Cargando…
Fragile X protein in newborn dried blood spots
BACKGROUND: The fragile X syndrome (FXS) results from mutation of the FMR1 gene that prevents expression of its gene product, FMRP. We previously characterized 215 dried blood spots (DBS) representing different FMR1 genotypes and ages with a Luminex-based immunoassay (qFMRP). We found variable FMRP...
Autores principales: | Adayev, Tatyana, LaFauci, Giuseppe, Dobkin, Carl, Caggana, Michele, Wiley, Veronica, Field, Michael, Wotton, Tiffany, Kascsak, Richard, Nolin, Sarah L, Glicksman, Anne, Hosmer, Nicole, Brown, W Ted |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412103/ https://www.ncbi.nlm.nih.gov/pubmed/25348928 http://dx.doi.org/10.1186/s12881-014-0119-0 |
Ejemplares similares
-
Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP)
por: LaFauci, Giuseppe, et al.
Publicado: (2016) -
Development of a Quantitative FMRP Assay for Mouse Tissue Applications
por: Adayev, Tatyana, et al.
Publicado: (2021) -
Optimization, validation and initial clinical implications of a Luminex-based immunoassay for the quantification of Fragile X Protein from dried blood spots
por: Boggs, Anna E., et al.
Publicado: (2022) -
Reduced vagal tone in women with the FMR1 premutation is associated with FMR1 mRNA but not depression or anxiety
por: Klusek, Jessica, et al.
Publicado: (2017) -
A Genotype-Phenotype Study of High-Resolution FMR1 Nucleic Acid and Protein Analyses in Fragile X Patients with Neurobehavioral Assessments
por: Budimirovic, Dejan B., et al.
Publicado: (2020)