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Thomas D Bird

Showing results (121-130 of 190) with videos related to

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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.
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.
American Journal of Human Genetics|June 4, 2016
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9LDong-Hui Chen, Jennifer E Below, Akiko Shimamura, et al.
The EMBO Journal|August 16, 2012
Upregulated function of mitochondria-associated ER membranes in Alzheimer diseaseEstela Area-Gomez, Maria Del Carmen Lara Castillo, Marc D Tambini, et al.
The American Journal of Pathology|October 17, 2009
Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondriaEstela Area-Gomez, Ad J C de Groof, Istvan Boldogh, et al.
American Journal of Human Genetics|March 20, 2003
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxiaDong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|October 11, 2024
Hereditary spastic paraplegia with thin corpus callosum and SPG11 mutation: A neuropathological evaluationKathryn P Scherpelz, Rebecca A Yoda, Suman Jayadev, et al.
Nature Structural & Molecular Biology|March 5, 2025
Tau filaments with the Alzheimer fold in human MAPT mutants V337M and R406WChao Qi, Sofia Lövestam, Alexey G Murzin, et al.
Pageof 19

Showing results (121-130 of 190) with videos related to

Sort By:
Pageof 19
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.
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.
American Journal of Human Genetics|June 4, 2016
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9LDong-Hui Chen, Jennifer E Below, Akiko Shimamura, et al.
The EMBO Journal|August 16, 2012
Upregulated function of mitochondria-associated ER membranes in Alzheimer diseaseEstela Area-Gomez, Maria Del Carmen Lara Castillo, Marc D Tambini, et al.
The American Journal of Pathology|October 17, 2009
Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondriaEstela Area-Gomez, Ad J C de Groof, Istvan Boldogh, et al.
American Journal of Human Genetics|March 20, 2003
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxiaDong-Hui Chen, Zoran Brkanac, Christophe L M J Verlinde, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|October 11, 2024
Hereditary spastic paraplegia with thin corpus callosum and SPG11 mutation: A neuropathological evaluationKathryn P Scherpelz, Rebecca A Yoda, Suman Jayadev, et al.
Nature Structural & Molecular Biology|March 5, 2025
Tau filaments with the Alzheimer fold in human MAPT mutants V337M and R406WChao Qi, Sofia Lövestam, Alexey G Murzin, et al.
Pageof 19