Human DICER1 Antigen Immunoaffinity Purified Polyclonal
- Known as:
- Human DICER1 Antigen Immunoaffinity Purified Polyclonal
- Catalog number:
- x2756p
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Exalpha
- Gene target:
- Human DICER1 Antigen Immunoaffinity Purified Polyclonal
Ask about this productRelated genes to: Human DICER1 Antigen Immunoaffinity Purified Polyclonal
- Gene:
- DICER1 NIH gene
- Name:
- dicer 1, ribonuclease III
- Previous symbol:
- MNG1
- Synonyms:
- Dicer, KIAA0928, K12H4.8-LIKE, HERNA
- Chromosome:
- 14q32.13
- Locus Type:
- gene with protein product
- Date approved:
- 2002-05-09
- Date modifiied:
- 2019-04-23
- Gene:
- DICER1-AS1 NIH gene
- Name:
- DICER1 antisense RNA 1
- Previous symbol:
- DICER1-AS
- Synonyms:
- FLJ45244
- Chromosome:
- 14q32.13
- Locus Type:
- RNA, long non-coding
- Date approved:
- 2011-09-16
- Date modifiied:
- 2018-05-18
Related products to: Human DICER1 Antigen Immunoaffinity Purified Polyclonal
Related articles to: Human DICER1 Antigen Immunoaffinity Purified Polyclonal
- The article "High levels of long non-coding RNA DICER1-AS1 are associated with poor clinical prognosis in patients with osteosarcoma" by X.-H. Hu, J. Dai, H.-L. Shang, Z.-X. Zhao, Y.-D. Hao, published in Eur Rev Med Pharmacol Sci 2018; 22 (22): 7640-7645-DOI: 10.26355/eurrev_201811_16379-PMID: 30536305 has been retracted in accordance with the Publisher and the Editor in Chief. Following some concerns raised on PubPeer (link: https://pubpeer.com/publications/2F91E52E0FA92A70237B1ECA287AF6), the Editor in Chief has started an investigation to assess the validity of the concerns raised. The journal's investigation identified that authors used primers specific to mouse genes for clinical samples, revealing ethical misconduct and data fabrication. The Editorial Team has contacted the authors to inform them of the ongoing investigation and to request the original data supporting the manuscript; however, the authors have not responded to these communications. Consequently, the Editor in Chief has decided to retract the article. This article has been retracted. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/16379. - Source: PubMed
Hu X-HDai JShang H-LZhao Z-XHao Y-D - - Source: PubMed
Publication date: 2024/01/30
Gu ZenghuiHou ZhenhaiZheng LongbaoWang XinqiangWu LiangbangZhang Cheng - [This retracts the article DOI: 10.2147/CMAR.S252786.]. - Source: PubMed
Publication date: 2023/07/26
- DICER1-AS1 is reported to promote the progression and disturb the cell cycle in osteosarcoma; however, its mechanism has rarely been studied. - Source: PubMed
Publication date: 2023/06/13
Fu LaihuaXu SongfengZhou YangHuang JingyangQiu JinHuang Pengzhou - Long non-coding RNAs (lncRNAs) are major genetic factors whose disruption lead to many diseases, including nervous system diseases. Bipolar disorder (BD) is a neuro-psychiatric disease with no definitive diagnosis and incomplete treatment. Regarding the role of NF-κB-associated lncRNAs in the neuro-psychiatric disorders, we examined the expression of three lncRNAs, DICER1-AS1, DILC, and CHAST, in BD patients. To assess lncRNA expression in peripheral blood mononuclear cells (PBMCs) of 50 BD patients and 50 healthy individuals, Real-time PCR was used. Additionally, some clinical characteristics of BD patients were investigated via an analysis of ROC curves and correlations. Based on our results, the expression level of CHAST increased significantly in BD patients in comparison with healthy people, in BD men compared with healthy men, as well as in BD women in comparison with control females (p < 0.05). A similar increase in expression was observed for DILC and DICER1-AS1 lncRNAs in female patients compared with healthy women. Whereas compared to healthy men, DILC was decreased in diseased men. Based on the results of the ROC curve, the area under the curve (AUC) for CHAST lncRNA was 0.83 with a P value of 0.0001. So, the expression level of CHAST lncRNA could play a role in the pathobiology of the BD and be considered a good putative biomarker for individuals with bipolar disorder. - Source: PubMed
Publication date: 2023/06/06
Pirbalouti Razieh GhasemiMohseni Mahdieh MehrabTaheri MohammadNeishabouri Seyedeh MorvaridShirvani-Farsani Zeinab