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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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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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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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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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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 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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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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Validation of an LC-MS/MS Method for Analysis of 58 Drugs of Abuse in Oral Fluid and Method Comparison with an Established LC-HRMS Method

Journal of analytical toxicology, 2024-11

2024

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Investigation of the metabolism and reductive activation of carcinogenic aristolochic acids in rats

Drug metabolism and disposition, 2007-06, Vol.35 (6), p.866-874

2007

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Catalytic Properties of ADAM19

The Journal of biological chemistry, 2003-06, Vol.278 (25), p.22331-22340

2003

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High prevalence of HIV-associated neurocognitive disorder in HIV-infected patients with a baseline CD4 count ≤ 350 cells/μL in Shanghai, China

BioScience Trends, 2013/12/31, Vol.7(6), pp.284-289

2013

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Validation of an automated UPLC-MS/MS method for methylmalonic acid in serum/plasma and its application on clinical samples

Scandinavian journal of clinical and laboratory investigation, 2022-07, Vol.82 (4), p.342-347

2022

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Organoids as a new model system to study neural tube defects

The FASEB journal, 2021-04, Vol.35 (4), p.e21545-n/a

2021

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Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli

The journal of obstetrics and gynaecology research, 2014-02, Vol.40 (2), p.501-508

2014

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Solid-Phase Extraction Procedure for Ethyl Glucuronide in Urine

Journal of analytical toxicology, 2008-11, Vol.32 (9), p.778-781

2008

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Chip-based CE coupled to a quadrupole TOF mass spectrometer for the analysis of a glycopeptide

Electrophoresis, 2007-05, Vol.28 (9), p.1305-1311

2007

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Detection of Drugs in Oral Fluid Samples Using a Commercially Available Collection Device: Agreement with Urine Testing and Evaluation of A and B Samples Obtained from Employees at Different Workplace Settings with Uncontrolled Sampling Procedures

Journal of analytical toxicology, 2021-01, Vol.44 (9), p.1004-1011

2021

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MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease

Clinical science (1979), 2018-12, Vol.132 (23), p.2483-2491

2018

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miR-377-3p Regulates Hippocampal Neurogenesis via the Zfp462-Pbx1 Pathway and Mediates Anxiety-Like Behaviors in Prenatal Hypoxic Offspring

Molecular neurobiology, 2024-04, Vol.61 (4), p.1920-1935

2024

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3' UTR lengthening as a novel mechanism in regulating cellular senescence

Genome research, 2018-03, Vol.28 (3), p.285-294

2018

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Robust H-infinity control for discrete-time T-S fuzzy systems with input delay

Journal of control theory and applications, 2011-05, Vol.9 (2), p.189-194

2011

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

Cell research, 2018-10, Vol.28 (10), p.1039-1041

2018

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Substrate‐selective protein ectodomain shedding by ADAM17 and iRhom2 depends on their juxtamembrane and transmembrane domains

The FASEB journal, 2020-04, Vol.34 (4), p.4956-4969

2020

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Metabolite Profiling of a NIST Standard Reference Material for Human Plasma (SRM 1950): GC-MS, LC-MS, NMR, and Clinical Laboratory Analyses, Libraries, and Web-Based Resources

Analytical chemistry (Washington), 2013-12, Vol.85 (24), p.11725-11731

2013

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Rare mutations in the autophagy‐regulating gene AMBRA1 contribute to human neural tube defects

Human mutation, 2020-08, Vol.41 (8), p.1383-1393

2020

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

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

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

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

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

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

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

Validation of an LC-MS/MS Method for Analysis of 58 Drugs of Abuse in Oral Fluid and Method Comparison with an Established LC-HRMS Method

Investigation of the metabolism and reductive activation of carcinogenic aristolochic acids in rats

Catalytic Properties of ADAM19

High prevalence of HIV-associated neurocognitive disorder in HIV-infected patients with a baseline CD4 count ≤ 350 cells/μL in Shanghai, China

Validation of an automated UPLC-MS/MS method for methylmalonic acid in serum/plasma and its application on clinical samples

Organoids as a new model system to study neural tube defects

Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli

Solid-Phase Extraction Procedure for Ethyl Glucuronide in Urine

Chip-based CE coupled to a quadrupole TOF mass spectrometer for the analysis of a glycopeptide

Detection of Drugs in Oral Fluid Samples Using a Commercially Available Collection Device: Agreement with Urine Testing and Evaluation of A and B Samples Obtained from Employees at Different Workplace Settings with Uncontrolled Sampling Procedures

MIB1 mutations reduce Notch signaling activation and contribute to congenital heart disease

miR-377-3p Regulates Hippocampal Neurogenesis via the Zfp462-Pbx1 Pathway and Mediates Anxiety-Like Behaviors in Prenatal Hypoxic Offspring

3' UTR lengthening as a novel mechanism in regulating cellular senescence

Robust H-infinity control for discrete-time T-S fuzzy systems with input delay

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

Substrate‐selective protein ectodomain shedding by ADAM17 and iRhom2 depends on their juxtamembrane and transmembrane domains

Metabolite Profiling of a NIST Standard Reference Material for Human Plasma (SRM 1950): GC-MS, LC-MS, NMR, and Clinical Laboratory Analyses, Libraries, and Web-Based Resources

Rare mutations in the autophagy‐regulating gene AMBRA1 contribute to human neural tube defects

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