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D Bird

Showing results (621-630 of 780) with videos related to

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Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Human Molecular Genetics|May 27, 2020
Ovotesticular disorders of sex development in FGF9 mouse models of human synostosis syndromesAnthony D Bird, Brittany M Croft, Masayo Harada, et al.
Acta Neuropathologica Communications|November 24, 2020
Adult onset pan-neuronal human tau tubulin kinase 1 expression causes severe cerebellar neurodegeneration in micePamela McMillan, Jeanna Wheeler, Rachel E Gatlin, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
The Journal of Physiology|August 19, 2025
The hyperaemic and metaboreflex response of the diaphragm during fatiguing diaphragmatic work in humansMegan L Lance, Christina D Bruce, Madison M Coyle, et al.
Neurology|May 29, 2001
Parkinson's disease, CYP2D6 polymorphism, and ageH Payami, N Lee, S Zareparsi, et al.
American Journal of Human Genetics|September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and femalesKen Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Pageof 78

Showing results (621-630 of 780) with videos related to

Sort By:
Pageof 78
Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Human Molecular Genetics|May 27, 2020
Ovotesticular disorders of sex development in FGF9 mouse models of human synostosis syndromesAnthony D Bird, Brittany M Croft, Masayo Harada, et al.
Acta Neuropathologica Communications|November 24, 2020
Adult onset pan-neuronal human tau tubulin kinase 1 expression causes severe cerebellar neurodegeneration in micePamela McMillan, Jeanna Wheeler, Rachel E Gatlin, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
The Journal of Physiology|August 19, 2025
The hyperaemic and metaboreflex response of the diaphragm during fatiguing diaphragmatic work in humansMegan L Lance, Christina D Bruce, Madison M Coyle, et al.
Neurology|May 29, 2001
Parkinson's disease, CYP2D6 polymorphism, and ageH Payami, N Lee, S Zareparsi, et al.
American Journal of Human Genetics|September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and femalesKen Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
Science (New York, N.Y.)|October 23, 1992
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14G D Schellenberg, T D Bird, E M Wijsman, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Pageof 78