(Q37342300)

English

Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving.

scientific article published on 10 September 2013

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scholarly article

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20 February 2020

Genes that escape X-inactivation in humans have high intraspecific variability in expression, are associated with mental impairment but are not slow evolving (English)

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20 February 2020

Laurence D. Hurst

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20 February 2020

Atahualpa Castillo-Morales

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20 February 2020

Araxi O. Urrutia

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20 February 2020

author name string

Yuchao Zhang

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20 February 2020

Min Jiang

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20 February 2020

Yufei Zhu

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20 February 2020

Landian Hu

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20 February 2020

Xiangyin Kong

7

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20 February 2020

publication date

10 September 2013

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20 February 2020

Molecular Biology and Evolution

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20 February 2020

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20 February 2020

2588-2601

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20 February 2020

12

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20 February 2020

maintained by WikiProject

WikiProject Ecology

1 reference

based on heuristic

inferred from title

Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective

1 reference

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6 September 2017

Genes that escape from X inactivation

1 reference

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6 September 2017

Strong purifying selection at genes escaping X chromosome inactivation

1 reference

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6 September 2017

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1 reference

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6 September 2017

Global survey of escape from X inactivation by RNA-sequencing in mouse

1 reference

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6 September 2017

Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome

1 reference

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6 September 2017

X-linked intellectual disability: unique vulnerability of the male genome

1 reference

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6 September 2017

Characterisation of inactivation domains and evolutionary strata in human X chromosome through Markov segmentation

1 reference

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6 September 2017

Triple X syndrome: a review of the literature

1 reference

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The genetic landscape of intellectual disability arising from chromosome X.

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TopHat: discovering splice junctions with RNA-Seq

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6 September 2017

RNA-Seq: a revolutionary tool for transcriptomics

1 reference

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6 September 2017

NCBI GEO: archive for high-throughput functional genomic data

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6 September 2017

Genome partitioning of genetic variation for height from 11,214 sibling pairs

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6 September 2017

The evolution of sex-biased genes and sex-biased gene expression

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6 September 2017

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6 September 2017

Dosage compensation in mammals: fine-tuning the expression of the X chromosome

1 reference

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6 September 2017

X-inactivation profile reveals extensive variability in X-linked gene expression in females

1 reference

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6 September 2017

Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse

1 reference

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6 September 2017

A gene atlas of the mouse and human protein-encoding transcriptomes

1 reference

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6 September 2017

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

1 reference

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6 September 2017

A stain upon the silence: genes escaping X inactivation

1 reference

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6 September 2017

Escape from X inactivation

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6 September 2017

Growth and ovarian function in girls with 48,XXXX karyotype--patient report and review of the literature

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6 September 2017

Escapees on the X chromosome

1 reference

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6 September 2017

Four evolutionary strata on the human X chromosome.

1 reference

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6 September 2017

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

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6 September 2017

A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome

1 reference

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6 September 2017

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26 June 2018

The UCSC Known Genes

1 reference

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2 September 2018

Genetic linkage of human height is confirmed to 9q22 and Xq24.

1 reference

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1 reference

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2 September 2018

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1 reference

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2 September 2018

Genetic Dissection of Human Stature in a Large Sample of Multiplex Pedigrees

1 reference

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A whole-genome linkage scan suggests several genomic regions potentially containing QTLs underlying the variation of stature

1 reference

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3 December 2018

[Triple X syndrome deviation with mild symptoms. The majority goes undiagnosed]

1 reference

https://pubmed.ncbi.nlm.nih.gov/24023392

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/MOLBEV/MST148

1 reference

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20 February 2020

1 reference

Europe PubMed Central

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20 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24023392%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

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