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Kinematic and static analysis of a novel tensegrity robot

Mechanism and machine theory, 2020-07, Vol.149, p.103788, Article 103788

2020

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Additive Manufacturing: Unlocking the Evolution of Energy Materials

Advanced science, 2017-10, Vol.4 (10), p.1700187-n/a

2017

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Novel Exon 7 Deletions in TSPAN12 in a Three-Generation FEVR Family: A Case Report and Literature Review

Genes, 2023-02, Vol.14 (3), p.587

2023

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Geometric accuracy design and error compensation of a one-translational and three-rotational parallel mechanism with articulated traveling plate

Proceedings of the Institution of Mechanical Engineers. Part B, Journal of engineering manufacture, 2018-10, Vol.232 (12), p.2083-2097

2018

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Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations

American journal of ophthalmology, 2021-03, Vol.223, p.160-168

2021

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Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1

Stem cell research, 2023-08, Vol.70, p.103131-103131, Article 103131

2023

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Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner

International journal of molecular sciences, 2023-12, Vol.24 (23), p.16928

2023

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MicroRNA-139-5p Promotes Functional Recovery and Reduces Pain Hypersensitivity in Mice with Spinal Cord Injury by Targeting Mammalian Sterile 20-like Kinase 1

Neurochemical research, 2021-02, Vol.46 (2), p.349-357

2021

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Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohort

Graefe's archive for clinical and experimental ophthalmology, 2021-10, Vol.259 (10), p.2929-2939

2021

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Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia

Journal of translational medicine, 2024-01, Vol.22 (1), p.75-18, Article 75

2024

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Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature

International journal of molecular sciences, 2023-03, Vol.24 (5), p.5012

2023

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Multi-locomotion transition of tensegrity mobile robot under different terrains

Science China. Technological sciences, 2024-02, Vol.67 (2), p.536-557

2024

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Grinding/Cutting Technology and Equipment of Multi-scale Casting Parts

Chinese journal of mechanical engineering, 2022-12, Vol.35 (1), p.97-9, Article 97

English ed., 2022

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Identification and extraction of lateral target signals in tunnel geological prediction with the Karhunen-Loéve beamforming method

Journal of applied geophysics, 2023-10, Vol.217, p.105167, Article 105167

2023

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Hypoxia preconditioning of adipose stem cell-derived exosomes loaded in gelatin methacryloyl (GelMA) promote type H angiogenesis and osteoporotic fracture repair

Journal of nanobiotechnology, 2024-03, Vol.22 (1), p.112-112, Article 112

2024

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Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic

Frontiers in immunology, 2023-08, Vol.14, p.1239886

2023

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New Insight into the Genotype-Phenotype Correlation of PRPH2 -Related Diseases Based on a Large Chinese Cohort and Literature Review

International journal of molecular sciences, 2023-04, Vol.24 (7), p.6728

2023

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Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis

PloS one, 2011-05, Vol.6 (5), p.e19458-e19458

2011

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Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands

Experimental eye research, 2016-05, Vol.146, p.252-258

2016

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Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families

Human genetics, 2020-08, Vol.139 (8), p.1057-1064

2020

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An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases

Translational vision science & technology, 2019-03, Vol.8 (2), p.21-21

2019

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Biomechanical evaluation of a healed acetabulum with internal fixators: finite element analysis

Journal of orthopaedic surgery and research, 2023-03, Vol.18 (1), p.251-251, Article 251

2023

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Development of a prediction model for predicting the prevalence of nonalcoholic fatty liver disease in Chinese nurses: the first-year follow data of a web-based ambispective cohort study

BMC gastroenterology, 2024-02, Vol.24 (1), p.72-72, Article 72

2024

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Design and Evaluation of Lyophilized Fibroblast Growth Factor 21 and Its Protection against Ischemia Cerebral Injury

Bioconjugate chemistry, 2018-02, Vol.29 (2), p.287-295

2018

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Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probands

Experimental eye research, 2016-08, Vol.149, p.93-99

2016

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Kinematic and static analysis of a novel tensegrity robot

Additive Manufacturing: Unlocking the Evolution of Energy Materials

Novel Exon 7 Deletions in TSPAN12 in a Three-Generation FEVR Family: A Case Report and Literature Review

Geometric accuracy design and error compensation of a one-translational and three-rotational parallel mechanism with articulated traveling plate

Clinical and Genetic Analysis of 63 Families Demonstrating Early and Advanced Characteristic Fundus as the Signature of CRB1 Mutations

Generation of an induced pluripotent stem cell line (ZSZOCi001-A) from a patient with Knobloch syndrome caused by biallelic mutations in the gene COL18A1

Defect of TIMP4 Is Associated with High Myopia and Participates in Rat Ocular Development in a Dose-Dependent Manner

MicroRNA-139-5p Promotes Functional Recovery and Reduces Pain Hypersensitivity in Mice with Spinal Cord Injury by Targeting Mammalian Sterile 20-like Kinase 1

Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohort

Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia

Variant Landscape of 15 Genes Involved in Corneal Dystrophies: Report of 30 Families and Comprehensive Analysis of the Literature

Multi-locomotion transition of tensegrity mobile robot under different terrains

Grinding/Cutting Technology and Equipment of Multi-scale Casting Parts

Identification and extraction of lateral target signals in tunnel geological prediction with the Karhunen-Loéve beamforming method

Hypoxia preconditioning of adipose stem cell-derived exosomes loaded in gelatin methacryloyl (GelMA) promote type H angiogenesis and osteoporotic fracture repair

Retinopathy as an initial sign of hereditary immunological diseases: report of six families and challenges in eye clinic

New Insight into the Genotype-Phenotype Correlation of PRPH2 -Related Diseases Based on a Large Chinese Cohort and Literature Review

Detection of variants in 15 genes in 87 unrelated Chinese patients with Leber congenital amaurosis

Molecular genetics of cone-rod dystrophy in Chinese patients: New data from 61 probands and mutation overview of 163 probands

Structural variations in a non-coding region at 1q32.1 are responsible for the NYS7 locus in two large families

An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases

Biomechanical evaluation of a healed acetabulum with internal fixators: finite element analysis

Development of a prediction model for predicting the prevalence of nonalcoholic fatty liver disease in Chinese nurses: the first-year follow data of a web-based ambispective cohort study

Design and Evaluation of Lyophilized Fibroblast Growth Factor 21 and Its Protection against Ischemia Cerebral Injury

Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probands

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