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Flora Tassone

Showing results (21-30 of 348) with videos related to

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Rheumatology (Oxford, England)|September 20, 2011
Fibromyalgia in fragile X mental retardation 1 gene premutation carriersMaureen A Leehey, Wendi Legg, Flora Tassone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2010
Parkinsonism and cognitive decline in a fragile X mosaic maleDeborah Hall, Laura Pickler, Karen Riley, et al.
Journal of Human Genetics|June 7, 2013
Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptionsCarolyn M Yrigollen, Guadalupe Mendoza-Morales, Randi Hagerman, et al.
The Biochemical Journal|August 25, 2016
Plasma metabolic profile delineates roles for neurodegeneration, pro-inflammatory damage and mitochondrial dysfunction in the FMR1 premutationCecilia Giulivi, Eleonora Napoli, Flora Tassone, et al.
Human Molecular Genetics|October 2, 2003
The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporterLi-Sheng Chen, Flora Tassone, Parminder Sahota, et al.
Frontiers in Molecular Neuroscience|August 30, 2016
Plasma Biomarkers for Monitoring Brain Pathophysiology in FMR1 Premutation CarriersCecilia Giulivi, Eleonora Napoli, Flora Tassone, et al.
Plos One|August 6, 2011
The role of AGG interruptions in the transcription of FMR1 premutation allelesCarolyn M Yrigollen, Federica Tassone, Blythe Durbin-Johnson, et al.
Intractable & Rare Diseases Research|September 12, 2015
Anxiety disorders in fragile X premutation carriers: Preliminary characterization of probands and non-probandsLisa Cordeiro, Floridette Abucayan, Randi Hagerman, et al.
Frontiers in Psychology|June 25, 2014
The development of cognitive control in children with chromosome 22q11.2 deletion syndromeHeather M Shapiro, Flora Tassone, Nimrah S Choudhary, et al.
BMJ Case Reports|July 26, 2022
Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosomeNattaporn Tassanakijpanich, Rachel Wright, Flora Tassone, et al.
Pageof 35

Showing results (21-30 of 348) with videos related to

Sort By:
Pageof 35
Rheumatology (Oxford, England)|September 20, 2011
Fibromyalgia in fragile X mental retardation 1 gene premutation carriersMaureen A Leehey, Wendi Legg, Flora Tassone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 23, 2010
Parkinsonism and cognitive decline in a fragile X mosaic maleDeborah Hall, Laura Pickler, Karen Riley, et al.
Journal of Human Genetics|June 7, 2013
Transmission of an FMR1 premutation allele in a large family identified through newborn screening: the role of AGG interruptionsCarolyn M Yrigollen, Guadalupe Mendoza-Morales, Randi Hagerman, et al.
The Biochemical Journal|August 25, 2016
Plasma metabolic profile delineates roles for neurodegeneration, pro-inflammatory damage and mitochondrial dysfunction in the FMR1 premutationCecilia Giulivi, Eleonora Napoli, Flora Tassone, et al.
Human Molecular Genetics|October 2, 2003
The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporterLi-Sheng Chen, Flora Tassone, Parminder Sahota, et al.
Frontiers in Molecular Neuroscience|August 30, 2016
Plasma Biomarkers for Monitoring Brain Pathophysiology in FMR1 Premutation CarriersCecilia Giulivi, Eleonora Napoli, Flora Tassone, et al.
Plos One|August 6, 2011
The role of AGG interruptions in the transcription of FMR1 premutation allelesCarolyn M Yrigollen, Federica Tassone, Blythe Durbin-Johnson, et al.
Intractable & Rare Diseases Research|September 12, 2015
Anxiety disorders in fragile X premutation carriers: Preliminary characterization of probands and non-probandsLisa Cordeiro, Floridette Abucayan, Randi Hagerman, et al.
Frontiers in Psychology|June 25, 2014
The development of cognitive control in children with chromosome 22q11.2 deletion syndromeHeather M Shapiro, Flora Tassone, Nimrah S Choudhary, et al.
BMJ Case Reports|July 26, 2022
Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosomeNattaporn Tassanakijpanich, Rachel Wright, Flora Tassone, et al.
Pageof 35