Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation. (Q35317411)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21783174%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation (English)

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8 February 2020

3

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8 February 2020

Kami Koldewyn

4

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8 February 2020

8

Flora Tassone

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8 February 2020

9

Paul J Hagerman

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8 February 2020

1

David Hessl

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8 February 2020

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Susan M Rivera

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8 February 2020

author name string

John M Wang

2

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8 February 2020

Lien Le

5

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8 February 2020

Christine Iwahashi

6

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8 February 2020

Katherine Cheung

7

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8 February 2020

language of work or name

English

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publication date

23 July 2011

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8 February 2020

published in

Biological Psychiatry

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8 February 2020

volume

70

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8 February 2020

issue

9

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8 February 2020

page(s)

859-865

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Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning

8 February 2020

cites work

1 reference

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Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers

12 July 2018

1 reference

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A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndrome

12 July 2018

1 reference

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Fragile X syndrome -- from genes to cognition

12 July 2018

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Examination of FMR1 transcript and protein levels among 74 premutation carriers

12 July 2018

1 reference

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12 July 2018

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Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population

12 July 2018

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A quantitative ELISA assay for the fragile x mental retardation 1 protein

12 July 2018

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A review of fragile X premutation disorders: expanding the psychiatric perspective

12 July 2018

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Aberrant brain activation during gaze processing in boys with fragile X syndrome

12 July 2018

1 reference

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A rapid polymerase chain reaction-based screening method for identification of all expanded alleles of the fragile X (FMR1) gene in newborn and high-risk populations.

12 July 2018

1 reference

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Correction of fragile X syndrome in mice.

12 July 2018

1 reference

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

12 July 2018

1 reference

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Therapeutic implications of the mGluR theory of fragile X mental retardation

12 July 2018

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A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity

12 July 2018

1 reference

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Intergenerational transmission of subthreshold autistic traits in the general population

12 July 2018

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A study of the distributional characteristics of FMR1 transcript levels in 238 individuals

12 July 2018

1 reference

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The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter

12 July 2018

1 reference

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Serotonin transporter genetic variation and the response of the human amygdala

12 July 2018

1 reference

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Thresholding of statistical maps in functional neuroimaging using the false discovery rate

12 July 2018

1 reference

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Automated Anatomical Labeling of Activations in SPM Using a Macroscopic Anatomical Parcellation of the MNI MRI Single-Subject Brain

12 July 2018

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Premature ovarian failure in the fragile X syndrome

12 July 2018

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Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

12 July 2018

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A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

12 July 2018

1 reference

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

12 July 2018

1 reference

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Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

12 July 2018

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Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

12 July 2018

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Mood and anxiety disorders in females with the FMR1 premutation

12 July 2018

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Fragile X-associated tremor/ataxia syndrome--an older face of the fragile X gene

26 September 2018

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Amygdala dysfunction in men with the fragile X premutation.

26 September 2018

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Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

26 September 2018

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

26 September 2018

1 reference

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Variation of human amygdala response during threatening stimuli as a function of 5'HTTLPR genotype and personality style

26 September 2018

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Autistic spectrum disorder and the fragile X premutation.

26 September 2018

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The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.

26 September 2018

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The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages.

26 September 2018

1 reference

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Clinical features of boys with fragile X premutations and intermediate alleles.

26 September 2018

1 reference

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Image distortion correction in EPI: comparison of field mapping with point spread function mapping

26 September 2018

1 reference

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Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

26 September 2018

1 reference

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The biomedical imaging resource at Mayo Clinic.

26 September 2018

1 reference

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Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3191264

Interactive display and analysis of 3-D medical images

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21783174

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Analyze: a comprehensive, operator-interactive software package for multidimensional medical image display and analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21783174

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.BIOPSYCH.2011.05.033

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21783174%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21783174%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

PubMed publication ID

21783174

1 reference