(Q51735502)

11 April 2018

title

Differential expression of Fmr-1 mRNA and FMRP in female mice brain during aging. (English)

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11 April 2018

author name string

Kanchan Singh

series ordinal

1

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11 April 2018

S Prasad

series ordinal

2

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11 April 2018

publication date

27 September 2007

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11 April 2018

Molecular Biology Reports

published in

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11 April 2018

volume

35

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11 April 2018

issue

4

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11 April 2018

page(s)

677-684

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11 April 2018

https://scigraph.springernature.com/pub.10.1007/s11033-007-9140-0

exact match

0 references

cites work

The fragile X syndrome: exploring its molecular basis and seeking a treatment.

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https://api.crossref.org/works/10.1007%2FS11033-007-9140-0

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation

21 January 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS11033-007-9140-0

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain

21 January 2018

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12 December 2020

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Synaptic regulation of protein synthesis and the fragile X protein

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The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter

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Analysis of neocortex in three males with the fragile X syndrome

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Occupancy and synergistic activation of the FMR1 promoter by Nrf-1 and Sp1 in vivo

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FXTAS: a progressive neurologic syndrome associated with Fragile X premutation

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Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

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Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation

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Age- and region-specific imbalances of basal amino acids and monoamine metabolism in limbic regions of female Fmr1 knock-out mice

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Age-dependent and selective impairment of long-term potentiation in the anterior piriform cortex of mice lacking the fragile X mental retardation protein.

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A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture

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Identification of three distinct tumor suppressor loci on the short arm of chromosome 9 in small cell lung cancer

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Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

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The pathophysiology of fragile x syndrome.

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Functional genomics, fragile X syndrome, and RNA interference.

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FMRP mediates mGluR5-dependent translation of amyloid precursor protein

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A decade of molecular studies of fragile X syndrome

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Fragile x mental retardation (Fmr-1) gene expression is down regulated in brain of mice during aging

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12 December 2020

The fragile X mental retardation protein has nucleic acid chaperone properties

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12 December 2020

Interaction of the transcription factors USF1, USF2, and alpha -Pal/Nrf-1 with the FMR1 promoter. Implications for Fragile X mental retardation syndrome

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Dendritic spine structural anomalies in fragile-X mental retardation syndrome

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The DNA-binding efficiency of Sp1 is affected by redox changes

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12 December 2020

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

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12 December 2020

mRNPs, polysomes or granules: FMRP in neuronal protein synthesis

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12 December 2020

Sp1 and AP2 transcription factors are required for the human fragile mental retardation promoter activity in SK-N-SH neuronal cells

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12 December 2020

Elevated FMR1 mRNA in premutation carriers is due to increased transcription.

1 reference

12 December 2020

Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.

1 reference

12 December 2020

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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12 December 2020

A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability

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12 December 2020

The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development.

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12 December 2020

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

12 December 2020

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12 December 2020

10.1007/S11033-007-9140-0

Identifiers

DOI

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11 April 2018

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11 April 2018