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Thomas D Bird

Showing results (61-70 of 190) 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|March 25, 2010
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 familiesElizabeth E Marchani, Thomas D Bird, Ellen J Steinbart, et al.
Archives of Neurology|September 13, 2006
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer diseaseKiri L Brickell, Ellen J Steinbart, Malia Rumbaugh, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 29, 2013
Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onsetWei Zhao, Elizabeth E Marchani, Charles Y K Cheung, et al.
Plos Genetics|December 14, 2019
Genome wide analysis reveals heparan sulfate epimerase modulates TDP-43 proteinopathyNicole F Liachko, Aleen D Saxton, Pamela J McMillan, et al.
Neurobiology of Disease|May 29, 2024
Evidence of mutant huntingtin and tau-related pathology within neuronal grafts in Huntington's disease casesShireen Salem, Mitchell D Kilgore, Mehwish Anwer, et al.
Muscle & Nerve|December 14, 2017
An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical featuresDong-Hui Chen, Maxwell Ma, Mena Scavina, et al.
American Journal of Human Genetics|May 5, 2009
IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23Zoran Brkanac, David Spencer, Jay Shendure, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2025
Presence of Alzheimer's disease variants in circular RNA of <i>PSEN1</i> and <i>PSEN2</i>Ian P Johnson, Tia M Peterson, Kathryn Gudsnuk, et al.
Brain : a Journal of Neurology|January 16, 2024
TREM2 variants that cause early dementia and increase Alzheimer's disease risk affect gene splicingKostantin Kiianitsa, Maria E Lukes, Brian J Hayes, et al.
Pageof 19

Showing results (61-70 of 190) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 25, 2010
Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 familiesElizabeth E Marchani, Thomas D Bird, Ellen J Steinbart, et al.
Archives of Neurology|September 13, 2006
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer diseaseKiri L Brickell, Ellen J Steinbart, Malia Rumbaugh, et al.
Archives of Neurology|December 17, 2003
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gammaIchiro Yabe, Hidenao Sasaki, Dong-Hui Chen, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 29, 2013
Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onsetWei Zhao, Elizabeth E Marchani, Charles Y K Cheung, et al.
Plos Genetics|December 14, 2019
Genome wide analysis reveals heparan sulfate epimerase modulates TDP-43 proteinopathyNicole F Liachko, Aleen D Saxton, Pamela J McMillan, et al.
Neurobiology of Disease|May 29, 2024
Evidence of mutant huntingtin and tau-related pathology within neuronal grafts in Huntington's disease casesShireen Salem, Mitchell D Kilgore, Mehwish Anwer, et al.
Muscle & Nerve|December 14, 2017
An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical featuresDong-Hui Chen, Maxwell Ma, Mena Scavina, et al.
American Journal of Human Genetics|May 5, 2009
IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23Zoran Brkanac, David Spencer, Jay Shendure, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2025
Presence of Alzheimer's disease variants in circular RNA of <i>PSEN1</i> and <i>PSEN2</i>Ian P Johnson, Tia M Peterson, Kathryn Gudsnuk, et al.
Brain : a Journal of Neurology|January 16, 2024
TREM2 variants that cause early dementia and increase Alzheimer's disease risk affect gene splicingKostantin Kiianitsa, Maria E Lukes, Brian J Hayes, et al.
Pageof 19