Health inequalities by gradients of access to water and sanitation between countries in the Americas, 1990 and 2010
Mújica, Oscar J.; Haeberer, Mariana; Teague, Jordan; Santos-Burgoa, Carlos; Galvão, Luiz Augusto Cassanha.
Rev Panam Salud Publica
; 38(5): 347-354, Nov. 2015. ilus, tab
Artigo em Inglês | LILACS | ID: lil-772129
Dysregulation and restoration of translational homeostasis in fragile X syndrome.
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex.
The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells.
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case report.
FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism.
Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).
Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies.
Gender and cell-type-specific effects of the transcription-coupled repair protein, ERCC6/CSB, on repeat expansion in a mouse model of the fragile X-related disorders.
CGG allele size somatic mosaicism and methylation in FMR1 premutation alleles.