Found: 26
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Genome-Wide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.01003
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- Publication type:
- Article
Telomere Length among Chinese Aged 75+ Years.
- Published in:
- Gerontology, 2023, v. 69, n. 12, p. 1414, doi. 10.1159/000534644
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- Publication type:
- Article
Effect of CYP2D6 and CYP3A4 Genotypes on the Efficacy of Cholinesterase Inhibitors in Southern Chinese Patients With Alzheimer's Disease.
- Published in:
- American Journal of Alzheimer's Disease & Other Dementias, 2019, v. 34, n. 5, p. 302, doi. 10.1177/1533317519848237
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- Publication type:
- Article
Pin1 gene expression is associated with MCI and Alzheimer's disease
- Published in:
- 2012
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- Publication type:
- Abstract
P1-292: Tagging SNPs of estrogen receptor α (ERα) gene is associated to the risk of Alzheimer’s disease in Chinese
- Published in:
- 2006
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- Publication type:
- Abstract
P1-292: Tagging SNPs of estrogen receptor α (ERα) gene is associated to the risk of Alzheimer’s disease in Chinese
- Published in:
- 2006
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- Publication type:
- Abstract
Lack of support for an association between CLEC4M homozygosity and protection against SARS coronavirus infection.
- Published in:
- 2007
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- Publication type:
- Letter
Genetic Associations of Type 2 Diabetes with Islet Amyloid Polypeptide Processing and Degrading Pathways in Asian Populations.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0062378
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- Article
The VNTR Polymorphism of the DC-SIGNR Gene and Susceptibility to HIV-1 Infection: A Meta-Analysis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0042972
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- Publication type:
- Article
The Origin and Evolution of Variable Number Tandem Repeat of CLEC4M Gene in the Global Human Population.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0030268
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- Publication type:
- Article
Polarized Secretion of Interleukin (IL)-6 and IL-8 by Human Airway Epithelia 16HBE14o- Cells in Response to Cationic Polypeptide Challenge.
- Published in:
- PLoS ONE, 2010, v. 5, n. 8, p. 1, doi. 10.1371/journal.pone.0012091
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- Article
Evidence for Positive Selection on the Osteogenin (BMP3) Gene in Human Populations.
- Published in:
- PLoS ONE, 2010, v. 5, n. 6, p. 1, doi. 10.1371/journal.pone.0010959
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- Publication type:
- Article
Re: Hormonal Markers and Hepatitis B Virus-Related Hepatocellular Carcinoma Risk: a Nested Case-Control Study Among Men.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2003, v. 95, n. 7, p. 559, doi. 10.1093/jnci/95.7.559
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- Article
Association between HLA-A Alleles and Alzheimer’s Disease in a Southern Chinese Community.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2008, v. 26, n. 5, p. 391, doi. 10.1159/000164275
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- Publication type:
- Article
Interferon response and profiling of interferon response genes in peripheral blood of vaccine-naive COVID-19 patients.
- Published in:
- Frontiers in Immunology, 2024, p. 01, doi. 10.3389/fimmu.2023.1315602
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- Publication type:
- Article
Renal Outcome in Type 2 Diabetic Patients With or Without Coexisting Nondiabetic Nephropathies.
- Published in:
- Diabetes Care, 2002, v. 25, n. 5, p. 900, doi. 10.2337/diacare.25.5.900
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- Publication type:
- Article
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.
- Published in:
- Nature Communications, 2015, v. 6, n. 9, p. 8355, doi. 10.1038/ncomms9355
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- Publication type:
- Article
Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 8, p. 1577, doi. 10.1093/hmg/ddx045
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- Publication type:
- Article
Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 19, p. 5271, doi. 10.1093/hmg/ddu224
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- Publication type:
- Article
A single nucleotide polymorphism in microRNA-146a is associated with the risk for nasopharyngeal carcinoma.
- Published in:
- Molecular Carcinogenesis, 2013, v. 52, p. 28, doi. 10.1002/mc.21937
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- Publication type:
- Article
Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation.
- Published in:
- Human Mutation, 2013, v. 34, n. 4, p. 655, doi. 10.1002/humu.22286
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- Publication type:
- Article
VCNet: vector-based gene co-expression network construction and its application to RNA-seq data.
- Published in:
- Bioinformatics, 2017, v. 33, n. 14, p. 2173, doi. 10.1093/bioinformatics/btx131
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- Publication type:
- Article
Cholesterol 24-hydroxylase (CYP46A1) polymorphisms are associated with faster cognitive deterioration in Chinese older persons: a two-year follow up study.
- Published in:
- International Journal of Geriatric Psychiatry, 2009, v. 24, n. 9, p. 921, doi. 10.1002/gps.2196
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- Publication type:
- Article
5-HT2A T102C receptor polymorphism and neuropsychiatric symptoms in Alzheimer's disease.
- Published in:
- 2004
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- Publication type:
- Journal Article
5-HT<sub>2A</sub> T102C receptor polymorphism and neuropsychiatric symptoms in Alzheimer's disease.
- Published in:
- International Journal of Geriatric Psychiatry, 2004, v. 19, n. 6, p. 523, doi. 10.1002/gps.1109
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- Publication type:
- Article
Peripheral Blood T Cell Gene Expression Responses to Exercise and HMB in Sarcopenia.
- Published in:
- Nutrients, 2021, v. 13, n. 7, p. 2313, doi. 10.3390/nu13072313
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- Publication type:
- Article