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
Messenger RNA
Medicine & Life Sciences
Fragile X Mental Retardation Protein
Medicine & Life Sciences
RNA
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 (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
Neuro Therapeutics Research Institute
9/15/07 → 6/30/12
Project: Research project › Linked Specialized Center Cooperative Agreement
Research Output 1969 2018
Autism phenotype in fragile X premutation males is not associated with FMR1 expression: A preliminary evaluation
Sumekar, T. A., Winarni, T. I., Mu, Y., Chonchaiya, W., Tassone, F., Iwahashi, C., Cheung, K., Faradz, S. M. H., Hagerman, P. J., Nguyen, D. V. & Hagerman, R. J., May 1 2018, In : Hiroshima Journal of Medical Sciences. 67, p. 166-173 8 p.Research output: Contribution to journal › Article
Autistic Disorder
Phenotype
Messenger RNA
Proteins
Communication
Fragile X syndrome and connective tissue dysregulation
Ramírez-Cheyne, J. A., Duque, G. A., Ayala-Zapata, S., Saldarriaga-Gil, W., Hagerman, P. J., Hagerman, R. J. & Payán-Gómez, C., Jan 1 2018, (Accepted/In press) In : Clinical Genetics.Research output: Contribution to journal › Article
Fragile X Syndrome
Connective Tissue
Extracellular Matrix
Fragile X Mental Retardation Protein
Urogenital System
Microglial cell activation and senescence are characteristic of the pathology FXTAS
Martínez Cerdeño, V., Hong, T., Amina, S., Lechpammer, M., Ariza, J., Tassone, F., Noctor, S. C., Hagerman, P. J. & Hagerman, R. J., Dec 1 2018, In : Movement Disorders. 33, 12, p. 1887-1894 8 p.Research output: Contribution to journal › Article
Cell Aging
Pathology
Fragile X Tremor Ataxia Syndrome
Iron
Intranuclear Inclusion Bodies
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