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Yu-Chi Liu

Showing results (191-200 of 200) with videos related to

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Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
The British Journal of Ophthalmology|July 10, 2021
Deep learning algorithms for automatic detection of pterygium using anterior segment photographs from slit-lamp and hand-held camerasXiaoling Fang, Mihir Deshmukh, Miao Li Chee, et al.
Frontiers in Bioengineering and Biotechnology|October 6, 2025
Evaluation of <i>in vitro</i> and <i>in vivo</i> release of recombinant human nerve growth factor from bioengineered human stromal lenticuleMolly Tzu-Yu Lin, Yu-Chi Liu, Isabelle Xin Yu Lee, et al.
Diabetes, Obesity & Metabolism|June 18, 2026
Diabetic Corneal Neuropathy as a Window Into Diabetic Foot Risk: A Large-Scale Association StudyChang Liu, Mingyi Yu, Isabelle Xin Yu Lee, et al.
The Journal of Clinical Endocrinology and Metabolism|January 29, 2026
Relationship between continuous glucose monitoring and corneal neuropathy in type 2 diabetesSuresh Rama Chandran, Jasmine Koh Shimin, Chang Liu, et al.
Transplantation and Cellular Therapy|November 20, 2025
One-Year Tear Proteomic Alterations with Topical Cyclosporine-A 0.1% Emulsion in Patients with Allogeneic Stem Cell TransplantChang Liu, Xinyue Wang, Sharon Wan Jie Yeo, et al.
Diabetes|November 29, 2022
Oral Peroxisome Proliferator-Activated Receptor-α Agonist Enhances Corneal Nerve Regeneration in Patients With Type 2 DiabetesCalesta Hui Yi Teo, Molly Tzu-Yu Lin, Isabelle Xin Yu Lee, et al.
Epilepsia Open|August 24, 2019
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in TasmaniaTyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain : a Journal of Neurology|July 5, 2022
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsyLuca Gozzelino, Gaga Kochlamazashvili, Sara Baldassari, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Pageof 20

Showing results (191-200 of 200) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 200 results.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
The British Journal of Ophthalmology|July 10, 2021
Deep learning algorithms for automatic detection of pterygium using anterior segment photographs from slit-lamp and hand-held camerasXiaoling Fang, Mihir Deshmukh, Miao Li Chee, et al.
Frontiers in Bioengineering and Biotechnology|October 6, 2025
Evaluation of <i>in vitro</i> and <i>in vivo</i> release of recombinant human nerve growth factor from bioengineered human stromal lenticuleMolly Tzu-Yu Lin, Yu-Chi Liu, Isabelle Xin Yu Lee, et al.
Diabetes, Obesity & Metabolism|June 18, 2026
Diabetic Corneal Neuropathy as a Window Into Diabetic Foot Risk: A Large-Scale Association StudyChang Liu, Mingyi Yu, Isabelle Xin Yu Lee, et al.
The Journal of Clinical Endocrinology and Metabolism|January 29, 2026
Relationship between continuous glucose monitoring and corneal neuropathy in type 2 diabetesSuresh Rama Chandran, Jasmine Koh Shimin, Chang Liu, et al.
Transplantation and Cellular Therapy|November 20, 2025
One-Year Tear Proteomic Alterations with Topical Cyclosporine-A 0.1% Emulsion in Patients with Allogeneic Stem Cell TransplantChang Liu, Xinyue Wang, Sharon Wan Jie Yeo, et al.
Diabetes|November 29, 2022
Oral Peroxisome Proliferator-Activated Receptor-α Agonist Enhances Corneal Nerve Regeneration in Patients With Type 2 DiabetesCalesta Hui Yi Teo, Molly Tzu-Yu Lin, Isabelle Xin Yu Lee, et al.
Epilepsia Open|August 24, 2019
Epidemiology and etiology of infantile developmental and epileptic encephalopathies in TasmaniaTyson L Ware, Shannon R Huskins, Bronwyn E Grinton, et al.
Brain : a Journal of Neurology|July 5, 2022
Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsyLuca Gozzelino, Gaga Kochlamazashvili, Sara Baldassari, et al.
American Journal of Human Genetics|November 4, 2017
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic EncephalopathiesFadi F Hamdan, Candace T Myers, Patrick Cossette, et al.
Pageof 20