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Jinhui Ding

Showing results (71-80 of 112) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's diseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's DiseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Neurobiology of Aging|August 9, 2014
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Cell Reports|August 1, 2019
Distinct Connectivity and Functionality of Aldehyde Dehydrogenase 1a1-Positive Nigrostriatal Dopaminergic Neurons in Motor LearningJunbing Wu, Justin Kung, Jie Dong, et al.
Neuron|January 13, 2010
Leucine-rich repeat kinase 2 regulates the progression of neuropathology induced by Parkinson's-disease-related mutant alpha-synucleinXian Lin, Loukia Parisiadou, Xing-Long Gu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 6, 2024
Intermediate <i>HTT</i> CAG repeats worsen disease severity in amyotrophic lateral sclerosisMaurizio Grassano, Antonio Canosa, Sandra D'Alfonso, et al.
Neurobiology of Aging|June 2, 2014
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 16, 2008
RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathwaysMarcel P van der Brug, Jeff Blackinton, Jayanth Chandran, et al.
Pageof 12

Showing results (71-80 of 112) with videos related to

Sort By:
Pageof 12
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's diseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's DiseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Neurobiology of Aging|August 9, 2014
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Cell Reports|August 1, 2019
Distinct Connectivity and Functionality of Aldehyde Dehydrogenase 1a1-Positive Nigrostriatal Dopaminergic Neurons in Motor LearningJunbing Wu, Justin Kung, Jie Dong, et al.
Neuron|January 13, 2010
Leucine-rich repeat kinase 2 regulates the progression of neuropathology induced by Parkinson's-disease-related mutant alpha-synucleinXian Lin, Loukia Parisiadou, Xing-Long Gu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 6, 2024
Intermediate <i>HTT</i> CAG repeats worsen disease severity in amyotrophic lateral sclerosisMaurizio Grassano, Antonio Canosa, Sandra D'Alfonso, et al.
Neurobiology of Aging|June 2, 2014
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
Neurobiology of Disease|June 18, 2016
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodiesJoshua T Geiger, Jinhui Ding, Barbara Crain, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 16, 2008
RNA binding activity of the recessive parkinsonism protein DJ-1 supports involvement in multiple cellular pathwaysMarcel P van der Brug, Jeff Blackinton, Jayanth Chandran, et al.
Pageof 12