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Performance evaluation of Stereo Vision aided Loosely Coupled GNSS/SINS Integration for land vehicle navigation in Different Urban Environments

IEEE sensors journal, 2023-02, Vol.23 (4), p.1-1

2023

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Enhance Pose and Extrinsic Accuracy with Online Spatial and Temporal Compensation in Monocular Camera-Aided GNSS/SINS Integration

IEEE transactions on instrumentation and measurement, 2024-01, Vol.73, p.1-1

2024

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A non-viral vector for potential DMD gene therapy study by targeting a minidystrophin-GFP fusion gene into the hrDNA locus

Acta biochimica et biophysica Sinica, 2009-12, Vol.41 (12), p.1053-1060

2009

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Improving battery safety by early detection of internal shorting with a bifunctional separator

Nature communications, 2014-10, Vol.5 (1), p.5193-5193, Article 5193

2014

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Designer exosomes for targeted and efficient ferroptosis induction in cancer via chemo-photodynamic therapy

Theranostics, 2021-01, Vol.11 (17), p.8185-8196

2021

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Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)

Clinical chemistry (Baltimore, Md.), 2015-01, Vol.61 (1), p.172-181

2015

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Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression

International journal of molecular sciences, 2022-07, Vol.23 (14), p.7941

2022

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Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem Cells

Human gene therapy, 2018-11, Vol.29 (11), p.1252-1263

2018

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O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells

International journal of molecular sciences, 2024-07, Vol.25 (14), p.7889

2024

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Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localization

Clinica chimica acta, 2021-12, Vol.523, p.297-303

2021

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Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read Sequencing

Clinical chemistry (Baltimore, Md.), 2022-07, Vol.68 (7), p.927-939

2022

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Sensitive and visual detection of SARS-CoV-2 using RPA-Cas12a one-step assay with ssDNA-modified crRNA

Analytica chimica acta, 2024-06, Vol.1309, p.342693-342693, Article 342693

2024

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Rapid and sensitive Cas12a-based one-step nucleic acid detection with ssDNA-modified crRNA

Analytica chimica acta, 2023-10, Vol.1276, p.341622-341622, Article 341622

2023

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Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism

International journal of molecular sciences, 2023-01, Vol.24 (1), p.786

2023

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Establishment and characterization of the third non-functional human pancreatic neuroendocrine tumor cell line

Human cell : official journal of Human Cell Research Society, 2022-07, Vol.35 (4), p.1248-1261

2022

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Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in ARSE

Frontiers in genetics, 2021-09, Vol.12, p.722694-722694

2021

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Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individuals

Human genomics, 2024-10, Vol.18 (1), p.111-12, Article 111

2024

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ssODN-Mediated In-Frame Deletion with CRISPR/Cas9 Restores FVIII Function in Hemophilia A-Patient-Derived iPSCs and ECs

Molecular therapy. Nucleic acids, 2019-09, Vol.17, p.198-209

2019

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Simultaneous Identification of Both MFSD8 and RDH12 Pathogenic Variants in a Chinese Family Affected With Retinitis Pigmentosa

Frontiers in genetics, 2021-09, Vol.12, p.715100-715100

2021

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Application of whole exome sequencing in carrier screening for high-risk families without probands

Frontiers in genetics, 2024-06, Vol.15, p.1415811

2024

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A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder

Cell reports (Cambridge), 2023-12, Vol.42 (12), p.113445-113445, Article 113445

2023

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PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation

Cell death & disease, 2024-11, Vol.15 (11), p.808-11, Article 808

2024

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Idea and Application to Explain Active Learning for Low-Carbon Sustainable AIoT

IEEE internet of things journal, 2024-09, p.1-1

2024

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Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families

Clinica chimica acta, 2022-07, Vol.532, p.53-60

2022

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Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1–2 years after initial analysis

Clinica chimica acta, 2021-12, Vol.523, p.163-168

2021

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Performance evaluation of Stereo Vision aided Loosely Coupled GNSS/SINS Integration for land vehicle navigation in Different Urban Environments

Enhance Pose and Extrinsic Accuracy with Online Spatial and Temporal Compensation in Monocular Camera-Aided GNSS/SINS Integration

A non-viral vector for potential DMD gene therapy study by targeting a minidystrophin-GFP fusion gene into the hrDNA locus

Improving battery safety by early detection of internal shorting with a bifunctional separator

Designer exosomes for targeted and efficient ferroptosis induction in cancer via chemo-photodynamic therapy

Noninvasive prenatal testing for Wilson disease by use of circulating single-molecule amplification and resequencing technology (cSMART)

Targeted-Deletion of a Tiny Sequence via Prime Editing to Restore SMN Expression

Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem Cells

O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells

Novel variants in OSGEP leading to Galloway-Mowat syndrome by altering its subcellular localization

Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read Sequencing

Sensitive and visual detection of SARS-CoV-2 using RPA-Cas12a one-step assay with ssDNA-modified crRNA

Rapid and sensitive Cas12a-based one-step nucleic acid detection with ssDNA-modified crRNA

Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism

Establishment and characterization of the third non-functional human pancreatic neuroendocrine tumor cell line

Prenatal Diagnosis in a Fetus With X-Linked Recessive Chondrodysplasia Punctata: Identification and Functional Study of a Novel Missense Mutation in ARSE

Comprehensive analysis of NGS-based expanded carrier screening and follow-up in southern and southwestern China: results from 3024 Chinese individuals

ssODN-Mediated In-Frame Deletion with CRISPR/Cas9 Restores FVIII Function in Hemophilia A-Patient-Derived iPSCs and ECs

Simultaneous Identification of Both MFSD8 and RDH12 Pathogenic Variants in a Chinese Family Affected With Retinitis Pigmentosa

Application of whole exome sequencing in carrier screening for high-risk families without probands

A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder

PIGK defects induce apoptosis in Purkinje cells and acceleration of neuroectodermal differentiation

Idea and Application to Explain Active Learning for Low-Carbon Sustainable AIoT

Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families

Increase in diagnostic yield achieved for 174 whole-exome sequencing cases reanalyzed 1–2 years after initial analysis

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