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Anna Richardson

Showing results (31-40 of 54) with videos related to

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Human Genetics|November 29, 2008
A genetic association study in the Gambia using tagging polymorphisms in the major histocompatibility complex class III region implicates a HLA-B associated transcript 2 polymorphism in severe malaria susceptibilityMahamadou Diakite, Taane G Clark, Sarah Auburn, et al.
Acta Neuropathologica Communications|July 2, 2017
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar DegenerationYvonne S Davidson, Andrew C Robinson, Louis Flood, et al.
Acta Neuropathologica|May 18, 2018
Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's diseaseDavid M A Mann, Yvonne S Davidson, Andrew C Robinson, et al.
Malaria Journal|March 17, 2009
TLR9 polymorphisms in African populations: no association with severe malaria, but evidence of cis-variants acting on gene expressionSusana Campino, Julian Forton, Sarah Auburn, et al.
Neurobiology of Aging|March 14, 2012
Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's diseaseSara Rollinson, Nicola Halliwell, Kate Young, et al.
Acta Neuropathologica Communications|April 23, 2017
Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 geneYvonne S Davidson, Louis Flood, Andrew C Robinson, et al.
Plos One|April 14, 2010
Further evidence supporting a role for gs signal transduction in severe malaria pathogenesisSarah Auburn, Andrew E Fry, Taane G Clark, et al.
Intensive & Critical Care Nursing|June 12, 2021
Intensive care nurse-family engagement from a global perspective: A qualitative multi-site explorationRahel Naef, Petra Brysiewicz, Natalie S Mc Andrew, et al.
Acta Neuropathologica|March 23, 2011
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS geneJulie S Snowden, Quan Hu, Sara Rollinson, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibilityTaane G Clark, Andrew E Fry, Sarah Auburn, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Human Genetics|November 29, 2008
A genetic association study in the Gambia using tagging polymorphisms in the major histocompatibility complex class III region implicates a HLA-B associated transcript 2 polymorphism in severe malaria susceptibilityMahamadou Diakite, Taane G Clark, Sarah Auburn, et al.
Acta Neuropathologica Communications|July 2, 2017
Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar DegenerationYvonne S Davidson, Andrew C Robinson, Louis Flood, et al.
Acta Neuropathologica|May 18, 2018
Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's diseaseDavid M A Mann, Yvonne S Davidson, Andrew C Robinson, et al.
Malaria Journal|March 17, 2009
TLR9 polymorphisms in African populations: no association with severe malaria, but evidence of cis-variants acting on gene expressionSusana Campino, Julian Forton, Sarah Auburn, et al.
Neurobiology of Aging|March 14, 2012
Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's diseaseSara Rollinson, Nicola Halliwell, Kate Young, et al.
Acta Neuropathologica Communications|April 23, 2017
Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 geneYvonne S Davidson, Louis Flood, Andrew C Robinson, et al.
Plos One|April 14, 2010
Further evidence supporting a role for gs signal transduction in severe malaria pathogenesisSarah Auburn, Andrew E Fry, Taane G Clark, et al.
Intensive & Critical Care Nursing|June 12, 2021
Intensive care nurse-family engagement from a global perspective: A qualitative multi-site explorationRahel Naef, Petra Brysiewicz, Natalie S Mc Andrew, et al.
Acta Neuropathologica|March 23, 2011
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS geneJulie S Snowden, Quan Hu, Sara Rollinson, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibilityTaane G Clark, Andrew E Fry, Sarah Auburn, et al.
Pageof 6