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Soraya Bardien

Showing results (1-10 of 103) with videos related to

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DNA and Cell Biology|November 28, 2018
Underappreciated Roles of the Translocase of the Outer and Inner Mitochondrial Membrane Protein Complexes in Human DiseaseThea Heinemeyer, Monique Stemmet, Soraya Bardien, et al.
Parkinsonism & Related Disorders|June 7, 2011
Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's diseaseSoraya Bardien, Suzanne Lesage, Alexis Brice, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 21, 2013
Screening of two indel polymorphisms in the 5'UTR of the DJ-1 gene in South African Parkinson's disease patientsBrigitte Glanzmann, Debbie Lombard, Jonathan Carr, et al.
Neurobiology of Aging|January 31, 2021
Can the interplay between autophagy and apoptosis be targeted as a novel therapy for Parkinson's disease?Minke Bekker, Shameemah Abrahams, Ben Loos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2011
An investigation into LOXL1 variants in black South African individuals with exfoliation syndromeRobyn M Rautenbach, Soraya Bardien, Justin Harvey, et al.
Neurobiology of Aging|October 2, 2013
EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South AfricaJanine Blanckenberg, Claudia Ntsapi, Jonathan A Carr, et al.
Open Biology|October 5, 2021
Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disordersKatelyn Cuttler, Maryam Hassan, Jonathan Carr, et al.
Frontiers in Bioengineering and Biotechnology|March 27, 2025
Mitochondria targeted nanoparticles for the treatment of mitochondrial dysfunction-associated brain disordersAmy Claire Buck, Gerald J Maarman, Admire Dube, et al.
Neuroscience Letters|March 23, 2016
Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patientsCelia van der Merwe, Jonathan Carr, Brigitte Glanzmann, et al.
Frontiers in Genetics|March 18, 2022
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s DiseaseNikita Simone Pillay, Owen A Ross, Alan Christoffels, et al.
Pageof 11

Showing results (1-10 of 103) with videos related to

Sort By:
Pageof 11
DNA and Cell Biology|November 28, 2018
Underappreciated Roles of the Translocase of the Outer and Inner Mitochondrial Membrane Protein Complexes in Human DiseaseThea Heinemeyer, Monique Stemmet, Soraya Bardien, et al.
Parkinsonism & Related Disorders|June 7, 2011
Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's diseaseSoraya Bardien, Suzanne Lesage, Alexis Brice, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 21, 2013
Screening of two indel polymorphisms in the 5'UTR of the DJ-1 gene in South African Parkinson's disease patientsBrigitte Glanzmann, Debbie Lombard, Jonathan Carr, et al.
Neurobiology of Aging|January 31, 2021
Can the interplay between autophagy and apoptosis be targeted as a novel therapy for Parkinson's disease?Minke Bekker, Shameemah Abrahams, Ben Loos, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2011
An investigation into LOXL1 variants in black South African individuals with exfoliation syndromeRobyn M Rautenbach, Soraya Bardien, Justin Harvey, et al.
Neurobiology of Aging|October 2, 2013
EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South AfricaJanine Blanckenberg, Claudia Ntsapi, Jonathan A Carr, et al.
Open Biology|October 5, 2021
Emerging evidence implicating a role for neurexins in neurodegenerative and neuropsychiatric disordersKatelyn Cuttler, Maryam Hassan, Jonathan Carr, et al.
Frontiers in Bioengineering and Biotechnology|March 27, 2025
Mitochondria targeted nanoparticles for the treatment of mitochondrial dysfunction-associated brain disordersAmy Claire Buck, Gerald J Maarman, Admire Dube, et al.
Neuroscience Letters|March 23, 2016
Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patientsCelia van der Merwe, Jonathan Carr, Brigitte Glanzmann, et al.
Frontiers in Genetics|March 18, 2022
Current Status of Next-Generation Sequencing Approaches for Candidate Gene Discovery in Familial Parkinson´s DiseaseNikita Simone Pillay, Owen A Ross, Alan Christoffels, et al.
Pageof 11