Publications by authors named "Jinjian Gao"

The growing microbial resistance to traditional medicines necessitates in-depth analysis of medicine-microbe interactions (MMIs) to develop new therapeutic strategies. Widely used artificial intelligence models are limited by sparse observational data and prevalent noise, leading to over-reliance on specific data for feature extraction and reduced generalization ability. To address these limitations, we integrate Kolmogorov-Arnold Networks (KANs), independent subspaces, and collaborative decoding techniques into the masked graph autoencoder (Mask GAE) framework, creating an innovative MMI prediction model with enhanced accuracy, generalization, and interpretability.

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Objectives: To explore the clinical diagnosis and treatment of special types of tracheobronchial foreign bodies in children and provide a reference for clinicians to formulate treatment plans.

Methods: Clinical data of 29 children with special types of tracheobronchial foreign bodies who were treated at The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University between June 2017 and June 2022 were collected and analyzed, and their diagnosis and treatment processes were reviewed.

Results: All 29 special types of foreign bodies were successfully removed using rigid bronchoscopy under general anesthesia, with no surgical complications.

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Congenital epiglottic cysts are rare disorders of the larynx with symptoms such as laryngeal stridor and inspiratory dyspnea and are life-threatening in severe cases. This study aimed to investigate the usefulness of low-temperature plasma radiofrequency ablation for congenital epiglottic cysts and provide a reference for clinicians to develop treatment options. The clinical data of children (n = 7, 4 males and 3 females) with congenital epiglottic cysts, who were admitted to the Second Affiliated Hospital of Wenzhou Medical University and Yuying Children's Hospital from March 2018 to March 2023, were analyzed retrospectively.

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Aim: To understand the degree of oncology patients' awareness of drug clinical trials and oncology patients' willingness to participate in drug clinical trials and the factors influencing them.

Methods: The differences in the relevant variables of patients' willingness to accept clinical trials were analyzed, and a descriptive analysis was done for the measurement data (mean and standard deviation). Pearson's correlation coefficient analysis was used to examine the correlation between willingness and the demographic variables.

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Article Synopsis
  • MYSM1 is a metalloprotease linked to colorectal cancer (CRC) that, when downregulated, negatively impacts patient survival and disease progression.
  • MYSM1 functions as a tumor suppressor by promoting apoptosis and inhibiting cancer cell proliferation, epithelial-mesenchymal transition (EMT), and metastasis.
  • The study suggests that targeting MYSM1 could be a promising strategy to improve CRC treatment and patient outcomes by enhancing the expression of specific microRNAs and modulating signaling pathways involved in tumor progression.
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Electromagnetic radiation has been proposed to non-aqueously stimulate shale formations, which can generate fractures and enhance the porosity of the matrix. The proposed method consumes electricity and thereby possesses significant advantages for sustainable and environmental hydrocarbon production. In this study, we investigate the pore structure variations of marine shale during electromagnetic radiation.

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Emerging evidence has indicated that microRNAs (miRs) are involved in the malignant behavior of cancer. The present study explored the role of miR‑193b in the development and metastasis of osteosarcoma. Compared with F4 osteosarcoma cells, which have a relatively low metastatic potential, highly metastatic F5M2 cells exhibited a lower expression of miR‑193b.

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  • Recent studies suggest genetic factors play a significant role in sudden sensorineural hearing loss (SSNHL), but findings have often been inconclusive.
  • A systematic review of 47 studies involving over 5,230 SSNHL patients identified 26 genes potentially linked to genetic susceptibility to the disorder.
  • There is a call for larger, multi-center studies to pinpoint definitive genetic risk factors, which could lead to improved prevention and treatment strategies for SSNHL.
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Article Synopsis
  • Complete blood count (CBC) tests are crucial for evaluating clinical outcomes in patients with sudden sensorineural hearing loss (SSNHL), with some indices showing potential prognostic value.
  • A meta-analysis of 10 studies involving 972 patients identified key haematological indices—namely the neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), neutrophil count, and lymphocyte count—associated with SSNHL prognosis.
  • The study concludes that these four indices could serve as cost-effective markers for predicting treatment outcomes in SSNHL patients.
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Background: Previous studies have described the protective effects of DADLE on myocardial injury in sepsis. Recently, autophagy has been shown to be an innate defense mechanism in sepsis-related myocardial injury. However, whether DADLE has an pro-autophagic effect is yet to be elucidated.

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The present study aimed to compare the efficacy and safety of subcutaneous immunotherapy with standardized extract administered in conventional and cluster immunotherapy regiments for patients with persistent allergic rhinitis. A total of 60 patients with moderate to severe allergic rhinitis caused by dust mites were treated for 1 year with either conventional immunotherapy (n=30) or cluster immunotherapy (n=30). Nasal conjunctival symptoms and signs were assessed to evaluate the clinical efficacy of the two regimens, and the incidence of local and systemic adverse reactions were also evaluated.

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Article Synopsis
  • Allergic rhinitis (AR) is a widespread issue worldwide, and sublingual immunotherapy (SLIT) has been found effective in treating persistent allergic rhinitis (PAR), though some studies question its efficacy when using house dust mite extracts.
  • The study performed a meta-analysis of randomized controlled trials (RCTs) to evaluate the effectiveness of SLIT for PAR, analyzing data from various medical databases up to May 2016, revealing significant symptom relief and reduced medication use.
  • The findings indicate that SLIT significantly alleviated symptoms (SMD=1.23) and decreased medication needs (SMD=-1.39), highlighting a need for further high-quality studies to confirm these outcomes and determine effective dosing.
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Objective: To investigate the alterations in the level of myocardial cells and mitochondrial autophagy during myocardial injury in lipopolysaccharide (LPS)-induced septic animal models.

Methods: Male C57BL/J mice were randomly divided into negative control group (NC), LPS treatment groups (6, 12, 24, 36 hours). The LPS treatment groups were subjected to LPS (10 mg/kg) injection intraperitoneally, and the NC group was injected intraperitoneally with the same amount of saline.

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Objective: To investigate the effect of miR-365 on the proliferation and apoptosis in SOSP-9607 osteosarcoma cells.

Methods: SOSP-9607 cells were transiently transfected with miR-365 mimic or miR-365 inhibitor which were artificially synthesized. The expression of miR-365 was detected by real-time PCR (qRT-PCR); the cell cycle and apoptosis was analyzed by flow cytometry; the cell proliferation was observed by MTT assay; and the level of KRAS was determined by qRT-PCR and Western blotting.

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It remains unclear whether the Glutathione S-transferase M1 (GSTM1) null genotype influence laryngeal cancer development. This study aimed to investigate the interactions among GSTM1 genotype with regard to laryngeal cancer development. We searched online electronic databases (PubMed, EMBASE and CNKI).

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Objective: This study was designed to explore the risk factors associated with severity of juvenile onset recurrent respiratory papillomatosis.

Method: A retrospective study was conducted to study determinants of severe forms of juvenile recurrent onset respiratory papillomatosis. The patients were separated into different groups based on the onset age, the first recurrence of age, the first recurrence of period, gender and incision of tracheal respectively.

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Objective: To investigate the correlation between nonsyndromic deafness and mitochondrial 12s rRNA A839G mutation.

Methods: According to the clinical manifestations of mitochondrial DNA sequencing and analysis to find and determine family containing mitochondrial 12s rRNA A839G mutation. Harvested its family members blood and transferred their lymphocytes into lymphoblastoid cell lines, followed by cells cultured, cell doubling experiment, susceptibility testing, cellular oxygen consumption rate experiment, ROS and mitochondrial membrane potential experimental tests were progressed to explore the correlation between the A839G mutation and nonsyndromic deafness.

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Objective: To assess the possible genotype-phenotype correlation for GJB2.

Methods: Retrospectively analyzed GJB2 gene mutations with non-syndromic hearing impairment (NSHI) patients and their families audiological data. Individuals were grouped, according to non-truncated mutant (non-truncating, NT) and truncating mutations (truncating, T), into T/T group, T/NT group and NT/NT group.

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Article Synopsis
  • A study evaluated the relationship between genetic mutations and the age of onset in nonsyndromic hearing impairment (NSHI) by analyzing 215 patients divided into four age groups based on when hearing loss first occurred.
  • The findings revealed that 18.14% had GJB2 mutations, primarily affecting infants, while 11.16% had mtDNA mutations, with a higher prevalence in adults.
  • The results indicated genetic mutations linked to congenital deafness (GJB2) and acquired deafness (mtDNA A1555G/C1494T), highlighting the need for early genetic testing and newborn hearing screening.
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Objective: To observe the changes of brain oxygen metabolism and neuroelectrophysiology after severe brain injury, and the effects of hypothermia on severe brain injury.

Methods: 148 patients with severe brain injury (GCS 3 - 8, admitted within 10 hours from injury) were selected for this study. Patients were divided into 3 groups, Group GCS 7 - 8, Group GCS 5 - 6 and Group GCS 3 - 4.

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Objective: To study the expression and significance of vascular permeability factor (VPF) in eosinophil, macrophage and plasma cell in nasal polyps.

Method: VPF in 12 nasal polyps was studied by immunohistochemistry, double immune-enzymatic staining technique and double MGG staining technique. Each section was observed under optical microscope.

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