Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Veikko Vuokila"'
1
Akademický článek
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette’s syndrome
Autor: Calwing Liao, Veikko Vuokila, Hélène Catoire, Fulya Akçimen, Jay P. Ross, Cynthia V. Bourassa, Patrick A. Dion, Inge A. Meijer, Guy A. Rouleau
Publikováno v: Communications Biology, Vol 5, Iss 1, Pp 1-6 (2022)
Calwing Liao and Veikko Vuokila et al. report a transcriptome-wide association study (TWAS) of Tourette’s Syndrome. They find increased expression of FLT3 in the dorsolateral prefrontal cortex and the lymphoblastoid cell lines in patients with Tour
Externí odkaz: https://doaj.org/article/c55de6f7799640e488bf9c601ff989c6
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2
Akademický článek
Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor
Autor: Calwing Liao, Faezeh Sarayloo, Veikko Vuokila, Daniel Rochefort, Fulya Akçimen, Simone Diamond, Gabrielle Houle, Alexandre D. Laporte, Dan Spiegelman, Qin He, Hélène Catoire, Patrick A. Dion, Guy A. Rouleau
Publikováno v: Frontiers in Genetics, Vol 11 (2020)
Objective: Essential tremor (ET) is a common movement disorder that has a high heritability. A number of genetic studies have associated different genes and loci with ET, but few have investigated the biology of any of these genes. STK32B was signifi
Externí odkaz: https://doaj.org/article/1b7dca9c79064eee9686d420cea20d75
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3
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome
Autor: Calwing Liao, Veikko Vuokila, Hélène Catoire, Fulya Akçimen, Jay P. Ross, Cynthia V. Bourassa, Patrick A. Dion, Inge A. Meijer, Guy A. Rouleau
Publikováno v: Communications biology. 5(1)
Tourette’s Syndrome (TS) is a neurodevelopmental disorder that is characterized by motor and phonic tics. A recent TS genome-wide association study (GWAS) identified a genome-wide significant locus. However, determining the biological mechanism of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6efde8ec92f9a63480fecc0a377dc935
https://pubmed.ncbi.nlm.nih.gov/35354918
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4
Increased expression of genetically-regulatedFLT3implicated in Tourette’s Syndrome
Autor: Veikko Vuokila, Patrick A. Dion, Inge A. Meijer, Calwing Liao, Hélène Catoire, Guy A. Rouleau, Cynthia V. Bourassa, Jay P. Ross, Fulya Akçimen
Tourette’s Syndrome (TS) is a neurodevelopmental disorder that is characterized by motor and phonic tics. A recent TS genome-wide association study (GWAS) identified a genome-wide significant locus. However, determining the biological mechanism of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a44d08cc288ed343d00469a1fe7bfb0
https://doi.org/10.1101/812420
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5
Akademický článek
Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.
Autor: Liao, Calwing1,2 (AUTHOR), Vuokila, Veikko2 (AUTHOR), Catoire, Hélène2 (AUTHOR), Akçimen, Fulya1,2 (AUTHOR), Ross, Jay P.1,2 (AUTHOR), Bourassa, Cynthia V.2 (AUTHOR), Dion, Patrick A.2,3 (AUTHOR), Meijer, Inge A.4 (AUTHOR), Rouleau, Guy A.1,2,3 (AUTHOR) guy.rouleau@mcgill.ca
Publikováno v: Communications Biology. 3/30/2022, Vol. 5 Issue 1, p1-6. 6p.
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