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Parasites & Vectors
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May 25, 2016
Molecular identification of different trypanosome species and subspecies in tsetse flies of northern Nigeria
Clement Isaac, Marc Ciosi, Alana Hamilton, et al.
Human Molecular Genetics
|
September 21, 2022
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease
Ainara Ruiz de Sabando, Edurne Urrutia Lafuente, Arkaitz Galbete, et al.
Brain : a Journal of Neurology
|
June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1
Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.
Journal of Huntington'S Disease
|
February 13, 2021
Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation
Marc Ciosi, Sarah A Cumming, Afroditi Chatzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 26, 2025
Cerebrospinal Fluid Proenkephalin Predicts Striatal Atrophy Decades before Clinical Motor Diagnosis in Huntington's Disease
Mena Farag, Michael J Murphy, Nicola Z Hobbs, 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.
Ebiomedicine
|
October 15, 2019
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes
Marc Ciosi, Alastair Maxwell, Sarah A Cumming, 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.
JAMA Ophthalmology
|
March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity
Siyin Liu, Amanda N Sadan, Nihar Bhattacharyya, 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.
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of 3
Search research articles
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Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Parasites & Vectors
|
May 25, 2016
Molecular identification of different trypanosome species and subspecies in tsetse flies of northern Nigeria
Clement Isaac, Marc Ciosi, Alana Hamilton, et al.
Human Molecular Genetics
|
September 21, 2022
Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease
Ainara Ruiz de Sabando, Edurne Urrutia Lafuente, Arkaitz Galbete, et al.
Brain : a Journal of Neurology
|
June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1
Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.
Journal of Huntington'S Disease
|
February 13, 2021
Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation
Marc Ciosi, Sarah A Cumming, Afroditi Chatzi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 26, 2025
Cerebrospinal Fluid Proenkephalin Predicts Striatal Atrophy Decades before Clinical Motor Diagnosis in Huntington's Disease
Mena Farag, Michael J Murphy, Nicola Z Hobbs, 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.
Ebiomedicine
|
October 15, 2019
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes
Marc Ciosi, Alastair Maxwell, Sarah A Cumming, 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.
JAMA Ophthalmology
|
March 13, 2025
Genetic and Demographic Determinants of Fuchs Endothelial Corneal Dystrophy Risk and Severity
Siyin Liu, Amanda N Sadan, Nihar Bhattacharyya, 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.
Page
of 3