Works matching AU Xu, Liangpu

Results: 124

Fujian Province β‐Thalassemia: A Molecular and Hematological Study in Southeastern China.

Published in:

Genetics Research, 2025, v. 2025, p. 1, doi. 10.1155/genr/8862095

By:

Zheng, Junhao;
Chen, Meihuan;
Zhang, Siwen;
Lv, Aixiang;
Zhang, Min;
Chen, Lingji;
Lin, Na;
Xu, Liangpu;
Huang, Hailong;
Ahmad, Irfan

Publication type:

Article

Upregulation of miR-17-3p is associated with HbF in patients with β-thalassemia and induces γ-globin expression by targeting BCL11A.

Published in:

Orphanet Journal of Rare Diseases, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13023-025-03806-0

By:

Zhang, Siwen;
Chen, Meihuan;
Zhao, Wantong;
Zheng, Junhao;
Zhang, Yanhong;
Lv, Aixiang;
Li, Jingmin;
Cao, Hua;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Fetal agenesis of corpus callosum: chromosomal copy number abnormalities and postnatal follow-up.

Published in:

2024

By:

Cai, Meiying;
Lin, Na;
Fu, Meimei;
Que, Yanting;
Huang, Hailong;
Xu, Liangpu

Publication type:

Case Study

Prenatal diagnosis and genetic analysis of small supernumerary marker chromosomes in the eastern chinese han population: A retrospective study of 36 cases.

Published in:

Chromosome Research, 2024, v. 32, n. 3, p. 1, doi. 10.1007/s10577-024-09754-y

By:

Jiang, Xiali;
Liang, Bin;
Chen, Bilian;
Wu, Xiaoqing;
Wang, Yan;
Lin, Na;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patients.

Published in:

European Journal of Pediatrics, 2024, v. 183, n. 3, p. 1367, doi. 10.1007/s00431-023-05398-y

By:

Chen, Meihuan;
Lv, Aixiang;
Zhang, Siwen;
Zheng, Junhao;
Lin, Na;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

The Clinical Values of Afamin, Triglyceride and PLR in Predicting Risk of Gestational Diabetes During Early Pregnancy.

Published in:

Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.723650

By:

Wang, Xuechun;
Zheng, Xiuqiong;
Yan, Jianying;
Xu, Rongli;
Xu, Mu;
Zheng, Lin;
Xu, Liangpu;
Lin, Zhi

Publication type:

Article

Copy number variations associated with fetal congenital kidney malformations.

Published in:

Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00481-7

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Chen, Xuemei;
Lin, Yuan;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0448-y

By:

Wu, Xiaoqing;
Xu, Liangpu;
Li, Ying;
Lin, Na;
Su, Linjuan;
Cai, Meiying;
Xie, Xiaorui;
Zheng, Lin;
Huang, Hailong;
Lin, Yuan

Publication type:

Article

Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0425-5

By:

Xue, Huili;
Huang, Hailong;
Wang, Yan;
An, Gang;
Zhang, Min;
Xu, Liangpu;
Lin, Yuan

Publication type:

Article

Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.

Published in:

Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0408-y

By:

Cai, Meiying;
Huang, Hailong;
Su, Linjuan;
Lin, Na;
Wu, Xiaoqing;
Xie, Xiaorui;
An, Gang;
Li, Ying;
Lin, Yuan;
Xu, Liangpu;
Cao, Hua

Publication type:

Article

Application of the BACs‐on‐Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.

Published in:

Molecular Reproduction & Development, 2018, v. 85, n. 2, p. 146, doi. 10.1002/mrd.22945

By:

Huang, Hailong;
Zhang, Min;
Wang, Yan;
Lin, Na;
He, Deqin;
Chen, Meihuan;
Chen, Lingji;
Lin, Yuan;
Xu, Liangpu

Publication type:

Article

PBX1, EMCN and ERG are associated with the sub-clusters and the prognosis of VHL mutant clear cell renal cell carcinoma.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13148-7

By:

Wang, Haiwei;
Wang, Xinrui;
Xu, Liangpu;
Zhang, Ji

Publication type:

Article

RUNX1 and REXO2 are associated with the heterogeneity and prognosis of IDH wild type lower grade glioma.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91382-1

By:

Wang, Haiwei;
Wang, Xinrui;
Xu, Liangpu;
Zhang, Ji;
Cao, Hua

Publication type:

Article

Biochemical and molecular features of tetrahydrobiopterin deficiency in Fujian Province, southeastern China.

Published in:

Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1250568

By:

Xiaolong Qiu;
Peiran Zhao;
Jinying Luo;
Guilin Li;
Lin Deng;
Yinglin Zeng;
Liangpu Xu;
Jinfu Zhou

Publication type:

Article

Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers.

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00870-w

By:

Cai, Meiying;
Lin, Na;
Chen, Xuemei;
Fu, Meimei;
Guo, Nan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele.

Published in:

Laboratory Medicine, 2023, v. 54, n. 1, p. 65, doi. 10.1093/labmed/lmac065

By:

Zhang, Min;
Lin, Zhaodong;
Chen, Meihuan;
Pan, Yali;
Zhang, Yanhong;
Chen, Lingji;
Lin, Na;
Ren, Yuanyuan;
Jia, Hongjin;
Cai, Meiying;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Activating transcription factor 4 in erythroid development and β-thalassemia: a powerful regulator with therapeutic potential.

Published in:

Annals of Hematology, 2024, v. 103, n. 8, p. 2659, doi. 10.1007/s00277-023-05508-8

By:

Li, Jingmin;
Lv, Aixiang;
Chen, Meihuan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.

Published in:

2022

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Xu, Shiyi;
Fu, Xianguo;
Xu, Liangpu;
Huang, Hailong

Publication type:

journal article

Molecular Spectrum of β-Thalassemia in Fujian Province, Southeastern China.

Published in:

Hemoglobin, 2013, v. 37, n. 4, p. 343, doi. 10.3109/03630269.2013.792274

By:

Huang, Hailong;
Xu, Liangpu;
Lin, Na;
He, Deqin;
Li, Yin;
Guo, Danhua;
Wang, Linshuo;
Wang, Yan;
Zhen, Lin;
Xu, Jinbang;
Lin, Yuan

Publication type:

Article

A New β-Thalassemia Deletion Mutation [Codon 36 (-C)] Observed in a Chinese Woman.

Published in:

Hemoglobin, 2010, v. 34, n. 6, p. 599, doi. 10.3109/03630269.2010.526841

By:

Huang, Hailong;
Xu, Liangpu;
Lin, Na;
Xu, Jinbang;
He, Deqin;
Li, Ying;
Zheng, Lin;
Liu, Hekun;
Lin, Yuan

Publication type:

Article

Molecular genetic analysis of 1,980 cases of male infertility.

Published in:

Experimental & Therapeutic Medicine, 2023, v. 26, n. 1, p. N.PAG, doi. 10.3892/etm.2023.12044

By:

Fu, Meimei;
Chen, Meihuan;
Guo, Nan;
Lin, Min;
Li, Ying;
Huang, Hailong;
Cai, Meiying;
Xu, Liangpu

Publication type:

Article

Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33668-0

By:

Cai, Meiying;
Lin, Na;
Guo, Nan;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
He, Shuqiong;
Fu, Xianguo;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Regulation of N<sup>6</sup>‐methyladenosine modification in erythropoiesis and thalassemia.

Published in:

Clinical Genetics, 2024, v. 106, n. 1, p. 3, doi. 10.1111/cge.14518

By:

Zheng, Yanping;
Lin, Siyang;
Chen, Meihuan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

A novel PLS1 c.981+1G>A variant causes autosomal‐dominant hereditary hearing loss in a family.

Published in:

Clinical Genetics, 2023, v. 103, n. 4, p. 413, doi. 10.1111/cge.14283

By:

Xu, Liangpu;
Wang, Xinrui;
Li, Jia;
Chen, Lingji;
Wang, Haiwei;
Xu, Shiyi;
Zhang, Yanhong;
Li, Wei;
Yao, Pengcheng;
Tan, Meihua;
Zhou, Si;
Chen, Meihuan;
Pan, Yali;
Chen, Xuemei;
Chen, Xiaolan;
Liu, Yunliang;
Lin, Na;
Huang, Hailong;
Cao, Hua

Publication type:

Article

Serum peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 in combination with C-reactive protein and white blood cell as novel predictors for infants with community-acquired pneumonia.

Published in:

European Journal of Inflammation, 2020, v. 18, p. 1, doi. 10.1177/2058739220942343

By:

Xue, Heng;
Liu, Hui;
Xu, Liangpu;
Liu, Qiaoling;
Zhuo, Bimin;
Dai, Meifeng;
Wu, Zhihui;
Chen, Min;
Chen, Qingquan

Publication type:

Article

Comparison and Agreement Analysis of ARCHITECT i2000SR and i-CHROMA™ Reader for Detecting Human Chorionic Gonadotropin Beta Subunit in Plasma.

Published in:

Clinical Laboratory, 2019, v. 65, n. 9, p. 1589, doi. 10.7754/Clin.Lab.2019.181237

By:

Mei Ma;
Mei Zhu;
Bimin Zhuo;
Xiuqing Wang;
Zhihui Wu;
Liangpu Xu

Publication type:

Article

Antimicrobial Resistance, Genetic Diversity and Virulence Genes of Salmonella Typhimurium Isolated in Infant with Acute Diarrhea in Fuzhou, China, 2015 - 2017.

Published in:

Clinical Laboratory, 2019, v. 65, n. 5, p. 779, doi. 10.7754/Clin.Lab.2018.181010

By:

Huiyu Chen;
Tengfei Shi;
Yanfang Lu;
Boqiu Zhang;
Hui Zhong;
Zhihui Wu;
Liangpu Xu;
Huahong Qiu

Publication type:

Article

Fetal congenital talipes equinovarus: genomic abnormalities and obstetric follow-up results.

Published in:

2024

By:

Cai, Meiying;
Lin, Jiansong;
Que, Yanting;
Xu, Liangpu;
Lin, Na;
Huang, Hailong

Publication type:

Case Study

Identification of a novel 91.5 kb-deletion (αα)<sup>FJ</sup> in the α-globin gene cluster using single-molecule real-time (SMRT) sequencing.

Published in:

Journal of Maternal-Fetal & Neonatal Medicine, 2023, v. 36, n. 2, p. 1, doi. 10.1080/14767058.2023.2254890

By:

Xu, Liangpu;
Chen, Meihuan;
Zheng, Junhao;
Zhang, Siwen;
Zhang, Min;
Chen, Lingji;
He, Qianqian;
Guo, Danhua;
Lin, Na;
Huang, Hailong

Publication type:

Article

TP53 and TP53-associated genes are correlated with the prognosis of paediatric neuroblastoma.

Published in:

BMC Genomic Data, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12863-022-01059-5

By:

Wang, Haiwei;
Wang, Xinrui;
Xu, Liangpu;
Zhang, Ji

Publication type:

Article

Retrospective analysis of the sex chromosomal copy number variations in 186 fetuses using single nucleotide polymorphism arrays.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.997757

By:

Haiwei Wang;
Bin Liang;
Yan Wang;
Hailong Huang;
Na Lin;
Liangpu Xu

Publication type:

Article

Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.941364

By:

Meihua Tan;
Xinrui Wang;
Hongjie Liu;
Xiaoyan Peng;
You Yang;
Haifei Yu;
Liangpu Xu;
Jia Li;
Hua Cao

Publication type:

Article

Global Trends on β-Thalassemia Research Over 10 Years: A Bibliometric Analysis.

Published in:

International Journal of General Medicine, 2024, v. 17, p. 3989, doi. 10.2147/IJGM.S479493

By:

Lv, Aixiang;
Li, Jingmin;
Chen, Meihuan;
Wang, Wei;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Different Cutoff Values for Increased Nuchal Translucency in First-Trimester Screening to Predict Fetal Chromosomal Abnormalities.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 8437, doi. 10.2147/IJGM.S330960

By:

Su, Linjuan;
Wu, Xiaoqing;
Lin, Na;
Xie, Xiaorui;
Cai, Meiying;
Wang, Meiying;
Zheng, Lin;
Xu, Liangpu

Publication type:

Article

Comprehensive Assessment of Fetal Bilateral Ventriculomegaly Based on Genetic Disorders, Cytomegalovirus Infection, Extra Prenatal Imaging and Pregnancy Outcomes in a Tertiary Referral Center.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 7719, doi. 10.2147/IJGM.S335011

By:

Guo, Danhua;
He, Deqin;
Shen, Qingmei;
Lin, Na;
He, Shuqiong;
Dai, Yifang;
Li, Ying;
Xu, Liangpu;
Wu, Xiaoqing

Publication type:

Article

Screening of Some Indicators for Alpha-Thalassemia in Fujian Province of Southern China.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 7329, doi. 10.2147/IJGM.S338419

By:

Zheng, Lin;
Huang, Hailong;
Wu, Xiaoqing;
Su, Linjuan;
Shen, Qingmei;
Wang, Meiying;
Lin, Na;
Xu, Liangpu

Publication type:

Article

Application of Single Nucleotide Polymorphism Microarray in Prenatal Diagnosis of Fetuses with Central Nervous System Abnormalities.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 4239, doi. 10.2147/IJGM.S323899

By:

Xie, Xiaorui;
Wu, Xiaoqing;
Su, Linjuan;
Cai, Meiying;
Li, Ying;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience.

Published in:

International Journal of General Medicine, 2021, v. 14, p. 1991, doi. 10.2147/IJGM.S311800

By:

Huang, Hailong;
Cai, Meiying;
Liu, Linyu;
Xu, Liangpu;
Lin, Na

Publication type:

Article

Molecular Epidemiology of Group B Streptococcus Isolates from Pregnant Women with Premature Rupture of Membranes in Fuzhou, China.

Published in:

Infection & Drug Resistance, 2023, v. 16, p. 269, doi. 10.2147/IDR.S393935

By:

Liang, Bin;
Chen, Huiyu;
Yu, Donghong;
Zhao, Wantong;
Cai, Xiaoling;
Qiu, Huahong;
Xu, Liangpu

Publication type:

Article

Molecular analysis and prenatal diagnosis of seven Chinese families with genetic epilepsy.

Published in:

Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1165601

By:

Bin Mao;
Na Lin;
Danhua Guo;
Deqin He;
Huili Xue;
Lingji Chen;
Qianqian He;
Min Zhang;
Meihuan Chen;
Hailong Huang;
Liangpu Xu

Publication type:

Article

Molecular Genetic and Clinical Characteristics of Fetuses With Chromosome 16 Short‐Arm Microdeletions/Microduplications.

Published in:

Journal of Clinical Laboratory Analysis, 2024, v. 38, n. 24, p. 1, doi. 10.1002/jcla.25132

By:

Cai, Meiying;
Lin, Na;
Guo, Nan;
Huang, Hailong;
Fan, Xiangqun;
Fu, Meimei;
Zhang, Min;
Xu, Liangpu

Publication type:

Article

Analysis of genotype-phenotype correlation in patients with α-thalassemia from Fujian province, Southeastern China.

Published in:

2022

By:

Pan, Yali;
Chen, Meihuan;
Zhang, YanHong;
Zhang, Min;
Chen, Lingji;
Lin, Na;
Xu, Liangpu;
Huang, Hailong

Publication type:

journal article

Genetic research and clinical analysis of β‐globin gene cluster deletions in the Chinese population of Fujian province: A 14‐year single‐center experience.

Published in:

Journal of Clinical Laboratory Analysis, 2022, v. 36, n. 2, p. 1, doi. 10.1002/jcla.24181

By:

Chen, Meihuan;
Zhang, Min;
Chen, Lingji;
Lin, Na;
Wang, Yan;
Xu, Liangpu;
Huang, Hailong

Publication type:

Article

Prenatal diagnosis of thalassemia in 695 pedigrees from southeastern China: a 10-year follow-up study.

Published in:

2021

By:

Huang, Hailong;
Chen, Meihuan;
Chen, Lingji;
Zhang, Min;
Wang, Yan;
Lin, Na;
Xu, Liangpu

Publication type:

journal article

Abnormal regulation of microRNAs and related genes in pediatric β‐thalassemia.

Published in:

Journal of Clinical Laboratory Analysis, 2021, v. 35, n. 9, p. 1, doi. 10.1002/jcla.23945

By:

Wang, Haiwei;
Chen, Meihuan;
Xu, Shiyi;
Pan, Yali;
Zhang, Yanhong;
Huang, Hailong;
Xu, Liangpu

Publication type:

Article

First report of the spectrum of δ‐globin gene mutations among women of reproductive age in Fujian area—Discrimination of δ‐thalassemia, α‐thalassemia, and Iron Deficiency Anemia.

Published in:

Journal of Clinical Laboratory Analysis, 2020, v. 34, n. 11, p. 1, doi. 10.1002/jcla.23479

By:

Chen, Meihuan;
Huang, Hailong;
Chen, Lingji;
Lin, Na;
Zhang, Min;
Lin, Yuan;
Xu, Liangpu

Publication type:

Article

Use of complete blood count for predicting preterm birth in asymptomatic pregnant women: A propensity score-matched analysis.

Published in:

2020

By:

Ma, Mei;
Zhu, Mei;
Zhuo, Bimin;
Li, Li;
Chen, Honglei;
Xu, Libo;
Wu, Zhihui;
Cheng, Feng;
Xu, Liangpu;
Yan, Jianying

Publication type:

journal article

X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations.

Published in:

2020

By:

Zhang, Min;
Huang, Hailong;
Lin, Na;
He, Shuqiong;
An, Gang;
Wang, Yan;
Chen, Meihuan;
Chen, Lingji;
Lin, Yuan;
Xu, Liangpu

Publication type:

journal article

Chromosomal microarray analysis for pregnancies with or without ultrasound abnormalities in women of advanced maternal age.

Published in:

2020

By:

Wu, Xiaoqing;
An, Gang;
Xie, Xiaorui;
Su, Linjuan;
Cai, Meiying;
Chen, Xuemei;
Li, Ying;
Lin, Na;
He, Deqin;
Wang, Meiying;
Huang, Hailong;
Xu, Liangpu

Publication type:

journal article

Detection of copy number disorders associated with congenital anomalies of the kidney and urinary tract in fetuses via single nucleotide polymorphism arrays.

Published in:

2020

By:

Cai, Meiying;
Lin, Na;
Su, Linjuan;
Wu, Xiaoqing;
Xie, Xiaorui;
Li, Ying;
Chen, Xuemei;
Dai, Yifang;
Lin, Yuan;
Huang, Hailong;
Xu, Liangpu

Publication type:

journal article