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S Brooks

Showing results (591-600 of 728) with videos related to

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Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|May 24, 2011
Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking AnalysisRebecca A Dragovic, Christopher Gardiner, Alexandra S Brooks, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresiaErwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
BMC Neurology|August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
Physical Review Letters|March 5, 2009
Chemical pressure induced spin freezing phase transition in kagome pr langasitesH D Zhou, C R Wiebe, Y-J Jo, et al.
Neurology|June 20, 2020
Longitudinal changes of brain microstructure and function in nonconcussed female rugby playersKathryn Y Manning, Jeffrey S Brooks, James P Dickey, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 13, 2015
Neuropathologic assessment of participants in two multi-center longitudinal observational studies: the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)Nigel J Cairns, Richard J Perrin, Erin E Franklin, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomaliesMax Krall, Stephanie Htun, Rhonda E Schnur, et al.
The Journal of Biological Chemistry|December 21, 2002
Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophyJohn B J Kwok, Glenda M Halliday, William S Brooks, et al.
Pageof 73

Showing results (591-600 of 728) with videos related to

Sort By:
Pageof 73
Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine|May 24, 2011
Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking AnalysisRebecca A Dragovic, Christopher Gardiner, Alexandra S Brooks, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
European Journal of Human Genetics : EJHG|January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresiaErwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
BMC Neurology|August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
Physical Review Letters|March 5, 2009
Chemical pressure induced spin freezing phase transition in kagome pr langasitesH D Zhou, C R Wiebe, Y-J Jo, et al.
Neurology|June 20, 2020
Longitudinal changes of brain microstructure and function in nonconcussed female rugby playersKathryn Y Manning, Jeffrey S Brooks, James P Dickey, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 13, 2015
Neuropathologic assessment of participants in two multi-center longitudinal observational studies: the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)Nigel J Cairns, Richard J Perrin, Erin E Franklin, et al.
European Journal of Human Genetics : EJHG|January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomaliesMax Krall, Stephanie Htun, Rhonda E Schnur, et al.
The Journal of Biological Chemistry|December 21, 2002
Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophyJohn B J Kwok, Glenda M Halliday, William S Brooks, et al.
Pageof 73