DIABETES RESEARCH AND CLINICAL PRACTICE

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If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know. Investigation of circulating lncRNAs as potential biomarkers in chronic respiratory diseases.

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Journal of Translational Medicine. Frontiers in Genetics. Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids in chronic inflammatory lung diseases. Scientific Reports.

Diabetes Research and Clinical Practice

Variation in the TEK gene is not associated with asthma but with allergic conjunctivitis. International Journal of Immunogenetics. Szalai C, et al. From genomes to diaries: a 3-year prospective, real-life study of ragweed-specific sublingual immunotherapy. Pharmacogenetic analysis of high-dose methotrexate treatment in children with osteosarcoma.

Pharmacogenetics of anthracyclines. VariantMetaCaller: automated fusion of variant calling pipelines for quantitative, precision-based filtering. Bmc Genomics. Plos One. Impact of single nucleotide polymorphisms of cytarabine metabolic genes on drug toxicity in childhood acute lymphoblastic leukemia.

In interaction with gender a common CYP3A4 polymorphism may influence the survival rate of chemotherapy for childhood acute lymphoblastic leukemia.

DIABETES RESEARCH AND CLINICAL PRACTICE

The Pharmacogenomics Journal. Genomic approach to complex diseases Ifmbe Proceedings. DOI: Associations of novel genetic variations in the folate-related and ARID5B genes with the pharmacokinetics and toxicity of high-dose methotrexate in paediatric acute lymphoblastic leukaemia.

British Journal of Haematology. Early repositioning through compound set enrichment analysis: a knowledge-recycling strategy. Future Medicinal Chemistry.

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Complex analysis of multiple single nucleotide polymorphisms diabetes mazi kezelése putative risk factors of tooth agenesis in the Hungarian population.

Acta Odontologica Scandinavica. Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Diabetes research clinical practice journal relevance and effect size analysis. Elevated complement diabetes research clinical practice journal H levels in asthmatic sputa. Journal of Clinical Immunology.

Candidate gene association study in pediatric acute lymphoblastic leukemia evaluated by Bayesian network based Bayesian multilevel analysis of relevance. Bmc Medical Genomics.

Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: association of galectin-8 F19Y occurrence with autoimmune diseases in a Caucasian population. Biochimica Et Biophysica Acta.

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Asthma endophenotypes and polymorphisms in the histamine receptor HRH4 gene. International Archives of Allergy and Immunology. Evaluation of a partial genome screening of two asthma susceptibility regions using bayesian network based bayesian multilevel analysis of relevance.

Clinical Practice Update in Endocrinology \u0026 Diabetes

Implication of BIRC5 in asthma pathogenesis. International Immunology.

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Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population. Journal of Community Genetics. ABCC1 polymorphisms in anthracycline-induced cardiotoxicity in childhood acute lymphoblastic leukaemia.

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Cell Biology International. Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia. Nature Genetics. Meta-analysis of adrenocortical tumour genomics data: novel pathogenic pathways revealed.

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Strengths and weaknesses of gene association studies in childhood acute lymphoblastic leukemia. Leukemia Research. Genomic background of asthma Lege Artis Medicinae. Gene expression profiling of experimental asthma reveals a possible role of paraoxonase-1 in the disease. Asthma from a pharmacogenomic point of view. British Journal of Pharmacology.

Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia. Frequency of carriers of 8. Immunological Investigations. CCR5 Delta 32 mutation, Mycoplasma pneumoniae infection, and asthma. The Journal of Allergy and Clinical Immunology.

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Chlamydophila pneumoniae infection status is dependent on the subtypes of asthma and allergy. The HLA 8.