Search Results - "Huang, Guoying"
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The reference curves of percentile for the length and head circumference of infants aged 0–1 year in Hainan Province, China
Published in Scientific reports (12-08-2024)“…We first established percentile reference curves for infant length and head circumference in Hainan Province based on gender and age in months and compared…”
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Identifying threshold sizes for enlarged abdominal lymph nodes in different age ranges from about 200,000 individual’s data
Published in Scientific reports (19-01-2021)“…The threshold size for enlarged abdominal lymph nodes (E-ALNs), a common pediatric disorder, has yet to be standardized. According to the maximum short-axis…”
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Author Correction: Identifying threshold sizes for enlarged abdominal lymph nodes in different age ranges from about 200,000 individual’s data
Published in Scientific reports (21-04-2021)“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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4
Characteristics and Workload of Pediatricians in China
Published in Pediatrics (Evanston) (01-07-2019)“…Although it is widely believed that China is facing a major shortage of pediatricians, the real situation of the current national status of pediatric human…”
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Paternal ethanol exposure and behavioral abnormities in offspring: Associated alterations in imprinted gene methylation
Published in Neuropharmacology (01-06-2014)“…Research confirms that maternal ethanol (EtOH) exposure can induce physical and mental disorders in offspring, yet the effect of paternal ethanol exposure on…”
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QKI is a critical pre-mRNA alternative splicing regulator of cardiac myofibrillogenesis and contractile function
Published in Nature communications (04-01-2021)“…The RNA-binding protein QKI belongs to the hnRNP K-homology domain protein family, a well-known regulator of pre-mRNA alternative splicing and is associated…”
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SMC3 contributes to heart development by regulating super-enhancer associated genes
Published in Experimental & molecular medicine (01-08-2024)“…Abnormal cardiac development has been observed in individuals with Cornelia de Lange syndrome (CdLS) due to mutations in genes encoding members of the cohesin…”
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Development and validation of a nomogram for predicting cardiovascular mortality risk for diffuse large B-cell lymphoma in children, adolescents, and adults
Published in Frontiers in pediatrics (07-02-2024)“…This study aimed to construct and validate a nomogram for predicting cardiovascular mortality (CVM) for child, adolescent, and adult patients with diffuse…”
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DNA methylation at CpG island shore and RXRα regulate NR2F2 in heart tissues of tetralogy of Fallot patients
Published in Biochemical and biophysical research communications (03-09-2020)“…The nuclear receptor subfamily 2 group F member 2 (NR2F2) gene encodes a ligand-inducible transcription factor involved in angiogenesis and heart development…”
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10
Current practice and awareness of pediatric off-label drug use in Shanghai, China -a questionnaire-based study
Published in BMC pediatrics (13-08-2019)“…Off-label drug use is widespread in pediatric drug treatment, and the implementation of guidelines on this topic remains challenging. The objective of this…”
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11
Randomized trial of different initial intravenous immunoglobulin regimens in Kawasaki disease
Published in Pediatrics international (01-07-2021)“…Background We aimed to assess the efficacy of different initial intravenous immunoglobulin (IVIG) regimens in Kawasaki disease (KD) patients to find more…”
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Noncardiac anomalies in children with congenital heart disease
Published in Frontiers in cardiovascular medicine (20-11-2023)“…Introduction Noncardiac anomalies (NCAs) in patients with congenital heart defects (CHDs) are crucial for perioperative management and etiology studies. This…”
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13
DNA methylation status of TBX20 in patients with tetralogy of Fallot
Published in BMC medical genomics (28-05-2019)“…TBX20 plays an important role in heart development; however, its epigenetic regulation in the pathogenesis of tetralogy of Fallot (TOF) remains unclear. The…”
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14
Loss of phosphatase CTDNEP1 potentiates aggressive medulloblastoma by triggering MYC amplification and genomic instability
Published in Nature communications (10-02-2023)“…MYC-driven medulloblastomas are highly aggressive childhood brain tumors, however, the molecular and genetic events triggering MYC amplification and malignant…”
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15
The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish
Published in PLoS genetics (15-08-2018)“…SMYD4 belongs to a family of lysine methyltransferases. We analyzed the role of smyd4 in zebrafish development by generating a smyd4 mutant zebrafish line…”
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16
Changes in peripheral perfusion index within 72 h of life in a cohort of very low birth weight infants
Published in Chinese medical journal (20-05-2022)“…Multiple linear regression with robust standard error was used to evaluate associations between baseline and measurement factors and the (log-transformed) pre-…”
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Identifying critical windows of air pollution exposure during preconception and gestational period on birthweight: a prospective cohort study
Published in Environmental health (19-10-2023)“…Few studies have assessed air pollution exposure association with birthweight during both preconception and gestational periods. Leveraging a preconception…”
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18
Single-Cell Lineage Tracing Reveals that Oriented Cell Division Contributes to Trabecular Morphogenesis and Regional Specification
Published in Cell reports (Cambridge) (05-04-2016)“…The cardiac trabeculae are sheet-like structures extending from the myocardium that function to increase surface area. A lack of trabeculation causes embryonic…”
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Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease
Published in Chinese medical journal (05-08-2024)“…Heterotaxy (HTX) is a thoracoabdominal organ anomaly syndrome and commonly accompanied by congenital heart disease (CHD). The aim of this study was to analyze…”
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Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation
Published in Journal of translational medicine (03-04-2017)“…Congenital heart disease (CHD) is a common birth defect, and most cases occur sporadically. Mutations in key genes that are responsible for cardiac development…”
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