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  • Yi, Huan  (16)
  • 2020-2024  (16)
  • 1
    In: Journal of Ethnopharmacology, Elsevier BV, Vol. 273 ( 2021-06), p. 113995-
    Type of Medium: Online Resource
    ISSN: 0378-8741
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
    detail.hit.zdb_id: 1491279-X
    SSG: 15,3
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  • 2
    In: Advanced Optical Materials, Wiley, Vol. 11, No. 19 ( 2023-10)
    Abstract: The self‐reduction of variable valence ions is known to be realized in the specific crystal structure with XO 4 groups. It may lead to some outstanding merits for phosphors, such as high thermal stability and easy popularization in industrial production. However, it has never been realized in the host with only planar XO 3 anionic groups before. Here, the self‐reduction from Mn 4+ to Mn 2+ is realized in a borate α ‐LiZnBO 3 , in which the planar triangle [BO 3 ] is the fundamental building unit. The borate‐based phosphor exhibits a typical Mn 2+ emission when it is prepared in the ambient atmosphere. The divalent state of doped ions is confirmed via X‐ray absorption fine structure and X‐ray photoelectron spectroscopy. Supported by electron paramagnetic resonance, thermoluminescence, and density functional theory, the oxygen vacancies formed during the synthesis process and the lithium ones introduced by heterovalent substitution are the decisive factors in the valence state‐transition of doped ions. In addition, the low‐valence activators can be stabilized in the lattice to offer the phosphor a good thermal stability of chromaticity coordinates. This study offers a new vision for the self‐reduction system, deepens the understanding of the self‐reduction mechanism, and broadens the choices for developing novel optical functional materials by defect control.
    Type of Medium: Online Resource
    ISSN: 2195-1071 , 2195-1071
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2708158-8
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  • 3
    In: Advanced Optical Materials, Wiley, Vol. 9, No. 19 ( 2021-10)
    Abstract: Self‐reduction behavior of doped activators and zero‐thermal‐quenching luminescence have received much more attention in the exploration of luminescent materials for phosphor‐converted white light‐emitting diodes. Here, a combination of the two properties is demonstrated in a Mn 2+ activated red phosphor, NaZn(PO 3 ) 3 :Mn 2+ , synthesized by a high temperature solid state reaction in ambient atmosphere, which is free from thermal quenching until 250 °C. By combined first‐principles calculation and experimental investigation, the self‐reduction mechanism from Mn 4+ to Mn 2+ and the anti‐thermal quenching are clarified. The unique properties originate from the cation vacancy defects and the thermally induced energy transfer from the defect energy levels to the Mn 2+ 3d excited state centers. This result will deepen the understanding of the effect of the crystal defect on luminescent materials, as well as inspiring more exploration on defect control to develop novel high thermal stability phosphors for practical application.
    Type of Medium: Online Resource
    ISSN: 2195-1071 , 2195-1071
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2708158-8
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  • 4
    In: Biomedicine & Pharmacotherapy, Elsevier BV, Vol. 133 ( 2021-01), p. 110984-
    Type of Medium: Online Resource
    ISSN: 0753-3322
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
    detail.hit.zdb_id: 1501510-5
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  • 5
    Online Resource
    Online Resource
    Frontiers Media SA ; 2020
    In:  Frontiers in Pharmacology Vol. 11 ( 2020-7-7)
    In: Frontiers in Pharmacology, Frontiers Media SA, Vol. 11 ( 2020-7-7)
    Type of Medium: Online Resource
    ISSN: 1663-9812
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2020
    detail.hit.zdb_id: 2587355-6
    SSG: 15,3
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  • 6
    Online Resource
    Online Resource
    Frontiers Media SA ; 2023
    In:  Frontiers in Cell and Developmental Biology Vol. 11 ( 2023-7-25)
    In: Frontiers in Cell and Developmental Biology, Frontiers Media SA, Vol. 11 ( 2023-7-25)
    Abstract: Objective: We aimed to explore the correlations between and possible mechanisms of common environmental endocrine disruptors, phthalates, and ovarian dysfunction in endometriosis. Methods: Subjects were included in the case group ( n = 107) who were diagnosed with endometriosis by postoperative pathology in Fujian Maternal and Child Hospital from February 2018 to February 2021, and the women who were excluded from endometriosis by surgery were as the control group ( n = 70). The demographic information of the subjects were evaluated by questionnaire, and the clinical characteristics were evaluated by medical records and 3-year follow-up results. Gas chromatography‒mass spectrometry was used to quantify 10 metabolites of phthalates, including dimethyl ortho-phthalate (DMP), mono-n-methyl phthalate (MMP), dioctyl ortho-phthalate (DEP), mono-ethyl phthalate (MEP), di-n-butyl ortho-phthalate (DBP), mono-butyl phthalate (MBP), benzylbutyl phthalate (BBzP), mono-benzyl; phthalate (MBzP), diethylhexyl phthalate (DEHP) and mono-ethylhexyl phthalate (MEHP), in the urine samples of the subjects. Furthermore, a total of 54 SD rats were exposed to DEHP 0, 5, 50, 100, 250, 500, 1,000, 2000, and 3,000 mg/kg/day for 2 weeks. The SD rats’ body weight, oestrus cycle changes, and serum anti-mullerian hormone (AMH) levels were evaluated. After sacrifice, the mass index of the rat uterus and bilateral ovaries were calculated. Finally, bioinformatics analysis of rat ovarian tissues was performed to explore the possible mechanism. SPSS 24.0 (IBM, United States) was used for data analysis. p -value & lt;0.05 was considered statistically significant. Results: The human urinary levels of DMP ( p & lt; 0.001), MMP ( p = 0.001), DEP ( p = 0.003), MEP ( p = 0.002), DBP ( p = 0.041), MBP ( p & lt; 0.001), BBzP ( p = 0.009), DEHP ( p & lt; 0.001), and MEHP ( p & lt; 0.001) were significantly higher in women with endometriosis than in controls. Notably, DEHP was a significant risk factor for endometriosis (OR: 11.0, 95% CI: 5.4–22.6). The area under the ROC curve increased when multiple phthalates were diagnosed jointly, reaching 0.974 as the highest value, which was helpful for the diagnosis of endometriosis. In vivo experiments showed that after DEHP exposure in rats, the mass index of the ovary and uterus decreased in a dose-dependent manner; the oestrus cycle of SD rats was irregularly prolonged and disordered; and the serum AMH level was negatively correlated with the DEHP exposure dose (Rho = −0.8, p & lt; 0.001). Bioinformatics analysis of rat ovarian tissues showed that seven genes involved in the steroid biosynthesis pathway were upregulated and may play a negative role in ovarian function. Conclusion: Exposure to phthalates, especially DEHP, is associated with the occurrence of endometriosis and affects women’s reproductive prognosis and ovarian function. The steroid biosynthesis pathway may be related to ovarian dysfunction. The detection of phthalate in urine may become a new biological target for the diagnosis of endometriosis.
    Type of Medium: Online Resource
    ISSN: 2296-634X
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2023
    detail.hit.zdb_id: 2737824-X
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  • 7
    In: Oxidative Medicine and Cellular Longevity, Hindawi Limited, Vol. 2021 ( 2021-6-23), p. 1-16
    Abstract: Metabolic diseases have become major public health issues worldwide. Searching for effective drugs for treating metabolic diseases from natural compounds has attracted increasing attention. Quercetin, an important natural flavonoid, is extensively present in fruits, vegetables, and medicinal plants. Due to its potentially beneficial effects on human health, quercetin has become the focus of medicinal attention. In this review, we provide a timely and comprehensive summary of the pharmacological advances and clinical data of quercetin in the treatment of three metabolic diseases, including diabetes, hyperlipidemia, and nonalcoholic fatty liver disease (NAFLD). Accumulating evidences obtained from animal experiments prove that quercetin has beneficial effects on these three diseases. It can promote insulin secretion, improve insulin resistance, lower blood lipid levels, inhibit inflammation and oxidative stress, alleviate hepatic lipid accumulation, and regulate gut microbiota disorders in animal models. However, human clinical studies on the effects of quercetin in diabetes, hyperlipidemia, and NAFLD remain scarce. More clinical trials with larger sample sizes and longer trial durations are needed to verify its true effectiveness in human subjects. Moreover, another important issue that needs to be resolved in future research is to improve the bioavailability of quercetin. This review may provide valuable information for the basic research, drug development, and clinical application of quercetin in the treatment of metabolic diseases.
    Type of Medium: Online Resource
    ISSN: 1942-0994 , 1942-0900
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2021
    detail.hit.zdb_id: 2455981-7
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  • 8
    In: Environmental Science: Nano, Royal Society of Chemistry (RSC), Vol. 10, No. 7 ( 2023), p. 1828-1841
    Abstract: Photo-Fenton catalytic oxidation is considered economical and eco-friendly technology for energy development and environmental protection. However, high-performance catalysts are vital in this process. Thus, in this study, an Fe-doped porous g-C 3 N 4 (Fe/PCN) nanomaterial was prepared via a one-step self-assembly strategy, which showed a large specific surface area, relatively negative conduction potential and intense visible light utilization, exhibiting an enhanced catalytic performance. As expected, in the photo-Fenton catalytic system, 99.24% oxytetracycline (OTC) degraded over Fe/PCN within 60 min, and the photo-Fenton degradation rate constant was up to 0.076 min −1 . Furthermore, a thimbleful of hydrogen peroxide (H 2 O 2 ) could meet the requirement in this photo-Fenton reaction system. The catalytic mechanism of Fe/PCN was discussed in depth, where Fe/PCN not only activated H 2 O 2 to generate hydroxyl radicals (˙OH), but also photo-generated superoxide radicals (˙O 2 − ) due to its more negative conduction potential (−0.78 eV vs. NHE) than E 0 (O 2 /˙O 2 − ) (−0.33 eV vs. NHE). Besides, the stability experiment showed that the precipitation of iron salts was prevented, which is conductive for practical applications. The possible degradation pathway of OTC was proposed and proven to be green according to the toxicity estimation software tool (TEST). The low consumption of H 2 O 2 , high tolerance to pH changes and coexisting ions and green degradation pathway of the prepared Fe/PCN make it a potential candidate for OTC removal. This work proposes a simple method to modulate the morphology and structure of g-C 3 N 4 to enhance the catalytic activity of Fenton-like reactions.
    Type of Medium: Online Resource
    ISSN: 2051-8153 , 2051-8161
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2758235-8
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  • 9
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2023
    In:  Journal of Clinical Oncology Vol. 41, No. 16_suppl ( 2023-06-01), p. e16252-e16252
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 41, No. 16_suppl ( 2023-06-01), p. e16252-e16252
    Abstract: e16252 Background: Homologous recombination deficiency (HRD) is associated with tumorigenesis and could predict the response of PARP inhibitor (PARPi) therapy and immunotherapy. Loss of function or deleterious mutations in homologous recombination-related (HRR) genes contribute to HRD phenotype. Methods: Tumor tissue samples from 669 Chinese patients with pancreatic cancer were sequenced with 551 cancer-related genes. Based on the clinical evidence, 15 HRR genes ( ATM, BRCA1, BRCA2, BARD1, BRIP1, CDK12, CHEK1, CHEK2, FANCL, PALB2, RAD51B, RAD51C, RAD51D, RAD54L, PPP2R2A) were selected. 495 patients with WES data from the TCGA datasets were included for analysis. Results: In the Chinese cohort, 10.46% (70/669) patients exhibited somatic HRR (sHRR) gene mutations. ATM (4%) was the most common mutant gene, followed by BRCA2 (3%), BARD1 (1%), BRCA1 (1%), BRIP1 (1%), RAD51D (1%), CHEK2(1%). The germline HRR (gHRR) gene mutations were identified in 55.67% (118/245) patients. BRCA2 (23%) was the most common mutant gene, followed by ATM (10%), BRCA1 (9%), BRIP1 (9%), PALB2 (8%), BARD1 (7%), FANCL (3%). 1.49% (10/669) patients carried both germline and somatic HRR gene mutations. The sHRR-Mut patients had a higher median TMB compared to the sHRR-WT patients (3.97 vs 2.13, p 〈 0.001). However, the median TMB was similar between the gHRR-Mut and the gHRR-WT patients (2.13 vs 2.13, p=0.49). In the TCGA cohort, 9.09% (45/495) patients exhibited sHRR gene mutations. The most common mutant gene was ATM (4%), followed by CDK12 (2%) BRCA2 (2%), BARD1 (1%). The sHRR-Mut patients had a higher median TMB compared to the sHRR-WT patients (1.03 vs 0.71, p 〈 0.001). Totally, the somatic mutant frequency of HRR genes was similar between Chinese cohort and TCGA cohort (10.46% vs 9.09%, p = 0.113). For the TCGA cohort, the patients with sHRR-Mut had a similar median progression free survival compared to the ones with sHRR-WT (74.4 months vs not reached, p = 0.299). Conclusions: Our data reported the genetic landscape of HRR gene in Chinese pancreatic cancer patients. Patients with somatic HRR gene mutations had a significantly elevated TMB level. Our data suggest that patients with altered HRR genes may be rational candidates for precision oncology treatment and provide new opportunities to predict the tumor response to multiple treatments.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2023
    detail.hit.zdb_id: 2005181-5
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  • 10
    In: Journal of Immunology Research, Hindawi Limited, Vol. 2022 ( 2022-3-29), p. 1-18
    Abstract: Objective. Ovarian cancer (OvCa) is the most lethal gynaecological malignancy worldwide. We aimed to illustrate the potential function and molecular mechanism of exosomal microRNA-543 (miR-543) in the oncogenesis and development of OvCa. Methods. Differentially expressed microRNAs in exosomes derived from OvCa cell lines were identified by bioinformatic analysis and verified by RT-PCR. Cell proliferation ability was estimated by clonogenic and 5-ethynyl-2 ′ -deoxyuridine assays in vitro and in vivo. Potential involved pathways and targets of exosomal miRNAs were analysed using DIANA and verified by pyrosequencing, glucose quantification, dual-luciferase reporter experiments, and functional rescue assays. Results. Bioinformatic analysis identified miR-543 and its potential target genes involved in the cancer-associated proteoglycan pathway. The expression of miR-543 was significantly decreased in exosomes derived from OvCa cell lines, patient serum, and OvCa tissues, while the mRNA levels of insulin-like growth factor 2 (IGF2) were increased. Furthermore, the overexpression of miR-543 resulted in the suppression of OvCa cell proliferation in vitro and in vivo. Moreover, miR-543 was significantly negatively correlated with IGF2 in OvCa tissues in comparison with paracarcinoma tissues. Notably, upregulation of miR-543 led to increased cell supernatant glucose levels and suppressed cell growth, which was rescued by overexpression of IGF2. Conclusions. Exosomal miR-543 participates in the proteoglycan pathway to suppress cell proliferation by targeting IGF2 in OvCa.
    Type of Medium: Online Resource
    ISSN: 2314-7156 , 2314-8861
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2022
    detail.hit.zdb_id: 2817541-4
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