Found: 13
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Exosomal MALAT1 Derived from High Glucose-Treated Macrophages Up-Regulates Resistin Expression via miR-150-5p Downregulation.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 3, p. 1095, doi. 10.3390/ijms23031095
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- Publication type:
- Article
Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor.
- Published in:
- Molecular Human Reproduction, 2012, v. 18, n. 3, p. 129, doi. 10.1093/molehr/gar065
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- Publication type:
- Article
A Refined Study of <i>FCRL</i> Genes from a Genome-Wide Association Study for Graves’ Disease.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0057758
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- Article
Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 661, doi. 10.1007/s00439-013-1404-2
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- Publication type:
- Article
Hyperbaric oxygen‐induced long non‐coding RNA MALAT1 exosomes suppress MicroRNA‐92a expression in a rat model of acute myocardial infarction.
- Published in:
- Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 22, p. 12945, doi. 10.1111/jcmm.15889
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- Publication type:
- Article
(-)-Epigallocatechin Gallate Promotes MicroRNA 145 Expression against Myocardial Hypoxic Injury through Dab2/Wnt3a/β-catenin.
- Published in:
- American Journal of Chinese Medicine, 2020, v. 48, n. 2, p. 341, doi. 10.1142/S0192415X20500172
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- Article
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 20, p. 5505
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- Publication type:
- Article
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 16, p. 3347
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- Publication type:
- Article
Chrysin boosts KLF2 expression through suppression of endothelial cell-derived exosomal microRNA-92a in the model of atheroprotection.
- Published in:
- European Journal of Nutrition, 2021, v. 60, n. 8, p. 4345, doi. 10.1007/s00394-021-02593-1
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- Article
G11R mutation in GJB6 gene causes hidrotic ectodermal dysplasia involving only hair and nails in a Chinese family.
- Published in:
- 2010
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- Publication type:
- Letter
The influence of the genetic and non-genetic factors on bone mineral density and osteoporotic fractures in Chinese women.
- Published in:
- Endocrine (1355008X), 2013, v. 43, n. 1, p. 127, doi. 10.1007/s12020-012-9726-8
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- Publication type:
- Article
Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 6, p. 1156, doi. 10.1093/hmg/ddn442
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- Publication type:
- Article
Dense mapping of IL2 RA shows no association with Graves' disease in Chinese Han population.
- Published in:
- Clinical Endocrinology, 2013, v. 79, n. 2, p. 267, doi. 10.1111/cen.12115
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- Publication type:
- Article