(Q51516247)

6 April 2018

title

Expression of selected genes escaping from X inactivation in the 41, XX(Y)* mouse model for Klinefelter's syndrome. (English)

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6 April 2018

author name string

Steffi Werler

1

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6 April 2018

Andreas Poplinski

2

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6 April 2018

Jörg Gromoll

3

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Joachim Wistuba

4

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language of work or name

English

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publication date

17 January 2011

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6 April 2018

published in

Acta Paediatrica

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6 April 2018

volume

100

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issue

6

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page(s)

885-891

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6 April 2018

cites work

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1 reference

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Klinefelter's syndrome and psychoneurologic function

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Klinefelter's syndrome, type 2 diabetes and the metabolic syndrome: the impact of body composition.

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Should non-mosaic Klinefelter syndrome men be labelled as infertile in 2009?

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Animal models for Klinefelter's syndrome and their relevance for the clinic

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XXY mice exhibit gonadal and behavioral phenotypes similar to Klinefelter syndrome.

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Genetic and hormonal control of bone volume, architecture, and remodeling in XXY mice

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Genetic, hormonal, and metabolomic influences on social behavior and sex preference of XXY mice

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Impaired recognition memory in male mice with a supernumerary X chromosome.

21 January 2018

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Male 41, XXY* mice as a model for klinefelter syndrome: hyperactivation of leydig cells.

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X-linked genes and mental functioning

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Severe XIST hypomethylation clearly distinguishes (SRY+) 46,XX-maleness from Klinefelter syndrome

21 January 2018

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

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

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

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

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Differential patterns of histone methylation and acetylation distinguish active and repressed alleles at X-linked genes.

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Crosstalk between histone modifications maintains the developmental pattern of gene expression on a tissue-specific locus.

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Identification of JmjC domain-containing UTX and JMJD3 as histone H3 lysine 27 demethylases

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Sexually dimorphic expression of the X-linked gene Eif2s3x mRNA but not protein in mouse brain.

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A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis.

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The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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

21 January 2018

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Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain

21 January 2018

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The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation.

21 January 2018

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A novel mutation in JARID1C gene associated with mental retardation

21 January 2018

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10.1111/J.1651-2227.2010.02112.X

21 January 2018

Identifiers

DOI

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6 April 2018

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6 April 2018