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Methods in Molecular Biology (Clifton, N.J.)
|
June 2, 2018
Methods for Assessing DNA Repair and Repeat Expansion in Huntington's Disease
Thomas Massey, Branduff McAllister, Lesley Jones
Scientific Reports
|
November 22, 2023
Mutant huntingtin confers cell-autonomous phenotypes on Huntington's disease iPSC-derived microglia
Nina Stöberl, Jasmine Donaldson, Caroline S Binda, et al.
Neurology
|
March 26, 2021
Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
Branduff McAllister, James F Gusella, G Bernhard Landwehrmeyer, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
TRACE: Open-Source Software for Quantifying Somatic Variation of Tandem Repeats by Capillary Electrophoresis
Andrew Jiang, Kevin Correia, Tammy Gillis, et al.
Journal of Huntington'S Disease
|
May 8, 2026
TRACE: Open-source software for quantifying somatic variation of tandem repeats by capillary electrophoresis
Andrew Jiang, Kevin Correia, Tammy Gillis, et al.
Journal of Huntington'S Disease
|
June 28, 2021
Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease
Eun Pyo Hong, Michael J Chao, Thomas Massey, et al.
NPJ Genomic Medicine
|
September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2024
Posttranscriptional regulation of <i>FAN1</i> by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease
Kyung-Hee Kim, Eun Pyo Hong, Yukyeong Lee, et al.
Brain Communications
|
March 7, 2024
Modification of Huntington's disease by short tandem repeats
Eun Pyo Hong, Eliana Marisa Ramos, N Ahmad Aziz, et al.
NAR Genomics and Bioinformatics
|
December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing
Alysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
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Search research articles
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
Methods in Molecular Biology (Clifton, N.J.)
|
June 2, 2018
Methods for Assessing DNA Repair and Repeat Expansion in Huntington's Disease
Thomas Massey, Branduff McAllister, Lesley Jones
Scientific Reports
|
November 22, 2023
Mutant huntingtin confers cell-autonomous phenotypes on Huntington's disease iPSC-derived microglia
Nina Stöberl, Jasmine Donaldson, Caroline S Binda, et al.
Neurology
|
March 26, 2021
Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
Branduff McAllister, James F Gusella, G Bernhard Landwehrmeyer, et al.
Biorxiv : the Preprint Server for Biology
|
February 6, 2026
TRACE: Open-Source Software for Quantifying Somatic Variation of Tandem Repeats by Capillary Electrophoresis
Andrew Jiang, Kevin Correia, Tammy Gillis, et al.
Journal of Huntington'S Disease
|
May 8, 2026
TRACE: Open-source software for quantifying somatic variation of tandem repeats by capillary electrophoresis
Andrew Jiang, Kevin Correia, Tammy Gillis, et al.
Journal of Huntington'S Disease
|
June 28, 2021
Association Analysis of Chromosome X to Identify Genetic Modifiers of Huntington's Disease
Eun Pyo Hong, Michael J Chao, Thomas Massey, et al.
NPJ Genomic Medicine
|
September 6, 2022
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
Sergey V Lobanov, Branduff McAllister, Mia McDade-Kumar, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2024
Posttranscriptional regulation of <i>FAN1</i> by miR-124-3p at rs3512 underlies onset-delaying genetic modification in Huntington's disease
Kyung-Hee Kim, Eun Pyo Hong, Yukyeong Lee, et al.
Brain Communications
|
March 7, 2024
Modification of Huntington's disease by short tandem repeats
Eun Pyo Hong, Eliana Marisa Ramos, N Ahmad Aziz, et al.
NAR Genomics and Bioinformatics
|
December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencing
Alysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Page
of 2