NAA10/ARD1 基因概述 NAA10 gene / cDNA is a protein-coding gene which located on Xq28. The NAA10 gene is conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, and frog.168 organisms have orthologs with human gene NAA10. ...
? 2024Introduction: We aimed to investigate the expression and prognostic role of NAA10 in clear cell renal cell carcinoma (ccRCC). Material and methods: We performed a gene expression and survival analysis based on the human cancer genome atlas database of ccRCC patients (TCGA-KIRC). Results:...
The NAA10 gene lies in the gene-rich region Xq28 and is composed of 8 exons (NM_003491.3; Figure 1a). It is highly expressed in the developing brain of mice embryos1 and shows a lower yet uniform and ubiquitous expression in adult mice.2 Complete knockout is lethal in Trypanosoma brucei...
价格￥1600.00￥960.00 包装100ul50ul 最小起订量50ul 发货地北京 更新日期2025-04-08 QQ交谈微信洽谈 产品详情 中文名称:Anti-NAA10 Polyclonal Antibody英文名称:Anti-NAA10 Polyclonal Antibody Gene ID:8260Public Immunogen Range:Recombinant protein of human NAA10 ...
Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants. 公司简介 北京索莱宝科技有限公司始创于2004年,是一家集产品研发、生产、销售和服务于一体综合性的*高新技术企业。 公司总部位于北京,拥有7000平米的研发和生产基地,并配有先进的仓储和物流系统...
De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females. Eur. J. Hum. Genet. 23, 602–609 (2015). Article CAS Google Scholar Johnston, J. J. et al. NAA10 polyadenylation signal variants cause syndromic microphthalmia. J. Med. ...
GeneWikiReview ThebiologicalfunctionsofNaa10—Fromamino-terminalacetylationto humandisease MaxJ.Dörfel a ,GholsonJ.Lyon a,b,c, ⁎ a StanleyInstituteforCognitiveGenomics,ColdSpringHarborLaboratory,NY,USA b DepartmentofPsychiatry,StonyBrookUniversity,StonyBrook,NY,USA c UtahFoundationforBiomedicalResearch...
4E). When FIH was silenced, the target gene expressions were enhanced due to the blockade of HIF-1α N803 hydroxylation. However, they were no more regulated by NAA10 knockdown because NAA10 was not capable of acetylating HIF-1α without FIH. Under hypoxia, the target genes were highly ...
The gene encoding hNaa16p originates from an early vertebrate duplication event from the common ancestor of hNAA15 and hNAA16. Immunoprecipitation coupled to mass spectrometry identified both endogenous hNaa15p and hNaa16p as distinct interaction partners of hNaa10p in HEK293 cells, thus ...
Ogden syndromeX-linked disorderOgden syndrome is an exceptionally rare X-linked disease caused by mutations in the NAA10 gene. Reported cases of this syndrome are approximately 20 children and are associated with facial dysmorphism, growth delay, developmental disorders, congenital heart disease, and ...