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Pathological characteristics analysis of children with intermittent and persistent hydronephrosis due to uretero-pelvic junction obstruction

Frontiers in pediatrics, 2024-07, Vol.12, p.1416789

2024

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Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes

Neural development, 2020-07, Vol.15 (1), p.1-8, Article 8

2020

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Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

The American journal of clinical nutrition, 2010-05, Vol.91 (5), p.1359-1367

2010

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Establishment and validation of a predictive nomogram for the risk of premalignant lesions in children with choledochal cyst

Frontiers in pediatrics, 2023-02, Vol.11, p.1108788-1108788

2023

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A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling

BMC pediatrics, 2023-03, Vol.23 (1), p.104-104, Article 104

2023

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Loss‐of‐Function of p21‐Activated Kinase 2 Links BMP Signaling to Neural Tube Patterning Defects

Advanced science, 2023-02, Vol.10 (4), p.e2204018-n/a

2023

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Detection of copy number variants reveals association of cilia genes with neural tube defects

PloS one, 2013-01, Vol.8 (1), p.e54492-e54492

2013

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Application of clinico-radiologic-pathologic diagnosis of diffuse parenchymal lung diseases in children in China

PloS one, 2015-01, Vol.10 (1), p.e0116930-e0116930

2015

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Association between PTCH1 polymorphisms and risk of neural tube defects in a Chinese population

Birth defects research. A Clinical and molecular teratology, 2013-06, Vol.97 (6), p.409-415

2013

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Short hairpin RNA targeting 2B gene of coxsackievirus B3 exhibits potential antiviral effects both in vitro and in vivo

BMC infectious diseases, 2012-08, Vol.12 (1), p.177-177, Article 177

2012

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Association Study of PARD3 Gene Polymorphisms With Neural Tube Defects in a Chinese Han Population

Reproductive sciences (Thousand Oaks, Calif.), 2012-07, Vol.19 (7), p.764-771

2012

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Wilms' tumor 1 and signal transducers and activators of transcription 3 synergistically promote cell proliferation : A possible mechanism in sporadic wilms' tumor

Cancer research (Chicago, Ill.), 2006-08, Vol.66 (16), p.8049-8057

2006

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Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model

Human molecular genetics, 2022-05, Vol.31 (10), p.1635-1650

2022

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The effect of folic acid deficiency on FGF pathway via Brachyury regulation in neural tube defects

The FASEB journal, 2019-04, Vol.33 (4), p.4688-4702

2019

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Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing

Scientific reports, 2017-11, Vol.7 (1), p.14796-11, Article 14796

2017

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Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects

Cellular and molecular neurobiology, 2018-04, Vol.38 (3), p.605-614

2018

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Rare Deleterious PARD3 Variants in the aPKC‐Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation

Human mutation, 2017-04, Vol.38 (4), p.378-389

2017

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MicroRNAs: Potential regulators involved in human anencephaly

The international journal of biochemistry & cell biology, 2010-02, Vol.42 (2), p.367-374

2010

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Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease

Experimental and molecular pathology, 2016-10, Vol.101 (2), p.241-248

2016

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Low folate concentration impacts mismatch repair deficiency in neural tube defects

Epigenomics, 2020-01, Vol.12 (1), p.5-18

2020

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Inhibition of IL-2 inducible T-cell kinase alleviates T-cell activation and murine myocardial inflammation associated with CVB3 infection

Molecular immunology, 2014-05, Vol.59 (1), p.30-38

2014

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MicroRNAs Regulate the Pathogenesis of CVB3-Induced Viral Myocarditis

Intervirology, 2013-01, Vol.56 (2), p.104-113

2013

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Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation: HUMAN MUTATION

Human mutation, 2017-04, Vol.38 (4), p.378-389

2017

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DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects

Birth defects research. A Clinical and molecular teratology, 2015-01, Vol.103 (1), p.37-44

2015

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Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study

Birth defects research. A Clinical and molecular teratology, 2010-07, Vol.88 (7), p.575-581

2010

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Pathological characteristics analysis of children with intermittent and persistent hydronephrosis due to uretero-pelvic junction obstruction

Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes

Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects

Establishment and validation of a predictive nomogram for the risk of premalignant lesions in children with choledochal cyst

A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling

Loss‐of‐Function of p21‐Activated Kinase 2 Links BMP Signaling to Neural Tube Patterning Defects

Detection of copy number variants reveals association of cilia genes with neural tube defects

Application of clinico-radiologic-pathologic diagnosis of diffuse parenchymal lung diseases in children in China

Association between PTCH1 polymorphisms and risk of neural tube defects in a Chinese population

Short hairpin RNA targeting 2B gene of coxsackievirus B3 exhibits potential antiviral effects both in vitro and in vivo

Association Study of PARD3 Gene Polymorphisms With Neural Tube Defects in a Chinese Han Population

Wilms' tumor 1 and signal transducers and activators of transcription 3 synergistically promote cell proliferation : A possible mechanism in sporadic wilms' tumor

Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model

The effect of folic acid deficiency on FGF pathway via Brachyury regulation in neural tube defects

Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing

Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects

Rare Deleterious PARD3 Variants in the aPKC‐Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation

MicroRNAs: Potential regulators involved in human anencephaly

Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease

Low folate concentration impacts mismatch repair deficiency in neural tube defects

Inhibition of IL-2 inducible T-cell kinase alleviates T-cell activation and murine myocardial inflammation associated with CVB3 infection

MicroRNAs Regulate the Pathogenesis of CVB3-Induced Viral Myocarditis

Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation: HUMAN MUTATION

DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects

Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study

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