Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism (Q35250287)

7 August 2017

title

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

1 reference

ORCID Public Data File 2021

7 August 2017

1 reference

author name string

Lau AW

1

1 reference

7 August 2017

Brown CJ

2

1 reference

7 August 2017

Peñaherrera M

3

1 reference

7 August 2017

Langlois S

4

1 reference

7 August 2017

Kalousek DK

5

1 reference

7 August 2017

Robinson WP

6

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 December 1997

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

61

1 reference

7 August 2017

issue

6

1 reference

7 August 2017

page(s)

1353-1361

1 reference

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

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

XIST expression and X-chromosome inactivation in human preimplantation embryos

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Meiotic origin of trisomy in confined placental mosaicism is correlated with presence of fetal uniparental disomy, high levels of trisomy in trophoblast, and increased risk of fetal intrauterine growth restriction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Requirement for Xist in X chromosome inactivation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Uniparental disomy for chromosome 16 in humans.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Nondisjunction of chromosome 15: origin and recombination

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

The effect of confined placental mosaicism on development of the human aneuploid conceptus.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Chromosomal mosaicism confined to the placenta in human conceptions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Mammalian X-chromosome inactivation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

X chromosome inactivation mosaicism in the mouse

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Restorative growth and its problems for morphogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Incomplete X chromosome dosage compensation in chorionic villi of human placenta

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

The production of mouse fetal-placental chimeras using trisomy 16 and euploid blastocysts

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Dinucleotide repeat polymorphism at the IGF2R locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

X-inactivation pattern in three cases of X/autosome translocation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Genetic control of X inactivation and processes leading to X-inactivation skewing.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Mosaicism in chorionic villus sampling: an analysis of incidence and chromosomes involved in 2612 consecutive cases

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Restricted distribution of tetraploid cells in mouse tetraploid<==>diploid chimaeras.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Murine trisomy: Developmental profiles of the embryo, and isolation of trisomic cellular systems

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716095

X-inactivation patterns in monozygotic and dizygotic female twins

26 September 2018

1 reference

12 December 2020

The influence of ploidy on the distribution of cells in chimaeric mouse blastocysts

1 reference

12 December 2020

Biological Sciences: X Chromosome Inactivation studied by Injection of a Single Cell into the Mouse Blastocyst

1 reference

12 December 2020

X-chromosome inactivation in cultured cells from human chorionic villi

1 reference

12 December 2020

X-chromosome inactivation in the human cytotrophoblast

1 reference

12 December 2020

Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism

1 reference

12 December 2020

Cytogenetic results from the U.S. Collaborative Study on CVS

1 reference

12 December 2020

X-chromosome inactivation occurs at different times in different tissues of the post-implantation mouse embryo

1 reference

12 December 2020

Distribution of mosaicism in human placentae

1 reference

12 December 2020

1 reference

12 December 2020

Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis

1 reference

12 December 2020

Identifiers

DOI

10.1086/301651

1 reference

7 August 2017

1 reference

7 August 2017

1 reference