VASP (phospho-Ser239) Antibody
- Known as:
- VASP (phosphorilated-Ser239) Antibody
- Catalog number:
- abx000239
- Product Quantity:
- EUR
- Category:
- -
- Supplier:
- Abbexa
- Gene target:
- VASP (phospho-Ser239) Antibody
Related genes to: VASP (phospho-Ser239) Antibody
- Gene:
- VASP NIH gene
- Name:
- vasodilator stimulated phosphoprotein
- Previous symbol:
- -
- Synonyms:
- -
- Chromosome:
- 19q13.32
- Locus Type:
- gene with protein product
- Date approved:
- 1996-06-07
- Date modifiied:
- 2017-06-13
Related products to: VASP (phospho-Ser239) Antibody
Related articles to: VASP (phospho-Ser239) Antibody
- Subtalar (ST) and talonavicular (TN) arthrodesis through a single medial approach is an established technique when dealing with common hindfoot conditions, but evidence of arthrodesis union usually relies on plain radiographs evaluation. The aims of this study were to determine long-term clinical and radiographic outcomes, including computed tomography scan (CT-scan) confirmed union rates, of ST and TN arthrodesis through a single medial approach. - Source: PubMed
Publication date: 2026/06/03
Saraiva DanielKnupp MarkusKim JaeyoungTulha JoséCadena MargalidaOliva Xavier Martín - To investigate the effect of the petroleum ether fraction of roots (PEFM) for relieving spasmodic abdominal pain in mice and its underlying mechanism. - Source: PubMed
Yang ShenghaiChen WentingChen XueqinTian KaiXiong YongSun JingxianHuang LinglingHuang XiangzhongWang Ziliang - Recent evidence has established a significant link between N4 acetylcytidine (ac4C) mRNA modification, mediated by N Acetyltransferase 10 (NAT10), and bone metabolism. Nonetheless, the precise role and regulatory targets of NAT10, along with its associated ac4C modification in human bone formation, remain inadequately characterized. This study employed bioinformatics analysis of transcriptomic datasets from primary osteoblasts of individuals with high versus low bone mineral density (BMD), alongside a curated set of ac4C-modified genes, to identify key differentially expressed genes (DEGs) regulated by this pathway within an osteogenic context. Overall, eleven key NAT10/ac4C-associated DEGs linked to BMD status were identified: CFD, CTSF, DCXR, FADS1, GOLIM4, IMPA2, MLEC, NCLN, NT5DC2, PTGFRN, and VASP. Notably, FADS1, NT5DC2, and PTGFRN emerged as crucial ac4C-modified genes across three machine learning models. Furthermore, the tri-gene signature (FADS1/NT5DC2/PTGFRN) showed excellent diagnostic performance in distinguishing different BMD statuses. In vitro validation using MC3T3-E1 osteoblastic cells revealed that the knockdown of NAT10 via lentiviral delivery markedly impaired cell proliferation and osteogenic differentiation. This impairment was evidenced by the results of the CCK-8 proliferation assay, alkaline phosphatase staining, and Alizarin Red staining. Additionally, qRT PCR analysis demonstrated a significant downregulation of FADS1 and NT5DC2 expression subsequent to NAT10 knockdown. These findings underscore the role of NAT10-mediated ac4C modification as a pivotal regulator of osteoblast activity and gene expression programs associated with BMD. This research offers novel insights into the regulation of bone metabolism and proposes potential diagnostic markers and therapeutic targets for osteoporosis. - Source: PubMed
Tang YWang QDong WJiang GLei MHu XWu YJiang WHao JHu Z - This study aims to evaluate the validity of the Visual Analog Scale-Tension (VAS-T). - Source: PubMed
Publication date: 2026/04/29
Erdoğru Demir TuğçeAlçalar Ayşe NiluferSertel Berk Hanife Özlem - To identify factors that enhance thermochemical redox reaction efficiency, we have investigated the thermochemical properties of transition-metal-doped cerium oxide. This study examines thermodynamic parameters using vibrational entropy rather than configurational entropy and investigates how microscopic changes in bonding states affect macroscopic properties. VASP calculations show that vibrational entropy increases slightly upon doping with transition metals (Mn, Fe, Co, Ni); however, the magnitude of this change is limited. Specifically, for 3.125 mol% Mn-doped ceria, the reaction temperature at which Gibbs free energy (Δ) becomes negative decreases and confirms a substantial improvement in redox reactivity. We further find that transition metal doping reduces the enthalpy required for oxygen vacancy formation, highlighting the dominant role of enthalpy over entropy in driving reaction feasibility when there are no significant changes in the crystal structure. Building on these findings, we present calculated results for ceria samples doped with 12.50 mol% and 25.00 mol% transition metals and compare them with the experimental data. These results provide a clear thermodynamic rationale for optimizing dopant species and concentration in solar redox materials. - Source: PubMed
Publication date: 2026/05/21
Nishimura TakakiKodama TatsuyaChiba KoujiSakane GentaTakashita TomokoYamamoto HirokiIshii Tomohiko