Dongxia Fu

ORCID: 0000-0002-3591-4422
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About
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Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Sexual Differentiation and Disorders
  • Diet and metabolism studies
  • Cancer-related molecular mechanisms research
  • Cancer, Hypoxia, and Metabolism
  • Cardiovascular Disease and Adiposity
  • Liver Disease Diagnosis and Treatment
  • Metal complexes synthesis and properties
  • Metabolism and Genetic Disorders
  • Circular RNAs in diseases
  • Metabolomics and Mass Spectrometry Studies
  • Bariatric Surgery and Outcomes
  • Alkaline Phosphatase Research Studies
  • Metabolism, Diabetes, and Cancer
  • Cardiovascular Health and Disease Prevention
  • bioluminescence and chemiluminescence research
  • Adipokines, Inflammation, and Metabolic Diseases
  • Genomics and Rare Diseases
  • Hedgehog Signaling Pathway Studies
  • Peripheral Artery Disease Management
  • Circadian rhythm and melatonin
  • Nutrition, Genetics, and Disease
  • Cancer Risks and Factors
  • Biochemical and Molecular Research

Zhengzhou Children's Hospital
2019-2025

Zhengzhou University
2018-2024

Cangzhou Central Hospital
2015-2021

Women's Hospital, School of Medicine, Zhejiang University
2018-2021

Hebei Medical University
2018

Huashan Hospital
2016

Fudan University
2016

People's Hospital of Cangzhou
2013

Home quarantine due to the global coronavirus disease 2019 (COVID-19) pandemic has had a significant impact on children. Lifestyle changes have led an increase in precocious puberty (PP) among girls, and underlying risk factors for this remain unclear. Thus, we aimed assess influence of environmental, genetic, nutritional, other lifestyle PP girls. We evaluated incidence new-onset girls during home COVID-19 analyzed potential factors. This was retrospective questionnaire medical record-based...

10.1155/2022/9229153 article EN cc-by International Journal of Endocrinology 2022-09-28

Introduction: To investigate the efficacy and safety of pulsatile gonadotropin-releasing hormone pump therapy in male infants with congenital hypogonadotropic hypogonadism. Methods: Seven hypogonadism who were treated a single center between 2019 2022 included. Each patient was by subcutaneous infusion 5 μg/90 min gonadorelin via for 3 to months. Data including age, drug dose, penile length, testicular volume, cryptorchidism collected. Serum testosterone, follicle-stimulating hormone,...

10.1530/ec-24-0655 article EN cc-by-nc-nd Endocrine Connections 2025-03-01

Background/Aims: Non-alcoholic fatty liver disease (NAFLD) is the most common cause of chronic disease. This study aims to investigate whether chloride channel 2 (ClC-2) involved in high fat diet (HFD)-induced NAFLD and possible molecular mechanisms. Methods: ClC-2 expression was liver-specifically downregulated using adeno-associated virus C57BL/6 mice treated with a chow or HFD for 12 weeks. Peripheral blood tissues were collected biochemical pathological estimation respectively. Western...

10.1159/000488164 article EN cc-by-nc-nd Cellular Physiology and Biochemistry 2018-01-01

OBJECTIVE: To evaluate the prevalence of Helicobacter pylori (H.pylori, HP) infection in subjects receiving routine physical examination and its associations with age, sex, body mass index (BMI) lipid profi les.MATERIALS AND METHODS: Clinical information 22,103 individuals who took examinations, including that on gender, height, weight, triglyceride, total cholesterol, high-density lipoprotein (HDL) low-density (LDL) cholesterol data HP were collected analyzed.RESULTS: H. rate taking was...

10.4149/bll_2016_103 article EN Bratislavské lekárske listy/Bratislava medical journal 2016-01-01

This study aims to investigate the value of high-resolution color Doppler ultrasonography (HR-CDU) in evaluation lower-extremity vasculopathy (LEV) and its related risk factors type 2 diabetes mellitus (T2DM) patients. Two hundred forty T2DM patients were selected, who underwent arterial HR-CDU. The divided into LEV group (V group) nonvasculopathy (A group). V was then mild (B group), moderate (C severe (D subgroups. relevant clinical parameters simultaneously recorded. results showed that...

10.4238/2015.april.27.8 article EN Genetics and Molecular Research 2015-01-01

To explore the clinical characteristics and genetic variants of two children with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency (HMGCLD).

10.3760/cma.j.cn511374-20221010-00677 article EN PubMed 2024-02-10

The clinical and molecular genetic characteristics of 46,XY disorders sex development caused by NR5A1 gene variants in 15 cases were analyzed to improve the understanding this disease.

10.3760/cma.j.cn511734-20221209-00853 article EN PubMed 2024-08-10

A series of m ‐ferrocenylbenzoylthiadiazole compounds, namely FcL 1 –FcL 7 , were synthesized using 3‐ferrocenylbenzoic acid and 2‐amino‐5‐aryl‐1,3,4‐thiadiazole as raw materials. These compounds characterized infrared NMR spectroscopies elemental analysis. The crystal structure was determined X‐ray diffraction. electrochemical behaviors revealed that the redox reactions on surface electrodes reversible with a single‐electron mechanism. Also, demonstrated certain responses to Pb 2+ Zn ....

10.1002/aoc.4265 article EN Applied Organometallic Chemistry 2018-01-19

Two metal–organic frameworks based on a multifunctional ligand 2-(5-bromo-pyridin-3-yl)-1H-imidazole-4,5-dicarboxylic acid (H3L), [Mn(HL)(C2H5OH)]n (1) and {[Zn(HL)(H2O)2]·H2O}n (2), have been hydro/solvothermally synthesized characterized by IR, elemental analyses, X-ray powder single-crystal diffractions, thermogravimetric analyses. In 1, (HL)2– ligands adopt the μ3-kN,O:kN′,O′:kN′′ coordination mode use their imidazoledicarboxylates to bis-chelate MnII into left- right-handed helixes...

10.1080/00958972.2019.1638509 article EN Journal of Coordination Chemistry 2019-06-03

To identify pathogenic mutation in a pedigree affected with brachydactyly and obesity.Peripheral blood sample was collected for extraction of genomic DNA. Exons capture combined next generation sequencing (NGS) carried out to potential mutation. Sanger used verify the results.NGS has identified novel heterozygous missense (c.125A>C, p.Gln42Pro) exon 1 PTHLH gene. The result verified by sequencing. mutations derived from his mother. His uncle sister have also same mutation.A gene been type E2 obesity.

10.3760/cma.j.issn.1003-9406.2019.03.016 article EN PubMed 2019-03-10

To explore the genetic basis for a girl featuring bone and tooth mineralization disorder, premature deciduous teeth, rickets short stature.Genomic DNA was extracted subjected to high-throughput whole exome sequencing. Suspected variants were confirmed by Sanger Impact of potential analyzed with bioinformatic software.The child found carry compound heterozygous missense ALPL gene, including c.1130C>T (p.A377V), known pathogenic mutation inherited from her father, c.1300G>A (p.V434M) mother,...

10.3760/cma.j.cn511374-20200414-00267 article EN PubMed 2021-05-10

: To analyze the clinical and genetic characteristics of children with Keishi-Bukuryo-Gan (KBG) syndrome. The data 5 KBG syndrome admitted in Children's Hospital Affiliated Zhengzhou University from November 2018 to September 2020 were retrospectively analyzed. Five all males who came four different families. All presented triangular face, bushy eyebrows, thin upper lip, large or delayed closure anterior fontanel, abnormal bone development. Four cases had growth retardation, ears, thick ear...

10.3724/zdxbyxb-2021-0268 article EN Journal of Zhejiang University (Medical Sciences) 2021-08-01

Objective To investigate the effect of gastrointestinal Roux-en-Y gastric bypass surgery on blood sugar and insulin function patients with type-2 diabetes mellitus.Methods Twenty-seven cases cancer undergone treatment in centre hospital Cangzhou were selected as our subject.Body mass index (BMI),Glycosylated hemoglobin (HBA1c),Fasting glucose (FPG),fasting (FINS),Fasting C-peptide (FCP) levels measured.Glucose (2 hPG),insulin hINS) hCP) detected after 2 h for oral use 75 g...

10.3760/cma.j.issn.1008-6315.2014.01.026 article EN 中国综合临床 2014-01-01

Objective To explore metabolic characteristics of and risk factors for newly diagnosed type 2 diabetes mellitus(T2DM) combined with non-alcoholic fatty liver disease (NAFLD).Methods One hundred forty-two cases T2DM were divided into two groups according to whether they have comorbid NAFLD:group A (without NAFLD,n =79) group B (combined =63).Data collected included body height,body weight,blood pressure,fasting plasma glucose (FPG),blood lipid,serum uric acid (UA),HbA1c fasting insulin,body...

10.3760/cma.j.issn.1008-6315.2013.03.004 article EN 中国综合临床 2013-03-01

Objective The present study aims to establish a professional knowledge structure for the family planning technical team at current stage in Zhejiang Province so as meet needs of training and offer reference evidences specific effective training. Methods This applied stratified cluster sampling method carry out self-administered questionnaire which was anonymous including general survey, situation training, well skill structure. This de-signed through literature review based on actual...

10.3760/cma.j.issn.2095-1485.2018.09.020 article EN Zhonghua yixue jiaoyu tansuo zazhi 2018-09-20
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