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SRPS associated protein WDR60 regulates the multipolar-to-bipolar transition of migrating neurons during cortical development

Cell death & disease, 2021-01, Vol.12 (1), p.75-75, Article 75

2021

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WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways

Journal of human genetics, 2020-11, Vol.65 (11), p.985-993

2020

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Molecular Species of the Alcohol Biomarker Phosphatidylethanol in Human Blood Measured by LC-MS

Clinical chemistry (Baltimore, Md.), 2009-07, Vol.55 (7), p.1395-1405

2009

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Embryonic Lethal Phenotyping to Identify Candidate Genes Related with Birth Defects

International journal of molecular sciences, 2024-08, Vol.25 (16), p.8788

2024

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Monitoring of the Alcohol Biomarkers PEth, CDT and EtG/EtS in an Outpatient Treatment Setting

Alcohol and alcoholism (Oxford), 2012-09, Vol.47 (5), p.552-557

2012

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High glucose causes developmental abnormalities in neuroepithelial cysts with actin and HK1 distribution changes

Frontiers in cell and developmental biology, 2023-01, Vol.10, p.1021284-1021284

2023

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Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

Cell research, 2021-04, Vol.31 (4), p.488-488

2021

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Deficiency of Wdr60 and Wdr34 cause distinct neural tube malformation phenotypes in early embryos

Frontiers in cell and developmental biology, 2023-05, Vol.11, p.1084245-1084245

2023

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Parental folate deficiency induces birth defects in mice accompanied with increased de novo mutations

Cell discovery, 2022-02, Vol.8 (1), p.18-18, Article 18

2022

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Diagnosis of liver cancer using HPLC-based metabonomics avoiding false-positive result from hepatitis and hepatocirrhosis diseases

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2004-12, Vol.813 (1), p.59-65

2004

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Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice

Cell death & disease, 2018-05, Vol.9 (5), p.520-12, Article 520

2018

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Genetic analysis of Wnt/PCP genes in neural tube defects

BMC medical genomics, 2018-04, Vol.11 (1), p.38-38, Article 38

2018

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Prevalence of anemia among adults with newly diagnosed HIV/AIDS in China

PloS one, 2013-09, Vol.8 (9), p.e73807-e73807

2013

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A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population

Translational psychiatry, 2019-01, Vol.9 (1), p.31-31, Article 31

2019

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Identification of functional mutations in GATA4 in patients with congenital heart disease

PloS one, 2013-04, Vol.8 (4), p.e62138

2013

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Interferon-gamma release assays for the diagnosis of active tuberculosis in HIV-infected patients: a systematic review and meta-analysis

PloS one, 2011-11, Vol.6 (11), p.e26827-e26827

2011

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Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

PloS one, 2011-01, Vol.6 (1), p.e14514-e14514

2011

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Ablation of Vacuole Protein Sorting 18 (Vps18) Gene Leads to Neurodegeneration and Impaired Neuronal Migration by Disrupting Multiple Vesicle Transport Pathways to Lysosomes

The Journal of biological chemistry, 2012-09, Vol.287 (39), p.32861-32873

2012

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Analysis and prediction of translation rate based on sequence and functional features of the mRNA

PloS one, 2011-01, Vol.6 (1), p.e16036-e16036

2011

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Combination of β-elimination and liquid chromatography/quadrupole time-of-flight mass spectrometry for the determination of O-glycosylation sites

Talanta (Oxford), 2009-04, Vol.78 (2), p.358-363

2009

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Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects

BMC medical genomics, 2021-01, Vol.14 (1), p.29-29, Article 29

2021

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Analysis of the clinical characteristics and treatment of two patients with avian influenza virus (H7N9)

BioScience Trends, 2013/04/30, Vol.7(2), pp.109-112

2013

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The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects

Molecular cytogenetics, 2019-02, Vol.12 (1), p.8-8, Article 8

2019

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Clinical findings for early human cases of influenza A(H7N9) virus infection, Shanghai, China

Emerging infectious diseases, 2013-07, Vol.19 (7), p.1142-1146

2013

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Prevalence of hyperglycemia among adults with newly diagnosed HIV/AIDS in China

BMC infectious diseases, 2013-02, Vol.13 (1), p.79-79, Article 79

2013

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SRPS associated protein WDR60 regulates the multipolar-to-bipolar transition of migrating neurons during cortical development

WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways

Molecular Species of the Alcohol Biomarker Phosphatidylethanol in Human Blood Measured by LC-MS

Embryonic Lethal Phenotyping to Identify Candidate Genes Related with Birth Defects

Monitoring of the Alcohol Biomarkers PEth, CDT and EtG/EtS in an Outpatient Treatment Setting

High glucose causes developmental abnormalities in neuroepithelial cysts with actin and HK1 distribution changes

Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants

Deficiency of Wdr60 and Wdr34 cause distinct neural tube malformation phenotypes in early embryos

Parental folate deficiency induces birth defects in mice accompanied with increased de novo mutations

Diagnosis of liver cancer using HPLC-based metabonomics avoiding false-positive result from hepatitis and hepatocirrhosis diseases

Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice

Genetic analysis of Wnt/PCP genes in neural tube defects

Prevalence of anemia among adults with newly diagnosed HIV/AIDS in China

A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population

Identification of functional mutations in GATA4 in patients with congenital heart disease

Interferon-gamma release assays for the diagnosis of active tuberculosis in HIV-infected patients: a systematic review and meta-analysis

Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

Ablation of Vacuole Protein Sorting 18 (Vps18) Gene Leads to Neurodegeneration and Impaired Neuronal Migration by Disrupting Multiple Vesicle Transport Pathways to Lysosomes

Analysis and prediction of translation rate based on sequence and functional features of the mRNA

Combination of β-elimination and liquid chromatography/quadrupole time-of-flight mass spectrometry for the determination of O-glycosylation sites

Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects

Analysis of the clinical characteristics and treatment of two patients with avian influenza virus (H7N9)

The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects

Clinical findings for early human cases of influenza A(H7N9) virus infection, Shanghai, China

Prevalence of hyperglycemia among adults with newly diagnosed HIV/AIDS in China

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