Works matching IS 14739542 AND DT 2019 AND VI 13 AND IP 1
Results: 58
Associations between microRNA (miR-25, miR-32, miR-125, and miR-222) polymorphisms and recurrent implantation failure in Korean women.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0246-y
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- Publication type:
- Article
Downregulation of miR-542-3p promotes osteogenic transition of vascular smooth muscle cells in the aging rat by targeting BMP7.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0245-z
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- Article
The multi-faceted functioning portrait of LRF/ZBTB7A.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0252-0
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- Article
Investigating RNA expression profiles altered by nicotinamide mononucleotide therapy in a chronic model of alcoholic liver disease.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0251-1
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- Article
Human genetics and genomics research in Ecuador: historical survey, current state, and future directions.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0249-8
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- Article
EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0238-y
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- Article
Factors affecting cell-free DNA fetal fraction: statistical analysis of 13,661 maternal plasmas for non-invasive prenatal screening.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0244-0
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- Article
Genetics and functions of the retinoic acid pathway, with special emphasis on the eye.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0248-9
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- Article
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 42,910 single pregnancies with different clinical features.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0250-2
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- Article
Transcriptomic analysis of monocytes from HIV-positive men on antiretroviral therapy reveals effects of tobacco smoking on interferon and stress response systems associated with depressive symptoms.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0247-x
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- Article
Association between polymorphism in CDKN2B-AS1 gene and its interaction with smoking on the risk of lung cancer in a Chinese population.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0240-4
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- Article
Common polymorphic inversions at 17q21.31 and 8p23.1 associate with cancer prognosis.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0242-2
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- Article
Genetic variants of VEGFR-1 gene promoter in acute myocardial infarction.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0243-1
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- Publication type:
- Article
Copy number of 8q24.3 drives HSF1 expression and patient outcome in cancer: an individual patient data meta-analysis.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0241-3
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- Article
Identification of key candidate genes and molecular pathways in white fat browning: an anti-obesity drug discovery based on computational biology.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0239-x
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- Article
lncRNA TUG1 modulates proliferation, apoptosis, invasion, and angiogenesis via targeting miR-29b in trophoblast cells.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0237-z
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- Publication type:
- Article
Novel analytical methods to interpret large sequencing data from small sample sizes.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0235-1
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- Article
Interplay Between the Host, the Human Microbiome, and Drug Metabolism.
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0211-9
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- Article
Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.
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- 2019
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- Publication type:
- Letter
Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.
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- 2019
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- Publication type:
- Letter
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patients.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0209-3
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- Article
Statement on bioinformatics and capturing the benefits of genome sequencing for society.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0208-4
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- Article
Three miRNAs cooperate with host genes involved in human cardiovascular disease.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0232-4
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- Article
Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0229-z
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- Article
Diversity of ATM gene variants: a population-based genome data analysis for precision medicine.
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- 2019
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- Publication type:
- Letter
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0231-5
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- Publication type:
- Article
Identification and potential mechanisms of a 4-lncRNA signature that predicts prognosis in patients with laryngeal cancer.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0230-6
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- Publication type:
- Article
Next-generation sequencing in liquid biopsy: cancer screening and early detection.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0220-8
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- Article
Meeting report: the Human Genome Meeting (HGM) 2019 in Seoul, Korea.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0218-2
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- Article
Identification of a novel long non-coding RNA within RUNX1 intron 5.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0219-1
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- Article
Helicobacter pylori infection, serum pepsinogens as markers of atrophic gastritis, and leukocyte telomere length: a population-based study.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0217-3
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- Article
Essential genetic findings in neurodevelopmental disorders.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0216-4
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- Publication type:
- Article
A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variants.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0213-7
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- Publication type:
- Article
Correction to: Evidence that DNA repair genes, a family of tumor suppressor genes, are associated with evolution rate and size of genomes.
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- 2019
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- Publication type:
- Correction Notice
Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0212-8
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- Article
What influences public views on forensic DNA testing in the criminal field? A scoping review of quantitative evidence.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0207-5
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- Publication type:
- Article
Association of genetic ancestry with colorectal tumor location in Puerto Rican Latinos.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0196-4
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- Publication type:
- Article
Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0205-7
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- Publication type:
- Article
Studies of liver tissue identify functional gene regulatory elements associated to gene expression, type 2 diabetes, and other metabolic diseases.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0204-8
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- Publication type:
- Article
Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0203-9
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- Publication type:
- Article
The significance of trisomy 7 mosaicism in noninvasive prenatal screening.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0201-y
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- Publication type:
- Article
Genetics of heart rate in heart failure patients (GenHRate).
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- Human Genomics, 2019, v. 13, n. 1, p. 1, doi. 10.1186/s40246-019-0206-6
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- Publication type:
- Article
Correction to: The evolutionary genetics of lactase persistence in seven ethnic groups across the Iranian plateau.
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- 2019
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- Publication type:
- Correction Notice
Transcriptome-wide analysis of differentially expressed chemokine receptors, SNPs, and SSRs in the age-related macular degeneration.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0199-1
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- Publication type:
- Article
Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0198-2
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- Publication type:
- Article
Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjects.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0197-3
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- Publication type:
- Article
Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0202-x
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- Publication type:
- Article
Update on the human and mouse lipocalin (LCN) gene family, including evidence the mouse Mup cluster is result of an "evolutionary bloom".
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0191-9
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- Article
Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0192-8
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- Publication type:
- Article
Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary study.
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- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-018-0186-y
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- Publication type:
- Article