Projects per year
Fingerprint Dive into the research topics where Paul J Hagerman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 9 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
- 12 Finished
Epigenetic regulation of the FMR1 gene
Hagerman, P. J., Tassone, F., Chedin, F. L., Chedin, F. & Tassone, F.
9/21/15 → 5/31/19
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
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
RNA
Small Interfering RNA
Oligonucleotides
Astrocytes
Glutamic Acid
Therapeutic Human Experimentation
Ataxia
Research
Neurodegenerative Diseases
Research Personnel
Research Output 1969 2019
1
Citation
(Scopus)
Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome
Ma, L., Herren, A. W., Espinal, G., Randol, J., McLaughlin, B., Martinez-Cerdeño, V., Pessah, I. N., Hagerman, R. J. & Hagerman, P. J., Sep 3 2019, In : Acta neuropathologica communications. 7, 1, 1 p.Research output: Contribution to journal › Article
Open Access
Intranuclear Inclusion Bodies
Peptides
Small Ubiquitin-Related Modifier Proteins
Flow Cytometry
Proteins
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
1
Citation
(Scopus)
Microglial cell activation and senescence are characteristic of the pathology FXTAS
Martinez-Cerdeno, 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
13
Citations
(Scopus)
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