Publications by authors named "Hong-guo Zhang"

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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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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Article Synopsis
  • 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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Article Synopsis
  • The text analyzes a model that describes how wild and sterile mosquitoes interact, focusing on different types of bifurcations that the model experiences.
  • It identifies various bifurcation types, such as saddle-node and Hopf bifurcations, revealing complex dynamics like monostability, bistability, or tristability in the populations.
  • The findings suggest that the initial numbers of wild and sterile mosquitoes significantly impact their future population states, providing insights for estimating how many sterile mosquitoes should be released.
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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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  • 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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  • MnFe(P,Ge) is a potential magnetocaloric material for refrigeration but suffers from large hysteresis and significant temperature/field range of paramagnetic and ferromagnetic coexistence, which lowers energy efficiency.
  • The research investigates the effects of Ge distribution on phase coexistence and hysteresis in MnFeP1-xGex compounds, finding that Ge shows a strong preference for the 2c crystallographic site and influences the temperature transition.
  • The study suggests that improving covalent bonding strengths may reduce heat hysteresis during phase transitions, enhancing the material's magnetic behavior and energy conversion efficiency.
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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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Objectives To investigate azoospermic factor (AZF) microdeletions in infertile men from northeastern China with karyotypic Y chromosome abnormalities. Methods G-banding of metaphase chromosomes and karyotype analysis were performed in all infertile male patients. Genomic DNA was isolated and used to analyze classical AZF microdeletions by PCR.

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Background: Previous researches about the effect of smoking on semen quality are contradictory, and the mechanism behind the harmful effect of smoking on semen quality still remains unclear until today.

Objective: The objectives of this study are evaluation of the relationship between smoking and fertility, investigation of the effects of cigarette smoking on sperm parameters and detection of presence of leukocytes within the semen of idiopathic infertile men from Northeastern China.

Materials And Methods: A retrospective study of 1512 infertile patients who visited affiliated hospitals of Jilin University from 2007-2010 were enrolled in this study.

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  • The study investigated a disagreement between a positive cell-free fetal DNA test for trisomy 13 and a standard cytogenetic diagnosis.
  • Cell-free fetal DNA testing was done using advanced sequencing, and conventional cytogenetic analysis confirmed the results with additional FISH testing on placental tissues.
  • Results indicated a positive DNA test for trisomy 13, but normal amniotic fluid and placental mosaicism suggest that DNA test results may not accurately represent the fetal genetic status, highlighting the need for further cytogenetic analysis in such cases.
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Objective: To determine the frequencies and the characteristics of Y chromosome microdeletion in infertile men from northeastern China to perform appropriate therapeutic choices.

Materials And Methods: The study included 1738 infertile men. Sperm concentration was measured according to standard methods and karyotype analysis was performed on peripheral blood lymphocytes with standard G-banding.

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Purpose: To explore the prevalence and clinical features, especially the reproductive function, of 45,X mosaicism patients in northeast China.

Methods: GTG-banding was performed on a series of 2,250 patients from our genetic counseling clinic. Each of these patients underwent a physical examination and was interviewed about their medical history and reproductive problems.

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Purpose: To compare the frequency of chromosomal heteromorphisms in reproductive failure and fertile control individuals in Northeast China, and investigate the impact on reproductive failure

Methods: 1751 males and 1424 couples with reproductive failure (n = 4599) and 777 fertile control individuals in Northeast China were enrolled. Chromosome karyotype analysis was performed on peripheral blood lymphocytes with standard G-banding. Additionally, C-banding was performed with heterochromatin heteromorphisms, and NORs-banding with satellites/stalks variations.

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Objective: To explore the mechanism of reinforcing function of moxibustion to spleen-stomach.

Methods: Forty healthy Sprague Dawley rats were randomly divided into 4 groups: group A (blank group), group B (model group), group C (moxibustion group) and group D (herbs group). The rat model of spleen-deficiency was established by intragastric administration with 200% Dahuang (Rhubarb) infusion.

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The two highly conserved NPA motifs (asparagine-proline-alanine, NPA) are the most important structural domains that play a crucial role in water-selective permeation in aquaporin water channels. However, the functions of NPA motifs in aquaporin (AQP) biogenesis remain largely unknown. Few AQP members with variations in NPA motifs such as AQP11 and AQP12 do not express in the plasma membrane, suggesting an important role of NPA motifs in AQP plasma membrane targeting.

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Aim: To develop a method for assessing sperm function by measuring released acrosin activity during the acrosome reaction (AR).

Methods: Human semen samples were obtained from 24 healthy donors with proven fertility after 3-7 days of sexual abstinence. After collection, samples were liquefied for 30 min at room temperature.

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Ca2+ is an important positive ion in the living body. Recently, there have been quite a few reports about the function of Ca2+ in sperm. Calcium is considered as a regulator of sperm motility, a participant in sperm capacitation, and an essential second messenger for acrosome reaction.

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Objective: To evaluate the relationship between sperm motility parameters and sperm morphology.

Methods: Seven hundred and eighty-three semen samples were tested. Sperm motility parameters were analyzed by computer-aided sperm analysis (CASA) , and sperm morphology assessed by automated sperm morphology analyzer (ASMA).

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