HINFP antibody
- Known as:
- HINFP (anti-)
- Catalog number:
- orb30645
- Product Quantity:
- 5 ug(Trial size)
- Category:
- -
- Supplier:
- Biorb
- Gene target:
- HINFP antibody
Related genes to: HINFP antibody
- Gene:
- HINFP NIH gene
- Name:
- histone H4 transcription factor
- Previous symbol:
- MIZF
- Synonyms:
- DKFZP434F162, HiNF-P, ZNF743
- Chromosome:
- 11q23.3
- Locus Type:
- gene with protein product
- Date approved:
- 2006-02-02
- Date modifiied:
- 2014-11-19
Related products to: HINFP antibody
Related articles to: HINFP antibody
- Hepatolithiasis (HL) is a prevalent condition in hepatobiliary surgery, often complicated by hepatatrophia. This study aimed to identify gene mutations in HL specimens with hepatatrophia and construct a mutation landscape using whole-exome sequencing (WES). - Source: PubMed
Publication date: 2026/04/09
Tang DanGu XuanyuLiu DanYang JialiZhao Lijin - Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder marked by cognitive decline, cholinergic dysfunction, synaptic loss, and neuroinflammation. Existing therapies such as Donepezil and estrogen replacement offer only symptomatic relief, failing to address the complexity of the disease due to their reductionist, single-targeted approach. In this study, we employed an integrative systems biology framework to evaluate the neurotherapeutic potential of Dioscorea bulbifera (DB), a core component of the US-patented polyherbal formulation BHD (comprising Bacopa monnieri, Hippophae rhamnoides, and DB), which has shown promising neuroprotective properties in preclinical models. We identified active phytoconstituents of DB-including Emodin, Beta-sitosterol, Diosgenin, Stigmasterol, Diosbulbin B, Jarnol, and Myricetin-and systematically assessed their interaction with Alzheimer's-relevant hub-bottleneck (H-B) genes using molecular docking, gene expression integration, network pharmacology, and molecular dynamics simulations. Our findings delineate a dual mechanistic model of DB's action: (1) an Estrogen Signaling Module centered around ESR1 and its key signaling associates (MAPK1, MAPK8, AKT1, EGFR, PIK3CA, and MAP2K1), forming a tightly interconnected, feedback-regulated pathway modulating memory, synaptic plasticity, neuroprotection, and inflammation; and (2) a Cholinergic Module involving direct inhibition of ACHE, providing rapid symptomatic relief. Molecular docking and dynamic simulations confirmed the strong and stable interactions of DB bioactives with both ESR1 and ACHE, showing comparable or superior stability to reference drugs (Estradiol and Donepezil). Regulatory network analysis revealed that ESR1 is one of the most connected genes in hippocampal-specific PPI networks and is co-regulated by numerous miRNAs and transcription factors. Co-expression analysis identified additional AD-relevant genes (e.g., PIK3R1, MAPK14, PTEN, DHODH, CAV1) involved in synaptic signaling, oxidative stress, and neurogenesis, while TF-miRNA coregulatory nodes such as miR-199a-3p, miR-181a-5p, GATA2, CREB1, and HINFP added further mechanistic layers to DB's network modulation. KEGG and GO enrichment analyses mapped DB-targeted genes to critical AD pathways, including Estrogen signaling, MAPK, PI3K-AKT, TNF, FoxO, and the Alzheimer's disease pathway itself. This multi-targeted, systems-level modulation by DB underscores its potential not only as a neuroprotective nutraceutical-especially for postmenopausal women vulnerable to estrogen loss-but also as a promising adjuvant to standard AD therapies. - Source: PubMed
Publication date: 2025/08/04
Chowdhury Mayank RoyVijaykumar Sudarshana Deepa - Alzheimer's disease (AD) and age-related macular degeneration (AMD) share similar pathological features, suggesting common genetic aetiologies between the two. Investigating gene associations between AD and AMD may provide useful insights into the underlying pathogenesis and inform integrated prevention and treatment for both diseases. - Source: PubMed
Publication date: 2024/04/15
Zhang XueliZhu ZhuotingHuang YuShang XianwenO'Brien Terence JKwan PatrickHa JasonWang WeiLiu ShunmingZhang XiayinKiburg KaterinaBao YiningWang JingYu HonghuaHe MingguangZhang Lei - Mice are routinely utilized as animal models of drug-induced liver injury (DILI), however, there are significant differences in the pathogenesis between mice and humans. This study aimed to compare gene expression between humans and mice in acetaminophen (APAP)-induced liver injury (AILI), and investigate the similarities and differences in biological processes between the two species. - Source: PubMed
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Publication date: 2024/03/04
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