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Matthew Harms

Showing results (21-30 of 38) with videos related to

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JAMA Neurology|April 17, 2013
C9orf72 hexanucleotide repeat expansions in clinical Alzheimer diseaseMatthew Harms, Bruno A Benitez, Nigel Cairns, et al.
Iscience|July 5, 2022
Lipoxins reduce obesity-induced adipose tissue inflammation in 3D-cultured human adipocytes and explant culturesMatúš Soták, Meenu Rohini Rajan, Madison Clark, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patientsBabi Ramesh Reddy Nallamilli, Samya Chakravorty, Akanchha Kesari, et al.
Journal of Neurology|June 24, 2015
Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1Alleene V Strickland, Maria Schabhüttl, Hans Offenbacher, et al.
Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|March 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|February 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 6, 2025
Toward therapeutic trials in primary lateral sclerosisErica Scirocco, Matti D Allen, Elisa Giacomelli, et al.
Neurology|October 4, 2019
Prospective natural history study of <i>C9orf72</i> ALS clinical characteristics and biomarkersAlexander J Cammack, Nazem Atassi, Theodore Hyman, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
JAMA Neurology|April 17, 2013
C9orf72 hexanucleotide repeat expansions in clinical Alzheimer diseaseMatthew Harms, Bruno A Benitez, Nigel Cairns, et al.
Iscience|July 5, 2022
Lipoxins reduce obesity-induced adipose tissue inflammation in 3D-cultured human adipocytes and explant culturesMatúš Soták, Meenu Rohini Rajan, Madison Clark, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patientsBabi Ramesh Reddy Nallamilli, Samya Chakravorty, Akanchha Kesari, et al.
Journal of Neurology|June 24, 2015
Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1Alleene V Strickland, Maria Schabhüttl, Hans Offenbacher, et al.
Nature Communications|October 11, 2018
A missense variant in SLC39A8 is associated with severe idiopathic scoliosisGabe Haller, Kevin McCall, Supak Jenkitkasemwong, et al.
American Journal of Human Genetics|December 22, 2020
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|March 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
American Journal of Human Genetics|February 5, 2021
Rare and de novo coding variants in chromodomain genes in Chiari I malformationBrooke Sadler, Jackson Wilborn, Lilian Antunes, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 6, 2025
Toward therapeutic trials in primary lateral sclerosisErica Scirocco, Matti D Allen, Elisa Giacomelli, et al.
Neurology|October 4, 2019
Prospective natural history study of <i>C9orf72</i> ALS clinical characteristics and biomarkersAlexander J Cammack, Nazem Atassi, Theodore Hyman, et al.
Pageof 4