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  • Wiley  (55)
  • Li, Hui  (55)
  • 1
    In: Addiction, Wiley, Vol. 116, No. 5 ( 2021-05), p. 1172-1185
    Abstract: Three to 10 minutes of smoking cessation advice by physicians is effective to increase quit rates, but is not routinely practised. We examined the effectiveness of physicians’ very brief (approximately 30 sec) smoking cessation intervention on quit rates among Chinese outpatient smokers. Design A pragmatic, open‐label, individually randomized controlled trial. Setting Seventy‐two medical outpatient departments of hospitals and/or community health centers in Guangdong, China. Participants Chinese adults who were daily cigarette smokers ( n  = 13 671, 99% males) were invited by their physician to participate during outpatient consultation. Smokers who were receiving smoking cessation treatment or were judged to need specialist treatment for cessation were excluded. Interventions The intervention group ( n  = 7015) received a 30‐sec intervention including physician's very brief advice, a leaflet with graphic warnings and a card with contact information of available cessation services. The control group ( n  = 6656) received a very brief intervention on consuming vegetables and fruit. A total of 3466 participants in the intervention group were further randomized to receive a brief booster advice from trained study personnel via telephone 1 month following their doctor visit. Measurements The primary outcome was self‐reported 7‐day point prevalence abstinence (PPA) in the intervention and control groups at the 12‐month follow‐up. Secondary outcomes included self‐reported 30‐day abstinence and biochemically validated abstinence at 12‐month follow‐up. Findings By intention‐to‐treat, the intervention (versus control) group had greater self‐reported 7‐day abstinence [9.1 versus 7.8%, odds ratio (OR) = 1.14, 95% confidence interval (CI) = 1.03–1.26, P  = 0.008] and 30‐day abstinence (8.0 versus 6.9%, OR = 1.14, 95% CI = 1.03–1.27, P  = 0.01) at 12‐month follow‐up. The effect size increased when only participants who received the intervention from compliant physicians were included (7‐day PPA, OR = 1.42, 95% CI = 1.11–1.74). The group difference in biochemically validated abstinence was small (0.8 versus 0.8%, OR = 1.00, 95% CI = 0.71–1.42, P  = 0.99). Conclusion A 30‐sec smoking cessation intervention increased self‐reported abstinence among mainly male smokers in China at 12‐month follow‐up (risk difference = 1.3%), and should be feasible to provide in most settings and delivered by all health‐care professionals.
    Type of Medium: Online Resource
    ISSN: 0965-2140 , 1360-0443
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2002997-4
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  • 2
    In: American Journal of Human Biology, Wiley, Vol. 33, No. 2 ( 2021-03)
    Abstract: Haplogroup C2a‐M48 is the predominant paternal lineage of Tungusic‐speaking populations, one of the largest population groups in Siberia. Up until now, the origins and dispersal of Tungusic‐speaking populations have remained unclear. In this study, the demographic history of Tungusic‐speaking populations was explored using the phylogenetic analysis of haplogroup C2a‐M86, the major subbranch of C2a‐M48. Materials and methods In total, 18 newly generated Y chromosome sequences from C2a‐M48 males and 20 previously available Y‐chromosome sequences from this haplogroup were analyzed. A highly revised phylogenetic tree of haplogroup C2a‐M86 with age estimates was reconstructed. Frequencies of this lineage in the literature were collected and a comprehensive analysis of this lineage in 13 022 individuals from 245 populations in Eurasia was performed. Results The distribution map of C2a‐M48 indicated the most probable area of origin and diffusion route of this paternal lineage in North Eurasia. Most C2a‐M86 samples from Tungusic‐speaking populations belonged to the sublineage C2a‐F5484, which emerged about 3300 years ago. We identified six unique sublineages corresponding to the Manchu, Evenks, Evens, Oroqen, and Daurpopulations; these sublineages diverged gradually over the past 1900 years. Notably, we observed a clear north‐south dichotomous structure for sublineages derived from C2a‐F5484, consistent with the internal north‐south divergence of Tungusic languages and ethnic groups. Conclusions We identified the important founding paternal haplogroup, C2a‐F5484, for Tungusic‐speaking populations as well as numerous unique subgroups of this haplogroup. We propose that the timeframe for the divergence of C2a‐F5484 corresponds with the early differentiation of ancestral Tungusic‐speaking populations.
    Type of Medium: Online Resource
    ISSN: 1042-0533 , 1520-6300
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2001218-4
    SSG: 12
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  • 3
    In: Small, Wiley, Vol. 20, No. 7 ( 2024-02)
    Abstract: Defect engineering is promising to tailor the physical properties of 2D semiconductors for function‐oriented electronics and optoelectronics. Compared with the extensively studied 2D binary materials, the origin of defects and their influence on physical properties of 2D ternary semiconductors are not clarified. Here, the effect of defects on the electronic structure and optical properties of few‐layer hexagonal Znln 2 S 4 is thoroughly studied via versatile spectroscopic tools in combination with theoretical calculations. It is demonstrated that the Zn–In antistructural defects induce the formation of a series of donor and acceptor energy levels and sulfur vacancies induce donor energy levels, leading to rich recombination paths for defect emission and extrinsic absorption. Impressively, the emission of donor–acceptor pair in Znln 2 S 4 can be significantly tailored by electrostatic gating due to efficient tunability of Fermi level ( E f ). Furthermore, the layer‐dependent dipole orientation of defect emission in Znln 2 S 4 is directly revealed by back focal plane imagining, where it presents obviously in‐plane dipole orientation within a dozen‐layer thickness of Znln 2 S 4 . These unique features of defects in Znln 2 S 4 including extrinsic absorption, rich recombination paths, gate tunability, and in‐plane dipole orientation are definitely a benefit to the advanced orientation‐functional optoelectronic applications.
    Type of Medium: Online Resource
    ISSN: 1613-6810 , 1613-6829
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 2168935-0
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  • 4
    Online Resource
    Online Resource
    Wiley ; 2016
    In:  Journal of Separation Science Vol. 39, No. 12 ( 2016-06), p. 2431-2437
    In: Journal of Separation Science, Wiley, Vol. 39, No. 12 ( 2016-06), p. 2431-2437
    Abstract: We describe a facile, general, and highly efficient approach to obtain polydopamine‐coated molecularly imprinted polymer based on halloysite nanotubes for bovine serum albumin. The method combined surface molecular imprinting and one‐step immobilized template technique. Hierarchically structured polymer was prepared in physiological conditions adopting dopamine as functional monomer. A thin layer of polydopamine can be coated on the surface of amino‐modified halloysite nanotubes by self‐polymerization, and the thickness of the imprinted shells can be controlled by the mass ratio of matrix and dopamine. The polymer was characterized by Fourier transform infrared spectrometry, transmission electron microscopy, and thermogravimetric analysis. The prepared material showed high binding capacity (45.4 mg/g) and specific recognition behavior toward the template protein. In addition, stability and regeneration analyses indicated that the imprinted polymer exhibited excellent reusability (relative standard deviation 〈 9% for batch‐to‐batch evaluation). Therefore, the developed polymer is effective for protein recognition and separation.
    Type of Medium: Online Resource
    ISSN: 1615-9306 , 1615-9314
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 2047990-6
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  • 5
    In: Catheterization and Cardiovascular Interventions, Wiley, Vol. 93, No. 7 ( 2019-06), p. 1194-1204
    Abstract: Dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) prevents ischemic events while increasing bleeding risk. Real‐world‐based metrics to accurately predict postdischarge bleeding (PDB) occurrence and its potential impact on postdischarge major cardiovascular event (MACE) remain undefined. This study sought to evaluate the impact of PDB on MACE occurrence, and to develop a score to predict PDB risk among Chinese acute coronary syndrome (ACS) patients after PCI. Methods and Results From May 2014 to January 2016, 2496 ACS patients who underwent PCI were recruited consecutively from 29 nationally representative Chinese tertiary hospitals. Among 2,381 patients (95.4%, 2,381/2,496) who completed 1‐year follow‐up, the cumulative incidence of PDB (bleeding academic research consortium type [BARC] ≥2) and postdischarge MACE (a composite of all‐cause death, nonfatal myocardial infarction, ischemic stroke, or urgent revascularization) was 4.9% ( n = 117) and 3.3% ( n = 79), respectively. The association between PDB and MACE during 1‐year follow‐up, as well as the impact of DAPT with ticagrelor or clopidogrel on PDB were evaluated. PDB was associated with higher risk of postdischarge MACE (7.7 vs. 3.1%; adjusted hazard ratio: 2.59 [95% confidence interval: 1.17–5.74]; p = .02). For ticagrelor versus clopidogrel, PDB risk was higher (8.0 vs. 4.4%; 2.05 [1.17–3.60]; p = .01), while MACE risk was similar (2.0 vs. 3.4%; 0.70 [0.25–1.93]; p = .49). Based on identified PDB predictors, the constructed bleeding risk in real world Chinese acute coronary syndrome patients (BRIC‐ACS) score for PDB was established. C‐statistic for the score for PDB was 0.67 (95% CI: 0.62–0.73) in the overall cohort, and 〉 0.70 in subgroups with non‐ST‐ and ST‐segment elevation myocardial infarction, diabetes and receiving more than two drug eluting stents. Conclusions In Chinese ACS patients, PDB with BARC ≥2 was associated with higher risk for MACE after PCI. The constructed BRIC‐ACS risk score provides a useful tool for PDB discrimination, particularly among high ischemic and bleeding risk patients.
    Type of Medium: Online Resource
    ISSN: 1522-1946 , 1522-726X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2001555-0
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2011
    In:  The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology Vol. 294, No. 11 ( 2011-11), p. 1809-1817
    In: The Anatomical Record: Advances in Integrative Anatomy and Evolutionary Biology, Wiley, Vol. 294, No. 11 ( 2011-11), p. 1809-1817
    Type of Medium: Online Resource
    ISSN: 1932-8486
    Language: English
    Publisher: Wiley
    Publication Date: 2011
    detail.hit.zdb_id: 2273240-8
    SSG: 12
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  • 7
    In: Plant Biotechnology Journal, Wiley, Vol. 20, No. 8 ( 2022-08), p. 1606-1621
    Abstract: Genetically enhancing drought tolerance and nutrient use efficacy enables sustainable and stable wheat production in drought‐prone areas exposed to water shortages and low soil fertility, due to global warming and declining natural resources. In this study, wheat plants, exhibiting improved drought tolerance and N‐use efficacy, were developed by introducing GmTDN1 , a gene encoding a DREB‐like transcription factor, into two modern winter wheat varieties, cv Shi4185 and Jimai22. Overexpressing GmTDN1 in wheat resulted in significantly improved drought and low‐N tolerance under drought and N‐deficient conditions in the greenhouse. Field trials conducted at three different locations over a period of 2–3 consecutive years showed that both Shi4185 and Jimai22 GmTDN1 transgenic lines were agronomically superior to wild‐type plants, and produced significantly higher yields under both drought and N‐deficient conditions. No yield penalties were observed in these transgenic lines under normal well irrigation conditions. Overexpressing GmTDN1 enhanced photosynthetic and osmotic adjustment capacity, antioxidant metabolism, and root mass of wheat plants, compared to those of wild‐type plants, by orchestrating the expression of a set of drought stress‐related genes as well as the nitrate transporter, NRT2.5 . Furthermore, transgenic wheat with overexpressed NRT2.5 can improve drought tolerance and nitrogen (N) absorption, suggesting that improving N absorption in GmTDN1 transgenic wheat may contribute to drought tolerance. These findings may lead to the development of new methodologies with the capacity to simultaneously improve drought tolerance and N‐use efficacy in cereal crops to ensure sustainable agriculture and global food security.
    Type of Medium: Online Resource
    ISSN: 1467-7644 , 1467-7652
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2136367-5
    SSG: 12
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  • 8
    In: Thoracic Cancer, Wiley, Vol. 10, No. 4 ( 2019-04), p. 918-929
    Abstract: Delanzomib, a novel proteasome inhibitor, has demonstrated promising efficacy and antitumor ability in human multiple myeloma cell lines and patient‐derived cells. However, the potential therapeutic effects of delanzomib on breast cancer remain unknown. In this study, we show that delanzomib has antitumor effects and synergizes with doxorubicin (Dox) in human breast cancer cell lines. Methods Cell proliferation assay and flow cytometry were used to evaluate cell viability and apoptosis in eight human breast cancer cell lines after treatment with delanzomib or Dox. Essential molecules of the p53, MAPK, and apoptosis signaling pathways were analyzed by Western blotting. Results Delanzomib induced cell death and demonstrated synergism with Dox in all tested breast cancer cell lines. In addition, delanzomib enhanced the Dox‐induced phosphorylation of p38/JNK and the expression of transcriptional target proteins of p53, such as p21, p27, NOXA, and PUMA. Conclusion The combined regimen of the proteasome inhibitor delanzomib with Dox chemotherapy may become an effective strategy for breast cancer therapy.
    Type of Medium: Online Resource
    ISSN: 1759-7706 , 1759-7714
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2559245-2
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  • 9
    In: CNS Neuroscience & Therapeutics, Wiley
    Abstract: Chronic hyperglycemia‐induced inflammation of the hippocampus is an important cause of cognitive deficits in diabetic patients. The receptor for advanced glycation end products (RAGE), which is widely expressed in the hippocampus, is a crucial factor in this inflammation and the associated cognitive deficits. We aimed to reveal the underlying mechanism by which RAGE regulates neuroinflammation in the pathogenesis of diabetes‐induced cognitive impairment. Methods We used db/db mice as a model for type 2 diabetes to investigate whether receptor‐interacting serine/threonine protein kinase 1 (RIPK1), which is expressed in microglia in the hippocampal region, is a key protein partner for RAGE. GST pull‐down assays and AutoDock Vina simulations were performed to identify the key structural domain in RAGE that binds to RIPK1. Western blotting, co‐immunoprecipitation (Co‐IP), and immunofluorescence (IF) were used to detect the levels of key proteins or interaction between RAGE and RIPK1. Cognitive deficits in the mice were assessed with the Morris water maze (MWM) and new object recognition (NOR) and fear‐conditioning tests. Results RAGE binds directly to RIPK1 via the amino acid sequence (AAs) 362–367, thereby upregulating phosphorylation of RIPK1, which results in activation of the NLRP3 inflammasome in microglia and ultimately leads to cognitive impairments in db/db mice. We mutated RAGE AAs 362–367 to reverse neuroinflammation in the hippocampus and improve cognitive function, suggesting that RAGE AAs 362–367 is a key structural domain that binds directly to RIPK1. These results also indicate that hyperglycemia‐induced inflammation in the hippocampus is dependent on direct binding of RAGE and RIPK1. Conclusion Direct interaction of RAGE and RIPK1 via AAs 362–367 is an important mechanism for enhanced neuroinflammation in the hyperglycemic environment and is a key node in the development of cognitive deficits in diabetes.
    Type of Medium: Online Resource
    ISSN: 1755-5930 , 1755-5949
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2423467-9
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  • 10
    In: Journal of Medical Virology, Wiley, Vol. 89, No. 7 ( 2017-07), p. 1215-1223
    Abstract: Vaccination against the hepatitis B virus (HBV) is extensively used as an effective method to prevent HBV infection. However, nearly 10% of healthy adults fail to produce a protective level of antibodies against the hepatitis B vaccine, and multiple genetic variants are known to affect the immune response to the hepatitis B vaccine. The aim of the present study was to investigate the association between polymorphisms in immunoresponsive gene 1 ( IRG1 ) gene and the immune response to hepatitis B vaccination in a Chinese Han population. Four single nucleotide polymorphisms (SNPs) located in the IRG1 gene were genotyped in 1230 high‐responders and 451 non‐responders to hepatitis B vaccination. The SNPs rs17470171 and rs17385627 were associated with the immune response to hepatitis B vaccination ( P  = 0.014 and 0.029, respectively). In addition, the haplotypes G‐A‐A‐A (rs614171‐rs17470171‐rs9530614‐rs17385627, P  = 0.0042, OR = 0.68) and A‐A (rs17470171‐rs17385627, P  = 0.0065, OR = 0.72) exerted a protective role in the immune response to hepatitis B vaccination. Allele ‘A’ of rs17470171 and allele ‘A’ of rs17385627 show higher levels of expression for the IRG1 gene compared with allele ‘C’ of rs17470171 and allele ‘T’ of rs17385627 as demonstrated by luciferase reporter and overexpression assays. In addition, we observed that IRG1 inhibited the HBV life cycle and that IRG1 rs17385627 allele ‘A’ was more effective than rs17385627 allele ‘T’ at eliminating HBV in HepG2.2.15 cells. These findings suggest that polymorphisms in the IRG1 gene are associated with the immune response to hepatitis B vaccination. The antiviral effect of IRG1 was confirmed using HBV infection cell models.
    Type of Medium: Online Resource
    ISSN: 0146-6615 , 1096-9071
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 752392-0
    detail.hit.zdb_id: 1475090-9
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