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  • 1
    In: Technology and Health Care, IOS Press, Vol. 31 ( 2023-04-28), p. 97-109
    Abstract: BACKGROUND: Unexplained recurrent spontaneous abortion (URSA) is difficult to diagnose and treat clinically due to its unknown cause OBJECTIVE: Changes in natural killer (NK) cells, T lymphocytes, and Th1(IFNγ)/Th2(IL-4) cytokines were investigated in the peripheral blood of patients with URSA to examine the pathogenesis, clinical diagnosis, and inform potential treatment strategies for this condition. METHODS: For this study, we selected patients with URSA as the case group and included normal women in the control group. Flow cytometry was performed to detect lymphocytes and cytokines in the peripheral blood of all subjects. RESULTS: The proportion of NK cells, Th1 cells, and the Th1/Th2 ratio were significantly higher in the URSA group compared to the control group; whereas the proportion of CD3+T cells was lower. Pairwise correlation analysis revealed a positive correlation between the percentage of NK cells and CD3+T cells, as well as CD3+CD4+T cells. Canonical correlation analysis indicated a significant correlation between NK cells and T cells, including their subgroups. CONCLUSION: Patients with URSA have immune balance disorders, characterised by an increased proportion of peripheral blood NK cells, Th1, and Th1/Th2 ratio along with a decreased proportion of CD3+T cells. The proportion of NK cells and CD3+T may serve as predictive factors for URSA, while NK cells are closely related to the regulation of CD3+T cells and their subsets. By regulating the level of IFN-γ, NK cells can influence the proportion of CD3+T cells and induce a Th1 (IFNγ)/Th2 (IL-4) imbalance.
    Type of Medium: Online Resource
    ISSN: 0928-7329 , 1878-7401
    Language: Unknown
    Publisher: IOS Press
    Publication Date: 2023
    detail.hit.zdb_id: 2043772-9
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  • 2
    In: Technology and Health Care, IOS Press, Vol. 30 ( 2022-03-02), p. 71-80
    Abstract: BACKGROUND: The etiology of polycystic ovary syndrome (PCOS) remains unclear with highly heterogeneous clinical manifestations, recently growing evidence revealing genetic variants play a crucial part in its pathogenesis. OBJECTIVE: This study aimed to examine the correlation between SNPs in miRNA-135a’s binding site of targeted gene IRS2 and clinical manifestations of PCOS in Chinese females. METHOD: A total of 126 Chinese women with PCOS and 109 healthy women were enrolled, divided into 4 groups based on different clinical features of hyperandrogenemia (HA), insulin resistance (IR), polycystic ovary morphology (PCOM) and obesity. We analyzed 2 single nucleotide polymorphisms (SNPs) of the IRS2 gene (rs2289046 and rs1865434) and clinical features’ laboratory measurements such as sex hormone, fasting plasma glucose (FPG), fasting plasma insulin (FINS). RESULTS: Located in miRNA-135a binding site of IRS2 gene, the rs2289046’s triple genotypes distribution showed a significant difference between PCOS/control group and PCOM/non-PCOM group (P 〈 0.05) while the rs1865434’s triple genotype distribution showed a significant difference between obesity/non-obesity group (P 〈 0.05). CONCLUSION: The results revealed the two SNPs as rs2289046 and rs1865434 in the IRS-2 binding region of miRNA-135a have correlations with the clinical features of PCOS in Chinese population.
    Type of Medium: Online Resource
    ISSN: 0928-7329 , 1878-7401
    Language: Unknown
    Publisher: IOS Press
    Publication Date: 2022
    detail.hit.zdb_id: 2043772-9
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  • 3
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Genetics Vol. 13 ( 2022-3-10)
    In: Frontiers in Genetics, Frontiers Media SA, Vol. 13 ( 2022-3-10)
    Abstract: Congenital contractural arachnodactyly (CCA) is a rare autosomal dominant disorder of connective tissue characterized by crumpled ears, arachnodactyly, camptodactyly, large joint contracture, and kyphoscoliosis. The nature course of CCA has not been well-described. We aim to decipher the genetic and phenotypic spectrum of CCA. The cohort was enrolled in Beijing Jishuitan Hospital and Peking Union Medical College Hospital, Beijing, China, based on Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study ( http://www.discostudy.org/ ). Exome sequencing was performed on patients’ blood DNA. A recent published CCA scoring system was validated in our cohort. Seven novel variants and three previously reported FBN2 variants were identified through exome sequencing. Two variants outside of the neonatal region of FBN2 gene were found. The phenotypes were comparable between patients in our cohort and previous literature, with arachnodactyly, camptodactyly and large joints contractures found in almost all patients. All patients eligible for analysis were successfully classified into likely CCA based on the CCA scoring system. Furthermore, we found a double disease-causing heterozygous variant of FBN2 and ANKRD11 in a patient with blended phenotypes consisting of CCA and KBG syndrome. The identification of seven novel variants broadens the mutational and phenotypic spectrum of CCA and may provide implications for genetic counseling and clinical management.
    Type of Medium: Online Resource
    ISSN: 1664-8021
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2606823-0
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  • 4
    In: Frontiers in Pharmacology, Frontiers Media SA, Vol. 11 ( 2020-12-18)
    Abstract: Purpose: N 6 -methyladenosine (m 6 A) mRNA methylation is affected by dietary factors and associated with lipid metabolism; however, whether the regulatory role of resveratrol in lipid metabolism is involved in m 6 A mRNA methylation remains unknown. Here, the objective of this study was to investigate the effect of resveratrol on hepatic lipid metabolism and m 6 A RNA methylation in the liver of mice. Methods: A total of 24 male mice were randomly allocated to LFD (low-fat diet), LFDR (low-fat diet + resveratrol), HFD (high-fat diet), and HFDR (high-fat diet + resveratrol) groups for 12 weeks ( n = 6/group). Final body weight of mice was measured before sacrificing. Perirhemtric fat, abdominal and epididymal fat, liver tissues, and serum were collected at sacrifice and analyzed. Briefly, mice phenotype, lipid metabolic index, and m 6 A modification in the liver were assessed. Results: Compared to the HFD group, dietary resveratrol supplementation reduced the body weight and relative abdominal, epididymal, and perirhemtric fat weight in high-fat-exposed mice; however, resveratrol significantly increased average daily feed intake in mice given HFD. The amounts of serum low-density lipoprotein cholesterol (LDL), liver total cholesterol (TC), and triacylglycerol (TAG) were significantly decreased by resveratrol supplementation. In addition, resveratrol significantly enhanced the levels of peroxisome proliferator-activated receptor alpha ( PPARα ), peroxisome proliferator-activated receptor beta/delta ( PPARβ/δ ), cytochrome P450, family 4, subfamily a, polypeptide 10/14 ( CYP4A10 / 14 ), acyl-CoA oxidase 1 ( ACOX1 ), and fatty acid-binding protein 4 ( FABP4 ) mRNA and inhibited acyl-CoA carboxylase ( ACC ) mRNA levels in the liver. Furthermore, the resveratrol in HFD increased the transcript levels of methyltransferase like 3 ( METTL3 ), alkB homolog 5 ( ALKBH5 ), fat mass and obesity associated protein ( FTO ), and YTH domain family 2 ( YTHDF2 ), whereas it decreased the level of YTH domain family 3 ( YTHDF3 ) and m 6 A abundance in mice liver. Conclusion: The beneficial effect of resveratrol on lipid metabolism disorder under HFD may be due to decrease of m 6 A RNA methylation and increase of PPARα mRNA, providing mechanistic insights into the function of resveratrol in alleviating the disturbance of lipid metabolism in mice.
    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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  • 5
    In: Annals of Joint, AME Publishing Company, Vol. 4 ( 2019-07), p. 30-30
    Type of Medium: Online Resource
    ISSN: 2415-6809
    Language: Unknown
    Publisher: AME Publishing Company
    Publication Date: 2019
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  • 6
    In: Physica Scripta, IOP Publishing, Vol. 99, No. 6 ( 2024-06-01), p. 065957-
    Abstract: Two-dimensional (2D) Ruddlesden–Popper (RP) perovskite is an ideal platform for building high-performance photodetectors due to its unique structure, excellent stability, and tunable bandgap. However, 2D perovskite heterojunction photodetectors are still less reported. In this work, the photodetector based on (PEA) 2 PbI 4 /P3HT heterojunction was prepared by the liquid-phase solution method under air conditions, which showed a responsivity (R) of 8.38 A W −1 and a specific detectivity (D*) of 6.53 × 10 11 Jones under 808 nm light. In addition, the device has a transient response time of 79.57 μ s/484 μ s and a high stability performance that maintains more than 95% of the photocurrent under continuous cycling tests and shows good cyclic stability after 30 days without encapsulation. This work provides a promising strategy for extending 2D perovskite photodetectors in the VIS to NIR spectral range.
    Type of Medium: Online Resource
    ISSN: 0031-8949 , 1402-4896
    Language: Unknown
    Publisher: IOP Publishing
    Publication Date: 2024
    detail.hit.zdb_id: 1477351-X
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