Results 131 to 140 of about 13,308 (213)

A cultura na FMRP-USP

open access: yesMedicina (Ribeirão Preto), 2002
Maria Alice Nunes Coelho   +1 more
openaire   +3 more sources

Contribution of astrocytic calcium signaling to auditory hypersensitivity in a mouse model of fragile X syndrome. [PDF]

open access: yesNeurobiol Dis
Bergdolt L   +12 more
europepmc   +1 more source

Lampbrush Chromosomes and Fragile X Mental Retardation Protein, FMRP

open access: yes, 2009
Fragile X Syndrome is the most common form of inherited mental retardation, occurring in 1/4000 males and 1/8000 females. This syndrome is caused by the lack of expression of the Fragile X mental retardation protein, or FMRP.
Miri Kim (2113432)
core  

Large-scale analysis of FMR1 CGG repeat length and risk of premature ovarian insufficiency in over 92 000 women. [PDF]

open access: yesHum Reprod
Morbey EJ   +7 more
europepmc   +1 more source

Circular RNA <i>circHomer1</i> mediates hippocampal functions via ribonucleoprotein granule transport and dendritic targeting of synaptic RNAs. [PDF]

open access: yesSci Adv
Cai Y   +15 more
europepmc   +1 more source

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