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  1. Article ; Online: Development of tryptophan metabolism patterns to predict prognosis and immunotherapeutic responses in hepatocellular carcinoma.

    Long, Guo / Wang, Dong / Tang, Jianing / Tang, Weifeng

    Aging

    2023  Volume 15, Issue 15, Page(s) 7593–7615

    Abstract: Tryptophan metabolism is associated with tumorigenesis and tumor immune response in various cancers. Liver is the main place where tryptophan catabolism is performed. However, the role of tryptophan metabolism in hepatocellular carcinoma (HCC) has not ... ...

    Abstract Tryptophan metabolism is associated with tumorigenesis and tumor immune response in various cancers. Liver is the main place where tryptophan catabolism is performed. However, the role of tryptophan metabolism in hepatocellular carcinoma (HCC) has not been well clarified. In the present study, we described the mutations of 42 tryptophan metabolism-related genes (TRPGs) in HCC cohorts. Then, HCC patients were well distributed into two subtypes based on the expression profiles of the 42 TRPGs. The clinicopathological characteristics and tumor microenvironmental landscape of the two subtypes were profiled. We also established a TRPGs scoring system and identified four hallmark TRPGs, including
    MeSH term(s) Humans ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/therapy ; Tryptophan ; Liver Neoplasms/genetics ; Liver Neoplasms/therapy ; Prognosis ; Immunotherapy ; Aldehyde Dehydrogenase, Mitochondrial
    Chemical Substances Tryptophan (8DUH1N11BX) ; ALDH2 protein, human (EC 1.2.1.3) ; Aldehyde Dehydrogenase, Mitochondrial (EC 1.2.1.3)
    Language English
    Publishing date 2023-08-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1945-4589
    ISSN (online) 1945-4589
    DOI 10.18632/aging.204928
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The mediating role of telomere length in multi-pollutant exposure associated with metabolic syndrome in adults.

    Tang, Weifeng / Zhan, Wenqiang / Chen, Qian

    Environmental science and pollution research international

    2023  Volume 30, Issue 34, Page(s) 82068–82082

    Abstract: Metabolic syndrome is a chronic and complex disease characterized by environmental and genetic factors. However, the underlying mechanisms remain unclear. This study assessed the relationship between exposure to a mixture of environmental chemicals and ... ...

    Abstract Metabolic syndrome is a chronic and complex disease characterized by environmental and genetic factors. However, the underlying mechanisms remain unclear. This study assessed the relationship between exposure to a mixture of environmental chemicals and metabolic syndrome (MetS) and further examined whether telomere length (TL) moderated these relationships. A total of 1265 adults aged > 20 years participated in the study. Data on multiple pollutants (polycyclic aromatic hydrocarbons, phthalates, and metals), MetS, leukocyte telomere length (LTL), and confounders were provided in the 2001-2002 National Health and Nutrition Examination Survey. The correlations between multi-pollutant exposure, TL, and MetS in the males and females were separately assessed using principal component analysis (PCA), logistic and extended linear regression models, Bayesian kernel machine regression (BKMR), and mediation analysis. Four factors were generated in PCA that accounted for 76.2% and 77.5% of the total environmental pollutants in males and females, respectively. The highest quantiles of PC2 and PC4 were associated with the risk of TL shortening (P < 0.05). We observed that the relationship between PC2, PC4, and MetS risk was significant in the participants with median TL levels (P for trend = 0.04 for PC2, and P for trend = 0.01 for PC4). Furthermore, mediation analysis revealed that TL could explain 26.1% and 17.1% of the effects of PC2 and PC4 associated with MetS in males, respectively. The results of BKMR model revealed that these associations were mainly driven by 1-PYE (cPIP = 0.65) and Cd (cPIP = 0.29) in PC2. Meanwhile, TL could explain 17.7% of the mediation effects of PC2 associated with MetS in the females. However, the relationships between pollutants and MetS were sparse and inconsistent in the females. Our findings suggest that the effects of the risk of MetS associated with mixed exposure to multiple pollutants are mediated by TL, and this mediating effect in the males is more pronounced than that in the females.
    MeSH term(s) Telomere ; Environmental Pollutants ; Metabolic Syndrome/epidemiology ; Environmental Pollution ; Humans ; Male ; Female ; Polycyclic Aromatic Hydrocarbons/analysis ; Environmental Exposure/statistics & numerical data ; Nutrition Surveys ; Metals
    Chemical Substances Environmental Pollutants ; Polycyclic Aromatic Hydrocarbons ; Metals
    Language English
    Publishing date 2023-06-15
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 1178791-0
    ISSN 1614-7499 ; 0944-1344
    ISSN (online) 1614-7499
    ISSN 0944-1344
    DOI 10.1007/s11356-023-28017-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Association of leptin receptor polymorphisms with susceptibility of non-small cell lung cancer: Evidence from 2249 subjects.

    Tang, Weifeng / Wang, Jian / Dai, Ting / Qiu, Hao / Liu, Chao / Chen, Shuchen / Hu, Zhendong

    Cancer medicine

    2024  Volume 13, Issue 8, Page(s) e7178

    Abstract: Non-small cell lung cancer (NSCLC) is increasing dramatically. It is believed that energy metabolism-related genes could play an important role in etiology of NSCLC. In this study, we sought to assess the correlation between three LEPR single nucleotide ... ...

    Abstract Non-small cell lung cancer (NSCLC) is increasing dramatically. It is believed that energy metabolism-related genes could play an important role in etiology of NSCLC. In this study, we sought to assess the correlation between three LEPR single nucleotide polymorphisms (rs1137101, rs1137100 and rs6588147) with NSCLS susceptibility. In total, 1193 NSCLC cases and 1056 controls were included. SNPscan™ genotyping method was used to analyze the genotypes of LEPR polymorphisms. Compared to rs6588147 GG in LEPR gene, this study identified a protective role of LEPR rs6588147 GA and GA/AA for the occurrence of NSCLC (GA vs. GG [p = 0.021] and GA/AA vs. GG [p = 0.030]). As well, we found that a protective role of LEPR rs6588147 for the occurrence of non-SCC subgroup (p < 0.05). By logistic regression analysis, we found that the rs6588147 A allele related genotypes might play a protective role for the occurrence of NSCLC in drinking, BMI ≥24 kg/m
    MeSH term(s) Humans ; Receptors, Leptin/genetics ; Carcinoma, Non-Small-Cell Lung/genetics ; Carcinoma, Non-Small-Cell Lung/pathology ; Polymorphism, Single Nucleotide ; Male ; Female ; Lung Neoplasms/genetics ; Middle Aged ; Genetic Predisposition to Disease ; Case-Control Studies ; Genotype ; Aged ; Alleles ; Genetic Association Studies
    Chemical Substances Receptors, Leptin ; LEPR protein, human
    Language English
    Publishing date 2024-04-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2659751-2
    ISSN 2045-7634 ; 2045-7634
    ISSN (online) 2045-7634
    ISSN 2045-7634
    DOI 10.1002/cam4.7178
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Evaluation of the Pharmacokinetics of Dapagliflozin in Patients With Chronic Kidney Disease With or Without Type 2 Diabetes Mellitus.

    Penland, Robert C / Melin, Johanna / Boulton, David W / Tang, Weifeng

    Journal of clinical pharmacology

    2023  Volume 63, Issue 5, Page(s) 551–559

    Abstract: Evidence shows that sodium-glucose cotransporter 2 inhibitors, such as dapagliflozin, can delay the progressive decline of kidney function in patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD). We used a population ... ...

    Abstract Evidence shows that sodium-glucose cotransporter 2 inhibitors, such as dapagliflozin, can delay the progressive decline of kidney function in patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD). We used a population pharmacokinetics (popPK) model to characterize the pharmacokinetics of dapagliflozin in patients with CKD and compare dapagliflozin systemic exposure in different populations, such as CKD with or without T2DM and T2DM without CKD. A 2-compartmental popPK model was developed from a previous popPK model. The final popPK model was based on 9715 dapagliflozin plasma concentrations from 3055 patients included in clinical studies involving adults with CKD with or without T2DM, adults with T2DM, healthy subjects, and pediatric patients with T2DM. Overall, the apparent clearance for patients treated with dapagliflozin was 21.6 L/h, similar to previous estimates in adults with T2DM and healthy subjects (22.9 L/h). Model-derived area under the plasma concentration-time curve (AUC) was not meaningfully different between patients with CKD with and without T2DM. Median AUC was 1.6-fold higher in adult patients with CKD with T2DM compared with adult patients with T2DM without CKD. Compared with patients with normal kidney function (estimated glomerular filtration rate ≥90 mL/min/1.73 m
    MeSH term(s) Adult ; Humans ; Child ; Diabetes Mellitus, Type 2/drug therapy ; Sodium-Glucose Transporter 2 Inhibitors/therapeutic use ; Glucosides/pharmacology ; Renal Insufficiency, Chronic/drug therapy ; Benzhydryl Compounds/pharmacokinetics ; Glomerular Filtration Rate
    Chemical Substances dapagliflozin (1ULL0QJ8UC) ; Sodium-Glucose Transporter 2 Inhibitors ; Glucosides ; Benzhydryl Compounds
    Language English
    Publishing date 2023-01-12
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 188980-1
    ISSN 1552-4604 ; 0091-2700 ; 0021-9754
    ISSN (online) 1552-4604
    ISSN 0091-2700 ; 0021-9754
    DOI 10.1002/jcph.2196
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Associations Between Different Dietary Vitamins and the Risk of Obesity in Children and Adolescents: A Machine Learning Approach.

    Tang, Weifeng / Zhan, Wenqiang / Wei, Mengdan / Chen, Qian

    Frontiers in endocrinology

    2022  Volume 12, Page(s) 816975

    Abstract: Backgrounds: Simultaneous dietary intake of vitamins is considered as a common and real scenario in daily life. However, limited prospective studies have evaluated the association between multivitamins intake and obesity in children and adolescents.: ... ...

    Abstract Backgrounds: Simultaneous dietary intake of vitamins is considered as a common and real scenario in daily life. However, limited prospective studies have evaluated the association between multivitamins intake and obesity in children and adolescents.
    Objectives: This study aimed to evaluate the relationship between the intake of different dietary vitamins and the risk of obesity in children (6-11 years) and adolescents (12-19 years).
    Methods: We conducted a cross-sectional study based on data from U.S. National Health and Nutrition Examination Survey, 2013-2016. A total of 3634 children and adolescents were included who had available data on dietary vitamins, obesity and covariates. We analyzed the dietary intake levels of nine vitamins, including vitamin A, vitamin B
    Results: In the multivariate logistic regression model, five vitamins (vitamin A, vitamin B
    Conclusions: We determine the combined effects of multivitamins on obesity in children and adolescents, and observe a significant interaction between vitamin B
    MeSH term(s) Adolescent ; Bayes Theorem ; Child ; Cross-Sectional Studies ; Humans ; Machine Learning ; Nutrition Surveys ; Pediatric Obesity/epidemiology ; Pediatric Obesity/etiology ; Prospective Studies ; Vitamin A ; Vitamin B 12 ; Vitamin D ; Vitamin K ; Vitamins
    Chemical Substances Vitamins ; Vitamin A (11103-57-4) ; Vitamin K (12001-79-5) ; Vitamin D (1406-16-2) ; Vitamin B 12 (P6YC3EG204)
    Language English
    Publishing date 2022-02-17
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2592084-4
    ISSN 1664-2392
    ISSN 1664-2392
    DOI 10.3389/fendo.2021.816975
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Vascular Niche Facilitates Acquired Drug Resistance to c-Met Inhibitor in Originally Sensitive Osteosarcoma Cells.

    Tang, Weifeng / Zhang, Yu / Zhang, Haixia / Zhang, Yan

    Cancers

    2022  Volume 14, Issue 24

    Abstract: Osteosarcoma (OS) is the most common primary bone tumor in children and adolescents characterized by drug resistance and poor prognosis. As one of the key oncogenes, c-Met is recognized as a promising therapeutic target for OS. In this report, we show ... ...

    Abstract Osteosarcoma (OS) is the most common primary bone tumor in children and adolescents characterized by drug resistance and poor prognosis. As one of the key oncogenes, c-Met is recognized as a promising therapeutic target for OS. In this report, we show that c-Met inhibitor PF02341066 specifically killed OS cells with highly phosphorylated c-Met in vitro. However, the inhibitory effect of PF02341066 was abrogated in vivo due to interference from the vascular niche. OS cells adjacent to microvessels or forming vascular mimicry suppressed c-Met expression and phosphorylation. Moreover, VEGFR2 was activated in OS cells and associated with acquired drug resistance. Dual targeting of c-Met and VEGFR2 could effectively shrink the tumor size in a xenograft model. c-Met-targeted therapy combined with VEGFR2 inhibition might be beneficial to achieve an ideal therapeutic effect in OS patients. Together, our results confirm the pivotal role of tumor heterogeneity and the microenvironment in drug response and reveal the molecular mechanism underlying acquired drug resistance to c-Met-targeted therapy.
    Language English
    Publishing date 2022-12-15
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14246201
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  7. Article ; Online: Which Anastomotic Techniques Is the Best Choice for Cervical Esophagogastric Anastomosis in Esophagectomy? A Bayesian Network Meta-Analysis.

    Chen, Boyang / Xia, Ping / Tang, Weifeng / Huang, Shijie

    Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract

    2022  Volume 27, Issue 2, Page(s) 422–432

    Abstract: Introduction: The optimal choice of anastomotic techniques for cervical esophagogastric anastomosis in esophagectomy remains unclear.: Methods: An electronic literature search of PubMed, Embase, and Web of Science (data up to April 2022) was ... ...

    Abstract Introduction: The optimal choice of anastomotic techniques for cervical esophagogastric anastomosis in esophagectomy remains unclear.
    Methods: An electronic literature search of PubMed, Embase, and Web of Science (data up to April 2022) was conducted and screened to compare hand sewn (HS), circular stapling (CS), side-to-side linear stapling (LS), and triangulating stapling (TS) for cervical esophagogastric anastomosis. Anastomotic leak, pulmonary complications, anastomotic stricture, and reflux esophagitis of the 4 anastomotic techniques were evaluated using a Bayesian network meta-analysis by R.
    Result: Twenty-nine studies were ultimately included, with a total of 5,020 patients from 9 randomized controlled trials, 7 prospect cohort studies, and 13 retrospective case-control studies in the meta-analysis. The present study demonstrates that the incidence of anastomotic leakage is lower in TS than HS and CS (TS vs. HS: odds ratio (OR) = 0.32, 95% CI: 0.1 to 0.9; TS vs. CS: OR = 0.37, 95% CI: 0.13 to 1.0), and the incidence of anastomotic stricture is lower in TS than in HS and CS (TS vs. HS: OR = 0.32, 95% CI: 0.11 to 0.86; TS vs. CS: OR = 0.23, 95% CI: 0.08 to 0.58). TS ranks best in terms of anastomotic leakage, pulmonary complication, anastomotic stricture, and reflux esophagitis.
    Conclusion: TS for cervical esophagogastric anastomosis of esophagectomy had a lower incidence of anastomotic leakage and stricture. TS should be preferentially recommended. Large-scale RCTs will be needed to provide more evidence in future studies.
    MeSH term(s) Humans ; Esophagectomy/adverse effects ; Esophagectomy/methods ; Anastomotic Leak/epidemiology ; Retrospective Studies ; Constriction, Pathologic/etiology ; Constriction, Pathologic/surgery ; Constriction, Pathologic/epidemiology ; Esophagitis, Peptic/surgery ; Bayes Theorem ; Network Meta-Analysis ; Surgical Stapling/adverse effects ; Esophageal Neoplasms/surgery ; Esophageal Neoplasms/complications ; Treatment Outcome ; Anastomosis, Surgical/adverse effects ; Anastomosis, Surgical/methods ; Postoperative Complications/epidemiology ; Postoperative Complications/etiology ; Postoperative Complications/surgery
    Language English
    Publishing date 2022-11-22
    Publishing country United States
    Document type Meta-Analysis ; Journal Article ; Review
    ZDB-ID 2012365-6
    ISSN 1873-4626 ; 1934-3213 ; 1091-255X
    ISSN (online) 1873-4626 ; 1934-3213
    ISSN 1091-255X
    DOI 10.1007/s11605-022-05482-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Bisphenol S exposure induces intestinal inflammation: An integrated metabolomic and transcriptomic study

    Ao, Junjie / Liu, Yongji / Tang, Weifeng / Zhang, Jun

    Chemosphere. 2022 Apr., v. 292 p.133510-

    2022  

    Abstract: As a typical substitute for bisphenol A (BPA), bisphenol S (BPS) is raising concerns due to the potential adverse effects on human health. Limit evidence is available to understand the toxicity of BPS to the digestive system, especially for intestine. In ...

    Abstract As a typical substitute for bisphenol A (BPA), bisphenol S (BPS) is raising concerns due to the potential adverse effects on human health. Limit evidence is available to understand the toxicity of BPS to the digestive system, especially for intestine. In this study, we aimed to investigate the potential effects and underlying mechanisms of BPS exposure on human colon mucosal epithelial cells (NCM460). Our results showed that BPS exposure significantly increased the production of pro-inflammatory cytokines, including tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ) and interleukin-17A (IL-17A). The tight junctions of the cells has been destroyed by BPS exposure, which was characterized by a down-regulation of the tight junction proteins (Claudin1 and zonula occluden 1 (ZO1)). A multi-omics study explored the underlying mechanisms based on the metabolomic and transcriptomic responses. A variety of neurotransmitters increased significantly after exposure to BPS. The top enriched pathway was “glutamatergic synapse”, which was activated by BPS exposure, resulting in the up-regulation of l-glutamine. Links were observed among the altered metabolites, genes and cytokines. Our results indicate that exposure to BPS may disturb the balance of gut-brain axis, leading to the production of inflammatory cytokines and the destruction of tight junction in NCM460 cells. It provides new clue for the development of intestinal inflammation in terms of the environmental pollutants.
    Keywords bisphenol A ; bisphenol S ; colon ; epithelium ; glutamine ; human health ; humans ; inflammation ; interleukin-17 ; metabolites ; metabolomics ; multiomics ; necrosis ; neoplasms ; neurotransmitters ; tight junctions ; toxicity ; transcriptomics ; Environmental endocrine disruptor ; Intestinal inflammation ; Metabolomic ; Transcriptomic
    Language English
    Dates of publication 2022-04
    Publishing place Elsevier Ltd
    Document type Article ; Online
    ZDB-ID 120089-6
    ISSN 1879-1298 ; 0045-6535 ; 0366-7111
    ISSN (online) 1879-1298
    ISSN 0045-6535 ; 0366-7111
    DOI 10.1016/j.chemosphere.2021.133510
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: A sensitive and robust method for the simultaneous determination of thirty-three legacy and emerging per- and polyfluoroalkyl substances in human plasma and serum

    Ao, Yan / Nian, Min / Tang, Weifeng / Zhang, Jun / Zhang, Qianlong / Ao, Junjie

    Anal Bioanal Chem. 2023 Jan., v. 415, no. 3 p.457-470

    2023  

    Abstract: Legacy and emerging per- and polyfluoroalkyl substances (PFAS) have attracted growing attention due to their potential adverse effects on humans. We developed a method to simultaneously determine thirty-three PFAS (legacy PFAS, precursors, and ... ...

    Abstract Legacy and emerging per- and polyfluoroalkyl substances (PFAS) have attracted growing attention due to their potential adverse effects on humans. We developed a method to simultaneously determine thirty-three PFAS (legacy PFAS, precursors, and alternatives) in human plasma and serum using solid phase extraction coupled to ultra-performance liquid chromatography-tandem mass spectrometry (SPE-UPLC-MS/MS). The method yielded good linearity (>0.995) and excellent limits of detection (LODs) (0.0005~0.012 ng mL⁻¹ in plasma and 0.002~0.016 ng mL⁻¹ in serum). The relative recoveries ranged from 80.1 to 116%, with intra- and inter-day precision less than 14.3%. The robustness of this method has been tested continuously for 10 months (coefficients of variation <14.9%). Our method was successfully applied to the PFAS analysis of 42 real human plasma and serum samples collected from women. The proposed method is attractive for the biomonitoring of multi-class PFAS in human health risk assessment and epidemiological studies.
    Keywords blood serum ; environmental monitoring ; health effects assessments ; human health ; humans ; liquid chromatography ; solid phase extraction ; tandem mass spectrometry
    Language English
    Dates of publication 2023-01
    Size p. 457-470.
    Publishing place Springer Berlin Heidelberg
    Document type Article ; Online
    ISSN 1618-2642
    DOI 10.1007/s00216-022-04426-4
    Database NAL-Catalogue (AGRICOLA)

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  10. Article ; Online: Association between miR-146a rs2910164, miR-196a2 rs11614913, and miR-499 rs3746444 polymorphisms and the risk of esophageal carcinoma: A case-control study.

    Liu, Chao / Gao, Wenhui / Shi, Yijun / Lv, Lu / Tang, Weifeng

    Cancer medicine

    2022  Volume 11, Issue 21, Page(s) 3949–3959

    Abstract: MicroRNAs (miRNAs) are a group of small, non-coding, and endogenous RNAs that regulate gene expression and over 50% of them are located at cancer-related genomic regions or fragile sites. According to previous studies there is significant association of ... ...

    Abstract MicroRNAs (miRNAs) are a group of small, non-coding, and endogenous RNAs that regulate gene expression and over 50% of them are located at cancer-related genomic regions or fragile sites. According to previous studies there is significant association of miRNA single nucleotide polymorphisms (SNPs) with tumorigenesis (e.g., esophageal cancer, hepatocellular cancer, gastric cancer, bladder cancer, breast cancer, lung cancer, and colon cancer), however, the conclusions have been inconsistent. To investigate the relationship between miR-146a rs2910164 C > G, miR-196a2 rs11614913 T > C, and miR-499 rs3746444 A > G polymorphisms and the susceptibility to esophageal squamous cell cancer (ESCC) in the Chinese Han nationality, we recruited 829 cases and 1522 controls in our study. In this case-control study, our results suggest that the rs3746444 GG genotype increased ESCC risk [homozygote model: adjusted odds ratio (OR), 2.26; 95% CI, 1.33-3.83; p = 0.003, recessive model: adjusted OR, 2.34; 95% CI, 1.38-3.96; p = 0.002], which remained consistent after Bonferroni correction. There was no association of rs11614913 and rs2910164 polymorphisms with ESCC. After adjusting by age, sex, smoking, and drinking status and body mass index (BMI), the multiple logistic analysis suggested that rs11614913 T → C variation reduced ESCC susceptibility in females and in the ≥63 years old subgroups, while rs2910164 C → G variation increased ESCC risk in both two BMI subgroups.
    MeSH term(s) Female ; Humans ; Middle Aged ; Carcinoma, Hepatocellular/genetics ; Case-Control Studies ; Esophageal Neoplasms/genetics ; Esophageal Squamous Cell Carcinoma/genetics ; Genetic Predisposition to Disease ; Genotype ; MicroRNAs/genetics ; Polymorphism, Single Nucleotide ; Male
    Chemical Substances MicroRNAs ; MIRN499 microRNA, human ; MIRN146 microRNA, human ; MIRN196 microRNA, human
    Language English
    Publishing date 2022-05-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2659751-2
    ISSN 2045-7634 ; 2045-7634
    ISSN (online) 2045-7634
    ISSN 2045-7634
    DOI 10.1002/cam4.4729
    Database MEDical Literature Analysis and Retrieval System OnLINE

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