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Showing results (471-480 of 480) with videos related to

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Plos Genetics|September 20, 2008
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisNicola J Rutherford, Yong-Jie Zhang, Matt Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2003
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic interventionBrian P Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
High-throughput mouse knockouts provide a functional analysis of the genomeC J Friddle, A Abuin, R Ramirez-Solis, et al.
Acta Neuropathologica|January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementiaMarka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Molecular Neurodegeneration|July 6, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypesCristina T Vicente, Tejasvi Niranjan, Elise Coopman, et al.
Nature Communications|June 17, 2015
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyNaomi Kouri, Owen A Ross, Beth Dombroski, et al.
The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
BMC Biology|February 6, 2025
Same data, different analysts: variation in effect sizes due to analytical decisions in ecology and evolutionary biologyElliot Gould, Hannah S Fraser, Timothy H Parker, et al.
Pageof 48

Showing results (471-480 of 480) with videos related to

Sort By:
Pageof 48
You have reached the last page of results.This site can display upto 480 results.
Plos Genetics|September 20, 2008
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosisNicola J Rutherford, Yong-Jie Zhang, Matt Baker, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 12, 2003
Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic interventionBrian P Zambrowicz, Alejandro Abuin, Ramiro Ramirez-Solis, et al.
Nature Communications|July 1, 2016
Prosaposin is a regulator of progranulin levels and oligomerizationAlexandra M Nicholson, NiCole A Finch, Marcio Almeida, et al.
Cold Spring Harbor Symposia on Quantitative Biology|September 2, 2004
High-throughput mouse knockouts provide a functional analysis of the genomeC J Friddle, A Abuin, R Ramirez-Solis, et al.
Acta Neuropathologica|January 4, 2014
TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementiaMarka van Blitterswijk, Bianca Mullen, Alexandra M Nicholson, et al.
Acta Neuropathologica|August 10, 2025
Brain transcriptomics highlight abundant gene expression and splicing alterations in non-neuronal cells in aFTLD-USara Alidadiani, Júlia Faura, Sarah Wynants, et al.
Molecular Neurodegeneration|July 6, 2025
Methylome analysis of FTLD patients with TDP-43 pathology identifies epigenetic signatures specific to pathological subtypesCristina T Vicente, Tejasvi Niranjan, Elise Coopman, et al.
Nature Communications|June 17, 2015
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsyNaomi Kouri, Owen A Ross, Beth Dombroski, et al.
The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
BMC Biology|February 6, 2025
Same data, different analysts: variation in effect sizes due to analytical decisions in ecology and evolutionary biologyElliot Gould, Hannah S Fraser, Timothy H Parker, et al.
Pageof 48