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Analysis of the impact of China’s energy industry on social development from the perspective of low-carbon policy

Energy reports, 2022-10, Vol.8, p.14-27

2022

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Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in China

BMC pediatrics, 2022-11, Vol.22 (1), p.1-666, Article 666

2022

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Segawa syndrome caused by TH gene mutation and its mechanism

Frontiers in genetics, 2022-12, Vol.13, p.1004307-1004307

2022

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Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome

Internal Medicine, 2021/12/01, Vol.60(23), pp.3721-3728

2021

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Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy

Molecular genetics & genomic medicine, 2023-09, Vol.11 (9), p.e2202-e2202

2023

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Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs28 (c.1507_1508del) in the ARX gene

Stem cell research, 2022-03, Vol.59, p.102621-102621, Article 102621

2022

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Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene

Stem cell research, 2022-07, Vol.62, p.102798-102798, Article 102798

2022

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Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency

Stem cell research, 2021-05, Vol.53, p.102292-102292, Article 102292

2021

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Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases

Frontiers in pediatrics, 2022-11, Vol.10, p.997088-997088

2022

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Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome

Stem cell research, 2020-07, Vol.46, p.101838-101838, Article 101838

2020

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Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan–Herndon–Dudley syndrome

Stem cell research, 2020-07, Vol.46, p.101872-101872, Article 101872

2020

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Clinical Study of 8 Cases of CHD2 Gene Mutation-Related Neurological Diseases and Their Mechanisms

Frontiers in cell and developmental biology, 2022-03, Vol.10, p.853127-853127

2022

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Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese Children

Frontiers in pediatrics, 2022-05, Vol.10, p.833371-833371

2022

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Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene

Frontiers in pediatrics, 2021-11, Vol.9, p.679342-679342

2021

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Research on non-linear input–output model based on production function theory and a new method to update IO coefficients matrix

Applied mathematics and computation, 2006-10, Vol.181 (1), p.478-486

2006

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Self-Assembly Reduced Graphene Oxide Nanosheet Hydrogel Fabrication by Anchorage of Chitosan/Silver and Its Potential Efficient Application toward Dye Degradation for Wastewater Treatments

ACS sustainable chemistry & engineering, 2015-12, Vol.3 (12), p.3130-3139

2015

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Graphene Oxide-Polymer Composite Langmuir Films Constructed by Interfacial Thiol-Ene Photopolymerization

Nanoscale research letters, 2017-12, Vol.12 (1), p.99-99, Article 99

2017

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Carbon‐based adsorbents for post‐combustion capture: a review

Greenhouse gases: science and technology, 2018-02, Vol.8 (1), p.11-36

2018

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Hydrothermal synthesis of hierarchical core–shell manganese oxide nanocomposites as efficient dye adsorbents for wastewater treatment

RSC advances, 2015-01, Vol.5 (69), p.56279-56285

2015

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FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndrome

Cell death and differentiation, 2023-10, Vol.30 (10), p.2351-2363

2023

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Biased adsorption of ethane over ethylene on low-cost hyper-crosslinked polymers

Journal of solid state chemistry, 2019-03, Vol.271, p.199-205

2019

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DWT-Net: Seizure Detection System with Structured EEG Montage and Multiple Feature Extractor in Convolution Neural Network

Journal of sensors, 2020-08, Vol.2020, p.1-13

2020

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Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13

Journal of the neurological sciences, 2020-09, Vol.416, p.116948-116948, Article 116948

2020

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Potassium Tethered Carbons with Unparalleled Adsorption Capacity and Selectivity for Low-Cost Carbon Dioxide Capture from Flue Gas

ACS applied materials & interfaces, 2018-01, Vol.10 (4), p.3495-3505

2018

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Preliminary Study on Clinical Characteristics and Pathogenesis of IQSEC2 Mutations Patients

Pharmacogenomics and personalized medicine, 2024-05, Vol.17, p.289-318

2024

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Analysis of the impact of China’s energy industry on social development from the perspective of low-carbon policy

Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in China

Segawa syndrome caused by TH gene mutation and its mechanism

Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome

Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy

Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs28 (c.1507_1508del) in the ARX gene

Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene

Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency

Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases

Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome

Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan–Herndon–Dudley syndrome

Clinical Study of 8 Cases of CHD2 Gene Mutation-Related Neurological Diseases and Their Mechanisms

Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese Children

Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene

Research on non-linear input–output model based on production function theory and a new method to update IO coefficients matrix

Self-Assembly Reduced Graphene Oxide Nanosheet Hydrogel Fabrication by Anchorage of Chitosan/Silver and Its Potential Efficient Application toward Dye Degradation for Wastewater Treatments

Graphene Oxide-Polymer Composite Langmuir Films Constructed by Interfacial Thiol-Ene Photopolymerization

Carbon‐based adsorbents for post‐combustion capture: a review

Hydrothermal synthesis of hierarchical core–shell manganese oxide nanocomposites as efficient dye adsorbents for wastewater treatment

FBXL4 mutations cause excessive mitophagy via BNIP3/BNIP3L accumulation leading to mitochondrial DNA depletion syndrome

Biased adsorption of ethane over ethylene on low-cost hyper-crosslinked polymers

DWT-Net: Seizure Detection System with Structured EEG Montage and Multiple Feature Extractor in Convolution Neural Network

Novel homozygous mutation in the FBXL4 gene is associated with mitochondria DNA depletion syndrome-13

Potassium Tethered Carbons with Unparalleled Adsorption Capacity and Selectivity for Low-Cost Carbon Dioxide Capture from Flue Gas

Preliminary Study on Clinical Characteristics and Pathogenesis of IQSEC2 Mutations Patients

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