Ask about this productRelated genes to: SLC9A7 antibody
- Gene:
- SLC9A7 NIH gene
- Name:
- solute carrier family 9 member A7
- Previous symbol:
- -
- Synonyms:
- NHE7
- Chromosome:
- Xp11.3
- Locus Type:
- gene with protein product
- Date approved:
- 2001-11-02
- Date modifiied:
- 2016-02-25
Related products to: SLC9A7 antibody
Related articles to: SLC9A7 antibody
- Endometrial Cancer (EC) is one of the most prevalent malignancies in the female reproductive system. Hypoxia is a hallmark of the tumor microenvironment that drives metabolic reprogramming, endoplasmic reticulum (ER) stress, and aggressive behavior in cancer cells. However, the underlying mechanisms remain incompletely understood. This study aimed to investigate hypoxia-mediated regulation of EC progression, focusing on the role of SLC9A7 (Solute Carrier Family 9 Member A7, NHE7). - Source: PubMed
Publication date: 2026/01/23
Yang ShizhouWu TingtingCao ZhuChen ZhengyunMa YuejiangWang TingQian LinhuaHuang Xiufeng - To evaluate the clinical significance of a hemizygous c.1042-10G>C variant of the SLC9A7 gene NM_001257291.2) previously identified in individuals with neurodevelopmental disorders, and to provide an evidence-based guidance for prenatal genetic counseling. - Source: PubMed
Wang JingyuanHuang JiaZhu HongjieZhou LingxiaoYang HengYang WenjieChen ShuaiLiu Hongyan - Cadmium (Cd), classified as an International Agency for Research on Cancer (IARC) Group 1 human carcinogen, is present in cigarette smoke. Recent studies have illustrated the potential role of genetics in influencing Cd biomarker levels. - Source: PubMed
Sullivan Shannon MMurphy Sharon EStram Daniel OWilkens Lynne RHaiman Christopher ALe Marchand LoïcStepanov IrinaPark S Lani - The X chromosome has remained enigmatic in Alzheimer disease (AD), yet it makes up 5% of the genome and carries a high proportion of genes expressed in the brain, making it particularly appealing as a potential source of unexplored genetic variation in AD. - Source: PubMed
Belloy Michael ELe Guen YannStewart IlariaWilliams KennedyHerz JoachimSherva RichardZhang RuiMerritt VictoriaPanizzon Matthew SHauger Richard LGaziano J MichaelLogue MarkNapolioni ValerioGreicius Michael D - To explore the clinical and genetic characteristics of a child with mental retardation, language and motor developmental delay and epilepsy. - Source: PubMed
Li WeiFu TianjiaoTamang SpanaWang YaoWang HuailiZhuo Zhihong