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Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517]

Stem cell research, 2022-07, Vol.62, p.102817-102817, Article 102817

2022

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SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

eLife, 2021-06, Vol.10

2021

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Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China

Frontiers in microbiology, 2018-06, Vol.9, p.1211-1211

2018

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Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

Frontiers in genetics, 2020-06, Vol.11, p.552-552

2020

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Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene

Stem cell research, 2021-10, Vol.56, p.102517-102517, Article 102517

2021

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Identification of a novel ANO5 missense mutation in a Chinese family with familial florid osseous dysplasia

Journal of human genetics, 2019-07, Vol.64 (7), p.599-607

2019

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Hemodynamic Effects of A Simplified Venturi Conduit for Fontan Circulation: A Pilot, In Silico Analysis

Scientific reports, 2020-01, Vol.10 (1), p.817-817, Article 817

2020

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Molecular Characteristic and Virulence Gene Profiles of Community-Associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China

Frontiers in microbiology, 2016-11, Vol.7, p.1818-1818

2016

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MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation

Journal of molecular medicine (Berlin, Germany), 2020-07, Vol.98 (7), p.1035-1048

2020

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The clinical application and laboratory management of molecular genetic diagnosis in children's hospital

Clinical and translational discovery, 2024-06, Vol.4 (3), p.n/a

2024

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Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

Orphanet journal of rare diseases, 2021-07, Vol.16 (1), p.334-334, Article 334

2021

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Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4

Molecular genetics and genomics : MGG, 2022-05, Vol.297 (3), p.671-687

2022

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A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

PloS one, 2016-07, Vol.11 (7), p.e0158904-e0158904

2016

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Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

BMC medical genomics, 2021-10, Vol.14 (1), p.243-243, Article 243

2021

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Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

BMC genomics, 2018-06, Vol.19 (1), p.485-485, Article 485

2018

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A Novel Nonsense GLI3 Variant Is Associated With Polydactyly and Syndactyly in a Family by Blocking the Sonic Hedgehog Signaling Pathway

Frontiers in genetics, 2020-11, Vol.11, p.542004-542004

2020

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Multifunctional superparamagnetic nanoshells: combining two-photon luminescence imaging, surface-enhanced Raman scattering and magnetic separation

Nanoscale, 2014-01, Vol.6 (23), p.14360-14370

2014

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FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically

Frontiers in cell and developmental biology, 2021-05, Vol.9, p.630634-630634

2021

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Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with 'non-syndromic' pre-axial polydactyly

Journal of human genetics, 2016-10, Vol.61 (10), p.907-910

2016

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Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

Communications biology, 2023-07, Vol.6 (1), p.735-735, Article 735

2023

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Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

Human genomics, 2018-09, Vol.12 (1), p.44-44, Article 44

2018

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Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease

Communications biology, 2023-02, Vol.6 (1), p.189-189, Article 189

2023

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Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection

Frontiers in genetics, 2018-11, Vol.9, p.559-559

2018

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The Fas/Fas ligand death receptor pathway contributes to phenylalanine-induced apoptosis in cortical neurons

PloS one, 2013-08, Vol.8 (8), p.e71553

2013

Volltextzugriff (PDF)

Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB

Frontiers in cell and developmental biology, 2021-05, Vol.9, p.660576-660576

2021

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Corrigendum to “Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene” [Stem Cell Res. 56 (2021) 102517]

SORBS2 is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

Molecular Characteristics of Community-Associated Staphylococcus aureus Isolates From Pediatric Patients With Bloodstream Infections Between 2012 and 2017 in Shanghai, China

Identification of miRNA–mRNA–TFs Regulatory Network and Crucial Pathways Involved in Tetralogy of Fallot

Generation of a homozygous CRISPR/Cas9-mediated knockout human iPSC line for PTCH1 gene

Identification of a novel ANO5 missense mutation in a Chinese family with familial florid osseous dysplasia

Hemodynamic Effects of A Simplified Venturi Conduit for Fontan Circulation: A Pilot, In Silico Analysis

Molecular Characteristic and Virulence Gene Profiles of Community-Associated Methicillin-Resistant Staphylococcus aureus Isolates from Pediatric Patients in Shanghai, China

MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation

The clinical application and laboratory management of molecular genetic diagnosis in children's hospital

Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation

Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease

Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting

A Novel Nonsense GLI3 Variant Is Associated With Polydactyly and Syndactyly in a Family by Blocking the Sonic Hedgehog Signaling Pathway

Multifunctional superparamagnetic nanoshells: combining two-photon luminescence imaging, surface-enhanced Raman scattering and magnetic separation

FGD5-AS1 Is a Hub lncRNA ceRNA in Hearts With Tetralogy of Fallot Which Regulates Congenital Heart Disease Genes Transcriptionally and Epigenetically

Exome sequencing reveals a novel nonsense mutation of GLI3 in a Chinese family with 'non-syndromic' pre-axial polydactyly

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies

Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

Copy number variation-associated lncRNAs may contribute to the etiologies of congenital heart disease

Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection

The Fas/Fas ligand death receptor pathway contributes to phenylalanine-induced apoptosis in cortical neurons

Long Noncoding RNA lnc-TSSK2-8 Activates Canonical Wnt/β-Catenin Signaling Through Small Heat Shock Proteins HSPA6 and CRYAB

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