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Natural Selection of ATP2B1 Underlies Susceptibility to Essential Hypertension.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.628516
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- Article
Genes Regulate Blood Pressure, but "Environments" Cause Hypertension.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.580443
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- Article
A network based covariance test for detecting multivariate eQTL in saccharomyces cerevisiae.
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- BMC Systems Biology, 2016, v. 10, p. 37, doi. 10.1186/s12918-015-0245-0
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- Article
Lack of Association between Tumour Necrosis Factor Receptor Superfamily Gene Polymorphisms and the Risk of Alzheimer's Disease in a Chinese Population.
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- Hong Kong Journal of Psychiatry, 2006, v. 16, n. 4, p. 128
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- Article
Shorter Telomere Length is Associated With Greater Decrease in Ankle-Brachial Index in Elderly Chinese Women but not Men.
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- Angiology, 2011, v. 62, n. 1, p. 87, doi. 10.1177/0003319710371618
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- Article
Association of disease-predisposition polymorphisms of the melatonin receptors and sunshine duration in the global human populations.
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- Journal of Pineal Research, 2010, v. 48, n. 2, p. 133, doi. 10.1111/j.1600-079X.2009.00736.x
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- Article
Dopamine Receptor D4 Gene −521C/T Polymorphism Is Associated with Opioid Dependence through Cold-Pain Responses.
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- Annals of the New York Academy of Sciences, 2008, v. 1139, p. 20, doi. 10.1196/annals.1432.054
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- Article
The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model.
- Published in:
- Scientific Reports, 2016, p. 38225, doi. 10.1038/srep38225
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- Article
CrossNorm: a novel normalization strategy for microarray data in cancers.
- Published in:
- Scientific Reports, 2016, p. 18898, doi. 10.1038/srep18898
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- Article
Chemotherapy-Related Amenorrhea and Menopause in Young Chinese Breast Cancer Patients: Analysis on Incidence, Risk Factors and Serum Hormone Profiles.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0140842
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- Article
European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations.
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- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013217
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- Article
Absence of association between angiotensin converting enzyme polymorphism and development of adult respiratory distress syndrome in patients with severe acute respiratory syndrome: a case control study.
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- BMC Infectious Diseases, 2005, v. 5, n. 1, p. 26, doi. 10.1186/1471-2334-5-26
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- Publication type:
- Article
Prognostic values of EORTC QLQ-C30 and QLQ-HCC18 index-scores in patients with hepatocellular carcinoma - clinical application of health-related quality-of-life data.
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- 2017
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- Publication type:
- journal article
Abnormal expressions of the subunits of the UDP- N-acetylglucosamine: lysosomal enzyme, N-acetylglucosamine-1-phosphotransferase, result in the formation of cytoplasmic vacuoles resembling those of the I-cells.
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- Journal of Molecular Medicine, 2007, v. 85, n. 4, p. 351, doi. 10.1007/s00109-006-0128-3
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- Article
Apolipoprotein E ε4 Allele Is Associated with Vascular Dementia.
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- Dementia & Geriatric Cognitive Disorders, 2006, v. 22, n. 4, p. 301, doi. 10.1159/000095246
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- Article
Mapping asthma-associated variants in admixed populations.
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- Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00292
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- Article
GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-09860-0
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- Article
Telomere length and cognitive function in southern Chinese community-dwelling male elders.
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- 2013
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- Publication type:
- Journal Article
Telomere length and cognitive function in southern Chinese community-dwelling male elders.
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- Age & Ageing, 2013, v. 42, n. 4, p. 450
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- Article
Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population.
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- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 525, doi. 10.1038/ejhg.2008.203
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- Article
MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study.
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- BMC Bioinformatics, 2009, v. 10, p. 1, doi. 1186/1471-2105-10-13
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- Article
Profiles of lipids, blood pressure and weight changes among premenopausal Chinese breast cancer patients after adjuvant chemotherapy.
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- 2017
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- Publication type:
- journal article
Association of SRD5A2 Variants and Serum Androstane-3α,17β-Diol Glucuronide Concentration in Chinese Elderly Men.
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- Clinical Chemistry, 2010, v. 56, n. 11, p. 1742, doi. 10.1373/clinchem.2010.150607
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- Publication type:
- Article
The association of liver function and quality of life of patients with liver cancer.
- Published in:
- 2019
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- Publication type:
- journal article
Older men with higher self-rated socioeconomic status have shorter telomeres.
- Published in:
- Age & Ageing, 2009, v. 38, n. 5, p. 553, doi. 10.1093/ageing/afp098
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- Article
Isolated persistent elevation of alanine transaminase for early diagnosis of pre-symptomatic Wilson’s disease in Chinese children.
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- World Journal of Pediatrics, 2013, v. 9, n. 4, p. 361, doi. 10.1007/s12519-013-0436-y
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- Publication type:
- Article
Functional Interaction Between SNPs and Microsatellite in the Transcriptional Regulation of Insulin-Like Growth Factor 1.
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- Human Mutation, 2013, v. 34, n. 9, p. 1289, doi. 10.1002/humu.22363
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- Article
Association of early growth response-1 gene polymorphisms with total IgE and atopy in asthmatic children.
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- Pediatric Allergy & Immunology, 2009, v. 20, n. 2, p. 142, doi. 10.1111/j.1399-3038.2008.00757.x
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- Article
Genetic association study between mbl2 and asthma phenotypes in Chinese children.
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- Pediatric Allergy & Immunology, 2006, v. 17, n. 7, p. 501, doi. 10.1111/j.1399-3038.2006.00446.x
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- Article
The C-159T polymorphism in the CD14 promoter is associated with serum total IgE concentration in atopic Chinese children.
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- Pediatric Allergy & Immunology, 2003, v. 14, n. 4, p. 255, doi. 10.1034/j.1399-3038.2003.00048.x
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- Publication type:
- Article
Thromboxane A2 receptor gene polymorphism is associated with the serum concentration of cat-specific immunoglobulin E as well as the development and severity of asthma in Chinese children.
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- Pediatric Allergy & Immunology, 2002, v. 13, n. 1, p. 10, doi. 10.1034/j.1399-3038.2002.01033.x
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- Article
Nonsense-Mediated Decay Targeted RNA (ntRNA): Proposal of a ntRNA–miRNA–lncRNA Triple Regulatory Network Usable as Biomarker of Prognostic Risk in Patients with Kidney Cancer.
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- Genes, 2022, v. 13, n. 9, p. 1656, doi. 10.3390/genes13091656
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- Article
A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait—A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis.
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- Genes, 2021, v. 12, n. 7, p. 1033, doi. 10.3390/genes12071033
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- Article
Direct Measurement of B Lymphocyte Gene Expression Biomarkers in Peripheral Blood Transcriptomics Enables Early Prediction of Vaccine Seroconversion.
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- Genes, 2021, v. 12, n. 7, p. 971, doi. 10.3390/genes12070971
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- Article
A network approach to exploring the functional basis of gene-gene epistatic interactions in disease susceptibility.
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- Bioinformatics, 2018, v. 34, n. 10, p. 1741, doi. 10.1093/bioinformatics/bty005
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- Article
Detecting two-locus associations allowing for interactions in genome-wide association studies.
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- Bioinformatics, 2010, v. 26, n. 20, p. 2517, doi. 10.1093/bioinformatics/btq486
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- Publication type:
- Article
Predictive rule inference for epistatic interaction detection in genome-wide association studies.
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- Bioinformatics, 2010, v. 26, n. 1, p. 30, doi. 10.1093/bioinformatics/btp622
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- Publication type:
- Article
The predisposition to thyrotoxic periodic paralysis ( TPP) is due to a genetic variant in the inward-rectifying potassium channel, KCNJ2.
- Published in:
- Clinical Endocrinology, 2014, v. 80, n. 5, p. 770, doi. 10.1111/cen.12277
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- Article
Haplotype effect in the IGF1 promoter accounts for the association between microsatellite and serum IGF1 concentration.
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- Clinical Endocrinology, 2011, v. 74, n. 4, p. 520, doi. 10.1111/j.1365-2265.2010.03962.x
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- Article
The α<sub>1S</sub> subunit of the L-type calcium channel is not a predisposition gene for thyrotoxic periodic paralysis.
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- Clinical Endocrinology, 2007, v. 66, n. 2, p. 229, doi. 10.1111/j.1365-2265.2006.02713.x
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- Article
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 4, p. 655, doi. 10.1093/hmg/8.4.655
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- Article