Search Results - "Chen, Riling"
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Pan-cancer integrated analysis of ANKRD1 expression, prognostic value, and potential implications in cancer
Published in Scientific reports (04-03-2024)“…There is substantial evidence demonstrating the crucial role of inflammation in oncogenesis. ANKRD1 has been identified as an anti-inflammatory factor and is…”
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Isolated steroid-resistant nephrotic syndrome in a Chinese child carrying a de novo mutation in WT1 gene:a case report and literature review
Published in BMC pediatrics (16-06-2022)“…Isolated steroid-resistant nephrotic syndrome (ISRNS) is caused by mutations in the Wilms' tumor-1 (WT1) gene, which encodes glomerular podocytes and podocyte…”
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Research progress of ankyrin repeat domain 1 protein: an updated review
Published in Cellular & molecular biology letters (17-10-2024)“…Ankyrin repeat domain 1 (Ankrd1) is an acute response protein that belongs to the muscle ankyrin repeat protein (MARP) family. Accumulating evidence has…”
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Mesenchymal Stem/Stromal Cells in Asthma Therapy: Mechanisms and Strategies for Enhancement
Published in Cell Transplantation (01-01-2023)“…Asthma is a complex and heterogeneous disease characterized by chronic airway inflammation, airway hyperresponsiveness, and airway remodeling. Most asthmatic…”
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miR-137: A Novel Therapeutic Target for Human Glioma
Published in Molecular therapy. Nucleic acids (04-09-2020)“…MicroRNA (miR)-137 is highly expressed in the brain and plays a crucial role in the development and prognosis of glioma. In this review, we aim to summarize…”
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The roles of sirtuins in ferroptosis
Published in Frontiers in physiology (20-04-2023)“…Ferroptosis represents a novel non-apoptotic form of regulated cell death that is driven by iron-dependent lipid peroxidation and plays vital roles in various…”
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Systematic analysis of prognostic and immunologic characteristics associated with coronavirus disease 2019 regulators in acute myeloid leukemia
Published in Frontiers in genetics (06-09-2022)“…The coronavirus disease 2019 (COVID-19) pandemic has so far damaged the health of millions and has made the treatment of cancer patients more complicated, and…”
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Case report: Familial glycogen storage disease type IV caused by novel compound heterozygous mutations in a glycogen branching enzyme 1 gene
Published in Frontiers in genetics (08-11-2022)“…Glycogen storage disease type IV (GSD IV), caused by a mutation in the glycogen branching enzyme 1 (GBE1) gene, is a rare metabolic disorder with an autosomal…”
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Association Between the miR-146a Rs2910164 Polymorphism and Childhood Acute Lymphoblastic Leukemia Susceptibility in an Asian Population
Published in Frontiers in genetics (02-10-2020)“…has been demonstrated to be involved in normal hematopoiesis and the pathogenesis of many hematological malignancies by inhibiting the expression of its…”
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The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-analysis
Published in Frontiers in genetics (27-09-2021)“…The dopamine transporter (DAT) is encoded by the SLC6A3 gene and plays an important role in the regulation of the neurotransmitter dopamine. The SLC6A3 gene…”
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Corrigendum: The 10-Repeat 3′-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson’s Disease: A Meta-Analysis
Published in Frontiers in genetics (21-10-2021)Get full text
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Association between the RETN -420C/G polymorphism and type 2 diabetes mellitus susceptibility: A meta-analysis of 23 studies
Published in Frontiers in endocrinology (Lausanne) (21-12-2022)“…The published findings on the link between the resistin (RETN) gene polymorphism and type 2 diabetes mellitus (T2DM) risk are still contradictory. Here,…”
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Different Associations Between the IREB2 Variants and Chronic Obstructive Pulmonary Disease Susceptibility
Published in Frontiers in genetics (16-11-2020)“…Background: Iron responsive element binding protein 2 ( IREB2 ) variants may be involved in the pathogenesis of chronic obstructive pulmonary disease (COPD)…”
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Congenital disorder of glycosylation type Ia in a Chinese family: Function analysis of a novel PMM2 complex heterozygosis mutation
Published in Molecular genetics and metabolism reports (01-06-2024)“…Congenital disorder of glycosylation type Ia (CDG-Ia) is an autosomal recessive genetic disease caused by a mutation in the phosphomannomutase 2 (PMM2) gene…”
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Positive Correlation Between LTA Expression and Overall Immune Activity Suggests an Increased Probability of Survival in Uterine Corpus Endometrial Carcinoma
Published in Frontiers in cell and developmental biology (28-01-2022)“…Mounting evidence indicates that immune status plays a crucial role in tumor progress and metastasis, while there are no effective and easily assayed…”
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Hypercalcemia as the first manifestation of childhood acute lymphoblastic leukemia: a case report
Published in Xīn yīxué (01-07-2023)“…Acute lymphoblastic leukemia (ALL) is a malignant tumor with the highest incidence during childhood. ALL is mainly characterized with fever, pale face, fatigue…”
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Potential Biomarker of Acute Anthracycline-induced Cardiotoxicity Among Children With Acute Lymphoblastic Leukemia: Cardiac Adriamycin-responsive Protein
Published in Journal of cardiovascular pharmacology (01-12-2023)“…This study aimed to investigate whether serum cardiac adriamycin-responsive protein (CARP) can serve as a sensitive and specific biomarker of anthracyclines…”
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Smad4 promotes diabetic nephropathy by modulating glycolysis and OXPHOS
Published in EMBO reports (05-02-2020)“…Diabetic nephropathy (DN) is the leading cause of end‐stage kidney disease. TGF‐β1/Smad3 signalling plays a major pathological role in DN; however, the…”
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Genetic variations in DOCK4 contribute to schizophrenia susceptibility in a Chinese cohort: A genetic neuroimaging study
Published in Behavioural brain research (12-04-2023)“…Emerging evidence suggests that the DOCK4 gene increases susceptibility to schizophrenia. However, no study has hitherto repeated this association in Chinese,…”
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