Ying Shi

ORCID: 0000-0001-8914-5510
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About
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Research Areas
  • Pregnancy and preeclampsia studies
  • Reproductive System and Pregnancy
  • MicroRNA in disease regulation
  • Sperm and Testicular Function
  • Birth, Development, and Health
  • Reproductive Biology and Fertility
  • Cancer-related molecular mechanisms research
  • Gestational Diabetes Research and Management
  • Ovarian function and disorders
  • Epigenetics and DNA Methylation
  • Hearing, Cochlea, Tinnitus, Genetics
  • Neonatal Respiratory Health Research
  • Immunodeficiency and Autoimmune Disorders
  • Pediatric health and respiratory diseases
  • Genomics, phytochemicals, and oxidative stress
  • Restraint-Related Deaths
  • Peptidase Inhibition and Analysis
  • Oral and Craniofacial Lesions
  • Ear Surgery and Otitis Media
  • Amyotrophic Lateral Sclerosis Research
  • Circular RNAs in diseases
  • Congenital heart defects research
  • Autophagy in Disease and Therapy
  • Cancer Genomics and Diagnostics
  • T-cell and Retrovirus Studies

Inner Mongolia Electric Power Survey & Design Institute (China)
2024

Third Affiliated Hospital of Zhengzhou University
2014-2023

Zhengzhou University
2014-2019

Zhongshan Hospital of Xiamen University
2016

Objective Breast cancer is the most common and high-incidence in women. It mainly treated by surgery combined with chemoradiation. The main challenge treating breast patients developing resistance to chemotherapeutics, so it urgent find potential strategies that can improve chemotherapy effect of patients. In this study, we aimed explore role GSDME methylation sensitivity for cancer. Methods Here, identified MCF-7 / Taxol cells models using quantitative real-time PCR (qRT-PCR), Western...

10.1371/journal.pone.0282244 article EN cc-by PLoS ONE 2023-03-03

Purpose: The aim of this study was to investigate the correlations and interactions between polymorphisms insulin resistance-related genes (ADIPOQ rs2241766), inflammation factors (TNF-α rs1800629, IL-6 rs1800795), obesity-related (GNB3 rs5443, ADRB rs1042714), risk for gestational diabetes mellitus (GDM) such as diet structure in development GDM.Materials methods: This research conducted among women who visited third-affiliate hospital Zhengzhou University pregnancy checkups from 1 June...

10.1080/14767058.2018.1446207 article EN The Journal of Maternal-Fetal & Neonatal Medicine 2018-03-08

Background Recent studies reported that serum anion gap could be regarded as a prognostic biomarker for patients admitted to intensive care units. However, the association between AG and mortality in cerebral infarction remained largely unknown.Methods Relevant clinical data were collected from Medical Information Mart Intensive Care III. Patients divided into three groups according tertiles of AG. Kaplan–Meier curve Cox proportional hazards models used evaluate levels all-cause mortality....

10.1080/1354750x.2020.1842497 article EN Biomarkers 2020-10-24

Objective: We aimed to investigate Th22 cells and their association with Th17 Treg in the etiology of severe preeclampsia (sPE).Methods: Thirty sPE patients 30 healthy pregnant women were recruited this study. The percentages Th17, Th22, regulatory T (Tregs) peripheral blood measured by flow cytometry. ELISA was used measure plasma concentrations interleukin (IL)-17, IL-22, IL-10.Results: IL-17 IL-22 significantly increased along a decreased percentage IL-10 concentration. There positive...

10.1080/10641955.2016.1239737 article EN Hypertension in Pregnancy 2016-11-11

Although Taxol has improved the survival of cancer patients as a first-line chemotherapeutic agent, an increasing number develop resistance to after prolonged treatment. The potential mechanisms cell are not completely clear. It been reported that microRNAs (miRNAs) involved in regulating sensitivity cells various agents. In this study, we aimed explore role miR-129-5p breast Taxol. Cell apoptosis and autophagy, MCF-7 were assessed with series vitro assays. Our results showed inhibition...

10.1590/1414-431x20198657 article EN cc-by Brazilian Journal of Medical and Biological Research 2019-01-01

The aim of this study was to investigate the roles oxygen free radicals and mitochondrial signaling in semen disorders, particular, how induces low concentrations reduced motility sperm. Ejaculate samples were obtained from 120 young adult males (mean age, 28.7±5.3 years) with normal (n=30), oligospermia asthenospermia (n=30) oligoasthenozoospermia (n=30). malondialdehyde (MDA) content, total superoxide dismutase (T‑SOD) activity glutathione peroxidase (GSH‑Px) sperm determined by enzymatic...

10.3892/mmr.2014.2428 article EN Molecular Medicine Reports 2014-07-29

Preeclampsia (PE) is a pregnancy-specific syndrome that has severe implications on perinatal mortality and morbidity. Excessive apoptosis of trophoblasts induced by hypoxia may be associated with the development PE, but exact pathogenesis unknown. Forkhead box O transcription factor 3a (FOXO3a) activated under hypoxic conditions. Furthermore, hypoxia‑inducible factor‑1α (HIF‑1α) sensitive to variations in partial oxygen pressure. Thus, aims present study were investigate expression levels...

10.3892/mmr.2020.11050 article EN cc-by-nc-nd Molecular Medicine Reports 2020-04-01

The goal of this study is to evaluate a new (18) F-labeled imaging agent for diagnosing high metastatic (aggressive) hepatocellular carcinoma using positron emission tomography (PET). [(18) F]AlF-NOTA-G-TMTP1 was synthesized and radiolabeled with F NOTA-AlF chelation method. tumor-targeting characteristics assessed in HepG2, SMCC-7721, HCC97L HCCLM3 xenografts. total synthesis time about 20 min radiochemical yield 25 ± 6%. specific activity 11.1-14.8 GBq/µmol at the end based on amount...

10.1002/cmmi.1688 article EN Contrast Media & Molecular Imaging 2016-03-01

Abstract Background The enlarged vestibular aqueduct (EVA) is the commonest malformation of inner ear accompanied by sensorineural hearing loss in children. Three genes SLC26A4 , FOXI1 and KCNJ10 have been associated with EVA, among them being most common. Yet, hotspot mutation screening can only diagnose a small number patients. Methods Thus, this study, we designed new molecular diagnosis panel for EVA based on multiplex PCR enrichment next‐generation sequencing exon flanking regions . A...

10.1002/mgg3.1734 article EN Molecular Genetics & Genomic Medicine 2021-06-25

Phenylketonuria (PKU, OMIM 261600) caused by phenylalanine hydroxylase (PAH) deficiency is an autosomal recessive disease that characterized abnormalities of metabolism. In this study, a total 77 patients, originating from the central region China and who were diagnosed with PAH at third affiliated hospital Zhengzhou University, enrolled in study. The 13 exons 12 flanking introns gene analyzed Sanger sequencing next generation sequencing. data aligned to hg19, PAHvdb HGMD databases...

10.1080/00365513.2018.1434898 article EN Scandinavian Journal of Clinical and Laboratory Investigation 2018-02-01

Abstract Immunophenotyping of blood lymphocytes has become an important tool in the diagnosis immunologic and hematologic disorders such as immunodeficiencies, lymphoproliferative autoimmune diseases. Lymphocyte subsets include total T‐cells (CD3 + ), TH (T helper, CD3 CD4 TC (cytotoxic T cells, CD8 B‐cells − CD19 NK‐cells CD16 CD56 ). Specific lymphocyte subset reference intervals should be locally established for meaningful comparison to obtain accurate interpretation results. Reference...

10.1002/cyto.a.22716 article EN Cytometry Part A 2015-07-07

Breast cancer (BC) is the most frequently diagnosed tumor in women worldwide. Although combination of surgery and Taxol chemotherapy can achieve a certain therapeutic effect, patients often develop drug-resistance, resulting poor prognosis. Therefore, it significative to seek molecular mechanism resistance. Recent studies have found that abnormal epigenetic regulation breast cells changes expression key genes, which lead occurrence, development, maintenance cancer, even related development...

10.1371/journal.pone.0241515 article EN cc-by PLoS ONE 2020-12-11
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