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International Journal of Molecular Sciences
|
March 27, 2025
Premutation Females with preFXTAS
Valentina Liani, Carme Torrents, Elisa Rolleri, et al.
Journal of Human Genetics
|
January 31, 2018
Genetic cluster of fragile X syndrome in a Colombian district
Wilmar Saldarriaga, Jose Vicente Forero-Forero, Laura Yuriko González-Teshima, et al.
Eneurologicalsci
|
October 4, 2017
Clinical and molecular correlates in fragile X premutation females
Poonnada Jiraanont, Stefan R Sweha, Reem R AlOlaby, et al.
Brain : a Journal of Neurology
|
October 16, 2004
The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy
Caroline J Moore, Eileen M Daly, Flora Tassone, et al.
Cell Reports
|
March 13, 2013
Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome
Chantal Sellier, Fernande Freyermuth, Ricardos Tabet, et al.
Neuron
|
July 17, 2015
Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome
Emanuela Pasciuto, Tariq Ahmed, Tina Wahle, et al.
Human Molecular Genetics
|
April 18, 2003
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
Rob Willemsen, Marianne Hoogeveen-Westerveld, Surya Reis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 24, 2021
Cerebral Microbleeds in Fragile X-Associated Tremor/Ataxia Syndrome
María Jimena Salcedo-Arellano, Jun Yi Wang, Yingratana A McLennan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 29, 2016
Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons
Ricardos Tabet, Enora Moutin, Jérôme A J Becker, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles
Sarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Page
of 35
Search research articles
Search
Showing results (301-310 of 348) with videos related to
Sort By:
Page
of 35
International Journal of Molecular Sciences
|
March 27, 2025
Premutation Females with preFXTAS
Valentina Liani, Carme Torrents, Elisa Rolleri, et al.
Journal of Human Genetics
|
January 31, 2018
Genetic cluster of fragile X syndrome in a Colombian district
Wilmar Saldarriaga, Jose Vicente Forero-Forero, Laura Yuriko González-Teshima, et al.
Eneurologicalsci
|
October 4, 2017
Clinical and molecular correlates in fragile X premutation females
Poonnada Jiraanont, Stefan R Sweha, Reem R AlOlaby, et al.
Brain : a Journal of Neurology
|
October 16, 2004
The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy
Caroline J Moore, Eileen M Daly, Flora Tassone, et al.
Cell Reports
|
March 13, 2013
Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome
Chantal Sellier, Fernande Freyermuth, Ricardos Tabet, et al.
Neuron
|
July 17, 2015
Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome
Emanuela Pasciuto, Tariq Ahmed, Tina Wahle, et al.
Human Molecular Genetics
|
April 18, 2003
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
Rob Willemsen, Marianne Hoogeveen-Westerveld, Surya Reis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 24, 2021
Cerebral Microbleeds in Fragile X-Associated Tremor/Ataxia Syndrome
María Jimena Salcedo-Arellano, Jun Yi Wang, Yingratana A McLennan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 29, 2016
Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons
Ricardos Tabet, Enora Moutin, Jérôme A J Becker, et al.
American Journal of Medical Genetics. Part A
|
February 28, 2013
Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles
Sarah L Nolin, Sachin Sah, Anne Glicksman, et al.
Page
of 35