Found: 16
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Activation of p38/HSP27 pathway counters melatonin-induced inhibitory effect on proliferation of human gastric cancer cells.
- Published in:
- Journal of Biomedical Research, 2019, v. 33, n. 5, p. 317, doi. 10.7555/JBR.33.20180066
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- Publication type:
- Article
Metabolic Abnormalities Linked to Auditory Pathways in ApoE -Knockout HEI-OC1 Cells: A Transcription-Metabolism Co-Analysis.
- Published in:
- Biomolecules (2218-273X), 2022, v. 12, n. 9, p. 1217, doi. 10.3390/biom12091217
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- Publication type:
- Article
Application of ultrasound in the closed reduction and percutaneous pinning in supracondylar humeral fractures.
- Published in:
- Journal of Orthopaedic Surgery & Research, 2021, v. 16, n. 1, p. 1, doi. 10.1186/s13018-021-02755-1
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- Publication type:
- Article
Dynamic expression analysis of armc10, the homologous gene of human GPRASP2, in zebrafish embryos.
- Published in:
- Molecular Medicine Reports, 2017, v. 16, n. 5, p. 5931, doi. 10.3892/mmr.2017.7357
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- Publication type:
- Article
Identification of a novel MYO6 mutation associated with autosomal dominant non-syndromic hearing loss in a Chinese family by whole-exome sequencing.
- Published in:
- Genes & Genetic Systems, 2018, v. 93, n. 5, p. 171, doi. 10.1266/ggs.18-00006
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- Publication type:
- Article
Deletion of OSBPL2 in auditory cells increases cholesterol biosynthesis and drives reactive oxygen species production by inhibiting AMPK activity.
- Published in:
- Cell Death & Disease, 2019, v. 10, n. 9, p. N.PAG, doi. 10.1038/s41419-019-1858-9
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- Publication type:
- Article
Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss.
- Published in:
- 2014
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- Publication type:
- journal article
Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
- Published in:
- Journal of Translational Medicine, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1479-5876-11-163
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- Publication type:
- Article
Genetic mutations of GJB2 and mitochondrial 12S rRNA in nonsyndromic hearing loss in Jiangsu Province of China.
- Published in:
- 2013
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- Publication type:
- journal article
A systematic review and meta-analysis of 235delC mutation of GJB2 gene.
- Published in:
- Journal of Translational Medicine, 2012, v. 10, n. 1, p. 136, doi. 10.1186/1479-5876-10-136
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- Publication type:
- Article
Oxysterol-binding protein-like 2 contributes to the developmental progression of preadipocytes by binding to β-catenin.
- Published in:
- Cell Death Discovery, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41420-021-00503-2
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- Publication type:
- Article
Probing the Effect of Two Heterozygous Mutations in Codon 723 of SLC26A4 on Deafness Phenotype Based on Molecular Dynamics Simulations.
- Published in:
- Scientific Reports, 2015, p. 10831, doi. 10.1038/srep10831
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- Publication type:
- Article
The association between abnormal microRNA-10b expression and cancer risk: a meta-analysis.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep07498
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- Publication type:
- Article
Identification of I411K, a novel missense EYA4 mutation causing autosomal dominant non-syndromic hearing loss.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 34, n. 6, p. 1467, doi. 10.3892/ijmm.2014.1939
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- Publication type:
- Article
A novel compound heterozygous mutation in the GJB2 gene causing non-syndromic hearing loss in a family.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 33, n. 2, p. 310, doi. 10.3892/ijmm.2013.1581
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- Publication type:
- Article
Clinical and Genetic Features in a Chinese Pedigree with Autosomal Dominant Auditory Neuropathy.
- Published in:
- ORL, 2007, v. 69, n. 2, p. 131, doi. 10.1159/000097981
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- Publication type:
- Article