Polymorphism in ficolin-1 (FCN1) gene is associated with an earlier onset of type 1 diabetes mellitus in children and adolescents from northeast Brazil-Reference-Cited by-同舟云学术

Polymorphism in ficolin-1 (FCN1) gene is associated with an earlier onset of type 1 diabetes mellitus in children and adolescents from northeast Brazil

Published:2016-12 Issue:4 Volume:95 Page:1031-1034
ISSN:0022-1333
Container-title:Journal of Genetics
language:en
Short-container-title:J Genet

Author:

DOS ANJOSA ZILMA PEREIRA,SILVA SANTOS MANUELLA MARIA,RODRIGUES NATASSIA JAVORSKI,NUNES DE LACERDA GLAUCIA ALYNE,ARAUJO JAQUELINE,DE AZEVÊDO SILVA JAQUELINE,DE ALENCAR CUNHA TAVARES NATHÁLIA,GUIMARÃES RAFAEL LIMA,CROVELLA SERGIO,CAVALCANTI BRANDÃO LUCAS ANDRÉ

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://link.springer.com/content/pdf/10.1007/s12041-016-0719-x.pdf

Reference20 articles.

1. Atkinson A. P., Cedzynski M., Szemraj J., St Swierzko A., Bak-Romaniszyn L., Banasik M. et al. 2004 L-ficolin in children with recurrent respiratory infections. Clin. Exp. Immunol. 138, 517–520.

2. Boniotto M., Braida L., Baldas V., Not T., Ventura A., Vatta S. et al. 2005 Evidence of a correlation between mannose binding lectin and celiac disease: a model for other autoimmune diseases. J. Mol. Med. (Berl). 83, 308–315.

3. Coelho A. V. C., Moura R. R., Cavalcanti C. A. J., Guimarães R. L., Sandrin-Garcia P., Crovella S. et al. 2015 A rapid screening of ancestry for genetic association studies in an admixed population from Pernambuco, Brazil. Genet. Mol. Res. 14, 2876–2884.

4. Garred P., Honoré C., Ma Y. J., Munthe-Fog L. and Hummelshøj T. 2009 MBL2, FCN1, FCN2 and FCN3-The genes behind the initiation of the lectin pathway of complement. Mol. Immunol. 46, 2737–2744.

5. Hansen T. K., Tarnow L., Thiel S., Steffensen R., Stehouwer C. D., Schalkwijk C. G. et al. 2004 Association between mannose-binding lectin and vascular complications in type 1 diabetes. Diabetes 53, 1570.

Cited by 12 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. Identification of novel prognostic targets in acute kidney injury using bioinformatics and next generation sequencing data analysis;2024-03-17

2. Bioinformatics and Next-Generation Data Analysis for Identification of Genes and Molecular Pathways Involved in Subjects with Diabetes and Obesity;Medicina;2023-02-07

3. Effect of Polymorphisms in the FCN1, FCN2, and FCN3 Genes on the Susceptibility to Develop Rheumatoid Arthritis: A Systematic Review;International Journal of Rheumatology;2022-12-15

4. Identification of hub genes and key pathways in pediatric Crohn’s disease using next generation sequencing and bioinformatics analysis;2022-07-28

5. Identification of biomarkers and pathways for focal segmental glomerulosclerosis using next generation sequencing data and bioinformatics analysis;2022-06-10