CARD6 (A2) pAb host: Rabbit
- Known as:
- CARD6 (A2) pAb production species: Rabbit
- Catalog number:
- bs1038
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Bioworld
- Gene target:
- CARD6 (A2) pAb host: Rabbit
Ask about this productRelated genes to: CARD6 (A2) pAb host: Rabbit
- Gene:
- A2MP1 NIH gene
- Name:
- alpha-2-macroglobulin pseudogene 1
- Previous symbol:
- A2MP
- Synonyms:
- -
- Chromosome:
- 12p13.31
- Locus Type:
- pseudogene
- Date approved:
- 1991-09-12
- Date modifiied:
- 2016-08-22
- Gene:
- AAR2 NIH gene
- Name:
- AAR2 splicing factor
- Previous symbol:
- C20orf4
- Synonyms:
- bA234K24.2
- Chromosome:
- 20q11.23
- Locus Type:
- gene with protein product
- Date approved:
- 2001-06-21
- Date modifiied:
- 2019-02-18
- Gene:
- ABHD17AP1 NIH gene
- Name:
- abhydrolase domain containing 17A pseudogene 1
- Previous symbol:
- FAM108A2, ABHD17AP2, FAM108A3, FAM108A11P, FAM108A3P
- Synonyms:
- C1orf47
- Chromosome:
- 1q21.2
- Locus Type:
- pseudogene
- Date approved:
- 2006-01-17
- Date modifiied:
- 2015-01-29
- Gene:
- ACBD5 NIH gene
- Name:
- acyl-CoA binding domain containing 5
- Previous symbol:
- -
- Synonyms:
- DKFZp434A2417, KIAA1996
- Chromosome:
- 10p12.1
- Locus Type:
- gene with protein product
- Date approved:
- 2003-11-11
- Date modifiied:
- 2014-11-19
- Gene:
- ACRV1 NIH gene
- Name:
- acrosomal vesicle protein 1
- Previous symbol:
- -
- Synonyms:
- SPACA2, SP-10, D11S4365
- Chromosome:
- 11q24.2
- Locus Type:
- gene with protein product
- Date approved:
- 1991-06-07
- Date modifiied:
- 2014-11-19
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- Lupus nephritis (LN) is a common complication of systemic lupus erythematosus (SLE) that symbolizes a primary contributor of morbidity and mortality. Dihydroartemisinin (DHA; artenimol) shows good therapeutic effects on LN. Its pharmacological target remains unclear. Proteolysis targeting chimeras (PROTAC) technology was used to identify the targets of DHA in LN treatment. - Source: PubMed
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Li HonglianNi ZhihaoRao YuzhenZhang JunzheGuo HuiyiYuan HaoxingYang HaoChen JiayunYang ChanWang JigangRao YuLiu Shuwen - The etiology of women with gestational diabetes mellitus (GDM) and a greater risk of developing type 2 diabetes (T2D) after delivery remains unknown. This study aimed to investigate the global gene expression in four postpartum women with previous GDM (pGDM), three with T2D, and three with a history of normoglycemic pregnancy (controls). Total RNA was extracted from whole blood between March and May 2020. Global mRNA expression was determined using an Affymetrix Human Gene 2.0 ST Array. The expression of the selected focused genes was validated by RT-PCR. The microarray revealed 140 transcripts ( < 0.05, fold change cut-off ≥ 2) in patients with pGDM compared to controls. We identified 583 gene-altered transcripts between patients with T2D and controls. Interestingly, 60 transcripts had genes shared by pGDM or T2D versus the controls. The selected upregulated genes involved in inflammatory response, glycosylation, and death-like domains, according to the functional network analysis of pGDM (, ) and T2D ( and ), showed similar trends to those obtained via microarray. Thus, these differentially expressed genes and their corresponding network and pathway analyses in women with pGDM and T2D offer valuable insights into the possible biological mechanisms of the progression of GDM to T2D. - Source: PubMed
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Xu BingyangYu BiaoXu ZiningYe ShuhongQing YuxinSun HongZhao BinWu NaWu Jiawen - Bruton tyrosine kinase inhibitor (BTKi) combined with rituximab-based chemotherapy benefits diffuse large B-cell lymphoma (DLBCL) patients. However, drug resistance is the major cause of relapse and death of DLBCL. In this study, we conducted a comprehensive analysis BTKi-resistance related genes (BRRGs) and established a 10-gene (CARD16, TRIP13, PSRC1, CASP1, PLBD1, CARD6, CAPG, CACNA1A, CDH15, and NDUFA4) signature for early identifying high-risk DLBCL patients. The resistance scores based on the BRRGs signature were associated with prognosis. Furthermore, we developed a nomogram incorporating the BRRGs signature, which demonstrated excellent performance in predicting the prognosis of DLBCL patients. Notably, tumor immune microenvironment, biological pathways, and chemotherapy sensitivity were different between high- and low-resistance score groups. Additionally, we identified TRIP13 as a key gene in our model. TRIP13 was found to be overexpressed in DLBCL and BTKi-resistant DLBCL cell lines, knocking down TRIP13 suppresses cell proliferation, promotes cell apoptosis, and enhances the apoptosis effect of BTKi on DLBCL cells by regulating the Wnt/β-catenin pathway. In conclusion, our study presents a novel BRRGs signature that could serve as a promising prognostic marker in DLBCL, and TRIP13 might be a potential therapeutic target for resistant DLBCL. - Source: PubMed
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Ding YangyangHuang KekeSun ChengLiu ZelinZhu JinliJiao XunyiLiao YaFeng XiangjiangGuo JingjingZhu ChunhuaZhai ZhiminXiong Shudao