Works matching AU Hyoung Doo Shin
Results: 138
Association of interleukin-18 gene polymorphisms with hepatitis B virus clearance.
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- 2010
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- Publication type:
- journal article
Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma.
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- 2017
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- Publication type:
- journal article
Scanning of genetic effects of alcohol metabolism gene ( ADH1B and ADH1C) polymorphisms on the risk of alcoholism.
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- Human Mutation, 2005, v. 26, n. 3, p. 224, doi. 10.1002/humu.20209
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- Article
Genetic polymorphisms in the transforming growth factor beta-induced gene associated with BMI.
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- Human Mutation, 2005, v. 25, n. 3, p. 322, doi. 10.1002/humu.9315
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- Article
Identification of novel variants in transforming growth factor-beta 1 (TGFB1) gene and association analysis with bone mineral density (Communicated by Michael Dean) Online Citation: Human Mutation, Mutation in Brief #641 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/641.pdf)
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- Human Mutation, 2003, v. 22, n. 3, p. 257, doi. 10.1002/humu.9170
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- Article
Association analysis of novel TBX21 variants with asthma phenotypes (Communicated by Michael Dean) Online Citation: Human Mutation, Mutation in Brief #640 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/640.pdf).
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- Human Mutation, 2003, v. 22, n. 3, p. 257, doi. 10.1002/humu.9169
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- Article
Identification of novel variants in transforming growth factor?beta 1 (TGFB1) gene and association analysis with bone mineral densityCommunicated by Michael DeanOnline Citation: Human Mutation, Mutation in Brief #641 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/641.pdf
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- Human Mutation, 2003, v. 22, n. 3, p. 257, doi. 10.1002/humu.9170
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- Article
Association analysis of novel TBX21 variants with asthma phenotypesCommunicated by Michael DeanOnline Citation: Human Mutation, Mutation in Brief #640 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/640.pdf.
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- Human Mutation, 2003, v. 22, n. 3, p. 257, doi. 10.1002/humu.9169
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- Publication type:
- Article
Polymorphisms in fatty acid-binding protein-3 (FABP3) putative association with type 2 diabetes mellitus (Communicated by Pui-Yan Kwok) Online Citation: Human Mutation, Mutation in Brief #639 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/639.pdf)
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- Human Mutation, 2003, v. 22, n. 2, p. 180, doi. 10.1002/humu.9168
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- Article
Polymorphisms in fatty acid?binding protein?3 (FABP3) – putative association with type 2 diabetes mellitusCommunicated by Pui?Yan KwokOnline Citation: Human Mutation, Mutation in Brief #639 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/639.pdf
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- Human Mutation, 2003, v. 22, n. 2, p. 180, doi. 10.1002/humu.9168
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- Publication type:
- Article
Identification of variants in NFKBIA and association analysis with hepatocellular carcinoma risk among chronic HBV patients(Communicated by Mark H. Paalman)Online Citation: Human Mutation, Mutation in Brief #617 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/617.pdf)
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- Human Mutation, 2003, v. 21, n. 6, p. 652, doi. 10.1002/humu.9146
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- Article
Identification of novel SNPs in the interleukin 6 receptor gene (IL6R) (Communicated by Michael Dean) Online Citation: Human Mutation, Mutation in Brief #601 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/601.pdf).
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- Human Mutation, 2003, v. 21, n. 4, p. 450, doi. 10.1002/humu.9130
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- Article
Identification of novel SNPs in the interleukin 6 receptor gene (IL6R)Communicated by Michael DeanOnline Citation: Human Mutation, Mutation in Brief #601 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/601.pdf.
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- Human Mutation, 2003, v. 21, n. 4, p. 450, doi. 10.1002/humu.9130
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- Article
Association of IL-15 Polymorphisms with Bone Mineral Density in Postmenopausal Korean Women.
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- Calcified Tissue International, 2009, v. 85, n. 5, p. 369, doi. 10.1007/s00223-009-9290-2
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- Article
TGFBR3 Polymorphisms and Its Haplotypes Associated with Chronic Hepatitis B Virus Infection and Age of Hepatocellular Carcinoma Occurrence.
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- Digestive Diseases, 2011, v. 29, n. 3, p. 278, doi. 10.1159/000327559
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- Article
Genome-wide association study with the risk of schizophrenia in a Korean population.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 257, doi. 10.1002/ajmg.b.32400
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- Article
Positive Association between Aspirin-Intolerant Asthma and Genetic Polymorphisms of FSIP1: a Case-Case Study.
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- BMC Pulmonary Medicine, 2010, v. 10, p. 34, doi. 10.1186/1471-2466-10-34
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- Article
A single nucleotide polymorphism in CAPN1 associated with marbling score in Korean cattle.
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- BMC Genetics, 2008, v. 9, p. 1, doi. 10.1186/1471-2156-9-33
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- Article
Growth hormone-releasing hormone (GHRH) polymorphisms associated with carcass traits of meat in Korean cattle.
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- BMC Genetics, 2006, v. 7, p. 35, doi. 10.1186/1471-2156-7-35
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- Article
Effect of Diffuse Panbronchiolitis Critical Region 1 Polymorphisms on the Risk of Aspirin-Exacerbated Respiratory Disease in Korean Asthmatics.
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- Respiratory Care, 2012, v. 57, n. 5, p. 758, doi. 10.4187/respcare.01480
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- Article
Potential Association of DDR1 Genetic Variant with FEV<sub>1</sub> Decline by Aspirin Provocation in Asthmatics.
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- Journal of Asthma, 2012, v. 49, n. 3, p. 237, doi. 10.3109/02770903.2012.661010
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- Article
Lack of Association between CD58 Genetic Variations and Aspirin-Exacerbated Respiratory Disease in a Korean Population.
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- Journal of Asthma, 2011, v. 48, n. 6, p. 539, doi. 10.3109/02770903.2011.589557
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- Article
Putative association of SMAPIL polymorphisms with risk of aspirin intolerance in asthmatics.
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- Journal of Asthma, 2010, v. 47, n. 9, p. 959, doi. 10.1080/02770903.2010.514637
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- Article
Global DNA Methylation Pattern of Fibroblasts in Idiopathic Pulmonary Fibrosis.
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- DNA & Cell Biology, 2019, v. 38, n. 9, p. 905, doi. 10.1089/dna.2018.4557
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- Article
Association Analysis of Member RAS Oncogene Family Gene Polymorphisms with Aspirin Intolerance in Asthmatic Patients.
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- DNA & Cell Biology, 2014, v. 33, n. 3, p. 155, doi. 10.1089/dna.2013.2213
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- Article
Contribution of the OBSCN Nonsynonymous Variants to Aspirin Exacerbated Respiratory Disease Susceptibility in Korean Population.
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- DNA & Cell Biology, 2012, v. 31, n. 6, p. 1001, doi. 10.1089/dna.2011.1436
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- Article
A non-synonymous variant rs12614 of complement factor B associated with risk of chronic hepatitis B in a Korean population.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01177-w
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- Article
A PHLDB1 variant associated with the nonfunctional pituitary adenoma.
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- Journal of Neuro-Oncology, 2019, v. 142, n. 2, p. 223, doi. 10.1007/s11060-018-03082-y
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- Article
Screening for 392 polymorphisms in 141 pharmacogenes.
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- Biomedical Reports, 2014, v. 2, n. 4, p. 463, doi. 10.3892/br.2014.272
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- Article
Common DNase I polymorphism associated with autoantibody production among systemic lupus erythematosus patients.
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- Human Molecular Genetics, 2004, v. 13, n. 20, p. 2343, doi. 10.1093/hmg/ddh275
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- Article
Association of tumor necrosis factor polymorphisms with asthma and serum total IgE.
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- Human Molecular Genetics, 2004, v. 13, n. 4, p. 397, doi. 10.1093/hmg/ddh036
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- Article
Association of TNF-α promoter polymorphisms with the clearance of hepatitis B virus infection.
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- Human Molecular Genetics, 2003, v. 12, n. 19, p. 2541, doi. 10.1093/hmg/ddg262
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- Article
Association of Eotaxin gene family with asthma and serum total IgE.
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- Human Molecular Genetics, 2003, v. 12, n. 16, p. 2083, doi. 10.1093/hmg/ddg205
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- Article
Association of Eotaxin gene family with asthma and serum total IgE.
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- Human Molecular Genetics, 2003, v. 12, n. 11, p. 1279, doi. 10.1093/hmg/ddg142
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- Publication type:
- Article
Interleukin 10 haplotype associated with increased risk of hepatocellular carcinoma.
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- Human Molecular Genetics, 2003, v. 12, n. 8, p. 901, doi. 10.1093/hmg/ddg104
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- Article
A functional SNP of the Interleukin-18 gene is associated with the presence of hepatocellular carcinoma in hepatitis B virus-infected patients.
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- 2009
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- Publication type:
- journal article
CD58 polymorphisms associated with the risk of neuromyelitis optica in a Korean population.
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- BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2377-14-57
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- Article
CD58 polymorphisms associated with the risk of neuromyelitis optica in a Korean population.
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- 2014
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- Publication type:
- journal article
Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.
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- Molecular Biology Reports, 2022, v. 49, n. 11, p. 10339, doi. 10.1007/s11033-022-07796-1
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- Article
SLC29A1 (ENT1) polymorphisms and outcome of complete remission in acute myeloid leukemia.
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- 2016
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- Publication type:
- journal article
Putative association between UBE2E2 polymorphisms and the risk of gestational diabetes mellitus.
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- Gynecological Endocrinology, 2013, v. 29, n. 10, p. 904, doi. 10.3109/09513590.2013.813465
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- Article
Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-23217-6
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- Article
Association of genetic polymorphisms in CD40 with susceptibility to SLE in the Korean population.
- Published in:
- 2013
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- Publication type:
- Journal Article
Association of genetic polymorphisms in CD40 with susceptibility to SLE in the Korean population.
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- Rheumatology, 2013, v. 52, n. 4, p. 623, doi. 10.1093/rheumatology/kes339
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- Article
A sequence variant on 17q21 is associated with age at onset and severity of asthma.
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- European Journal of Human Genetics, 2010, v. 18, n. 8, p. 902, doi. 10.1038/ejhg.2010.38
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- Article
Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease.
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- Neonatology (16617800), 2015, v. 108, n. 3, p. 164, doi. 10.1159/000435874
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- Article
Epigenetic repression of CHCHD2 enhances survival from single cell dissociation through attenuated Rho A kinase activity.
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- Cellular & Molecular Life Sciences, 2024, v. 81, n. 1, p. 1, doi. 10.1007/s00018-023-05060-8
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- Article
Possible Association of SLC22A2 Polymorphisms with Aspirin-Intolerant Asthma.
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- International Archives of Allergy & Immunology, 2011, v. 155, n. 4, p. 395, doi. 10.1159/000321267
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- Article
Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases.
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- Allergy & Asthma Proceedings, 2017, v. 38, n. 1, p. e4, doi. 10.2500/aap.2017.38.4014
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- Article
Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.
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- Liver International, 2018, v. 38, n. 9, p. 1576, doi. 10.1111/liv.13675
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- Publication type:
- Article