Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sex-specific childhood leukemia risk
Author:
Publisher
Informa UK Limited
Subject
Immunology,Immunology and Allergy
Link
http://www.tandfonline.com/doi/pdf/10.3109/08916930903567492
Reference41 articles.
1. Unravelling an HLA-DR Association in Childhood Acute Lymphoblastic Leukemia
2. The C282Y Mutation of HFE Is Another Male-Specific Risk Factor for Childhood Acute Lymphoblastic Leukemia
3. A male-specific increase in the HLA-DRB4 (DR53) frequency in high-risk and relapsed childhood ALL
4. Evidence that an HLA-DQA1-DQB1 haplotype influences susceptibility in childhood common acute lymphoblastic leukaemia in boys provides further support for an infection-related aetiology
5. Genetic susceptibility to childhood common acute lymphoblastic leukaemia is associated with polymorphic peptide-binding pocket profiles in HLA-DPB1*0201
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1. HLA DRB1 alleles, IFN-γ and TGF-β Gene Variants in childhood ALL patients;Turkish Journal of Biochemistry;2022-05-24
2. Allergies, genetic polymorphisms of Th2 interleukins, and childhood acute lymphoblastic leukemia: The ESTELLE study;Pediatric Blood & Cancer;2021-10-18
3. Multi-Omics Analysis of Acute Lymphoblastic Leukemia Identified the Methylation and Expression Differences Between BCP-ALL and T-ALL;Frontiers in Cell and Developmental Biology;2021-01-21
4. Sex-specific differences in peripheral blood leukocyte transcriptional response to LPS are enriched for HLA region and X chromosome genes;Scientific Reports;2021-01-13
5. Association of HLA-DRA and IL2RA Polymorphisms with the Severity and Relapses Rate of Multiple Sclerosis in an Iranian Population;Reports of Biochemistry and Molecular Biology;2020-06-01
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