Projects per year
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- 8 Similar Profiles
Fragile X Syndrome
Medicine & Life Sciences
Intellectual Disability
Medicine & Life Sciences
Tremor
Medicine & Life Sciences
Alleles
Medicine & Life Sciences
Genes
Medicine & Life Sciences
RNA
Medicine & Life Sciences
Messenger RNA
Medicine & Life Sciences
Fragile X Mental Retardation Protein
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects 1980 2019
Epigenetic regulation of the FMR1 gene
Hagerman, P. J., Tassone, F. & Chedin, F. L.
9/21/15 → 5/31/19
Project: Research project › Research Project
Epigenomics
Methylation
Gene Silencing
Double-Stranded DNA Breaks
Genes
Human iPSC neuronal models for early and late phases of FXTAS neurodegeneration
9/30/09 → 8/31/11
Project: Research project › NIH Challenge Grants and Partnerships Program
Induced Pluripotent Stem Cells
Intellectual Disability
Alleles
Fibroblasts
Gait Ataxia
Development of targeted therapeutic agents for the treatment of FXTAS (2 of 6)
9/30/07 → 6/30/12
Project: Research project › Linked Research project Grant
RNA
Small Interfering RNA
Oligonucleotides
Astrocytes
Glutamic Acid
Neuro Therapeutics Research Institute
9/15/07 → 6/30/12
Project: Research project › Linked Specialized Center Cooperative Agreement
Neuro Therapeutics Research Institute (1 of 6)
9/15/07 → 6/30/12
Project: Research project › Linked Specialized Center Cooperative Agreement
Therapeutic Human Experimentation
Ataxia
Research
Neurodegenerative Diseases
Research Personnel
Research Output 1969 2017
Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome
Robin, G., López, J. R., Espinal, G. M., Hulsizer, S., Hagerman, P. J. & Pessah, I. N., Jul 15 2017, In : Human Molecular Genetics. 26, 14, p. 2649-2666 18 p.Research output: Contribution to journal › Article
DNA Damage
Calcium
Brain
Dantrolene
Intranuclear Inclusion Bodies
Clinical and molecular correlates in fragile X premutation females
Jiraanont, P., Sweha, S. R., AlOlaby, R. R., Silva, M., Tang, H. T., Durbin-Johnson, B., Schneider, A., Espinal, G. M., Hagerman, P. J., Rivera, S. M., Hessl, D. R., Hagerman, R. J., Chutabhakdikul, N. & Tassone, F., Jun 1 2017, In : eNeurologicalSci. 7, p. 49-56 8 p.Research output: Contribution to journal › Article
Phenotype
Anxiety
Executive Function
Depression
Messenger RNA
Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: Report of two cases
Lechpammer, M., Martinez-Cerdeno, V., Hunsaker, M. R., Hah, M., Gonzales, H., Tisch, S., Joffe, R., Pamphlett, R., Tassone, F., Hagerman, P. J., Bolitho, S. J. & Hagerman, R. J., Aug 1 2017, In : Croatian Medical Journal. 58, 4, p. 310-315 6 p.Research output: Contribution to journal › Article
Inclusion Body Myositis
Fragile X Syndrome
Fatal Outcome
Tremor
Ataxia
Fragile X syndrome
Hagerman, R. J., Berry-Kravis, E., Hazlett, H. C., Bailey, D. B., Moine, H., Kooy, R. F., Tassone, F., Gantois, I., Sonenberg, N., Mandel, J. L. & Hagerman, P. J., Sep 29 2017, In : Nature reviews. Disease primers. 3, 1 p.Research output: Contribution to journal › Review article
Fragile X Mental Retardation Protein
Fragile X Syndrome
Trinucleotide Repeats
Language Development
Neuronal Plasticity
Iron accumulation and dysregulation in the putamen in fragile X-associated tremor/ataxia syndrome
Ariza, J., Rogers, H., Hartvigsen, A., Snell, M., Dill, M., Judd, D., Hagerman, P. J. & Martinez-Cerdeno, V., 2017, (Accepted/In press) In : Movement Disorders.Research output: Contribution to journal › Article
Putamen
Iron
Ceruloplasmin
Iron-Binding Proteins
Transferrin