X-chromosome inactivation: molecular mechanisms from the human perspective (Q37873373)

24 August 2017

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title

X-chromosome inactivation: molecular mechanisms from the human perspective (English)

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24 August 2017

Allison M Cotton

5

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Carolyn J. Brown

object named as

Carolyn J Brown

6

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author name string

Christine Yang

1

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PubMed ID

21553122

24 August 2017

Andrew G Chapman

2

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PubMed ID

21553122

24 August 2017

Angela D Kelsey

3

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PubMed ID

21553122

24 August 2017

Jakub Minks

4

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24 August 2017

7 May 2011

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24 August 2017

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24 August 2017

130

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24 August 2017

2

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24 August 2017

175-185

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https://scigraph.springernature.com/pub.10.1007/s00439-011-0994-9

24 August 2017

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cites work

A general mechanism for network-dosage compensation in gene circuits

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X chromosome-inactivation patterns of 1,005 phenotypically unaffected females

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Sensing X chromosome pairs before X inactivation via a novel X-pairing region of the Xic.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Transient colocalization of X-inactivation centres accompanies the initiation of X inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

RNF12 activates Xist and is essential for X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

A morphological distinction between neurones of the male and female, and the behaviour of the nucleolar satellite during accelerated nucleoprotein synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Escape from X inactivation in mice and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The physical phenotype of girls and women with Turner syndrome is not X-imprinted.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Identification of regulatory elements flanking human XIST reveals species differences

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Genome-wide distribution of macroH2A1 histone variants in mouse liver chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X inactivation and the complexities of silencing a sex chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Characterization of expression at the human XIST locus in somatic, embryonal carcinoma, and transgenic cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Inducible XIST-dependent X-chromosome inactivation in human somatic cells is reversible

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

LINE-1 activity in facultative heterochromatin formation during X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Functional analysis of the DXPas34 locus, a 3' regulator of Xist expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Identification of a Ctcf cofactor, Yy1, for the X chromosome binary switch.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The pluripotency factor Oct4 interacts with Ctcf and also controls X-chromosome pairing and counting

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Variations of X chromosome inactivation occur in early passages of female human embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

PHOG, a candidate gene for involvement in the short stature of Turner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Mammalian oocytes: X chromosome activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Boundaries between chromosomal domains of X inactivation and escape bind CTCF and lack CpG methylation during early development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Mammalian X-chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Molecular and cytogenetic analysis of the spreading of X inactivation in a girl with microcephaly, mild dysmorphic features and t(X;5)(q22.1;q31.1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Inactive X chromosome-specific histone H3 modifications and CpG hypomethylation flank a chromatin boundary between an X-inactivated and an escape gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Sex chromosome specialization and degeneration in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

How the gene content of human sex chromosomes evolved

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Unbalanced X;autosome translocations provide evidence for sequence specificity in the association of XIST RNA with chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Meiosis and sex chromosome aneuploidy: how meiotic errors cause aneuploidy; how aneuploidy causes meiotic errors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X-inactivation reveals epigenetic anomalies in most hESC but identifies sublines that initiate as expected

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X-inactivation status varies in human embryonic stem cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Evidence for the existence of the human "super female".

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

A cytogenetic survey of 11,680 newborn infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Large-scale population study of human cell lines indicates that dosage compensation is virtually complete

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

RNF12 is an X-Encoded dose-dependent activator of X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

H4 acetylation, XIST RNA and replication timing are coincident and define x;autosome boundaries in two abnormal X chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Histone H4 acetylation analyses in patients with polysomy X: implications for the mechanism of X inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Tsix, a gene antisense to Xist at the X-inactivation centre

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Derivation of pre-X inactivation human embryonic stem cells under physiological oxygen concentrations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Escape from X chromosome inactivation is an intrinsic property of the Jarid1c locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X-chromosome inactivation: a repeat hypothesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Phenotype of triploid embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Is Tsix repression of Xist specific to mouse?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Getting to the center of X-chromosome inactivation: the role of transgenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Is the prevalence of Klinefelter syndrome increasing?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Molecular coupling of Xist regulation and pluripotency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Dosage compensation of the active X chromosome in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Xite, X-inactivation intergenic transcription elements that regulate the probability of choice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Requirement for Xist in X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Identification of a cluster of X-linked imprinted genes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Female-biased expression of long non-coding RNAs in domains that escape X-inactivation in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X inactivation, differentiation, and DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The DNA sequence of the human X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Methylation of two Homo sapiens-specific X-Y homologous genes in Klinefelter's syndrome (XXY).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X-autosome translocations: A review of 122 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Non-inactivation of an X-Chromosome Locus in Man

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Maternal Rnf12/RLIM is required for imprinted X-chromosome inactivation in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X-chromosome inactivation and epigenetic fluidity in human embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

MAOA and GYG2 are submitted to X chromosome inactivation in human fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Defining molecular cornerstones during fibroblast to iPS cell reprogramming in mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Mortality and incidence in women with 47,XXX and variants.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Characterization of Xpr (Xpct) reveals instability but no effects on X-chromosome pairing or Xist expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Mortality in patients with Klinefelter syndrome in Britain: a cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Mortality and cancer incidence in women with extra X chromosomes: a cohort study in Britain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X chromosome gene expression in human tissues: male and female comparisons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Female human iPSCs retain an inactive X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The long noncoding RNA, Jpx, is a molecular switch for X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X chromosome inactivation is initiated in human preimplantation embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Evidence of influence of genomic DNA sequence on human X chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

RNA-Seq: a revolutionary tool for transcriptomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Xist function: bridging chromatin and stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

RNA sequencing shows no dosage compensation of the active X-chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Transient homologous chromosome pairing marks the onset of X inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Application of microarrays to the analysis of the inactivation status of human X-linked genes expressed in lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the α-galactosidase A gene in the Czech and Slovak population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

The human X-inactivation centre is not required for maintenance of X-chromosome inactivation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-0994-9

eXIST with matrix-associated proteins

21 January 2018

1 reference

12 December 2020

The behavior of sex chromosomes in two human X-autosome translocations: failure of extensive X-inactivation spreading.

1 reference

12 December 2020

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia

1 reference

12 December 2020

Late replicating X chromosomes in human triploidy

1 reference

12 December 2020

No evidence that skewing of X chromosome inactivation patterns is transmitted to offspring in humans

1 reference

12 December 2020

Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine

1 reference

12 December 2020

X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X

1 reference

12 December 2020

Human X inactivation center induces random X chromosome inactivation in male transgenic mice

1 reference

12 December 2020

The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression

1 reference

12 December 2020

Localizing DNA and RNA within nuclei and chromosomes by fluorescence in situ hybridization

1 reference

12 December 2020

Maternally inherited X chromosome is not inactivated in mouse blastocysts due to parental imprinting

1 reference

12 December 2020

X chromosome inactivation during induced differentiation of a female mouse embryonal carcinoma cell line

1 reference

12 December 2020

Xist-deficient mice are defective in dosage compensation but not spermatogenesis

1 reference

12 December 2020

Cytogenetic and molecular analysis of an unbalanced translocation (X;7) (q28;p15) in a dysmorphic girl

1 reference

12 December 2020

Controlling elements in the mouse X chromosome

1 reference

12 December 2020

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

1 reference

12 December 2020

An unusual sex chromatin pattern in three mentally deficient subjects

1 reference

12 December 2020

Mapping of the distal boundary of the X-inactivation center in a rearranged X chromosome from a female expressing XIST

1 reference

12 December 2020

Sex chromatin and gene action in the mammalian X-chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

X-chromosome deletions in embryo-derived (EK) cell lines associated with lack of X-chromosome inactivation

1 reference

12 December 2020

10.1007/S00439-011-0994-9

Identifiers

DOI

1 reference

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30 July 2022

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Fatcat

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https://api.fatcat.wiki/v0/release/23j3whfvenforobhq53nvz3ahy

30 July 2022