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Anna Richardson

Showing results (21-30 of 54) with videos related to

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Neurobiology of Aging|January 25, 2011
Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosisSara Rollinson, Simon Mead, Julie Snowden, et al.
Genome Biology|April 19, 2003
Haplotypic analysis of the TNF locus by association efficiency and entropyHans Ackerman, Stanley Usen, Richard Mott, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 17, 2015
Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutationsJulie S Snowden, Jennifer Adams, Jennifer Harris, et al.
Practical Neurology|July 26, 2024
Time Shelter by <i>Georgi Gospodinov</i>Christopher Hutchcroft, Daniel Whittam, Stephanie Azzopardi, et al.
Plos One|January 1, 2009
Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populationsSusana Campino, Julian Forton, Srilakshmi Raj, et al.
Neurobiology of Aging|December 2, 2014
Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degenerationLinda Gibbons, Sara Rollinson, Jennifer C Thompson, et al.
Neurobiology of Aging|December 1, 2014
p62/SQSTM1 analysis in frontotemporal lobar degenerationLouise Miller, Sara Rollinson, Janis Bennion Callister, et al.
Acta Neuropathologica|January 19, 2011
Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathologyAyoub Dakson, Osamu Yokota, Margaret Esiri, et al.
Creative Nursing|September 3, 2024
Collaborative International Nursing Writing Group: A Nonpatriarchal ApproachSandy Richardson, Louisa Krueger, Anna Richardson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutationStuart Pickering-Brown, Matt Baker, Thomas Bird, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Neurobiology of Aging|January 25, 2011
Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosisSara Rollinson, Simon Mead, Julie Snowden, et al.
Genome Biology|April 19, 2003
Haplotypic analysis of the TNF locus by association efficiency and entropyHans Ackerman, Stanley Usen, Richard Mott, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 17, 2015
Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutationsJulie S Snowden, Jennifer Adams, Jennifer Harris, et al.
Practical Neurology|July 26, 2024
Time Shelter by <i>Georgi Gospodinov</i>Christopher Hutchcroft, Daniel Whittam, Stephanie Azzopardi, et al.
Plos One|January 1, 2009
Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populationsSusana Campino, Julian Forton, Srilakshmi Raj, et al.
Neurobiology of Aging|December 2, 2014
Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degenerationLinda Gibbons, Sara Rollinson, Jennifer C Thompson, et al.
Neurobiology of Aging|December 1, 2014
p62/SQSTM1 analysis in frontotemporal lobar degenerationLouise Miller, Sara Rollinson, Janis Bennion Callister, et al.
Acta Neuropathologica|January 19, 2011
Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathologyAyoub Dakson, Osamu Yokota, Margaret Esiri, et al.
Creative Nursing|September 3, 2024
Collaborative International Nursing Writing Group: A Nonpatriarchal ApproachSandy Richardson, Louisa Krueger, Anna Richardson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutationStuart Pickering-Brown, Matt Baker, Thomas Bird, et al.
Pageof 6