Add to ORKGFragile X Syndrome (FXS), the most common cause of inherited mental retardation and autism, is caused by transcriptional silencing of Fmr1, which encodes the translational repressor protein FMRP. FMRP and CPEB, an activator of translation, are present in neuronal dendrites, are Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research
textabstractThe FMR1 gene, located on the X chromosome, harbours a CGG-trinucleotide repeat in a DNA...
The Fragile X syndrome (FXS) is the most frequent form of inherited mental retardation and also cons...
The final product of FMR1 gene transcription, Fragile X Mental Retardation Protein 1 (FMRP), is an R...
Fragile X syndrome (FXS), the most common cause of inherited mental retardation and autism, is cause...
Fragile X syndrome, an X-linked dominant disorder with reduced penetrance, is associated with intell...
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans and perhaps t...
Fragile X syndrome (FXS) is the leading genetic cause of autism. Mutations in Fmr1 (fragile X mental...
Fragile X syndrome (FXS) is caused by inactivation of FMR1 gene and loss of its encoded product the ...
Abstract Fragile X syndrome (FXS) is caused by an expanded CGG repeat (>200 repeats) in the 5 ′ u...
Fragile X syndrome (FXS) is caused by an expanded CGG repeat (>200 repeats) in the 5' un-translat...
Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism. The F...
International audienceThe Fragile X Mental Retardation Protein (FMRP) is an RNA-binding protein esse...
The Fragile X syndrome (FXS) is a leading cause of intellectual disability (ID) and autism. The dise...
FMRP loss of function causes Fragile X syndrome (FXS) and autistic features. FMRP is a polyribosome-...
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gen...
textabstractThe FMR1 gene, located on the X chromosome, harbours a CGG-trinucleotide repeat in a DNA...
The Fragile X syndrome (FXS) is the most frequent form of inherited mental retardation and also cons...
The final product of FMR1 gene transcription, Fragile X Mental Retardation Protein 1 (FMRP), is an R...
Fragile X syndrome (FXS), the most common cause of inherited mental retardation and autism, is cause...
Fragile X syndrome, an X-linked dominant disorder with reduced penetrance, is associated with intell...
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans and perhaps t...
Fragile X syndrome (FXS) is the leading genetic cause of autism. Mutations in Fmr1 (fragile X mental...
Fragile X syndrome (FXS) is caused by inactivation of FMR1 gene and loss of its encoded product the ...
Abstract Fragile X syndrome (FXS) is caused by an expanded CGG repeat (>200 repeats) in the 5 ′ u...
Fragile X syndrome (FXS) is caused by an expanded CGG repeat (>200 repeats) in the 5' un-translat...
Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism. The F...
International audienceThe Fragile X Mental Retardation Protein (FMRP) is an RNA-binding protein esse...
The Fragile X syndrome (FXS) is a leading cause of intellectual disability (ID) and autism. The dise...
FMRP loss of function causes Fragile X syndrome (FXS) and autistic features. FMRP is a polyribosome-...
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gen...
textabstractThe FMR1 gene, located on the X chromosome, harbours a CGG-trinucleotide repeat in a DNA...
The Fragile X syndrome (FXS) is the most frequent form of inherited mental retardation and also cons...
The final product of FMR1 gene transcription, Fragile X Mental Retardation Protein 1 (FMRP), is an R...