Publications by authors named "Rui-zhi Liu"

Zn-air batteries (ZABs) present high energy density and high safety but suffer from low oxygen reaction reversibility and dendrite growth at Zn electrode in alkaline electrolytes. Non-alkaline electrolytes have been considered recently for improving the interfacial processes in ZABs. However, the dynamic evolution and reaction mechanisms regulated by electrolytes at both the positive and Zn negative electrodes remain elusive.

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Long-term continual straw return can enhance soil quality and increase crop yields by perpetually altering the soil environment. However, little is known about how different straw return methods affect soil physicochemical properties, enzymatic processes, and crop yields. The study aims to determine how different straw return practices improve soil structure, nutrients, enzyme activities, and maize yields.

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Article Synopsis
  • This study looked at how chromothripsis, a type of DNA damage, could help doctors understand more about pancreatic tumors.
  • They studied 30 patients with high-grade tumors and compared them to 25 with lower-grade tumors.
  • The findings showed that chromothripsis is linked to worse outcomes and can help tell apart aggressive tumors from less serious ones.
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Lithium-carbon dioxide (Li-CO ) battery technology presents a promising opportunity for carbon capture and energy storage. Despite tremendous efforts in Li-CO batteries, the complex electrode/electrolyte/CO triple-phase interfacial processes remain poorly understood, in particular at the nanoscale. Here, using in situ atomic force microscopy and laser confocal microscopy-differential interference contrast microscopy, we directly observed the CO conversion processes in Li-CO batteries at the nanoscale, and further revealed a laser-tuned reaction pathway based on the real-time observations.

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Research Question: What are the potential clinical benefits of embryo culture and assessment in a time-lapse incubator compared with a standard incubator using static assessment?

Design: This large multicentre, single-blinded, randomized controlled study included 1224 participants randomly assigned (1:1) to the time-lapse or standard incubator group. In all patients one or two embryos were transferred on day 3. The primary outcome was the implantation rate in the first embryo transfer cycle.

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Background: Raltitrexed plus S-1 (RS) and regorafenib both showed considerable efficacy for metastatic colorectal cancer (mCRC) patients. This study aims to compare the effectiveness and safety of two different regimens in patients with refractory mCRC.

Methods: This retrospective cohort study included mCRC patients who were treated with RS or regorafenib from February 2017 to June 2021.

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Body mass index (BMI) has been increasing globally in recent decades. Previous studies reported that BMI was associated with sex hormone levels, but the results were generated via linear regression or logistic regression, which would lose part of information. Quantile regression analysis can maximize the use of variable information.

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Objective: We report a prenatal case of male fetus with a 2q13 deletion and an Xq27.3q28 duplication, presenting nasal bone dysplasia by ultrasound examination. And we compare the similarities of clinical features of cases consisting of similar 2q deletion and Xq duplication.

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Purpose: Immune-related pneumonitis (IRP) has attracted extensive attention, owing to its increased mortality rate. Conventional chemotherapy (C) has been considered as an immunosuppressive agent and may thus reduce IRP's risk when used in combination with PD-1/L1 inhibitors. This study aimed to assess the risk of IRP with PD-1/L1 inhibitors plus chemotherapy (I+C) versus PD-1/L1 inhibitors alone (I) in solid cancer treatment.

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Bone morphogenetic protein 6 (BMP6) and connective tissue growth factor (CTGF) are critical growth factors required for normal follicular development and luteal function. Cluster of Differentiation 68 (CD68) is an intraovarian marker of macrophages that plays an important role in modulating the physiological regression of the corpus luteum. The aim of this study was to investigate the effect of BMP6 on the expression of CTGF and the subsequent increase in CD68 expression as well as its underlying mechanisms.

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Background: Down syndrome (DS) is one of the most common chromosomal aneuploidy diseases. Prenatal screening and diagnostic tests can aid the early diagnosis, appropriate management of these fetuses, and give parents an informed choice about whether or not to terminate a pregnancy. In recent years, investigations have been conducted to achieve a high detection rate (DR) and reduce the false positive rate (FPR).

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Objective: To diagnose the ring chromosome 13 (r(13)) in a fetus, and analyze the genotype-phenotype correlation.

Case Report: A 26-year-old woman who was second pregnancy, underwent amniocentesis at 18 weeks of gestation because of the increased nuchal translucency (NT). Prenatal ultrasound showed the NT thickness was 3.

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BACKGROUND In pregnant women with advanced maternal age (AMA) and fetuses with ultrasonographic (USG) soft markers it is always challenging to decide whether to implement chromosomal microarray analysis (CMA) or not. It is unclear whether CMA should be used in the fetuses with isolated USG soft markers, and there is still a lack of extensive sample research. MATERIAL AND METHODS We enrolled 1521 cases in our research and divided them into 3 groups as follows: pregnant women with isolated AMA (group 1, n=633), pregnant women whose fetuses had isolated USG soft markers (group 2, n=750), and pregnant women with AMA whose fetuses had isolated USG soft markers (group 3, n=138).

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Article Synopsis
  • The study focuses on a small supernumerary marker chromosome (sSMC) from chromosome 15, analyzing a case involving a 29-year-old woman who underwent amniocentesis due to a potential Down syndrome risk.* -
  • Genetic tests revealed that the woman had a chromosomal abnormality, specifically a marker chromosome inherited from her, while the father's chromosomes were normal.* -
  • Advanced molecular techniques like fluorescence in situ hybridization (FISH) and chromosomal microarray analysis (CMA) were crucial in identifying the sSMC, aiding in genetic counseling and prenatal diagnostics, and the delivery resulted in a healthy infant.*
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Objective: To retrospectively analyze the incidence of chromosomal polymorphisms in prenatal cytogenetic diagnostic cases and the effect of the clinical manifestation of these fetuses.

Materials And Methods: 490 fetuses with chromosomal polymorphisms among 9996 pregnant women who underwent prenatal cytogenetic diagnosis were included in this study and were set as group 1. Other 500 pregnant women, whose fetuses were with normal karyotypes, were randomly selected from the remaining pregnant women and set as group 2.

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  • The study aimed to indigenize the median screening markers for Down syndrome in first and second trimester pregnancies and evaluate the impact on screening efficiency.
  • Data was analyzed through a retrospective study, comparing multiple of median (MoM) values derived from indigenized medians against built-in median data using regression models.
  • Results showed that indigenized parameters improved detection rates in screening, with a 100% detection rate for first trimester screenings and a 16.13% increase in effectiveness for second trimester screenings compared to built-in parameters, highlighting the importance of using localized data in prenatal screenings.
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Objective: This study aimed to re-evaluate the clinical value of a 4% cut-off threshold of sperm morphology in fertilization (IVF) in a cohort of a Northeastern Chinese population.

Methods: A total of 375 IVF cycles that met strict inclusion criteria were included. These cycles were conducted with semen analysis and oocyte fertilization.

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Bone morphogenetic protein 6 (BMP6) and transforming growth factor-β1 (TGF-β1) are key intraovarian regulators that play essential roles in regulating mammalian follicular function and promoting oocyte maturation. Furin, a member of the subtilisin-like proprotein convertase family, promotes the activation of diverse functional proteins by cleaving protein precursors in the secretory pathway. The aim of this study was to investigate the effect and underlying molecular mechanisms by which BMP6 regulates the expression of furin to increase TGF-β1 production.

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  • The study investigates cases where infertile men inherited Y chromosome microdeletions from their fertile fathers, highlighting potential genetic transmission.
  • Three patients were analyzed: two had normal karyotypes with specific Y chromosome deletions, while one and his father had a different karyotype with a duplication.
  • The findings indicate that certain Y chromosome deletions or duplications may lead to further structural instability, potentially increasing the risk of more extensive genetic issues being passed on.
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Bone morphogenetic protein (BMP) 6 is a critical regulator of follicular development that is expressed in mammalian oocytes and granulosa cells. Glial cell line‒derived neurotrophic factor (GDNF) is an intraovarian neurotrophic factor that plays an essential role in regulating mammalian oocyte maturation. The aim of this study was to investigate the effect of BMP6 on the regulation of GDNF expression and the potential underlying mechanisms.

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Background: Balanced translocations may cause the loss of genetic material at the breakpoints and may result in failure of spermatogenesis. However, carriers of reciprocal translocation may naturally conceive. Genetic counseling of male carriers of translocations remains challenging.

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  • The study aimed to explore azoospermic factor (AZF) microdeletions in infertile men from northeastern China with specific Y chromosome abnormalities.
  • Researchers conducted chromosome analysis and genetic testing, identifying AZF microdeletions in 35 out of 190 men, particularly common in patients with 46,X,Yqh- abnormalities.
  • Findings suggest that screening for AZF microdeletions is essential for men with Y chromosome abnormalities, as 38.5% of these individuals exhibited such microdeletions.
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Objective: To evaluate the frequency of azoospermia factor (AZFa) microdeletions among infertile men and establish a new high-throughput sequencing method to detect novel deletion types.

Materials And Methods: A total of 3731 infertile men were included. Karyotype analysis was performed using G-band staining of peripheral blood lymphocytes.

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Article Synopsis
  • - A male patient with a complete deletion of the azoospermia factor b (AZFb) gene experienced severe difficulty in sperm production but was able to father a child through intracytoplasmic sperm injection (ICSI).
  • - Genetic tests confirmed the patient's normal male karyotype (46,XY) and the absence of specific markers indicating the AZFb deletion, which the patient successfully passed on to his son.
  • - This case highlights that men with AZFb deletions can still produce viable sperm and father children, emphasizing the importance of genetic counseling for those with such microdeletions.
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