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Items: 1 to 20 of 101

1.

NOD2 and CCDC122-LACC1 genes are associated with leprosy susceptibility in Brazilians.

Sales-Marques C, Salomão H, Fava VM, Alvarado-Arnez LE, Amaral EP, Cardoso CC, Dias-Batista IM, da Silva WL, Medeiros P, da Cunha Lopes Virmond M, Lana FC, Pacheco AG, Moraes MO, Mira MT, Pereira Latini AC.

Hum Genet. 2014 Dec;133(12):1525-32. doi: 10.1007/s00439-014-1502-9. Epub 2014 Nov 4.

PMID:
25367361
2.

Association between genetic variants in NOD2, C13orf31, and CCDC122 genes and leprosy among the Chinese Yi population.

Xiong JH, Mao C, Sha XW, Jin Z, Wang H, Liu YY, Ning Y.

Int J Dermatol. 2016 Jan;55(1):65-9. doi: 10.1111/ijd.12981. Epub 2015 Jul 31.

PMID:
26235265
3.

Crohn's disease susceptibility genes are associated with leprosy in the Vietnamese population.

Grant AV, Alter A, Huong NT, Orlova M, Van Thuc N, Ba NN, Thai VH, Abel L, Schurr E, Alcais A.

J Infect Dis. 2012 Dec 1;206(11):1763-7. doi: 10.1093/infdis/jis588. Epub 2012 Sep 14.

PMID:
22984114
4.

Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.

Zhang F, Liu H, Chen S, Low H, Sun L, Cui Y, Chu T, Li Y, Fu X, Yu Y, Yu G, Shi B, Tian H, Liu D, Yu X, Li J, Lu N, Bao F, Yuan C, Liu J, Liu H, Zhang L, Sun Y, Chen M, Yang Q, Yang H, Yang R, Zhang L, Wang Q, Liu H, Zuo F, Zhang H, Khor CC, Hibberd ML, Yang S, Liu J, Zhang X.

Nat Genet. 2011 Oct 23;43(12):1247-51. doi: 10.1038/ng.973.

PMID:
22019778
5.

Polymorphisms of NOD2 and the risk of tuberculosis: a validation study in the Chinese population.

Pan H, Dai Y, Tang S, Wang J.

Int J Immunogenet. 2012 Jun;39(3):233-40. doi: 10.1111/j.1744-313X.2011.01079.x. Epub 2012 Jan 2.

PMID:
22212192
6.

Genetic polymorphisms of the IL6 and NOD2 genes are risk factors for inflammatory reactions in leprosy.

Sales-Marques C, Cardoso CC, Alvarado-Arnez LE, Illaramendi X, Sales AM, Hacker MA, Barbosa MGM, Nery JADC, Pinheiro RO, Sarno EN, Pacheco AG, Moraes MO.

PLoS Negl Trop Dis. 2017 Jul 17;11(7):e0005754. doi: 10.1371/journal.pntd.0005754. eCollection 2017 Jul.

7.

Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese.

Wang D, Fan Y, Malhi M, Bi R, Wu Y, Xu M, Yu XF, Long H, Li YY, Zhang DF, Yao YG.

Am J Hum Genet. 2018 May 3;102(5):794-805. doi: 10.1016/j.ajhg.2018.03.006. Epub 2018 Apr 26.

8.

Common polymorphisms in the NOD2 gene region are associated with leprosy and its reactive states.

Berrington WR, Macdonald M, Khadge S, Sapkota BR, Janer M, Hagge DA, Kaplan G, Hawn TR.

J Infect Dis. 2010 May 1;201(9):1422-35. doi: 10.1086/651559.

9.

Gene expression analysis of leprosy by using a multiplex branched DNA assay.

Sun Y, Liu H, Yu G, Chen X, Liu H, Tian H, Zhou G, Zhang F.

Exp Dermatol. 2011 Jun;20(6):520-2. doi: 10.1111/j.1600-0625.2011.01270.x.

PMID:
21585556
10.

The TLR1 gene is associated with higher protection from leprosy in women.

Alvarenga Niitsuma EN, Fernandes GDR, Lana FCF.

PLoS One. 2018 Oct 5;13(10):e0205234. doi: 10.1371/journal.pone.0205234. eCollection 2018.

11.

An association study of TOLL and CARD with leprosy susceptibility in Chinese population.

Liu H, Bao F, Irwanto A, Fu X, Lu N, Yu G, Yu Y, Sun Y, Low H, Li Y, Liany H, Yuan C, Li J, Liu J, Chen M, Liu H, Wang N, You J, Ma S, Niu G, Zhou Y, Chu T, Tian H, Chen S, Zhang X, Liu J, Zhang F.

Hum Mol Genet. 2013 Nov 1;22(21):4430-7. doi: 10.1093/hmg/ddt286. Epub 2013 Jun 19.

12.

Absence of nucleotide-binding oligomerization domain-containing protein 2 variants in patients with leprosy and tuberculosis.

Singh V, Gaur R, Mittal M, Biswas SK, Das R, Girdhar BK, Bajaj B, Katoch VM, Kumar A, Mohanty KK.

Int J Immunogenet. 2012 Aug;39(4):353-6. doi: 10.1111/j.1744-313X.2012.01085.x. Epub 2012 Jan 31.

PMID:
22289211
13.

LRRK2 and RIPK2 variants in the NOD 2-mediated signaling pathway are associated with susceptibility to Mycobacterium leprae in Indian populations.

Marcinek P, Jha AN, Shinde V, Sundaramoorthy A, Rajkumar R, Suryadevara NC, Neela SK, van Tong H, Balachander V, Valluri VL, Thangaraj K, Velavan TP.

PLoS One. 2013 Aug 28;8(8):e73103. doi: 10.1371/journal.pone.0073103. eCollection 2013.

14.

Linkage disequilibrium pattern and age-at-diagnosis are critical for replicating genetic associations across ethnic groups in leprosy.

Alter A, Fava VM, Huong NT, Singh M, Orlova M, Van Thuc N, Katoch K, Thai VH, Ba NN, Abel L, Mehra N, Alcaïs A, Schurr E.

Hum Genet. 2013 Jan;132(1):107-16. doi: 10.1007/s00439-012-1227-6. Epub 2012 Sep 29.

PMID:
23052943
15.

IL12B SNPs and copy number variation in IL23R gene associated with susceptibility to leprosy.

Ali S, Srivastava AK, Chopra R, Aggarwal S, Garg VK, Bhattacharya SN, Bamezai RN.

J Med Genet. 2013 Jan;50(1):34-42. doi: 10.1136/jmedgenet-2012-101214.

PMID:
23240095
16.

Association of IL10 Polymorphisms and Leprosy: A Meta-Analysis.

Alvarado-Arnez LE, Amaral EP, Sales-Marques C, Durães SM, Cardoso CC, Nunes Sarno E, Pacheco AG, Lana FC, Moraes MO.

PLoS One. 2015 Sep 4;10(9):e0136282. doi: 10.1371/journal.pone.0136282. eCollection 2015.

17.

The GATA3 gene is involved in leprosy susceptibility in Brazilian patients.

Medeiros P, da Silva WL, de Oliveira Gimenez BB, Vallezi KB, Moraes MO, de Souza VNB, Latini ACP.

Infect Genet Evol. 2016 Apr;39:194-200. doi: 10.1016/j.meegid.2016.01.015. Epub 2016 Jan 23.

PMID:
26807920
18.

Examining ERBB2 as a candidate gene for susceptibility to leprosy (Hansen's disease) in Brazil.

Araújo SR, Jamieson SE, Dupnik KM, Monteiro GR, Nobre ML, Dias MS, Trindade Neto PB, Queiroz Mdo C, Gomes CE, Blackwell JM, Jeronimo SM.

Mem Inst Oswaldo Cruz. 2014 Apr;109(2):182-8. Epub 2014 Mar 5.

19.

Stepwise replication identifies a low-producing lymphotoxin-alpha allele as a major risk factor for early-onset leprosy.

Alcaïs A, Alter A, Antoni G, Orlova M, Nguyen VT, Singh M, Vanderborght PR, Katoch K, Mira MT, Vu HT, Ngyuen TH, Nguyen NB, Moraes M, Mehra N, Schurr E, Abel L.

Nat Genet. 2007 Apr;39(4):517-22. Epub 2007 Mar 11.

PMID:
17353895
20.

The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants.

Glas J, Seiderer J, Tillack C, Pfennig S, Beigel F, Jürgens M, Olszak T, Laubender RP, Weidinger M, Müller-Myhsok B, Göke B, Ochsenkühn T, Lohse P, Diegelmann J, Czamara D, Brand S.

PLoS One. 2010 Dec 30;5(12):e14466. doi: 10.1371/journal.pone.0014466.

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