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Association analysis of ILVBL gene polymorphisms with aspirin-exacerbated respiratory disease in asthma.
- Published in:
- 2017
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- Publication type:
- journal article
Association of interleukin-18 gene polymorphisms with hepatitis B virus clearance.
- Published in:
- 2010
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- Publication type:
- journal article
Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases.
- Published in:
- Allergy & Asthma Proceedings, 2017, v. 38, n. 1, p. e4, doi. 10.2500/aap.2017.38.4014
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
MicroRNA-196A-2 polymorphisms and hepatocellular carcinoma in patients with chronic hepatitis B.
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- Journal of Medical Virology, 2014, v. 86, n. 3, p. 446, doi. 10.1002/jmv.23848
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- Publication type:
- Article
Association of polymorphism in MicroRNA 219-1 with clearance of hepatitis B virus infection.
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- Journal of Medical Virology, 2013, v. 85, n. 5, p. 808, doi. 10.1002/jmv.23551
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- Publication type:
- Article
Lack of association of RAD51 genetic variations with hepatitis B virus clearance and occurrence of hepatocellular carcinoma in a Korean population.
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- Journal of Medical Virology, 2011, v. 83, n. 11, p. 1892, doi. 10.1002/jmv.22122
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- Publication type:
- Article
Epigenome-Wide Association Analysis of Differentially Methylated Signals in Blood Samples of Patients with Non-Small-Cell Lung Cancer.
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- Journal of Clinical Medicine, 2019, v. 8, n. 9, p. 1307, doi. 10.3390/jcm8091307
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- Publication type:
- 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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- Publication type:
- Article
Association analysis of formyl peptide receptor 2 (FPR2) polymorphisms and Aspirin exacerbated respiratory diseases.
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- Journal of Human Genetics, 2012, v. 57, n. 4, p. 247, doi. 10.1038/jhg.2012.12
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- Publication type:
- Article
UBE3C genetic variations as potent markers of nasal polyps in Korean asthma patients.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 797, doi. 10.1038/jhg.2011.104
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- Publication type:
- Article
Genetic association analysis of TAP1 and TAP2 polymorphisms with aspirin exacerbated respiratory disease and its FEV1 decline.
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- Journal of Human Genetics, 2011, v. 56, n. 9, p. 652, doi. 10.1038/jhg.2011.75
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- Publication type:
- Article
Screening of genetic variations of SLC15A2, SLC22A1, SLC22A2 and SLC22A6 genes.
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- Journal of Human Genetics, 2011, v. 56, n. 9, p. 666, doi. 10.1038/jhg.2011.77
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- Publication type:
- Article
Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage.
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- Journal of Human Genetics, 2010, v. 55, n. 11, p. 726, doi. 10.1038/jhg.2010.97
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- Publication type:
- Article
CCND2 polymorphisms associated with clearance of HBV Infection.
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- Journal of Human Genetics, 2010, v. 55, n. 7, p. 416, doi. 10.1038/jhg.2010.36
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- Publication type:
- Article
A new association between polymorphisms of the SLC6A7 gene in the chromosome 5q31–32 region and asthma.
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- Journal of Human Genetics, 2010, v. 55, n. 6, p. 358, doi. 10.1038/jhg.2010.34
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- Publication type:
- Article
Association analysis of COMT polymorphisms with schizophrenia and smooth pursuit eye movement abnormality.
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- Journal of Human Genetics, 2009, v. 54, n. 12, p. 709, doi. 10.1038/jhg.2009.102
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- Publication type:
- Article
Association study of TP53 polymorphisms with lung cancer in a Korean population.
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- Journal of Human Genetics, 2008, v. 53, n. 6, p. 508, doi. 10.1007/s10038-008-0278-y
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- Publication type:
- Article
Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean women.
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- Journal of Human Genetics, 2007, v. 52, n. 6, p. 502, doi. 10.1007/s10038-007-0143-4
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- Publication type:
- Article
Polymorphisms in interleukin 8 and its receptors ( IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 781, doi. 10.1007/s10038-006-0021-5
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- Publication type:
- Article
Polymorphisms in the leptin receptor (LEPR)—putative association with obesity and T2DM.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 85, doi. 10.1007/s10038-005-0327-8
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- Publication type:
- Article
Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women.
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- Journal of Human Genetics, 2006, v. 51, n. 2, p. 112, doi. 10.1007/s10038-005-0331-z
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- Publication type:
- Article
Highly polymorphic human CYP4A11 gene.
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- Journal of Human Genetics, 2005, v. 50, n. 5, p. 259, doi. 10.1007/s10038-005-0245-9
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- Publication type:
- Article
Association of eotaxin-2 gene polymorphisms with plasma eotaxin-2 concentration.
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- Journal of Human Genetics, 2005, v. 50, n. 3, p. 118, doi. 10.1007/s10038-005-0230-3
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- Publication type:
- Article
Interleukin 3 (IL3) polymorphisms associated with decreased risk of asthma and atopy.
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- Journal of Human Genetics, 2004, v. 49, n. 10, p. 517, doi. 10.1007/s10038-004-0184-x
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- Publication type:
- Article
Identification of variants in cyclin D1 (CCND1) and B-Cell CLL/lymphoma 2 (BCL2).
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 8, p. 449, doi. 10.1007/s10038-004-0173-0
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- Publication type:
- Article
Association of interleukin-6 promoter variant with bone mineral density in pre-menopausal women.
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- Journal of Human Genetics, 2003, v. 48, n. 5, p. 243, doi. 10.1007/s10038-003-0020-8
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- Publication type:
- Article
Association Analysis of Neuregulin 3 Gene with Schizophrenia in a Korean Population.
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- Korean Journal of Biological Psychiatry, 2012, v. 19, n. 3, p. 128
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- Publication type:
- 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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- Publication type:
- Article
Association of FLT3 Polymorphisms With Low BMD and Risk of Osteoporotic Fracture in Postmenopausal Women.
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- Journal of Bone & Mineral Research, 2007, v. 22, n. 11, p. 1752, doi. 10.1359/jbmr.070705
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- Publication type:
- Article
Association of the OSCAR Promoter Polymorphism With BMD in Postmenopausal Women.
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- Journal of Bone & Mineral Research, 2005, v. 20, n. 8, p. 1342, doi. 10.1359/JBMR.050320
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- Publication type:
- Article
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.
- Published in:
- Nature Genetics, 2010, v. 42, n. 10, p. 864, doi. 10.1038/ng.660
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
TPX2 prompts mitotic survival via the induction of BCL2L1 through YAP1 protein stabilization in human embryonic stem cells.
- Published in:
- Experimental & Molecular Medicine EMM, 2023, v. 55, n. 1, p. 32, doi. 10.1038/s12276-022-00907-9
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- Publication type:
- Article
Positive Association between Aspirin-Intolerant Asthma and Genetic Polymorphisms of FSIP1: a Case-Case Study.
- Published in:
- BMC Pulmonary Medicine, 2010, v. 10, p. 34, doi. 10.1186/1471-2466-10-34
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- Publication type:
- Article
Independent Association of Tumor Necrosis Factor Polymorphism with Type 1 Diabetes Susceptibility.
- Published in:
- Annals of the New York Academy of Sciences, 2008, v. 1150, p. 76, doi. 10.1196/annals.1447.059
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- Publication type:
- Article
TGFBR3 Polymorphisms and Its Haplotypes Associated with Chronic Hepatitis B Virus Infection and Age of Hepatocellular Carcinoma Occurrence.
- Published in:
- Digestive Diseases, 2011, v. 29, n. 3, p. 278, doi. 10.1159/000327559
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- Publication type:
- Article
No associations of polymorphisms in ADPRT with hepatitis B virus clearance and hepatocellular carcinoma occurrence in a Korean population.
- Published in:
- Hepatology Research, 2011, v. 41, n. 3, p. 250, doi. 10.1111/j.1872-034X.2010.00772.x
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- Publication type:
- Article
Exonic Variants Associated with Development of Aspirin Exacerbated Respiratory Diseases.
- Published in:
- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111887
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- Publication type:
- Article
A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0110292
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- Publication type:
- Article
Targeted Next-Generation Sequencing at Copy-Number Breakpoints for Personalized Analysis of Rearranged Ends in Solid Tumors.
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- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100089
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- Publication type:
- Article
A Genome-Wide Association Study of Total Serum and Mite-Specific IgEs in Asthma Patients.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071958
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- Publication type:
- Article
Frequent Amplification of CENPF, GMNN and CDK13 Genes in Hepatocellular Carcinomas.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043223
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- Publication type:
- Article
Association of Polymorphism in Pri-microRNAs-371-372-373 with the Occurrence of Hepatocellular Carcinoma in Hepatitis B Virus Infected Patients.
- Published in:
- PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0041983
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- Publication type:
- Article
Loss of ATF2 Function Leads to Cranial Motoneuron Degeneration during Embryonic Mouse Development.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019091
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- Publication type:
- Article
The Genetic Effect of Copy Number Variations on the Risk of Type 2 Diabetes in a Korean Population.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019091
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- Publication type:
- Article
Genome-Wide and Follow-Up Studies Identify CEP68 Gene Variants Associated with Risk of Aspirin-Intolerant Asthma.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013818
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- Publication type:
- Article