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The Journal of Clinical Investigation|June 15, 1996
Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI geneD R Booth, S Y Tan, S E Booth, et al.
Gynecologic Oncology|August 21, 2017
Family history of cancer predicts endometrial cancer risk independently of Lynch Syndrome: Implications for genetic counsellingSharon E Johnatty, Yen Y Tan, Daniel D Buchanan, et al.
Frontiers in Immunology|July 3, 2020
Targeting Nuclear LSD1 to Reprogram Cancer Cells and Reinvigorate Exhausted T Cells via a Novel LSD1-EOMES SwitchWen Juan Tu, Robert D McCuaig, Abel H Y Tan, et al.
European Heart Journal Open|June 3, 2025
Cardiac function after catheter ablation of ventricular arrhythmias in patients with arrhythmogenic right ventricular cardiomyopathyFatima M Ezzeddine, Nathaniel E Davis, Samuel J Asirvatham, et al.
Investigative Ophthalmology & Visual Science|April 14, 2026
Bruch's Membrane Contributes to the Structural Integrity of the Normal Human EyeRoyston K Y Tan, Swati Sharma, Anita S Y Chan, et al.
The Lancet. Respiratory Medicine|January 20, 2020
Safety and efficacy of nazartinib (EGF816) in adults with EGFR-mutant non-small-cell lung carcinoma: a multicentre, open-label, phase 1 studyDaniel S-W Tan, Natasha B Leighl, Gregory J Riely, et al.
Human Mutation|November 10, 2020
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10Guy Helman, Alison G Compton, Daniella H Hock, et al.
Nature Communications|December 19, 2013
Observation of possible topological in-gap surface states in the Kondo insulator SmB6 by photoemissionJ Jiang, S Li, T Zhang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 31, 2018
ASPRE trial: incidence of preterm pre-eclampsia in patients fulfilling ACOG and NICE criteria according to risk by FMF algorithmL C Poon, D L Rolnik, M Y Tan, et al.
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