Neurodevelopmental effects of the FMR-1 full mutation in humans. (Q52019051)

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21 October 2019

title

Neurodevelopmental effects of the FMR-1 full mutation in humans (English)

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21 October 2019

4

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21 October 2019

author name string

A L Reiss

1

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21 October 2019

M T Abrams

2

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21 October 2019

R Greenlaw

3

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21 October 2019

M B Denckla

5

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21 October 2019

language of work or name

English

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publication date

1 February 1995

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21 October 2019

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21 October 2019

volume

1

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21 October 2019

issue

2

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21 October 2019

page(s)

159-167

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Neuropsychological dimensions of the fragile X syndrome: support for a non-dominant hemisphere dysfunction hypothesis

21 October 2019

cites work

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Neuroanatomy of fragile X syndrome: the temporal lobe

21 January 2018

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Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

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Frontal-subcortical circuits and human behavior

21 January 2018

1 reference

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The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

21 January 2018

1 reference

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KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism

21 January 2018

1 reference

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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

21 January 2018

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Programmed cell death: implications for neuropsychiatric disorders

21 January 2018

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Mechanisms and Functions of Cell Death

21 January 2018

1 reference

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C. elegans cell survival gene ced-9 encodes a functional homolog of the mammalian proto-oncogene bcl-2.

21 January 2018

1 reference

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Lithium induces apoptosis in immature cerebellar granule cells but promotes survival of mature neurons

21 January 2018

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Frequency and stability of the fragile X premutation.

21 January 2018

1 reference

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7 January 2021

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

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

The trajectory of cognitive development in males with fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Longitudinal changes in IQ among fragile X females: a preliminary multicenter analysis

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Longitudinal IQ changes in fragile X males

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Fragile X syndrome: genetic predisposition to psychopathology

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Syntactic delay and pragmatic deviance in the language of fragile X males.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Cognitive profiles associated with the fra(X) syndrome in males and females.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Cognitive profiles of boys with the fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Individual variation and specific cognitive deficits in the fra(X) syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Behavior problems of young girls with fragile X syndrome: factor scores on the Conners' Parent's Questionnaire

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Fragile X syndrome: growth, development, and intellectual function

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Analysis of neocortex in three males with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Adult fragile X syndrome. Clinico-neuropathologic findings

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Neuroanatomy of fragile X syndrome: the posterior fossa

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

The young adult human brain: an MRI-based morphometric analysis

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Molecular-neurobehavioral associations in females with the fragile X full mutation.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Individual-specific ‘fingerprints’ of human DNA

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https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

MRI-based hippocampal volume measurements in epilepsy

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Developmental implications of changing trajectories of IQ in males with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation

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https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Alternative splicing in the fragile X gene FMR1.

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Fine structure of the human FMR1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Molecular genetics of cell death in the nematode Caenorhabditis elegans

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Prevention of programmed cell death in Caenorhabditis elegans by human bcl-2

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

The effects of X monosomy on brain development: monozygotic twins discordant for Turner's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNM0295-159

7 January 2021

Identifiers

DOI

10.1038/NM0295-159

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7585014%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference