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Sheng Liao

Showing results (471-480 of 512) with videos related to

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Journal of the American Chemical Society|March 10, 2023
Bifunctional Electron-Transporting Agent for Red Colloidal Quantum Dot Light-Emitting DiodesYa-Kun Wang, Haoyue Wan, Jian Xu, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 19, 2025
Dual-Functional Surface Engineering of Single-Crystal NMC Cathodes via Residue-to-Coating Conversion for Enhanced Interface StabilityShadab Ali Ahmed, Tripti Agnihotri, Ashok Ranjan, et al.
National Science Review|February 5, 2026
Singlet and triplet harvesting enable efficient NIR-II quantum-dot electroluminescenceWan-Shan Shen, Sam Teale, Yang Liu, et al.
National Science Review|May 8, 2025
Radical-activable charge-transfer cocrystals for solar thermoelectric generator toward information conversionSheng Zhuo, Yu Dong Zhao, Yan-Xin Liu, et al.
ACS Applied Materials & Interfaces|February 15, 2024
Boosting the Interfacial Stability of the Li<sub>6</sub>PS<sub>5</sub>Cl Electrolyte with a Li Anode via In Situ Formation of a LiF-Rich SEI Layer and a Ductile Sulfide Composite Solid ElectrolyteGashahun Gobena Serbessa, Bereket Woldegbreal Taklu, Yosef Nikodimos, et al.
International Journal of Cancer|February 1, 2014
A new insight into fecal hemoglobin concentration-dependent predictor for colorectal neoplasiaAmy Ming-Fang Yen, Sam Li-Sheng Chen, Sherry Yueh-Hsia Chiu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemiaKai-Ying He, Hong-Ping Yu, Jing Zou, et al.
Science Bulletin|November 2, 2023
Thickness-variation-insensitive near-infrared quantum dot LEDsWan-Shan Shen, Yang Liu, Luke Grater, et al.
Annals of Hematology|March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case reportJian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.
Journal of Medical Genetics|July 19, 2023
Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndromeHong-Hong Pan, Dan-Dan Ruan, Min Wu, et al.
Pageof 52

Showing results (471-480 of 512) with videos related to

Sort By:
Pageof 52
Journal of the American Chemical Society|March 10, 2023
Bifunctional Electron-Transporting Agent for Red Colloidal Quantum Dot Light-Emitting DiodesYa-Kun Wang, Haoyue Wan, Jian Xu, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 19, 2025
Dual-Functional Surface Engineering of Single-Crystal NMC Cathodes via Residue-to-Coating Conversion for Enhanced Interface StabilityShadab Ali Ahmed, Tripti Agnihotri, Ashok Ranjan, et al.
National Science Review|February 5, 2026
Singlet and triplet harvesting enable efficient NIR-II quantum-dot electroluminescenceWan-Shan Shen, Sam Teale, Yang Liu, et al.
National Science Review|May 8, 2025
Radical-activable charge-transfer cocrystals for solar thermoelectric generator toward information conversionSheng Zhuo, Yu Dong Zhao, Yan-Xin Liu, et al.
ACS Applied Materials & Interfaces|February 15, 2024
Boosting the Interfacial Stability of the Li<sub>6</sub>PS<sub>5</sub>Cl Electrolyte with a Li Anode via In Situ Formation of a LiF-Rich SEI Layer and a Ductile Sulfide Composite Solid ElectrolyteGashahun Gobena Serbessa, Bereket Woldegbreal Taklu, Yosef Nikodimos, et al.
International Journal of Cancer|February 1, 2014
A new insight into fecal hemoglobin concentration-dependent predictor for colorectal neoplasiaAmy Ming-Fang Yen, Sam Li-Sheng Chen, Sherry Yueh-Hsia Chiu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 18, 2024
A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemiaKai-Ying He, Hong-Ping Yu, Jing Zou, et al.
Science Bulletin|November 2, 2023
Thickness-variation-insensitive near-infrared quantum dot LEDsWan-Shan Shen, Yang Liu, Luke Grater, et al.
Annals of Hematology|March 21, 2024
Adult type I Gaucher disease with splenectomy caused by a compound heterozygous GBA1 mutation in a Chinese patient: a case reportJian-Hui Zhang, Hui Chen, Dan-Dan Ruan, et al.
Journal of Medical Genetics|July 19, 2023
Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndromeHong-Hong Pan, Dan-Dan Ruan, Min Wu, et al.
Pageof 52