Publications by authors named "YeJuan Li"

Article Synopsis
  • Asthenozoospermia is a type of male infertility caused by problems with sperm mitochondria, and scientists want to find more markers and understand its causes better.
  • Researchers looked at several gene data sets to find differences in gene expression between normal sperm and sperm from men with asthenozoospermia, identifying important genes and pathways.
  • They discovered a specific gene network that may be important for understanding asthenozoospermia, but more experiments are needed to figure out exactly how it works.
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  • Researchers found that a molecule called miR-19b is lower in women with polycystic ovary syndrome (PCOS).
  • They studied how miR-19b interacts with another molecule called BBOX1-AS1, which is higher in PCOS and is important in ovarian cancer.
  • The study suggests that BBOX1-AS1 may stop miR-19b from doing its job in stopping cell growth, which could help in treating PCOS.
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Introduction: To investigate the expression and treatment of chemokine CXCL12 and its receptor CXCR4/CXCR7.

Methods: The liver cirrhosis hypersplenism model of rats was made with CCL4, and then was detected by immunohistochemistry, Western blot and qRT-PCR.

Results: The area of spleen fibrosis in the model group was significantly larger than that in the control group ( < 0.

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Objective: Patients with cirrhosis and splenomegaly often have coagulation dysfunction which affects treatment and prognosis. This study explores the status, grading, and treatment strategies of coagulation dysfunction in patients with liver cirrhosis and splenomegaly.

Methods: A retrospective cohort study was conducted on the clinical data on consecutive patients with cirrhosis and splenomegaly treated at Hainan General Hospital, China, from January 2000 to December 2020.

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Polycystic ovary syndrome (PCOS) is a perplexing condition in females of reproductive age. Dysplasia of ovarian granulosa cell (GC) is implicated in PCOS. Follicular fluid (FF)-extracellular vesicles (Evs) are important in cell-cell communication during follicular development.

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Article Synopsis
  • Follicular fluid-derived exosomes (FF-Evs) can affect a condition called polycystic ovary syndrome (PCOS) in rats.
  • Researchers treated PCOS rats with FF-Evs and looked for changes in hormones, blood sugar, and other health markers.
  • The study found that FF-Evs helped improve the symptoms of PCOS by affecting a specific RNA (LINC00092) that regulates another gene (PTEN), helping to keep more healthy cells in the ovaries.
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Background: Hypersplenism associated with cirrhotic portal hypertension is a common condition often resulting from hepatitis B-related cirrhosis. However, the levels of immunoglobulin (Ig) and complement in patients with hypersplenism associated with cirrhotic portal hypertension remain unclear. This study was undertaken to determine the levels of Ig and complement in these patients, the relationship between these levels and Child-Pugh class and their clinical significance.

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Small RNA sequences in follicular fluid (FF)-derived exosomes (extracellular vesicles contain proteins, DNA, and RNA) vitally function in the development of polycystic ovary syndrome (PCOS). It has been identified that microRNA (miR)-18b-5p is one of miRs that differ between control and PCOS women that passed the false discovery rate, and phosphatase and tensin homolog deleted on chromosome 10 (PTEN) is an important modifier of biological functions of ovarian granulosa cells (GCs) in PCOS. However, whether miR-18b-5p could functionally mediate the progression of PCOS via PTEN was not clarified completely, which was the issue we wanted to solve in our research.

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Objectives: To evaluate the Th1/Th2 cell profile in spleens of cirrhotic and hypersplenic rats by investigating the expression of Th1-associated chemokine receptors CXCR3, CCR5 and Th2-associated chemokine receptor CCR3.

Methods: Experimental liver cirrhosis and hypersplenism were induced in rats by the intragastric administration of carbon tetrachloride (CCl; 40% solution [0.3 ml/100g, twice/week for 8 weeks]) and confirmed by pathology and hemogram.

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Article Synopsis
  • * 478 individuals were found to carry thalassemia gene mutations, leading to a gene-carrying rate of 13.72%, with α-thalassemia being the most common type at 9.56%.
  • * The findings suggest a high incidence of thalassemia in Ding'an, highlighting the need for government action to enhance screening efforts to prevent congenital thalassemia.
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The aim of the present study was to evaluate the prevalence and causes of spontaneous remission of obstructive jaundice in rats. Healthy male and female Wistar rats (180-220 g) were randomly assigned to receive common bile duct ligation (CBDL) and transection (group A), CBDL only (group B), or CBD dissection without ligation or transection (control group C; n=36 in each group). There was a difference in eye and skin jaundice prevalence between groups A and B from 14 days after surgery.

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Objectives To investigate peripheral cytopenia in patients with splenomegaly due to hepatitis B-related cirrhotic portal hypertension (HBRCPH) by comparing blood cell counts from enlarged spleens with peripheral blood. Methods This prospective study involved patients undergoing splenectomy at the Nangfang Hospital from June 2013 to December 2015. Blood cell counts from peripheral blood were compared with those from splenic blood taken during splenectomies.

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The clinical data of 183 patients with hepatitic cirrhosis and portal hypertensive splenomegaly complicated by peripheral cytopenia were retrospectively analyzed to investigate the causes of peripheral cytopenia, as well as the proportion of the causes in these patients. All patients underwent splenectomy. Before operation, these patients had one or more types of peripheral cytopenia (cumulative cytopenia: 390 patient-times).

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Hypersplenism is a common disorder characterized by an enlarged spleen which causes rapid and premature destruction of blood cells. This review summarizes the history of hypersplenism, discuss its classification and pathogenesis, and examines its diagnosis and treatment options. We performed a comprehensive literature search using PubMed, Web of Knowledge and the China National Knowledge Infrastructure (CNKI) database, reviewed hypersplenism-related articles and summarized the major findings.

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This study investigates peripheral cytopenias in patients with splenomegaly caused by nonalcoholic cirrhotic portal hypertension. Data from 330 splenomegaly cases caused by nonalcoholic cirrhotic portal hypertension were collected and analyzed using univariate and multivariate analysis. The cytopenias were scored and graded according to the F value of the multiple linear regression equation.

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Article Synopsis
  • The study looked at 358 patients with a condition that caused their spleens to be enlarged (called splenomegaly) due to liver problems.
  • Out of these patients, a large part (90%) had low blood cell counts, which can lead to health issues.
  • After surgery to remove the spleen (splenectomy), some patients showed improvement in their blood cell counts, but not everyone, suggesting that this surgery can help those with low blood cells caused by spleen issues.
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