5. Mannose-binding lectin gene (MBL-2) polymorphism in oral lichen planus;Barkokebas A;Clin Oral Investig,2011
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3. Review of the current evidence of non-HLA gene polymorphism in oral lichen planus;Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology;2021-05
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