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Lesley Jones

Showing results (71-80 of 138) with videos related to

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Brain Research. Molecular Brain Research|January 18, 2003
Insoluble TATA-binding protein accumulation in Huntington's disease cortexWilleke M C van Roon-Mom, Suzanne J Reid, A Lesley Jones, et al.
Pharmacogenetics and Genomics|January 21, 2006
A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's diseaseDenise Harold, Stuart Macgregor, Cathryn E Patterson, et al.
Palliative Medicine|May 2, 2023
'It's tough. It is hard': A qualitative interview study of staff and volunteers caring for hospice in-patients with deliriumImogen Featherstone, Najma Siddiqi, Lesley Jones, et al.
International Journal of Audiology|September 28, 2011
Hearing help-seeking and rehabilitation: perspectives of adults with hearing impairmentAriane Laplante-Lévesque, Line V Knudsen, Jill E Preminger, et al.
Plos One|April 6, 2013
Time's up. descriptive epidemiology of multi-morbidity and time spent on health related activity by older Australians: a time use surveyTanisha Jowsey, Ian S McRae, Jose M Valderas, et al.
Brain : a Journal of Neurology|June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.
Plos Genetics|April 24, 2007
Conservation of regional gene expression in mouse and human brainAndrew D Strand, Aaron K Aragaki, Zachary C Baquet, et al.
PLOS Global Public Health|September 21, 2023
Views and experiences of opioid access amongst palliative care providers and public representatives in a low-resource setting: A qualitative interview studyJoseph Clark, Naveen Salins, Sunitha Daniel, et al.
BMC Genomics|December 23, 2015
Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalenceZubeyde Bayram-Weston, Timothy C Stone, Peter Giles, et al.
Human Molecular Genetics|October 26, 2018
FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeatRobert Goold, Michael Flower, Davina Hensman Moss, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
Brain Research. Molecular Brain Research|January 18, 2003
Insoluble TATA-binding protein accumulation in Huntington's disease cortexWilleke M C van Roon-Mom, Suzanne J Reid, A Lesley Jones, et al.
Pharmacogenetics and Genomics|January 21, 2006
A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's diseaseDenise Harold, Stuart Macgregor, Cathryn E Patterson, et al.
Palliative Medicine|May 2, 2023
'It's tough. It is hard': A qualitative interview study of staff and volunteers caring for hospice in-patients with deliriumImogen Featherstone, Najma Siddiqi, Lesley Jones, et al.
International Journal of Audiology|September 28, 2011
Hearing help-seeking and rehabilitation: perspectives of adults with hearing impairmentAriane Laplante-Lévesque, Line V Knudsen, Jill E Preminger, et al.
Plos One|April 6, 2013
Time's up. descriptive epidemiology of multi-morbidity and time spent on health related activity by older Australians: a time use surveyTanisha Jowsey, Ian S McRae, Jose M Valderas, et al.
Brain : a Journal of Neurology|June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.
Plos Genetics|April 24, 2007
Conservation of regional gene expression in mouse and human brainAndrew D Strand, Aaron K Aragaki, Zachary C Baquet, et al.
PLOS Global Public Health|September 21, 2023
Views and experiences of opioid access amongst palliative care providers and public representatives in a low-resource setting: A qualitative interview studyJoseph Clark, Naveen Salins, Sunitha Daniel, et al.
BMC Genomics|December 23, 2015
Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalenceZubeyde Bayram-Weston, Timothy C Stone, Peter Giles, et al.
Human Molecular Genetics|October 26, 2018
FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeatRobert Goold, Michael Flower, Davina Hensman Moss, et al.
Pageof 14