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Impact of Time-Restricted Feeding on Adaptation to a 6-Hour Delay Phase Shift or a 12-Hour Phase Shift in Mice

Nutrients, 2022-07, Vol.14 (15), p.3025

2022

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Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the JAM3 gene

Frontiers in genetics, 2022-10, Vol.13

2022

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Identification of four TTN variants in three families with fetal akinesia deformation sequence

BMC medical genomics, 2024-06, Vol.17 (1), p.170-7, Article 170

2024

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Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene

Stem cell research, 2020-05, Vol.45, p.101791-101791, Article 101791

2020

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The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies

Molecular cytogenetics, 2018-12, Vol.11 (1), p.59-59, Article 59

2018

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Soft Actor-Critic-Based Multi-User Multi-TTI MIMO Precoding in Multi-Modal Real-Time Broadband Communications

IEEE transactions on wireless communications, 2024-09, p.1-1

2024

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An On-board Adaptive Modelling Approach based on MIRLS-MA Extended Kalman filter for Aero-engines

IEEE transactions on aerospace and electronic systems, 2024-08, p.1-16

2024

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A robust adaptive linear parameter-varying gain-scheduling controller for aeroengines

Aerospace science and technology, 2023-07, Vol.138, p.108319, Article 108319

2023

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Long-Stroke Hydraulic Robot Motion Control With Incremental Nonlinear Dynamic Inversion

IEEE/ASME transactions on mechatronics, 2019-02, Vol.24 (1), p.304-314

2019

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Time-Delay Margin and Robustness of Incremental Nonlinear Dynamic Inversion Control

Journal of guidance, control, and dynamics, 2022-02, Vol.45 (2), p.394-404

2022

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Lack of MECP2 gene transcription on the duplicated alleles of two related asymptomatic females with Xq28 duplications and opposite X‐chromosome inactivation skewing

Human mutation, 2021-11, Vol.42 (11), p.1429-1442

2021

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Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings

Clinica chimica acta, 2022-01, Vol.525, p.23-28

2022

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Expression and localization of HSD17B13 along mouse urinary tract

American journal of physiology. Renal physiology, 2024-07, Vol.327 (1), p.F146-F157

2024

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A large‐scale production of mesenchymal stem cells and their exosomes for an efficient treatment against lung inflammation

Biotechnology journal, 2024-02, Vol.19 (2), p.e2300174-n/a

2024

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Self-attention reinforcement learning for multi-beam combining in mmWave 3D-MIMO systems

Science China. Information sciences, 2023-06, Vol.66 (6), p.162304, Article 162304

2023

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Pathogenic mutations in two Chinese patients exhibiting severe early-onset obesity

Science China. Life sciences, 2019-11, Vol.62 (11), p.1554-1556

2019

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Genetic study of a family of neuronal ceroid lipofuscinosis caused by a heterozygous mutation of CLN6 gene

Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban, 2019-06, Vol.48 (4), p.373-377

2019

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Database-Driven Safe Flight-Envelope Protection for Impaired Aircraft

Journal of aerospace information systems, 2021-01, Vol.18 (1), p.14-25

2021

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Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression

Frontiers of medicine, 2020-06, Vol.14 (3), p.305-317

2020

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Germline intergenic duplications at Xq26.1 underlie Bazex–Dupré–Christol basal cell carcinoma susceptibility syndrome

British journal of dermatology (1951), 2022-12, Vol.187 (6), p.948-961

2022

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Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia

Genetic testing and molecular biomarkers, 2018-08, Vol.22 (8), p.487-491

2018

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Genetic analysis and prenatal diagnosis of a sporadic family with neurofibromatosis type 1

Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban, 2019-06, Vol.48 (4), p.367-372

2019

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Research on Chinese Font Size of Automobile Central Control Interface Driving

HCI in Mobility, Transport, and Automotive Systems, p.210-223

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Biological, immunological and regenerative characteristics of placenta-derived mesenchymal stem cell isolated using a time-gradient attachment method

Stem cell research, 2012-09, Vol.9 (2), p.110-123

2012

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Identification of a novel mutation of DSPP gene in a Chinese family affected with dentinogenesis imperfecta shields type II

Zhonghua yi xue yi chuan xue za zhi, 2016-02, Vol.33 (1), p.34

2016

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Impact of Time-Restricted Feeding on Adaptation to a 6-Hour Delay Phase Shift or a 12-Hour Phase Shift in Mice

Case report: Prenatal diagnosis of fetal intracranial hemorrhage due to compound mutations in the JAM3 gene

Identification of four TTN variants in three families with fetal akinesia deformation sequence

Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene

The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies

Soft Actor-Critic-Based Multi-User Multi-TTI MIMO Precoding in Multi-Modal Real-Time Broadband Communications

An On-board Adaptive Modelling Approach based on MIRLS-MA Extended Kalman filter for Aero-engines

A robust adaptive linear parameter-varying gain-scheduling controller for aeroengines

Long-Stroke Hydraulic Robot Motion Control With Incremental Nonlinear Dynamic Inversion

Time-Delay Margin and Robustness of Incremental Nonlinear Dynamic Inversion Control

Lack of MECP2 gene transcription on the duplicated alleles of two related asymptomatic females with Xq28 duplications and opposite X‐chromosome inactivation skewing

Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings

Expression and localization of HSD17B13 along mouse urinary tract

A large‐scale production of mesenchymal stem cells and their exosomes for an efficient treatment against lung inflammation

Self-attention reinforcement learning for multi-beam combining in mmWave 3D-MIMO systems

Pathogenic mutations in two Chinese patients exhibiting severe early-onset obesity

Genetic study of a family of neuronal ceroid lipofuscinosis caused by a heterozygous mutation of CLN6 gene

Database-Driven Safe Flight-Envelope Protection for Impaired Aircraft

Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression

Germline intergenic duplications at Xq26.1 underlie Bazex–Dupré–Christol basal cell carcinoma susceptibility syndrome

Mutation Screening of the EDA Gene in Seven Chinese Families with X-Linked Hypohidrotic Ectodermal Dysplasia

Genetic analysis and prenatal diagnosis of a sporadic family with neurofibromatosis type 1

Research on Chinese Font Size of Automobile Central Control Interface Driving

Biological, immunological and regenerative characteristics of placenta-derived mesenchymal stem cell isolated using a time-gradient attachment method

Identification of a novel mutation of DSPP gene in a Chinese family affected with dentinogenesis imperfecta shields type II

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