Investigation of the eotaxin gene −426C→T, −384A→G and 67G→A single-nucleotide polymorphisms and atopic dermatitis in Italian children using family-based association methods

2008 ◽  
Vol 33 (3) ◽  
pp. 316-321 ◽  
Author(s):  
L. Rigoli ◽  
L. Caminiti ◽  
C. Di Bella ◽  
V. Procopio ◽  
C. Cuppari ◽  
...  
Keyword(s):  
Atopic Dermatitis ◽  
Single Nucleotide Polymorphisms ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Family Based ◽  
Italian Children

Hint for association of single nucleotide polymorphisms and haplotype in SPINK5 gene with atopic dermatitis in Koreans

2010 ◽  
Vol 19 (12) ◽  
pp. 1048-1053 ◽  
Author(s):  
Jung-Hyun Namkung ◽  
Jong-Eun Lee ◽  
Eugene Kim ◽  
Ji-Yeon Byun ◽  
Sook Kim ◽  
...  
Keyword(s):  
Atopic Dermatitis ◽  
Single Nucleotide Polymorphisms ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

scholarly journals Chromosome 9p21.3 is Associated with Early-Onset Coronary Heart Disease in the Irish Population

2008 ◽  
Vol 25 (2) ◽  
pp. 81-85 ◽  
Author(s):  
Weihua Meng ◽  
Anne E. Hughes ◽  
Chris C. Patterson ◽  
Christine Belton ◽  
Frank Kee ◽  
...  
Keyword(s):  
Coronary Heart Disease ◽  
Heart Disease ◽  
Single Nucleotide Polymorphisms ◽  
Cause Of Death ◽  
Early Onset ◽  
Nucleotide Polymorphisms ◽  
Irish Population ◽  
Single Nucleotide ◽  
The World ◽  
Family Based

Coronary heart disease (CHD) remains a leading cause of death across the world. A region on chromosome 9p21.3 has been recently reported to be associated with CHD. We evaluated 3 SNPs and 3 common haplotypes in the 9p21.3 region in 1494 individuals from 580 Irish families, where at least 1 member had early-onset (males ≤55yr, females ≤60yr) CHD. Genotypes were determined by multiplex SNaPshot technology. Using the combined TDT/S-TDT test, the 3 single nucleotide polymorphisms (SNP), rs10757274, rs2383206 and rs1333049, were strongly associated with early-onset CHD (p= 2.7 × 10-6, 2.7 × 10-6, 3.8 × 10-7, respectively). Analysis of haplotypes by the TRANSMIT program also showed that the GGC haplotype was associated with early-onset CHD (p= 7.9 × 10-7). In conclusion, using a family-based approach in the Irish population, we have confirmed previous reports of association between a region on chromosome 9p21.3 and early-onset CHD.

Association of single nucleotide polymorphisms of interleukin-1 family with atopic dermatitis

2014 ◽  
Vol 42 (3) ◽  
pp. 212-215 ◽  
Author(s):  
N. Behniafard ◽  
M. Gharagozlou ◽  
S. Sotoudeh ◽  
E. Farhadi ◽  
M. Khaledi ◽  
...  
Keyword(s):  
Atopic Dermatitis ◽  
Single Nucleotide Polymorphisms ◽  
Interleukin 1 ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

Association of β-Defensin 1 Single Nucleotide Polymorphisms with Atopic Dermatitis

2006 ◽  
Vol 142 (3) ◽  
pp. 211-218 ◽  
Author(s):  
Ernesto Prado-Montes de Oca ◽  
Alejandro García-Vargas ◽  
Reymundo Lozano-Inocencio ◽  
Martha Patricia Gallegos-Arreola ◽  
Lucila Sandoval-Ramírez ◽  
...  
Keyword(s):  
Atopic Dermatitis ◽  
Single Nucleotide Polymorphisms ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide

scholarly journals Association of Single-Nucleotide Polymorphisms of theMBL2with Atopic Dermatitis in Korean Patients

2017 ◽  
Vol 29 (5) ◽  
pp. 571 ◽  
Author(s):  
Jung Soo Kim ◽  
Soo Young Lee ◽  
Hyung Jin Hahn ◽  
Young Bok Lee ◽  
Dong Soo Yu ◽  
...  
Keyword(s):  
Atopic Dermatitis ◽  
Single Nucleotide Polymorphisms ◽  
Nucleotide Polymorphisms ◽  
Single Nucleotide ◽  
Korean Patients
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