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Phuc Nguyen

Showing results (361-370 of 481) with videos related to

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Frontiers in Oncology|September 26, 2022
Broad genomic workup including optical genome mapping uncovers a <i>DDX3X</i>: <i>MLLT10</i> gene fusion in acute myeloid leukemiaVerena Nilius-Eliliwi, Marco Tembrink, Wanda Maria Gerding, et al.
European Journal of Neurology|January 11, 2024
Association of the neonatal Fc receptor promoter variable number of tandem repeat polymorphism with immunoglobulin response in patients with chronic inflammatory demyelinating polyneuropathyAnna Lena Fisse, Emelie Schäfer, Alina Hieke, et al.
ACS Nano|May 27, 2024
Multimodal Imaging-Guided Stem Cell Ocular TreatmentVan Phuc Nguyen, Athanasios J Karoukis, Wei Qian, et al.
Journal of Neuropathology and Experimental Neurology|June 11, 2010
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington diseaseMahesh Kandasamy, Sebastien Couillard-Despres, Kerstin A Raber, et al.
BMC Medical Genetics|October 21, 2018
Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in VietnamHoa Giang, Vu T Nguyen, Sinh D Nguyen, et al.
International Journal of Cancer|January 22, 2022
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patientsWanda M Gerding, Marco Tembrink, Verena Nilius-Eliliwi, et al.
Cells|June 19, 2019
Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington DiseaseLibo Yu-Taeger, Janice Stricker-Shaver, Katrin Arnold, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 13, 2010
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytesMarta Valenza, Valerio Leoni, Joanna M Karasinska, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2025
Evolved microbial diversity enables combinatoric biosensing in complex environmentsAlyssa Jasmine Chiang, Nicholas Csicsery, Richard O'Laughlin, et al.
Investigative Ophthalmology & Visual Science|July 2, 2026
Müller Glia-Exclusive CLRN1 Expression Drives Non-Cell-Autonomous Photoreceptor Degeneration in Usher Syndrome Type 3AYeachan Lee, Yuanyuan Gao, Van Phuc Nguyen, et al.
Pageof 49

Showing results (361-370 of 481) with videos related to

Sort By:
Pageof 49
Frontiers in Oncology|September 26, 2022
Broad genomic workup including optical genome mapping uncovers a <i>DDX3X</i>: <i>MLLT10</i> gene fusion in acute myeloid leukemiaVerena Nilius-Eliliwi, Marco Tembrink, Wanda Maria Gerding, et al.
European Journal of Neurology|January 11, 2024
Association of the neonatal Fc receptor promoter variable number of tandem repeat polymorphism with immunoglobulin response in patients with chronic inflammatory demyelinating polyneuropathyAnna Lena Fisse, Emelie Schäfer, Alina Hieke, et al.
ACS Nano|May 27, 2024
Multimodal Imaging-Guided Stem Cell Ocular TreatmentVan Phuc Nguyen, Athanasios J Karoukis, Wei Qian, et al.
Journal of Neuropathology and Experimental Neurology|June 11, 2010
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington diseaseMahesh Kandasamy, Sebastien Couillard-Despres, Kerstin A Raber, et al.
BMC Medical Genetics|October 21, 2018
Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in VietnamHoa Giang, Vu T Nguyen, Sinh D Nguyen, et al.
International Journal of Cancer|January 22, 2022
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patientsWanda M Gerding, Marco Tembrink, Verena Nilius-Eliliwi, et al.
Cells|June 19, 2019
Intranasal Administration of Mesenchymal Stem Cells Ameliorates the Abnormal Dopamine Transmission System and Inflammatory Reaction in the R6/2 Mouse Model of Huntington DiseaseLibo Yu-Taeger, Janice Stricker-Shaver, Katrin Arnold, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 13, 2010
Cholesterol defect is marked across multiple rodent models of Huntington's disease and is manifest in astrocytesMarta Valenza, Valerio Leoni, Joanna M Karasinska, et al.
Biorxiv : the Preprint Server for Biology|April 8, 2025
Evolved microbial diversity enables combinatoric biosensing in complex environmentsAlyssa Jasmine Chiang, Nicholas Csicsery, Richard O'Laughlin, et al.
Investigative Ophthalmology & Visual Science|July 2, 2026
Müller Glia-Exclusive CLRN1 Expression Drives Non-Cell-Autonomous Photoreceptor Degeneration in Usher Syndrome Type 3AYeachan Lee, Yuanyuan Gao, Van Phuc Nguyen, et al.
Pageof 49