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Possible roles of genetic variations in chemotherapy related cardiotoxicity in pediatric acute lymphoblastic leukemia and osteosarcoma

BMC cancer, 2018-07, Vol.18 (1), p.704-704, Article 704

2018

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Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis

PloS one, 2013-08, Vol.8 (8), p.e69843-e69843

2013

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MiR-128-3p as blood based liquid biopsy biomarker in childhood acute lymphoblastic leukemia

Molecular and cellular probes, 2023-02, Vol.67, p.101893-101893, Article 101893

2023

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Subgroups of Paediatric Acute Lymphoblastic Leukaemia Might Differ Significantly in Genetic Predisposition to Asparaginase Hypersensitivity

PloS one, 2015-10, Vol.10 (10), p.e0140136-e0140136

2015

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Two tagging single‐nucleotide polymorphisms to capture HLA‐DRB107:01–DQA102:01–DQB102:02 haplotype associated with asparaginase hypersensitivity

British journal of clinical pharmacology, 2021-06, Vol.87 (6), p.2542-2548

2021

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Implication of BIRC5 in asthma pathogenesis

International immunology, 2012-05, Vol.24 (5), p.293-301

2012

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Investigation of the Possible Role of the Hippo/YAP1 Pathway in Asthma and Allergy

Allergy, 2017, Asthma & Immunology Research, 9(3), , pp.247-256

2017

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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, 2012-10, Vol.1820 (10), p.1512-1518

2012

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Gene expression profiling of experimental asthma reveals a possible role of paraoxonase-1 in the disease

International immunology, 2009-08, Vol.21 (8), p.967-975

2009

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Asthma Endophenotypes and Polymorphisms in the Histamine Receptor HRH4 Gene

International archives of allergy and immunology, 2012-01, Vol.159 (2), p.109-120

2012

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Investigation of circulating lncRNAs as potential biomarkers in chronic respiratory diseases

Journal of translational medicine, 2020-11, Vol.18 (1), p.422-422, Article 422

2020

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Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia

Leukemia research, 2008-08, Vol.32 (8), p.1214-1220

2008

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Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population

Journal of community genetics, 2012-01, Vol.3 (1), p.25-33

2012

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Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

Journal of translational medicine, 2019-11, Vol.17 (1), p.372-372, Article 372

2019

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MicroRNA-181a as novel liquid biopsy marker of central nervous system involvement in pediatric acute lymphoblastic leukemia

Journal of translational medicine, 2020-06, Vol.18 (1), p.250-250, Article 250

2020

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Lack of evidence for association of two functional SNPs of CHI3L1 gene (HC-gp39) with rheumatoid arthritis

Rheumatology international, 2011-08, Vol.31 (8), p.1003-1007

2011

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Strengths and weaknesses of gene association studies in childhood acute lymphoblastic leukemia

Leukemia research, 2010-03, Vol.34 (3), p.269-271

2010

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Pharmacogenetic analysis of high-dose methotrexate treatment in children with osteosarcoma

Oncotarget, 2017-02, Vol.8 (6), p.9388-9398

2017

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Co-Detection of VEGF-A and Its Regulator, microRNA-181a, May Indicate Central Nervous System Involvement in Pediatric Leukemia

Pathology oncology research, 2022-04, Vol.28, p.1610096-1610096

2022

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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, 2014-08, Vol.166 (3), p.410-420

2014

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

BMC medical genomics, 2012-09, Vol.5 (1), p.42-42, Article 42

2012

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ABCC1 polymorphisms in anthracycline-induced cardiotoxicity in childhood acute lymphoblastic leukaemia

Cell biology international, 2012-01, Vol.36 (1), p.79-86

2012

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The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia

Cellular immunology, 2006-12, Vol.244 (2), p.121-124

2006

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Pharmacogenetics of the Central Nervous System—Toxicity and Relapse Affecting the CNS in Pediatric Acute Lymphoblastic Leukemia

Cancers, 2021-05, Vol.13 (10), p.2333

2021

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Possible roles of genetic variations in chemotherapy related cardiotoxicity in pediatric acute lymphoblastic leukemia and osteosarcoma

Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis

MiR-128-3p as blood based liquid biopsy biomarker in childhood acute lymphoblastic leukemia

Subgroups of Paediatric Acute Lymphoblastic Leukaemia Might Differ Significantly in Genetic Predisposition to Asparaginase Hypersensitivity

Two tagging single‐nucleotide polymorphisms to capture HLA‐DRB107:01–DQA102:01–DQB102:02 haplotype associated with asparaginase hypersensitivity

Implication of BIRC5 in asthma pathogenesis

Investigation of the Possible Role of the Hippo/YAP1 Pathway in Asthma and Allergy

Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: Association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population

Gene expression profiling of experimental asthma reveals a possible role of paraoxonase-1 in the disease

Asthma Endophenotypes and Polymorphisms in the Histamine Receptor HRH4 Gene

Investigation of circulating lncRNAs as potential biomarkers in chronic respiratory diseases

Association of some rare haplotypes and genotype combinations in the MDR1 gene with childhood acute lymphoblastic leukaemia

Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population

Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

MicroRNA-181a as novel liquid biopsy marker of central nervous system involvement in pediatric acute lymphoblastic leukemia

Lack of evidence for association of two functional SNPs of CHI3L1 gene (HC-gp39) with rheumatoid arthritis

Strengths and weaknesses of gene association studies in childhood acute lymphoblastic leukemia

Pharmacogenetic analysis of high-dose methotrexate treatment in children with osteosarcoma

Co-Detection of VEGF-A and Its Regulator, microRNA-181a, May Indicate Central Nervous System Involvement in Pediatric Leukemia

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

Evaluation of a partial genome screening of two asthma susceptibility regions using bayesian network based bayesian multilevel analysis of relevance

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

ABCC1 polymorphisms in anthracycline-induced cardiotoxicity in childhood acute lymphoblastic leukaemia

The role of ABC-transporter gene polymorphisms in chemotherapy induced immunosuppression, a retrospective study in childhood acute lymphoblastic leukaemia

Pharmacogenetics of the Central Nervous System—Toxicity and Relapse Affecting the CNS in Pediatric Acute Lymphoblastic Leukemia

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