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Genetic background of idiopathic neurodevelopmental delay patients with significant brain deviation volume

Chinese medical journal, 2023-04, Vol.136 (7), p.807-814

2023

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PRMT3 drives glioblastoma progression by enhancing HIF1A and glycolytic metabolism

Cell death & disease, 2022-11, Vol.13 (11), p.943-943, Article 943

2022

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High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population

Chinese medical journal, 2022-03, Vol.135 (5), p.625-627

2022

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Modeling photocatalytic conversion of carbon dioxide in bubbling twin reactor

Energy conversion and management, 2017-10, Vol.149, p.514-525

2017

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IL‐18‐dependent NKG2D ligand upregulation on accessory cells is mediated by the PI3K/GSK‐3 pathway

Journal of leukocyte biology, 2017-06, Vol.101 (6), p.1317-1323

2017

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A multi-omic approach reveals utility of CD45 expression in prognosis and novel target discovery

Frontiers in genetics, 2022-08, Vol.13, p.928328-928328

2022

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Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information

Frontiers in genetics, 2021-07, Vol.12, p.689071-689071

2021

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Transcriptional Networks Identify BRPF1 as a Potential Drug Target Based on Inflammatory Signature in Primary Lower-Grade Gliomas

Frontiers in oncology, 2021-12, Vol.11, p.766656-766656

2021

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Comprehensive assessment of the genetic characteristics of small for gestational age newborns in NICU: from diagnosis of genetic disorders to prediction of prognosis

Genome medicine, 2023-12, Vol.15 (1), p.112-15, Article 112

2023

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Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2 -Related Disorders

Frontiers in molecular neuroscience, 2022-04, Vol.15, p.809810-809810

2022

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The performance of the practices associated with the occurrence of severe intraventricular hemorrhage in the very premature infants: data analysis from the Chinese neonatal network

BMC pediatrics, 2024-06, Vol.24 (1), p.394-10

2024

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Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome

Computational and structural biotechnology journal, 2022, Vol.20, p.5047-5053

2022

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Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication

Frontiers in genetics, 2021-05, Vol.12, p.615072-615072

2021

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Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay

Frontiers in pediatrics, 2022-10, Vol.10

2022

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“Going global” and FDI inflows in China: “One Belt & One Road” initiative as a quasi‐natural experiment

World economy, 2019-06, Vol.42 (6), p.1654-1672

2019

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Data-driven financial transmission right scenario generation and speculation

Energy (Oxford), 2022-01, Vol.238, p.122056, Article 122056

2022

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Zinc-Finger Protein ZFP488 Regulates the Timing of Oligodendrocyte Myelination and Remyelination

The Journal of neuroscience, 2024-09, Vol.44 (39), p.e0141242024

2024

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KIF5C deficiency causes abnormal cortical neuronal migration, dendritic branching, and spine morphology in mice

Pediatric research, 2022-10, Vol.92 (4), p.995-1002

2022

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Lipidomic analysis and diagnosis of glioblastoma multiforme with rapid evaporative ionization mass spectrometry

Electrophoresis, 2021-10, Vol.42 (19), p.1965-1973

2021

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Enhanced photocatalytic reduction of carbon dioxide in optical fiber monolith reactor with transparent glass balls

Applied energy, 2018-11, Vol.230, p.1403-1413

2018

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The role of oligodendrocyte progenitor cells in the spatiotemporal vascularization of the human and mouse neocortex

Glia, 2024-10

2024

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Engineering Electron–Phonon Coupling of Quantum Defects to a Semiconfocal Acoustic Resonator

Nano letters, 2019-10, Vol.19 (10), p.7021-7027

2019

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Automatic Noise Generation and Reduction for Text Classification

IEEE/ACM transactions on audio, speech, and language processing, 2024, Vol.32, p.139-150

2024

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Exploring the barriers and facilitators of palliative care in the adult intensive care unit from nurses' perspectives in China: A qualitative study

Nursing in critical care, 2024-07, Vol.29 (4), p.756-764

2024

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mTOR pathway repressing expression of FoxO3 is a potential mechanism involved in neonatal white matter dysplasia

Human molecular genetics, 2022-08, Vol.31 (15), p.2508-2520

2022

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Genetic background of idiopathic neurodevelopmental delay patients with significant brain deviation volume

PRMT3 drives glioblastoma progression by enhancing HIF1A and glycolytic metabolism

High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population

Modeling photocatalytic conversion of carbon dioxide in bubbling twin reactor

IL‐18‐dependent NKG2D ligand upregulation on accessory cells is mediated by the PI3K/GSK‐3 pathway

A multi-omic approach reveals utility of CD45 expression in prognosis and novel target discovery

Bronchopulmonary Dysplasia Predicted by Developing a Machine Learning Model of Genetic and Clinical Information

Transcriptional Networks Identify BRPF1 as a Potential Drug Target Based on Inflammatory Signature in Primary Lower-Grade Gliomas

Comprehensive assessment of the genetic characteristics of small for gestational age newborns in NICU: from diagnosis of genetic disorders to prediction of prognosis

Clinical Study of 30 Novel KCNQ2 Variants/Deletions in KCNQ2 -Related Disorders

The performance of the practices associated with the occurrence of severe intraventricular hemorrhage in the very premature infants: data analysis from the Chinese neonatal network

Rare-variant collapsing analyses identified risk genes for neonatal acute respiratory distress syndrome

Overdosage of HNF1B Gene Associated With Annular Pancreas Detected in Neonate Patients With 17q12 Duplication

Case report: A novel truncating variant of BCL11B associated with rare feature of craniosynostosis and global developmental delay

“Going global” and FDI inflows in China: “One Belt & One Road” initiative as a quasi‐natural experiment

Data-driven financial transmission right scenario generation and speculation

Zinc-Finger Protein ZFP488 Regulates the Timing of Oligodendrocyte Myelination and Remyelination

KIF5C deficiency causes abnormal cortical neuronal migration, dendritic branching, and spine morphology in mice

Lipidomic analysis and diagnosis of glioblastoma multiforme with rapid evaporative ionization mass spectrometry

Enhanced photocatalytic reduction of carbon dioxide in optical fiber monolith reactor with transparent glass balls

The role of oligodendrocyte progenitor cells in the spatiotemporal vascularization of the human and mouse neocortex

Engineering Electron–Phonon Coupling of Quantum Defects to a Semiconfocal Acoustic Resonator

Automatic Noise Generation and Reduction for Text Classification

Exploring the barriers and facilitators of palliative care in the adult intensive care unit from nurses' perspectives in China: A qualitative study

mTOR pathway repressing expression of FoxO3 is a potential mechanism involved in neonatal white matter dysplasia

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