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Flora Tassone

Showing results (181-190 of 348) with videos related to

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Human Molecular Genetics|October 22, 2005
Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cellsDolores Garcia Arocena, Christine K Iwahashi, Nelly Won, et al.
Brain & Development|March 1, 2017
Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndromeReem Rafik AlOlaby, Stefan R Sweha, Marisol Silva, et al.
Neurobiology of Disease|February 4, 2026
The apolipoprotein gene: A modulating role on brain volume and cognitive function in carriers of the fragile X premutationPoonnada Jiraanont, Jun Yi Wang, Blythe Durbin-Johnson, et al.
Frontiers in Genetics|September 11, 2018
Curvilinear Association Between Language Disfluency and Jessica Klusek, Anna Porter, Leonard Abbeduto, et al.
Neurobiology of Disease|May 21, 2026
Corrigendum to "The apolipoprotein gene: a modulating role on brain volume and cognitive function in carriers of the fragile X premutation" [Neurobiology of Disease 2026 Feb 2; 220:107292, Page 1-13]Poonnada Jiraanont, Jun Yi Wang, Blythe Durbin-Johnson, et al.
Nucleic Acids Research|April 12, 2011
Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation allelesFlora Tassone, Silvia De Rubeis, Chiara Carosi, et al.
Epidemiology (Cambridge, Mass.)|May 26, 2011
Prenatal vitamins, one-carbon metabolism gene variants, and risk for autismRebecca J Schmidt, Robin L Hansen, Jaana Hartiala, et al.
Brain and Cognition|February 8, 2011
Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairmentsNaomi J Goodrich-Hunsaker, Ling M Wong, Yingratana McLennan, et al.
Movement Disorders Clinical Practice|May 7, 2020
Parkinsonism Versus Concomitant Parkinson's Disease in Fragile X-Associated Tremor/Ataxia SyndromeMaría Jimena Salcedo-Arellano, Marisol Wendy Wolf-Ochoa, Tiffany Hong, et al.
Early Human Development|June 16, 2015
Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE StudyRebecca J Schmidt, Robin L Hansen, Jaana Hartiala, et al.
Pageof 35

Showing results (181-190 of 348) with videos related to

Sort By:
Pageof 35
Human Molecular Genetics|October 22, 2005
Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cellsDolores Garcia Arocena, Christine K Iwahashi, Nelly Won, et al.
Brain & Development|March 1, 2017
Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndromeReem Rafik AlOlaby, Stefan R Sweha, Marisol Silva, et al.
Neurobiology of Disease|February 4, 2026
The apolipoprotein gene: A modulating role on brain volume and cognitive function in carriers of the fragile X premutationPoonnada Jiraanont, Jun Yi Wang, Blythe Durbin-Johnson, et al.
Frontiers in Genetics|September 11, 2018
Curvilinear Association Between Language Disfluency and Jessica Klusek, Anna Porter, Leonard Abbeduto, et al.
Neurobiology of Disease|May 21, 2026
Corrigendum to "The apolipoprotein gene: a modulating role on brain volume and cognitive function in carriers of the fragile X premutation" [Neurobiology of Disease 2026 Feb 2; 220:107292, Page 1-13]Poonnada Jiraanont, Jun Yi Wang, Blythe Durbin-Johnson, et al.
Nucleic Acids Research|April 12, 2011
Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation allelesFlora Tassone, Silvia De Rubeis, Chiara Carosi, et al.
Epidemiology (Cambridge, Mass.)|May 26, 2011
Prenatal vitamins, one-carbon metabolism gene variants, and risk for autismRebecca J Schmidt, Robin L Hansen, Jaana Hartiala, et al.
Brain and Cognition|February 8, 2011
Young adult female fragile X premutation carriers show age- and genetically-modulated cognitive impairmentsNaomi J Goodrich-Hunsaker, Ling M Wong, Yingratana McLennan, et al.
Movement Disorders Clinical Practice|May 7, 2020
Parkinsonism Versus Concomitant Parkinson's Disease in Fragile X-Associated Tremor/Ataxia SyndromeMaría Jimena Salcedo-Arellano, Marisol Wendy Wolf-Ochoa, Tiffany Hong, et al.
Early Human Development|June 16, 2015
Selected vitamin D metabolic gene variants and risk for autism spectrum disorder in the CHARGE StudyRebecca J Schmidt, Robin L Hansen, Jaana Hartiala, et al.
Pageof 35