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Hoa Huu Phuc Nguyen

Showing results (1-10 of 15) with videos related to

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Cells|March 27, 2024
Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological ChangesLibo Yu-Taeger, Ali El-Ayoubi, Pengfei Qi, et al.
Neuropharmacology|February 4, 2017
Dysregulation of gene expression in the striatum of BACHD rats expressing full-length mutant huntingtin and associated abnormalities on molecular and protein levelsLibo Yu-Taeger, Michael Bonin, Janice Stricker-Shaver, et al.
Genes|June 27, 2024
Optical Genome Mapping Reveals Disruption of the <i>RASGRF2</i> Gene in a Patient with Developmental Delay Carrying a De Novo Balanced Reciprocal TranslocationRosa Catalina Lederbogen, Sabine Hoffjan, Charlotte Thiels, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 8, 2026
Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse modelPengfei Qi, Libo Yu-Taeger, Hezhou Han, et al.
Genes|October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular DystrophyNatalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2020
Site-specific ubiquitination of pathogenic huntingtin attenuates its deleterious effectsVicky Hakim-Eshed, Ayub Boulos, Chen Cohen-Rosenzweig, et al.
International Journal of Molecular Sciences|April 27, 2024
AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse ModelAnna Niewiadomska-Cimicka, Lorraine Fievet, Magdalena Surdyka, et al.
Neurobiology of Disease|January 5, 2024
Loss-of-function of GNAL dystonia gene impairs striatal dopamine receptors-mediated adenylyl cyclase/ cyclic AMP signaling pathwayIlham El Atiallah, Giulia Ponterio, Maria Meringolo, et al.
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.
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.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Cells|March 27, 2024
Intravenous MSC-Treatment Improves Impaired Brain Functions in the R6/2 Mouse Model of Huntington's Disease via Recovered Hepatic Pathological ChangesLibo Yu-Taeger, Ali El-Ayoubi, Pengfei Qi, et al.
Neuropharmacology|February 4, 2017
Dysregulation of gene expression in the striatum of BACHD rats expressing full-length mutant huntingtin and associated abnormalities on molecular and protein levelsLibo Yu-Taeger, Michael Bonin, Janice Stricker-Shaver, et al.
Genes|June 27, 2024
Optical Genome Mapping Reveals Disruption of the <i>RASGRF2</i> Gene in a Patient with Developmental Delay Carrying a De Novo Balanced Reciprocal TranslocationRosa Catalina Lederbogen, Sabine Hoffjan, Charlotte Thiels, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 8, 2026
Prevention of ubiquitination at K6 and K9 in mutant huntingtin exacerbates disease pathology in a knock-in mouse modelPengfei Qi, Libo Yu-Taeger, Hezhou Han, et al.
Genes|October 27, 2022
Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular DystrophyNatalie Pluta, Sabine Hoffjan, Frederic Zimmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 18, 2020
Site-specific ubiquitination of pathogenic huntingtin attenuates its deleterious effectsVicky Hakim-Eshed, Ayub Boulos, Chen Cohen-Rosenzweig, et al.
International Journal of Molecular Sciences|April 27, 2024
AAV-Mediated CAG-Targeting Selectively Reduces Polyglutamine-Expanded Protein and Attenuates Disease Phenotypes in a Spinocerebellar Ataxia Mouse ModelAnna Niewiadomska-Cimicka, Lorraine Fievet, Magdalena Surdyka, et al.
Neurobiology of Disease|January 5, 2024
Loss-of-function of GNAL dystonia gene impairs striatal dopamine receptors-mediated adenylyl cyclase/ cyclic AMP signaling pathwayIlham El Atiallah, Giulia Ponterio, Maria Meringolo, et al.
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.
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.
Pageof 2