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D Bird

Showing results (671-680 of 780) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 13, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 26, 2021
Severity of central sleep apnea does not affect sleeping oxygen saturation during ascent to high altitudeJordan D Bird, Anne Kalker, Alexander N Rimke, et al.
Archives of Neurology|March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disordersIgnacio F Mata, Ali Samii, Seth H Schneer, et al.
Annals of Neurology|February 24, 2001
Quantitative neuropathological changes in presymptomatic Huntington's diseaseE Gómez-Tortosa, M E MacDonald, J C Friend, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Aβ and tau prions feature in the neuropathogenesis of Down syndromeCarlo Condello, Alison M Maxwell, Erika Castillo, et al.
Journal of Geriatric Psychiatry and Neurology|March 19, 2003
Familial dementia with Lewy bodies with an atypical clinical presentationLauren T Bonner, Debby W Tsuang, Monique M Cherrier, et al.
Human Mutation|August 2, 2018
Mutant NR5A1/SF-1 in patients with disorders of sex development shows defective activation of the SOX9 TESCO enhancerRajini Sreenivasan, Louisa Ludbrook, Brett Fisher, et al.
Plos Genetics|December 5, 2014
The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43Nicole F Liachko, Pamela J McMillan, Timothy J Strovas, et al.
Human Molecular Genetics|July 2, 2009
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolatesWeiva Sieh, Yoonha Choi, Nicola H Chapman, et al.
Neurology. Genetics|March 27, 2020
Heterozygous <i>STUB1</i> missense variants cause ataxia, cognitive decline, and STUB1 mislocalizationDong-Hui Chen, Caitlin Latimer, Mayumi Yagi, et al.
Pageof 78

Showing results (671-680 of 780) with videos related to

Sort By:
Pageof 78
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 13, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|August 26, 2021
Severity of central sleep apnea does not affect sleeping oxygen saturation during ascent to high altitudeJordan D Bird, Anne Kalker, Alexander N Rimke, et al.
Archives of Neurology|March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disordersIgnacio F Mata, Ali Samii, Seth H Schneer, et al.
Annals of Neurology|February 24, 2001
Quantitative neuropathological changes in presymptomatic Huntington's diseaseE Gómez-Tortosa, M E MacDonald, J C Friend, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Aβ and tau prions feature in the neuropathogenesis of Down syndromeCarlo Condello, Alison M Maxwell, Erika Castillo, et al.
Journal of Geriatric Psychiatry and Neurology|March 19, 2003
Familial dementia with Lewy bodies with an atypical clinical presentationLauren T Bonner, Debby W Tsuang, Monique M Cherrier, et al.
Human Mutation|August 2, 2018
Mutant NR5A1/SF-1 in patients with disorders of sex development shows defective activation of the SOX9 TESCO enhancerRajini Sreenivasan, Louisa Ludbrook, Brett Fisher, et al.
Plos Genetics|December 5, 2014
The tau tubulin kinases TTBK1/2 promote accumulation of pathological TDP-43Nicole F Liachko, Pamela J McMillan, Timothy J Strovas, et al.
Human Molecular Genetics|July 2, 2009
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolatesWeiva Sieh, Yoonha Choi, Nicola H Chapman, et al.
Neurology. Genetics|March 27, 2020
Heterozygous <i>STUB1</i> missense variants cause ataxia, cognitive decline, and STUB1 mislocalizationDong-Hui Chen, Caitlin Latimer, Mayumi Yagi, et al.
Pageof 78