Associated Papers
Genetic Variants of Interleukin-8 and Interleukin-16 and Their Association with Cervical Cancer Risk.
Watrowski R et al.
Life (basel, Switzerland), 2025
Association of the Single Nucleotide Polymorphisms rs11556218, rs4778889, rs4072111, and rs1131445 of the Interleukin-16 Gene with Ovarian Cancer.
Watrowski R et al.
International Journal of Molecular Sciences, 2024
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
38790902 (PubMed )
Supplement: biomedicines-12-00940-s001.zip › biomedicines-2930173-supplementary.pdf
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
37292598 (PubMed )
Supplement: media-1.xlsx › Variants
The role of IL‑16 gene polymorphisms in endometriosis.
Matalliotakis M et al.
International Journal of Molecular Medicine, 2018
Genetic association study in a three-generation family with seven members with endometriosis.
Matalliotakis M et al.
Molecular Medicine Reports, 2017
A variant of the CXCL11 gene may influence susceptibility to contact allergy, particularly in polysensitized patients.
Westphal GA et al.
Contact Dermatitis, 2016
Association of interleukin 16 gene polymorphisms and plasma IL16 level with osteosarcoma risk.
Tang YJ et al.
Scientific Reports, 2016
Association of interleukin-16 polymorphisms with disease progression and susceptibility in endometriosis.
Azimzadeh P et al.
International Journal of Immunogenetics, 2016
modPDZpep: a web resource for structure based analysis of human PDZ-mediated interaction networks.
Sain N et al.
Biology Direct, 2016
27655048 (PubMed )
Supplement: 13062_2016_151_MOESM1_ESM.xls › Sheet4
Genetic variants in apoptosis and immunoregulation-related genes are associated with risk of chronic lymphocytic leukemia.
Enjuanes A et al.
Cancer Research, 2008
Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis.
Sellick GS et al.
Blood, 2008
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