43 results match your criteria: "and Sichuan University[Affiliation]"

EyeHealer: A large-scale anterior eye segment dataset with eye structure and lesion annotations.

Precis Clin Med

June 2021

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.

Anterior segment eye diseases account for a significant proportion of presentations to eye clinics worldwide, including diseases associated with corneal pathologies, anterior chamber abnormalities (e.g. blood or inflammation), and lens diseases.

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Article Synopsis
  • The study aimed to understand how people with arthritis perceive wearables to monitor their physical activity by analyzing qualitative research findings.
  • After reviewing over 4,300 articles, seven studies were included that explored participants' experiences with wearable technology related to arthritis management.
  • Key themes emerged from the data, including improved communication with healthcare providers through sharing data, mixed feelings about how wearables influence self-awareness and motivation for physical activity, and the desire for wearable designs that fit seamlessly into daily life without causing embarrassment.
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Background: Some autoimmune hepatitis (AIH) patients have elevated serum IgG4 levels, and the clinical characteristics of such patients are currently incompletely characterized.

Aim: To analyze the clinical features and possible pathogenesis of AIH with elevated serum IgG4 levels.

Methods: According to their serum IgG4 value, patients were divided into elevated IgG4 (IgG4 > 1.

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This review provides a snapshot of the current state-of-the-art of drying cells and spermatozoa. The major successes and pitfalls of the most relevant literature are described separately for spermatozoa and cells. Overall, the data published so far indicate that we are closer to success in spermatozoa, whereas the situation is far more complex with cells.

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Introduction: The Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder. The obstetric course of women with KTS varies. Complications include bleeding, disseminated intravascular coagulation (DIC), thromboembolic events, etc.

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Evaluating the effectiveness of a disaster preparedness nursing education program in Chengdu, China.

Public Health Nurs

March 2020

MSc. Graduated from School of Nursing and Institute of Disaster Management and Reconstruction (IDMR), The Hong Kong Polytechnic University and Sichuan University, Chendu, China.

Objective: To develop and evaluate a disaster nursing preparedness training program to improve nursing students' ability in disaster fundamentals, triage, and family preparedness when facing a disaster.

Design And Sample: An experimental study was applied using a pretest and post-test control group design. Participants were randomly assigned to the experimental (n = 31) and control (n = 32) groups.

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Despite initial progress in preclinical models, most known histone deacetylase inhibitors (HDACis) used as a single agent have failed to show clinical benefits in nearly all types of solid tumours. Hence, the efficacy of HDACis in solid tumours remains uncertain. Herein, we developed a hybrid HDAC inhibitor that sensitized solid tumours to HDAC-targeted treatment.

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Background: Many effects of statins on non-cardiovascular disease (non-CVD) outcomes have been reported.

Purpose: To evaluate the quantity, validity, and credibility of evidence regarding associations between statins and non-CVD outcomes and the effects of statins on these outcomes.

Data Sources: MEDLINE and EMBASE (English terms only, inception to 28 May 2018).

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As a result of societal expectations and to avoid societal homophobia, many lesbians and gay men in China marry heterosexual partners and do not disclose their own sexual orientation. This study used qualitative methods to explore why gay men enter into such marriages of convenience. A total of 17 in-depth interviews were conducted with lesbians and gay men who had entered "formality marriages.

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Spontaneous expulsion of a huge cervical leiomyoma from the vagina after cesarean: A case report with literature review.

Medicine (Baltimore)

August 2018

Department of Gynecology and Obstetrics, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital Department of Gynecology and Obstetrics, West China Second University Hospital and Sichuan University, China.

Rationale: As more and more women delay their child bearing age, the prevalence of uterine fibroids during pregnancy is likely to increase.

Patient Concerns & Lessons: We report a Chinese Tibetan case with spontaneous expulsion of a huge cervical myoma after cesarean. Decreased blood supply of the myoma and the uterine contraction may contribute to the spontaneous expulsion.

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High-Throughput Sequencing of the Expressed Torafugu () Antibody Sequences Distinguishes IgM and IgT Repertoires and Reveals Evidence of Convergent Evolution.

Front Immunol

March 2019

Laboratory of Aquatic Molecular Biology and Biotechnology, Department of Aquatic Bioscience, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.

B-cell antigen receptor (BCR) or antibody diversity arises from somatic recombination of immunoglobulin (Ig) gene segments and is concentrated within the Ig heavy (H) chain complementarity-determining region 3 (CDR-H3). We performed high-throughput sequencing of the expressed antibody heavy-chain repertoire from adult torafugu. We found that torafugu use between 70 and 82% of all possible V (variable), D (diversity), and J (joining) gene segment combinations and that they share a similar frequency distribution of these VDJ combinations.

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Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.

Proc Natl Acad Sci U S A

November 2015

Institute for Genomic Medicine and Shiley Eye Institute, University of California, San Diego, La Jolla, CA 92328; Molecular Medicine Research Center, State Key Laboratory of Biotherapy, West China Hospital and Sichuan University, Chengdu 610041, China; Veterans Administration Healthcare System, San Diego, CA 92161

Noninvasive prenatal testing (NIPT) using sequencing of fetal cell-free DNA from maternal plasma has enabled accurate prenatal diagnosis of aneuploidy and become increasingly accepted in clinical practice. We investigated whether NIPT using semiconductor sequencing platform (SSP) could reliably detect subchromosomal deletions/duplications in women carrying high-risk fetuses. We first showed that increasing concentration of abnormal DNA and sequencing depth improved detection.

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A designed low aggregated magnetic polyethyleneimine/DNA (MPD-cc) complex showed efficient transfection in serum-containing medium for PEI-mediated gene transfection in vitro and in vivo, but the mechanism remains unclear. The present study provides an insight into the extracellular and intracellular fates of the magnetic gene complexes, evaluates their transfection efficiency and body distribution after systemic administration assisted by fluorescent imaging technology. The PEI cationic complexes in our study switched to be negatively charged in the serum-containing medium due to protein corona formation, and the complexes displayed negligible aggregation from transmission electron microscopy observation and dynamic light scattering analysis.

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Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.

Proc Natl Acad Sci U S A

May 2014

Institute for Genomic Medicine and Department of Ophthalmology, University of California, San Diego, La Jolla, CA 92328;Molecular Medicine Research Center, State Key Laboratory of Biotherapy, West China Hospital and Sichuan University, Chengdu 610041, China; andVeterans Administration Healthcare System, San Diego, CA 92161

Massively parallel sequencing (MPS) of cell-free fetal DNA from maternal plasma has revolutionized our ability to perform noninvasive prenatal diagnosis. This approach avoids the risk of fetal loss associated with more invasive diagnostic procedures. The present study developed an effective method for noninvasive prenatal diagnosis of common chromosomal aneuploidies using a benchtop semiconductor sequencing platform (SSP), which relies on the MPS platform but offers advantages over existing noninvasive screening techniques.

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Entropic stabilization of nanoscale voids in materials under tension.

Phys Rev Lett

May 2013

Theoretical Division T-1, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA.

While preexisting defects are known to act as nucleation sites for plastic deformation in shocked materials, the kinetics of the early stages of plastic yield are still poorly understood. We use atomistic simulation techniques to investigate the kinetics of plastic yield around small preexisting voids in copper single crystals under uniaxial tensile strain. We demonstrate that at finite temperatures, these voids are stabilized by strong entropic effects that confer them significant lifetimes even when the static mechanical instability limit is exceeded.

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Targeting the kynurenine pathway as a potential strategy to prevent and treat Alzheimer's disease.

Med Hypotheses

September 2011

Department of Urology, The Second Hospital of Chengdu, and Sichuan University, Chengdu, Sichuan 610017, PR China.

Alzheimer's disease (AD) is a progressive neurodegenerative disorder of the elderly accounting for the vast majority of dementia. Recently, many studies have implicated the role of inflammatory response, especially neuroinflammatory response in the development and progression of AD. However, the underlying mechanism of how inflammatory response induces AD is unknown.

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Article Synopsis
  • The study aimed to investigate the frequency of genetic variants at Xmn I and Msp I sites of the ApoAI-CIII-AIV gene cluster and their link to cholesterol gallstones in Chinese patients.
  • Restriction fragment length polymorphisms (RFLP) were analyzed in 161 patients with cholesterol gallstones and 94 healthy subjects via polymerase chain reaction (PCR).
  • Results indicated that while some genetic variations were common in both groups, a notable increase in the X2 allele mutation was found in female patients with gallstones compared to healthy females, suggesting a potential association between the gene variants and cholesterol gallstones.
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