Issue Information.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3251
- Publication type:
- Article
Works matching IS 1099498X AND DT 2020 AND VI 22 AND IP 8
Results: 15
1
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miR‐129‐5p attenuates hypoxia‐induced apoptosis in rat H9c2 cardiomyocytes by activating autophagy.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3200
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- Publication type:
- Article
3
Clinical experience regarding the accuracy of NIPT in the detection of sex chromosome abnormality.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3199
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- Publication type:
- Article
4
Cnidium lactone prevents bone loss in an ovariectomized rat model through the estrogen‐α/BMP‐2/Smad signaling pathway.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3198
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- Publication type:
- Article
5
Triple diagnosis of Wiedemann‐Steiner, Waardenburg and DLG3‐related intellectual disability association found by WES: A case report.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3197
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- Publication type:
- Article
6
A homozygous missense variant in the homeobox domain of the NKX6‐2 results in progressive spastic ataxia type 8 associated with lower limb weakness and neurological manifestations.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3196
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- Publication type:
- Article
7
Zinc finger protein 750(ZNF750), negatively regulated by miR‐17‐5p, inhibits proliferation, motility and invasion of colonic cancer cells.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3195
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- Publication type:
- Article
8
The impact of catalase and glutathione peroxidase‐1 genetic polymorphisms on their enzyme activities among Egyptian patients with keratoconus.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3192
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- Publication type:
- Article
9
A novel UBE2A mutation in a Chinese family with X‐linked intellectual disability.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3191
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- Publication type:
- Article
10
Association of MYC gene polymorphisms with neuroblastoma risk in Chinese children: A four‐center case–control study.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3190
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- Publication type:
- Article
11
TFPI2 and NDRG4 gene promoter methylation analysis in peripheral blood mononuclear cells are novel epigenetic noninvasive biomarkers for colorectal cancer diagnosis.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3189
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- Publication type:
- Article
12
MiR‐96‐5p promotes breast cancer migration by activating MEK/ERK signaling.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3188
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- Publication type:
- Article
13
Andrographolide mitigates cartilage damage via miR‐27‐3p‐modulated matrix metalloproteinase13 repression.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3187
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- Publication type:
- Article
14
TIMD4 exhibits regulatory capability on the proliferation and apoptosis of diffuse large B‐cell lymphoma cells via the Wnt/β‐catenin pathway.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3186
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- Publication type:
- Article
15
Compound heterozygous mutations in ABCG5 or ABCG8 causing Chinese familial Sitosterolemia.
- Published in:
- Journal of Gene Medicine, 2020, v. 22, n. 8, p. 1, doi. 10.1002/jgm.3185
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- Publication type:
- Article