Yingyu Wang
Wenzhou, 325027, China
Last Updated: 09/26/2026
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Found 19 publications
Buried interface anchored octahedra for efficient sky-blue perovskite light-emitting diodes.
Journal: Chemical communications (Cambridge, England)
Published: September 03, 2025
Application of Skin Barrier Monitoring Technology in the Early Prediction of Incontinence-Associated Dermatitis: A Prospective Observational Study.
Journal: Dermatology (Basel, Switzerland)
Published: May 26, 2025
Improved Photovoltaic Performance of Inverted Two-Dimensional Perovskite Solar Cells via a Simple Molecular Bridge on Buried Interface.
Journal: Langmuir : the ACS journal of surfaces and colloids
Published: February 16, 2024
Color-stable blue light-emitting diodes with defect management by sulfonate.
Journal: Chemical communications (Cambridge, England)
Published: April 25, 2023
Solvent polishing engineering for quasi-two-dimensional perovskite blue light-emitting diodes.
Journal: Chemical communications (Cambridge, England)
Published: June 07, 2022
A case of a severe factor XI deficiency in a Chinese woman with heavy menorrhagia.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: February 06, 2019
Homozygous missense mutation p.Val298Met of F10 gene causing hereditary coagulation factor X deficiency in a Chinese pedigree
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: June 07, 2016
Severe coagulation factor VII deficiency caused by a novel homozygous mutation (p. Trp284Gly) in loop 140s.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: January 14, 2016
Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 15, 2015
Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivation.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: October 31, 2015
Identification of Genetic Defects Underlying FXII Deficiency in Four Unrelated Chinese Patients.
Journal: Acta haematologica
Published: September 07, 2015
A novel gene insertion combined with a missense mutation causing factor VII deficiency in two unrelated Chinese families.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: June 18, 2015
Last Updated: 09/26/2026