Diabetes research clinical practice journal


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Journal of Translational Medicine. Frontiers in Genetics. Plasma neutrophil extracellular trap level is modified by disease severity and inhaled corticosteroids diabetes research clinical practice journal chronic inflammatory lung diseases.

Scientific Reports. 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.

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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. 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.

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Early repositioning through compound set enrichment analysis: a knowledge-recycling strategy. Future Medicinal Chemistry. Complex analysis of multiple single nucleotide polymorphisms as 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 Bayesian relevance and effect size analysis. Elevated complement factor 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.

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Diabetes research clinical practice journal Et Biophysica Acta. 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. Implication of BIRC5 in asthma pathogenesis. International Immunology.

Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population. Cukorbetegség diabetikus nefropátia kezelésére of Community Genetics.

ABCC1 polymorphisms in anthracycline-induced cardiotoxicity in childhood acute lymphoblastic leukaemia. Cell Biology International. Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia.

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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.

Implementing a Diabetes Risk Assessment Tool into Clinical Practice

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.

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Immunological Investigations. CCR5 Delta 32 mutation, Mycoplasma pneumoniae infection, and asthma. The Journal of Allergy and Clinical Immunology. Chlamydophila pneumoniae infection status is dependent on the subtypes of asthma and allergy. The HLA 8. Haplotype-independent association of the C allele with high hemoglobinA1C levels in diabetic patients.

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Molecular Immunology. The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia. Cellular Immunology. Involvement of TNFalpha A promoter polymorphism in the development of asthma in children infected with Chlamydophila pneumoniae. Pediatric Research. Pediatric asthmatic patients have low serum levels of monocyte chemoattractant protein Orvosi Hetilap.

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PMID 0. Frequencies of two common mutations c. International Journal of Molecular Medicine. Genetic basis of tobacco smoking: strong association of a specific major histocompatibility complex haplotype on chromosome 6 with smoking behavior.

Polymorphism in the promoter region of the apolipoprotein A5 gene is associated with an increased susceptibility for coronary artery disease. The development of asthma in children infected with Chlamydia pneumoniae is dependent on the modifying effect of mannose-binding lectin. Diversity in intrinsic strengths of the human complement system: serum C4 protein concentrations correlate with C4 gene size and polygenic variations, hemolytic activities, and body mass index. Journal of Immunology Baltimore, Md.

Histamine deficiency in gene-targeted mice strongly reduces antigen-induced airway hyper-responsiveness, eosinophilia and allergen-specific IgE. Relationship between the tumor necrosis factor alpha polymorphism and the serum C-reactive protein levels in inflammatory bowel disease. Evolution of the thyrotropin receptor: a G protein coupled receptor with an intrinsic capacity to dimerize. Molecular Genetics and Metabolism. Human Immunology. Histidine decarboxylase deficiency in gene knockout mice elevates male sex steroid production.

The Journal of Endocrinology. Differences in the genetic background of latent autoimmune diabetes in adults LADA and type 1 diabetes mellitus. Immunology Letters. Histamine genomics in silico: polymorphisms of the human genes involved in the synthesis, action and degradation of histamine.

Bone marrow-derived mast cell differentiation is strongly reduced in histidine decarboxylase knockout, histamine-free mice. Association of plasma lipid levels with apolipoprotein E polymorphism in Type 2 diabetes. Diabetes Research and Clinical Practice. Association of polymorphisms and diabetes research clinical practice journal combinations in the tumour necrosis factor-α-complement MHC region with coronary artery disease [3] Journal of Medical Genetics.

Functional genomics: Potentials, hopes and post-genomic realism Lege Artis Medicinae. Polymorphism in the gene regulatory region of MCP-1 is associated with asthma susceptibility and severity Journal of Allergy and Clinical Immunology.

Involvement of polymorphisms in the chemokine system in the susceptibility for coronary artery disease CAD. Hepatic regeneration induces transient acute phase reaction: Systemic elevation of acute phase az impotencia cukorbetegség kezelésének and soluble cytokine receptors Cell Biology International. The association of serum lipoprotein a levels, apolipoprotein a size diabetes research clinical practice journal TTTTA n polymorphism with coronary heart disease.

Frequency of the RQ mutation of the apolipoprotein B gene in a sample screened clinically for familial hypercholesterolemia in Hungary. Histidine decarboxylase expression in human melanoma Journal of Investigative Dermatology. H1 histamine receptor antagonist inhibits constitutive growth of Jurkat T cells and antigen-specific proliferation of ovalbumin-specific murine T cells.

Seminars in Cancer Biology.

Kapcsolódó fájlok:

Biosynthesis of interleukin-6, an autocrine growth factor for melanoma, is regulated by melanoma-derived histamine. Influence of apolipoprotein E genotypes on serum lipid parameters in a biracial sample of children European Journal of Pediatrics.

Interleukininduced production of type II acute phase proteins and expression of junB gene are downregulated by human recombinant growth hormone in vitro Cell Biology International. Exon-intron organization of the human gp gene Gene. Angiotensin II type 1 receptor gene polymorphism and mitral valve prolapse syndrome American Heart Journal. Keratin 9 mutations in the coil 1A region in epidermolytic palmoplantar keratoderma Pediatric Dermatology.

Histamine and histamine-receptor antagonists modify gene expression and biosynthesis of interferon γ in peripheral human blood mononuclear cells and in CDdepleted cell subsets Immunology Letters. Elevated hepatic glucocorticoid receptor expression during liver regeneration in rats Pathology and Oncology Research.

Genetic investigation of patients with hypercholesterolemia type IIa [4] Clinical Genetics. Growth hormone receptor gene expression on human lymphocytic and monocytic cell lines Cell Biology International. Mutations in brief no. Online Human Mutation.