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Heming Wei

Showing results (81-90 of 99) with videos related to

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Clinical Biochemistry|December 14, 2004
Platelet-endothelial cell adhesion molecule-1 gene polymorphism and its soluble level are associated with severe coronary artery stenosis in Chinese SingaporeanHeming Wei, Lu Fang, Sanual H Chowdhury, et al.
Frontiers in Endocrinology|October 18, 2021
MIRAGE Syndrome Caused by a <i>De Novo</i> c.3406G>C (p. Glu1136Gln) Mutation in the <i>SAMD9</i> Gene Presenting With Neonatal Adrenal Insufficiency and Recurrent Intussusception: A Case ReportXinyi Chin, Aravind Venkatesh Sreedharan, Ene Choo Tan, et al.
Scientific Reports|September 15, 2017
Erratum: Identification of Na<sup>+</sup>/K<sup>+</sup>-ATPase inhibition-independent proarrhythmic ionic mechanisms of cardiac glycosidesCai Hong Koh, Jianjun Wu, Ying Ying Chung, et al.
Scientific Reports|May 28, 2017
Identification of Na+/K+-ATPase inhibition-independent proarrhythmic ionic mechanisms of cardiac glycosidesCai Hong Koh, Jianjun Wu, Ying Ying Chung, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Mouse models and genetic modifiers in X-linked adrenoleukodystrophyAnn K Heinzer, Martina C McGuinness, Jyh-Feng Lu, et al.
International Journal of Cardiology|September 4, 2013
Modeling type 3 long QT syndrome with cardiomyocytes derived from patient-specific induced pluripotent stem cellsDongrui Ma, Heming Wei, Yongxing Zhao, et al.
Annals of the Academy of Medicine, Singapore|January 2, 2023
Rapid exome sequencing to aid diagnostics in genetic disorders: Implementation and challenges in the Singapore contextNikki Fong, Jiin Ying Lim, Breana Cham, et al.
Molecular Genetics & Genomic Medicine|December 27, 2021
A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvementEne-Choo Tan, Shi Yun Chia, Khadijah Rafi'ee, et al.
Journal of Cellular and Molecular Medicine|July 1, 2014
iPSC-derived human mesenchymal stem cells improve myocardial strain of infarcted myocardiumQingfeng Miao, Winston Shim, Nicole Tee, et al.
American Journal of Medical Genetics. Part A|December 1, 2020
Self-improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast AsiaPriya Bishnoi, Yi Zhen Ng, Heming Wei, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Clinical Biochemistry|December 14, 2004
Platelet-endothelial cell adhesion molecule-1 gene polymorphism and its soluble level are associated with severe coronary artery stenosis in Chinese SingaporeanHeming Wei, Lu Fang, Sanual H Chowdhury, et al.
Frontiers in Endocrinology|October 18, 2021
MIRAGE Syndrome Caused by a <i>De Novo</i> c.3406G>C (p. Glu1136Gln) Mutation in the <i>SAMD9</i> Gene Presenting With Neonatal Adrenal Insufficiency and Recurrent Intussusception: A Case ReportXinyi Chin, Aravind Venkatesh Sreedharan, Ene Choo Tan, et al.
Scientific Reports|September 15, 2017
Erratum: Identification of Na<sup>+</sup>/K<sup>+</sup>-ATPase inhibition-independent proarrhythmic ionic mechanisms of cardiac glycosidesCai Hong Koh, Jianjun Wu, Ying Ying Chung, et al.
Scientific Reports|May 28, 2017
Identification of Na+/K+-ATPase inhibition-independent proarrhythmic ionic mechanisms of cardiac glycosidesCai Hong Koh, Jianjun Wu, Ying Ying Chung, et al.
Advances in Experimental Medicine and Biology|January 10, 2004
Mouse models and genetic modifiers in X-linked adrenoleukodystrophyAnn K Heinzer, Martina C McGuinness, Jyh-Feng Lu, et al.
International Journal of Cardiology|September 4, 2013
Modeling type 3 long QT syndrome with cardiomyocytes derived from patient-specific induced pluripotent stem cellsDongrui Ma, Heming Wei, Yongxing Zhao, et al.
Annals of the Academy of Medicine, Singapore|January 2, 2023
Rapid exome sequencing to aid diagnostics in genetic disorders: Implementation and challenges in the Singapore contextNikki Fong, Jiin Ying Lim, Breana Cham, et al.
Molecular Genetics & Genomic Medicine|December 27, 2021
A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvementEne-Choo Tan, Shi Yun Chia, Khadijah Rafi'ee, et al.
Journal of Cellular and Molecular Medicine|July 1, 2014
iPSC-derived human mesenchymal stem cells improve myocardial strain of infarcted myocardiumQingfeng Miao, Winston Shim, Nicole Tee, et al.
American Journal of Medical Genetics. Part A|December 1, 2020
Self-improving dystrophic epidermolysis bullosa: First report of clinical, molecular, and genetic characterization of five patients from Southeast AsiaPriya Bishnoi, Yi Zhen Ng, Heming Wei, et al.
Pageof 10