The fragile X syndrome results from transcriptional silencing of the FMR1 gene and the absence of its encoded FMRP protein. Two autosomal homologues of the FMR1 gene, FXR1 and FXR2, have been identified and the overall structures of the corresponding proteins are very similar to that of FMRP. Using antibodies raised against FXR1P, we observed that two major protein isoforms of relative MW of 78 and 70 kDa are expressed in different mammalian cell lines and in the majority of mouse tissues. In mammalian cells grown in culture as well as in brain extracts, both P78 and P70 isoforms are associated with mRNPs within translating poly-ribosomes, similarly to their closely related FMRP homologues. In muscle tissues as well as in murine myoblastic ...
THE fragile X syndrome is the most frequent form of inherited mental retardation after Down's syndro...
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism ...
Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism. The F...
The Fragile X Mental Retardation-Related 1 (FXR1) gene belongs to the Fragile X Related family, that...
The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (Fmr1), like many transc...
The final product of FMR1 gene transcription, Fragile X Mental Retardation Protein 1 (FMRP), is an R...
AbstractFragile X syndrome results from the absence of the RNA binding FMR protein. Here, mRNA was c...
Fragile X syndrome, the most frequent form of inherited mental retardation, is due to the absence of...
textabstractThe absence of fragile-X mental-retardation protein (FMRP) results in fragile-...
<div><p>The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (<i>Fmr1</i>), l...
The loss of FMR1 expression due to trinucleotide repeat expansion leads to fragile X syndrome, a cau...
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gen...
The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (Fmr1), like many transc...
Expansion of the CGG trinucleotide repeat in the 5′-untranslated region of the FMR1, fragile X menta...
textabstractLack of expression of the fragile X mental retardation protein (FMRP) results in m...
THE fragile X syndrome is the most frequent form of inherited mental retardation after Down's syndro...
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism ...
Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism. The F...
The Fragile X Mental Retardation-Related 1 (FXR1) gene belongs to the Fragile X Related family, that...
The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (Fmr1), like many transc...
The final product of FMR1 gene transcription, Fragile X Mental Retardation Protein 1 (FMRP), is an R...
AbstractFragile X syndrome results from the absence of the RNA binding FMR protein. Here, mRNA was c...
Fragile X syndrome, the most frequent form of inherited mental retardation, is due to the absence of...
textabstractThe absence of fragile-X mental-retardation protein (FMRP) results in fragile-...
<div><p>The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (<i>Fmr1</i>), l...
The loss of FMR1 expression due to trinucleotide repeat expansion leads to fragile X syndrome, a cau...
Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation 1 gen...
The primary transcript of the mammalian Fragile X Mental Retardation-1 gene (Fmr1), like many transc...
Expansion of the CGG trinucleotide repeat in the 5′-untranslated region of the FMR1, fragile X menta...
textabstractLack of expression of the fragile X mental retardation protein (FMRP) results in m...
THE fragile X syndrome is the most frequent form of inherited mental retardation after Down's syndro...
Fragile X syndrome (FXS) is a multi-organ disease that leads to mental retardation, macro-orchidism ...
Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism. The F...