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M Bui

Showing results (401-410 of 540) with videos related to

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Nature Ecology & Evolution|January 19, 2021
Spontaneous cell fusions as a mechanism of parasexual recombination in tumour cell populationsDaria Miroshnychenko, Etienne Baratchart, Meghan C Ferrall-Fairbanks, et al.
Neuro-Ophthalmology (Aeolus Press)|September 14, 2013
<i>De novo</i> malignant optic chiasm glioma with initial clinical response to steroidsJoann J Kang, Joshua H Hou, Kelly M Bui, et al.
Journal of Cardiac Failure|May 4, 2026
Patient Perspectives on Cardiac Gene Therapy: A Survey of Knowledge, Attitudes, and Educational NeedsElizabeth Silver, Adam Taub, Vivian Bui, et al.
Heliyon|September 26, 2024
MLAFP-XN: Leveraging neural network model for development of antifungal peptide identification toolMd Fahim Sultan, Md Shazzad Hossain Shaon, Tasmin Karim, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 9, 2025
Toward Optimizing the Impact of Digital Pathology and Augmented Intelligence on Issues of Diagnosis, Grading, Staging, and ClassificationLewis A Hassell, Marika L Forsythe, Ami Bhalodia, et al.
Sarcoma|November 28, 2013
Rapid screening of novel agents for combination therapy in sarcomasChristopher L Cubitt, Jiliana Menth, Jana Dawson, et al.
Biomed Research International|May 9, 2022
Discovering Common Pathophysiological Processes between COVID-19 and Cystic Fibrosis by Differential Gene Expression Pattern AnalysisMd Tanvir Hasan, Lway Faisal Abdulrazak, Mohammad Khursheed Alam, et al.
Dalton Transactions (Cambridge, England : 2003)|May 4, 2022
Enhancing the remarkable adsorption of Pb<sup>2+</sup> in a series of sulfonic-functionalized Zr-based MOFs: a combined theoretical and experimental study for elucidating the adsorption mechanismCuong C Tran, Hieu C Dong, Vy T N Truong, et al.
Nature Genetics|October 31, 2001
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaX Zhao, D Alvarado, S Rainier, et al.
BMC Cancer|April 10, 2017
Myoepithelial carcinoma with RB1 mutation: remarkable chemosensitivity to carcinoma of unknown origin therapyTimothy M Hoggard, Evita Henderson-Jackson, Marilyn M Bui, et al.
Pageof 54

Showing results (401-410 of 540) with videos related to

Sort By:
Pageof 54
Nature Ecology & Evolution|January 19, 2021
Spontaneous cell fusions as a mechanism of parasexual recombination in tumour cell populationsDaria Miroshnychenko, Etienne Baratchart, Meghan C Ferrall-Fairbanks, et al.
Neuro-Ophthalmology (Aeolus Press)|September 14, 2013
<i>De novo</i> malignant optic chiasm glioma with initial clinical response to steroidsJoann J Kang, Joshua H Hou, Kelly M Bui, et al.
Journal of Cardiac Failure|May 4, 2026
Patient Perspectives on Cardiac Gene Therapy: A Survey of Knowledge, Attitudes, and Educational NeedsElizabeth Silver, Adam Taub, Vivian Bui, et al.
Heliyon|September 26, 2024
MLAFP-XN: Leveraging neural network model for development of antifungal peptide identification toolMd Fahim Sultan, Md Shazzad Hossain Shaon, Tasmin Karim, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 9, 2025
Toward Optimizing the Impact of Digital Pathology and Augmented Intelligence on Issues of Diagnosis, Grading, Staging, and ClassificationLewis A Hassell, Marika L Forsythe, Ami Bhalodia, et al.
Sarcoma|November 28, 2013
Rapid screening of novel agents for combination therapy in sarcomasChristopher L Cubitt, Jiliana Menth, Jana Dawson, et al.
Biomed Research International|May 9, 2022
Discovering Common Pathophysiological Processes between COVID-19 and Cystic Fibrosis by Differential Gene Expression Pattern AnalysisMd Tanvir Hasan, Lway Faisal Abdulrazak, Mohammad Khursheed Alam, et al.
Dalton Transactions (Cambridge, England : 2003)|May 4, 2022
Enhancing the remarkable adsorption of Pb<sup>2+</sup> in a series of sulfonic-functionalized Zr-based MOFs: a combined theoretical and experimental study for elucidating the adsorption mechanismCuong C Tran, Hieu C Dong, Vy T N Truong, et al.
Nature Genetics|October 31, 2001
Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaX Zhao, D Alvarado, S Rainier, et al.
BMC Cancer|April 10, 2017
Myoepithelial carcinoma with RB1 mutation: remarkable chemosensitivity to carcinoma of unknown origin therapyTimothy M Hoggard, Evita Henderson-Jackson, Marilyn M Bui, et al.
Pageof 54