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Translational Neurodegeneration
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November 2, 2023
NLRP3 inflammasome in cognitive impairment and pharmacological properties of its inhibitors
Yi Xu, Yanling Yang, Xi Chen, et al.
Journal of Colloid and Interface Science
|
March 21, 2021
Bi<sub>2</sub>O<sub>3</sub>/BiVO<sub>4</sub>@graphene oxide van der Waals heterostructures with enhanced photocatalytic activity toward oxygen generation
Yaxin Bi, Yanling Yang, Xiao-Lei Shi, et al.
Journal of Colloid and Interface Science
|
April 21, 2020
Amorphous carbon coated SnO<sub>2</sub> nanohseets on hard carbon hollow spheres to boost potassium storage with high surface capacitive contributions
Dan Li, Jiaqi Zhang, Syed Musab Ahmed, et al.
Journal of Colloid and Interface Science
|
July 5, 2020
Tuning wall thickness of TiO<sub>2</sub> microtubes for an enhanced photocatalytic activity with thickness-dependent charge separation efficiency
Xinxin Zou, Yanling Yang, Huajun Chen, et al.
BMC Medical Genomics
|
June 11, 2024
Clinical features and ALDH5A1 gene findings in 13 Chinese cases with succinic semialdehyde dehydrogenase deficiency
Hui Dong, Xue Ma, Zhehui Chen, et al.
Bioorganic Chemistry
|
May 24, 2024
Design and synthesis of sulfonamide phenothiazine derivatives as novel ferroptosis inhibitors and their therapeutic effects in spinal cord injury
Xinyue Bai, Yanling Yang, Yilin Luo, et al.
Orphanet Journal of Rare Diseases
|
December 24, 2024
Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees
Yaojun Xie, Keyi Li, Li Yang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 4, 2019
One potential hotspot ACADVL mutation in Chinese patients with very-long-chain acyl-coenzyme A dehydrogenase deficiency
Xiyuan Li, Rui Ma, Yi Liu, et al.
BMC Pediatrics
|
December 12, 2025
Functional identification of two variants in unrelated Chinese patients with DNM1L-related mitochondrial disorders
Zhenkun Zhang, Zhehui Chen, Xiaofan Bie, et al.
BMC Pediatrics
|
February 10, 2024
A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review
Zhenkun Zhang, Xiaofan Bie, Zhehui Chen, et al.
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of 38
Search research articles
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Showing results (281-290 of 376) with videos related to
Sort By:
Page
of 38
Translational Neurodegeneration
|
November 2, 2023
NLRP3 inflammasome in cognitive impairment and pharmacological properties of its inhibitors
Yi Xu, Yanling Yang, Xi Chen, et al.
Journal of Colloid and Interface Science
|
March 21, 2021
Bi<sub>2</sub>O<sub>3</sub>/BiVO<sub>4</sub>@graphene oxide van der Waals heterostructures with enhanced photocatalytic activity toward oxygen generation
Yaxin Bi, Yanling Yang, Xiao-Lei Shi, et al.
Journal of Colloid and Interface Science
|
April 21, 2020
Amorphous carbon coated SnO<sub>2</sub> nanohseets on hard carbon hollow spheres to boost potassium storage with high surface capacitive contributions
Dan Li, Jiaqi Zhang, Syed Musab Ahmed, et al.
Journal of Colloid and Interface Science
|
July 5, 2020
Tuning wall thickness of TiO<sub>2</sub> microtubes for an enhanced photocatalytic activity with thickness-dependent charge separation efficiency
Xinxin Zou, Yanling Yang, Huajun Chen, et al.
BMC Medical Genomics
|
June 11, 2024
Clinical features and ALDH5A1 gene findings in 13 Chinese cases with succinic semialdehyde dehydrogenase deficiency
Hui Dong, Xue Ma, Zhehui Chen, et al.
Bioorganic Chemistry
|
May 24, 2024
Design and synthesis of sulfonamide phenothiazine derivatives as novel ferroptosis inhibitors and their therapeutic effects in spinal cord injury
Xinyue Bai, Yanling Yang, Yilin Luo, et al.
Orphanet Journal of Rare Diseases
|
December 24, 2024
Expanding the phenotypic and genetic spectrum of GTPBP3 deficiency: findings from nine Chinese pedigrees
Yaojun Xie, Keyi Li, Li Yang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 4, 2019
One potential hotspot ACADVL mutation in Chinese patients with very-long-chain acyl-coenzyme A dehydrogenase deficiency
Xiyuan Li, Rui Ma, Yi Liu, et al.
BMC Pediatrics
|
December 12, 2025
Functional identification of two variants in unrelated Chinese patients with DNM1L-related mitochondrial disorders
Zhenkun Zhang, Zhehui Chen, Xiaofan Bie, et al.
BMC Pediatrics
|
February 10, 2024
A novel variant of DNM1L expanding the clinical phenotypic spectrum: a case report and literature review
Zhenkun Zhang, Xiaofan Bie, Zhehui Chen, et al.
Page
of 38