Associated Papers
Hereditary predisposition to malignant myeloid hemopathies: Caution in use of saliva and guideline based on our experience.
Perani A et al.
Frontiers in Oncology, 2023
36923434 (PubMed )
Supplement: DataSheet_1.zip › Data_Sheet_1 › Table_S3.xlsx › 1_Patient_4
Polymorphisms in genes involved in breast cancer among Iranian patients.
Farnoosh G et al.
Personalized Medicine, 2021
cDNA-Based Mutation Screening Using a Combination of High-Resolution Melting Curve and Fragment Analysis Facilitates Efficient CCR4 Mutation Analysis in Adult T-Cell Leukemia/Lymphoma.
Mizuta S et al.
American Journal of Clinical Pathology, 2020
Single Nucleotide Variants Associated with Colorectal Cancer Among Iranian Patients: A Narrative Review.
Jamshidi M et al.
Pharmacogenomics and Personalized Medicine, 2020
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
25671699 (PubMed )
Supplement: pgen.1004955.s006.xlsx › SNVs
CCR4 C1014T and CCL22 C16A genetic variations in the Iranian patients with colorectal adenocarcinoma.
Erfani N et al.
Iranian Journal of Allergy, Asthma, and Immunology, 2014
Genetic Polymorphisms of CCL22 and CCR4 in Patients with Lung Cancer.
Erfani N et al.
Iranian Journal of Medical Sciences, 2014
Genetic susceptibility to atopic dermatitis.
Kiyohara C et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2008
Association screen for atopic dermatitis candidate gene regions using microsatellite markers in pooled DNA samples.
Hoffjan S et al.
International Journal of Immunogenetics, 2006
Lack of association of CCR4 single nucleotide polymorphism with atopic dermatitis in Japanese patients.
Tsunemi Y et al.
Acta Dermato-venereologica, 2004
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