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Nancy Johnson

Showing results (51-60 of 58) with videos related to

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Acta Neuropathologica|October 14, 2009
Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degenerationPenelope G Foulds, Yvonne Davidson, Manjari Mishra, et al.
The ISME Journal|June 10, 2018
Microbial island biogeography: isolation shapes the life history characteristics but not diversity of root-symbiotic fungal communitiesJohn Davison, Mari Moora, Maarja Öpik, et al.
Archives of Neurology|October 15, 2008
Association of GSK3B with Alzheimer disease and frontotemporal dementiaBarbara A J Schaffer, Lars Bertram, Bruce L Miller, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humansTrygve E Bakken, J Cooper Roddey, Srdjan Djurovic, et al.
Geroscience|January 31, 2025
Dynamic proportional loss of functional connectivity revealed change of left superior frontal gyrus in subjective cognitive decline: an explanatory study based on Chinese and Western cohortsLuyao Wang, Wenjing Hu, Fan Dong, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Acta Neuropathologica|October 14, 2009
Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degenerationPenelope G Foulds, Yvonne Davidson, Manjari Mishra, et al.
The ISME Journal|June 10, 2018
Microbial island biogeography: isolation shapes the life history characteristics but not diversity of root-symbiotic fungal communitiesJohn Davison, Mari Moora, Maarja Öpik, et al.
Archives of Neurology|October 15, 2008
Association of GSK3B with Alzheimer disease and frontotemporal dementiaBarbara A J Schaffer, Lars Bertram, Bruce L Miller, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Nature Genetics|April 5, 2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's diseaseAdam C Naj, Gyungah Jun, Gary W Beecham, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 21, 2012
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humansTrygve E Bakken, J Cooper Roddey, Srdjan Djurovic, et al.
Geroscience|January 31, 2025
Dynamic proportional loss of functional connectivity revealed change of left superior frontal gyrus in subjective cognitive decline: an explanatory study based on Chinese and Western cohortsLuyao Wang, Wenjing Hu, Fan Dong, et al.
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