(Q36395394)

English

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

13 August 2017

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others (English)

1 reference

Europe PubMed Central

13 August 2017

author name string

L Carrel

1

1 reference

Europe PubMed Central

13 August 2017

H F Willard

2

1 reference

Europe PubMed Central

13 August 2017

language of work or name

0 references

publication date

1 June 1999

1 reference

Europe PubMed Central

13 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

13 August 2017

96

1 reference

Europe PubMed Central

13 August 2017

13

1 reference

Europe PubMed Central

13 August 2017

7364-7369

1 reference

Europe PubMed Central

13 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC22091/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Stabilization and localization of Xist RNA are controlled by separate mechanisms and are not sufficient for X inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Genomic imprinting in mammals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Escape from X inactivation of two new genes associated with DXS6974E and DXS7020E

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Expression of genes from the human active and inactive X chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Use of flow cytometry and RT-PCR for detecting gene expression by single cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

X inactivation of the FMR1 fragile X mental retardation gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Prediction of the coding sequences of unidentified human genes. IV. The coding sequences of 40 new genes (KIAA0121-KIAA0160) deduced by analysis of cDNA clones from human cell line KG-1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

cDNA cloning of component A of Rab geranylgeranyl transferase and demonstration of its role as a Rab escort protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Retinal degeneration in choroideremia: deficiency of rab geranylgeranyl transferase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Chromatin domains as potential units of eukaryotic gene function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Isolation of new genes in distal Xq28: transcriptional map and identification of a human homologue of the ARD1 N-acetyl transferase of Saccharomyces cerevisiae

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Escape from X inactivation in human and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Reactivation of inactive X-linked genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Differential expression of steroid sulphatase locus on active and inactive human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrier

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Cloning of a gene that is rearranged in patients with choroideraemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Inactivation of the Zfx gene on the mouse X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

X-chromosome inactivation may explain the difference in viability of XO humans and mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

The NT 1311 polymorphism of G6PD: G6PD Mediterranean mutation may have originated independently in Europe and Asia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

'Touchdown' PCR to circumvent spurious priming during gene amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Localized Derepression on the Human Inactive X Chromosone in Mouse-Human Cell Hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Non-inactivation of an X-Chromosome Locus in Man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

The role of insulator elements in defining domains of gene expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Direct detection of non-random X chromosome inactivation by use of a transcribed polymorphism in the XIST gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

Effect of ageing on reactivation of the human X-linked HPRT locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

30 September 2017

The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

X-chromosome inactivation in mammals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

Mosaic and polymorphic imprinting of the WT1 gene in humans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

X;14 translocation:an exception to the critical region hypothesis on the human X-chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

X-linked retinal disorders and the Lyon hypothesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

Two point mutations are responsible for G6PD polymorphism in Sardinia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

Pericentromeric structure of human X "isochromosomes": evidence for molecular heterogeneity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

28 June 2018

Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Escape from X inactivation of Smcx is preceded by silencing during mouse development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Physical and genetic mapping of the human X chromosome centromere: repression of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

X inactivation in females with X-linked disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Differential expression pattern of XqPAR-linked genes SYBL1 and IL9R correlates with the structure and evolution of the region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Mutation analysis in Canadian families with choroideremia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Inactivation of the Rps4 gene on the mouse X chromosome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=22091

21 September 2018

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.13.7364

21 January 2018

Stability of X Chromosomal Inactivation in Human Somatic Cells

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.13.7364

21 January 2018

Epigenetic and Chromosomal Control of Gene Expression: Molecular and Genetic Analysis of X Chromosome Inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-6-phosphate dehydrogenase as a probe for the study of X-chromosome inactivation in hunan females

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional enhancers act in cis to suppress position-effect variegation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphic functional imprinting of the human IGF2 gene among individuals, in blood cells, is associated with H19 expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

It's raining SNPs, hallelujah?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X Inactivation in Females with X-Linked Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.96.13.7364

1 reference

Europe PubMed Central

13 August 2017

1999PNAS...96.7364C

0 references

1 reference

Europe PubMed Central

13 August 2017

1 reference

Europe PubMed Central

13 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36395394&oldid=1658506944"