(Q51547585)

English

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation.

scientific article published on 7 July 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Spread of X-chromosome inactivation into chromosome 15 is associated with Prader-Willi syndrome phenotype in a boy with a t(X;15)(p21.1;q11.2) translocation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Prader–Willi syndrome

1 reference

based on heuristic

inferred from title

author name string

Satoru Sakazume

1

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Hirofumi Ohashi

2

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Yuki Sasaki

3

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Naoki Harada

4

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Katsumi Nakanishi

5

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Hidenori Sato

6

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Mitsuru Emi

7

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Kazushi Endoh

8

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Ryoichi Sohma

9

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Yasuhiro Kido

10

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Toshiro Nagai

11

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

Takeo Kubota

12

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

publication date

7 July 2011

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

131

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

1

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

121-130

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

https://scigraph.springernature.com/pub.10.1007/s00439-011-1051-4

0 references

Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Mammalian X-chromosome inactivation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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).

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Xist has properties of the X-chromosome inactivation centre

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

The proportion of cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Long-range cis effects of ectopic X-inactivation centres on a mouse autosome

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

A 450 kb transgene displays properties of the mammalian X-inactivation center.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

X-chromosome inactivation: a repeat hypothesis

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Microphthalmia with linear skin defects syndrome in a mosaic female infant with monosomy for the Xp22 region: molecular analysis of the Xp22 breakpoint and the X-inactivation pattern.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features.

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Attenuated spread of X-inactivation in an X;autosome translocation

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Isochromosome consisting of terminal short arm and proximal long arm X in a girl with short stature

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Aberrant patterns of X chromosome inactivation in bovine clones

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

Nuclear reprogramming of cloned embryos and its implications for therapeutic cloning

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

The Mouse Pink-Eyed Dilution Gene: Association with Hypopigmentation in Prader-Willi and Angelman Syndromes and with Human OCA2

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1051-4

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Switch in X-inactivation in a JAK2 V617F-negative case of polycythemia vera with two acquired X-autosome translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CpG Islands in Human X-Inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detrimental effects of two active X chromosomes on early mouse development.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromatin and gene action in the mammalian X-chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21735174

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-011-1051-4

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 April 2018

http://europepmc.org/abstract/MED/21735174

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