Publications by authors named "Sheng Yi"

Normal embryo development is a complex process that requires normal sperm to fertilize normal oocytes. Abnormal embryogenesis can be caused by either abnormal oocytes or abnormal sperm. However, the impact of sperm-associated factors is often underappreciated.

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Schwann cells are specific peripheral glial cells with remarkable plasticity following peripheral nerve injury. Injury responses stimulate c-Jun activation in Schwann cells, drive epithelial-mesenchymal transition and cellular phenotypic changes, and induce the generation of reprogrammed repair Schwann cells to orchestrate peripheral nerve regeneration process. Schwann cells and/or Schwann cell-derived molecules are commonly used as supporting cells and/or neurotrophic factors to construct Schwann cell-based tissue-engineered nerve grafts for repairing severe peripheral nerve injury with long defects.

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Background: The 10q26 microdeletion syndrome (OMIM #609625) is a distinct genomic disorder characterized by a spectrum of clinical features including craniofacial anomalies, developmental delay (DD)/intellectual disability (ID), hypotonia, cardiovascular, and urogenital malformations. Despite the identification of critical regions within 10q26 linked to the syndrome's phenotype, the specific genes responsible for the associated facial characteristics, microcephaly, cognitive issues, and growth deficiencies remain elusive. Interstitial deletions at 10q25.

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Objective: This study aims to investigate the utility of chromosomal microarray analysis (CMA) and whole exome sequencing (WES) in fetuses diagnosed with talipes equinovarus (TE), as well as to explore the genetic factors contributing to TE.

Methods: The study reviewed a total of 241 fetuses with TE between January 2015 and December 2023, categorizing them into two groups based on the absence or presence of additional ultrasound anomalies: 163 cases (67.6%) in the isolated TE group and 78 cases (32.

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This study investigates the effects of electrical stimulation (EMS) combined with strength training on lower limb muscle activation and badminton jump performance, specifically during the "jump smash" movement. A total of 25 male badminton players, with a minimum of three years of professional training experience and no history of lower limb injuries, participated in the study. Participants underwent three distinct conditions: baseline testing, strength training, and EMS combined with strength training.

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(1) Background: Attention Deficit Hyperactivity Disorder (ADHD) is a common mental health condition in children that can significantly impact their quality of life. In this study, we compared the effectiveness of virtual reality (VR) technology with traditional rehabilitation training through meta-analysis, aiming to provide a basis for the clinical optimization of rehabilitation strategies. (2) Methods: The study was registered in PROSPERO, and a search was conducted using the subject terms "virtual reality" and "attention deficit hyperactivity disorder" across six databases.

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Background: The extracellular matrix (ECM) provides essential physical support and biochemical cues for diverse biological activities, including tissue remodelling and regeneration, and thus is commonly applied in the construction of artificial peripheral nerve grafts. Nevertheless, the specific functions of essential peripheral nerve ECM components have not been fully determined. Our research aimed to differentially represent the neural activities of main components of ECM on peripheral nerve regeneration.

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The special AT-rich sequence-binding (SATB) protein DVE-1 is widely recognized for its pivotal involvement in orchestrating the retrograde mitochondrial unfolded protein response (mitoUPR) in C. elegans. In our study of downstream factors contributing to lifespan extension in sensory ciliary mutants, we find that DVE-1 is crucial for this longevity effect independent of its canonical mitoUPR function.

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Injury to the peripheral nervous system disconnects targets to the central nervous system, disrupts signal transmission, and results in functional disability. Although surgical and therapeutic treatments improve nerve regeneration, it is generally hard to achieve fully functional recovery after severe peripheral nerve injury. A better understanding of pathological changes after peripheral nerve injury helps the development of promising treatments for nerve regeneration.

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Article Synopsis
  • Mutations in the WD repeat structural domain 26 gene are linked to Skraban-Deardorff syndrome, a genetic disorder causing intellectual and developmental challenges, hypotonia, epilepsy, and distinctive facial features.
  • This study analyzed two Chinese patients with the syndrome using whole-exome sequencing to identify novel pathogenic variants in the gene, confirming them through Sanger sequencing.
  • The findings reveal clinical diversity among patients, including new severe behavioral complications in one case, and emphasize that symptoms may worsen with age.
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This study investigated whether lower extremity stiffness plays a role in the enhancement of change of direction speed (CODS) and the duration of this enhancement after dynamic loaded warm-up (DLWU). Fifteen badminton athletes underwent DLWU, and CODS, individual muscle and tendon stiffness, and vertical stiffness were measured before DLWU and 6, 12, and 18 min after DLWU. The data were analyzed using ANOVA and covariance analysis.

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The intestinal barrier, an indispensable guardian of gastrointestinal health, mediates the intricate exchange between internal and external environments. Anchored by evolutionarily conserved junctional complexes, this barrier meticulously regulates paracellular permeability in essentially all living organisms. Disruptions in intestinal junctional complexes, prevalent in inflammatory bowel diseases and irritable bowel syndrome, compromise barrier integrity and often lead to the notorious "leaky gut" syndrome.

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Aim: This study aimed to investigate the associations of serum lactate level [within and after 24 h of the intensive care unit (ICU) admission] and lactate clearance rate with delirium and assess associations of lactate and lactate clearance rate with 30-day mortality in delirium patients.

Methods: Data in this retrospective cohort study were extracted from the Medical Information Mart for Intensive Care IV (MIMIC-IV) database in 2012-2019. The associations of lactate and lactate clearance rate with delirium were explored through univariable and multivariable logistic regression analyses, whereas the associations of lactate and lactate clearance rate with 30-day mortality in delirium patients were investigated using univariable and multivariable Cox regression analyses.

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Objective: This study aims to use structural equation modeling to explore the pathways and effect sizes of factors influencing the adherence of postoperative patients with digestive tract tumor to oral nutritional supplements, providing a theoretical basis for future nursing intervention measures.

Methods: A total of 300 postoperative patients with digestive tract tumor within 30 days after surgery were conveniently sampled. Surveys were conducted using a General Information Questionnaire, Morisky Medication Adherence Scale, Digestive System Tumor Patient Nutrition Knowledge-Attitude-Behavior Questionnaire, Multidimensional Social Perception Scale, Beliefs about Medical Questionnaire, and General Self-Efficacy Scale.

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Background: Serum lactate dehydrogenase (LDH) is a nonspecific inflammatory biomarker and has been reported to be associated with pneumonia prognosis. This study aimed to evaluate the relationship between LDH levels and ventilator-associated pneumonia (VAP) risk in intensive care unit (ICU) patients.

Methods: This retrospective cohort study used data from the Multiparameter Intelligent Monitoring in Intensive Care database from 2001 to 2019.

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Article Synopsis
  • Mitochondrial stress in GABAergic neurons can influence lifespan, stress tolerance, and reproductive health, showing their significant impact on overall health.
  • This stress leads to changes in mitochondrial function, including increased mitochondrial mass, energy production, and higher reactive oxygen species levels.
  • The research highlights that GABA signaling and mitochondrial stress in these neurons work together to cause broader effects on the organism's aging and stress responses.
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  • Autosomal recessive intellectual developmental disorder-3 is linked to mutations in a specific gene, resulting in intellectual disability and autism spectrum disorder, with limited genetic variants identified so far in affected patients.
  • A case study describes a Chinese patient with severe intellectual disability and autism, where whole-exome sequencing revealed a significant mutation, along with the discovery of six new likely pathogenic variants.
  • The research enhances understanding of the genetic and clinical features of this disorder, aiming to improve awareness, genetic testing, and counseling for affected families.
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  • TNRC6B deficiency syndrome is a rare genetic disorder marked by developmental delays, speech issues, ADHD, and distinctive facial features, caused by mutations in the TNRC6B gene.
  • The study involved two Chinese patients with this syndrome, identifying novel genetic variants that broaden the known genetic variations associated with the condition.
  • The results highlight not only the genetic complexity of TNRC6B deficiency syndrome but also the need for ongoing monitoring of patients for growth and metabolic issues and the development of targeted treatments.
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Article Synopsis
  • - Kleefstra syndrome (KLEFS) is a rare neurodevelopmental disorder with symptoms like intellectual disability, language and motor delays, and distinctive facial features, divided into two subtypes (KLEFS1 and KLEFS2) based on genetic causes.
  • - This study identified five unrelated Chinese patients with KLEFS2, each showing different genetic variants in a specific gene linked to the disorder, all exhibiting similar clinical profiles.
  • - The research found a broad range of associated phenotypes in KLEFS2 patients, including intellectual disability and behavioral issues, and highlighted that factors like sex may influence the severity of these symptoms, contributing to a better understanding of the disorder's genetic and phenotypic diversity. *
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Article Synopsis
  • Mega-corpus-callosum syndrome is a rare neurological disorder characterized by brain malformations, caused by mutations in the MAST1 gene, essential for neuron development.
  • A 26-year-old woman was referred for prenatal assessment after ultrasound showed significant brain abnormalities in her fetus, including enlarged ventricles and underdeveloped cerebellum.
  • Whole-exome sequencing revealed a specific mutation in the MAST1 gene, marking the first reported prenatal case of this disorder in the Chinese population and contributing to better understanding of the gene's mutation spectrum.
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Article Synopsis
  • The study investigates the genetic basis of nephronophthisis-related ciliopathies in a 3-year-old boy, identifying two significant mutations in a specific gene linked to multiple disorders including NPHP13 and Caroli disease.
  • Researchers performed whole-exome sequencing to analyze the boy's genetic variations, which included one novel splice-donor variant and a recurrent missense variant, as well as compound heterozygous variants.
  • The findings broaden the understanding of the genetic mutations associated with these disorders and emphasize the clinical diversity, aiding in genetic counseling and screening efforts within affected populations.
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A central question in neural tissue engineering is how the tissue-engineered nerve (TEN) translates detailed transcriptional signals associated with peripheral nerve regeneration into meaningful biological processes. Here, we report a skin-derived precursor-induced Schwann cell (SKP-SC)-mediated chitosan/silk fibroin-fabricated tissue-engineered nerve graft (SKP-SCs-TEN) that can promote sciatic nerve regeneration and functional restoration nearly to the levels achieved by autologous nerve grafts according to behavioral, histological, and electrophysiological evidence. For achieving better effect of neuroregeneration, this is the first time to jointly apply a dynamic perfusion bioreactor and the ascorbic acid to stimulate the SKP-SCs secretion of extracellular matrix (ECM).

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Objectives: This study aimed to explore the value of the Charlson comorbidity index (CCI) in predicting ICU admission in patients with aortic aneurysm (AA).

Methods: The clinical data of patients were obtained from the Medical Information Mart for Intensive Care-IV database. The association between CCI and ICU admission was explored by restricted cubic spline (RCS), threshold effect analysis, generalized linear model, logistic regression, interaction, and mediation analyses.

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