(Q50305534)

PubMed publication ID

16167093

2 March 2018

http://europepmc.org/abstract/MED/16167093

title

Brief report: non-random X chromosome inactivation in females with autism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

author name string

Z Talebizadeh

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

D C Bittel

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

N Kibiryeva

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

M G Butler

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

language of work or name

English

0 references

publication date

1 October 2005

1 reference

PubMed publication ID

16167093

2 March 2018

http://europepmc.org/abstract/MED/16167093

published in

Journal of Autism and Developmental Disorders

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

volume

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

page(s)

675-681

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s10803-005-0011-z

12 May 2020

exact match

0 references

cites work

Heritability of X chromosome--inactivation phenotype in a large family

1 reference

12 December 2020

Non-random X chromosome inactivation in mammalian cells.

1 reference

12 December 2020

Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts

1 reference

12 December 2020

Expression of genes from the human active and inactive X chromosomes

1 reference

12 December 2020

X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease

1 reference

12 December 2020

Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion

1 reference

12 December 2020

Localization of the X inactivation centre on the human X chromosome in Xq13.

1 reference

12 December 2020

A genomewide screen of 345 families for autism-susceptibility loci

1 reference

12 December 2020

The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus

1 reference

12 December 2020

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

12 December 2020

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism

1 reference

12 December 2020

Analysis of the distribution of CAG repeats and X-chromosome inactivation status of HUMARA gene in healthy female subjects using improved fluorescence-based assay.

1 reference

12 December 2020

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease

1 reference

12 December 2020

Xp deletions associated with autism in three females.

1 reference

12 December 2020

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

12 December 2020

Sex differences in pervasive developmental disorders

1 reference

12 December 2020

A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation

1 reference

12 December 2020

X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes

1 reference

12 December 2020

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene

1 reference

12 December 2020

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

1 reference

12 December 2020

Requirement for Xist in X chromosome inactivation

1 reference

12 December 2020

A first-generation X-inactivation profile of the human X chromosome

1 reference

12 December 2020

Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy

1 reference

12 December 2020

Mammalian X-chromosome action: inactivation limited in spread and region of origin

1 reference

12 December 2020

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

12 December 2020

Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation

1 reference

12 December 2020

Molecular cytogenetic analysis of a duplication Xp in a male: further delineation of a possible sex influencing region on the X chromosome.

1 reference

12 December 2020

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders

1 reference

12 December 2020

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita

1 reference

12 December 2020

10.1007/S10803-005-0011-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6744835&resulttype=core&format=json

12 May 2020

PubMed publication ID

16167093

1 reference