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Christos Proukakis

Showing results (31-40 of 64) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2022
CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy-like PhenotypeRamita Dewan, Zane Jaunmuktane, Monica Emili Garcia-Segura, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 23, 2014
Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutationsChristos Proukakis, Maryiam Shoaee, James Morris, et al.
Molecular Genetics & Genomic Medicine|January 15, 2019
Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinIONMelissa Leija-Salazar, Fritz J Sedlazeck, Marco Toffoli, et al.
Brain : a Journal of Neurology|June 13, 2014
Visual short-term memory deficits associated with GBA mutation and Parkinson's diseaseNahid Zokaei, Alisdair McNeill, Christos Proukakis, et al.
Communications Biology|October 9, 2024
Single-cell somatic copy number variants in brain using different amplification methods and reference genomesEster Kalef-Ezra, Zeliha Gozde Turan, Diego Perez-Rodriguez, et al.
Biorxiv : the Preprint Server for Biology|August 23, 2023
Single-cell somatic copy number variants in brain using different amplification methods and reference genomesEster Kalef-Ezra, Zeliha Gozde Turan, Diego Perez-Rodriguez, et al.
Plos One|July 7, 2017
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimationElizabeth Nacheva, Katya Mokretar, Aynur Soenmez, et al.
Brain : a Journal of Neurology|June 20, 2018
Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brainsKatya Mokretar, Daniel Pease, Jan-Willem Taanman, et al.
Acta Neuropathologica|February 14, 2013
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Aoife P Kiely, Yasmine T Asi, Eleanna Kara, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2022
CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy-like PhenotypeRamita Dewan, Zane Jaunmuktane, Monica Emili Garcia-Segura, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 23, 2014
Analysis of Parkinson's disease brain-derived DNA for alpha-synuclein coding somatic mutationsChristos Proukakis, Maryiam Shoaee, James Morris, et al.
Molecular Genetics & Genomic Medicine|January 15, 2019
Evaluation of the detection of GBA missense mutations and other variants using the Oxford Nanopore MinIONMelissa Leija-Salazar, Fritz J Sedlazeck, Marco Toffoli, et al.
Brain : a Journal of Neurology|June 13, 2014
Visual short-term memory deficits associated with GBA mutation and Parkinson's diseaseNahid Zokaei, Alisdair McNeill, Christos Proukakis, et al.
Communications Biology|October 9, 2024
Single-cell somatic copy number variants in brain using different amplification methods and reference genomesEster Kalef-Ezra, Zeliha Gozde Turan, Diego Perez-Rodriguez, et al.
Biorxiv : the Preprint Server for Biology|August 23, 2023
Single-cell somatic copy number variants in brain using different amplification methods and reference genomesEster Kalef-Ezra, Zeliha Gozde Turan, Diego Perez-Rodriguez, et al.
Plos One|July 7, 2017
DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimationElizabeth Nacheva, Katya Mokretar, Aynur Soenmez, et al.
Brain : a Journal of Neurology|June 20, 2018
Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brainsKatya Mokretar, Daniel Pease, Jan-Willem Taanman, et al.
Acta Neuropathologica|February 14, 2013
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?Aoife P Kiely, Yasmine T Asi, Eleanna Kara, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Single cell long read whole genome sequencing reveals somatic transposon activity in human brainMichal B Izydorczyk, Ester Kalef-Ezra, Dominic W Horner, et al.
Pageof 7