Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation (Q35195259)

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scientific article published on January 1, 1992

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English	Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation	scientific article published on January 1, 1992

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

title

Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

main subject

CpG island

1 reference

based on heuristic

inferred from title

restriction fragment length polymorphism

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

author

Stefano Rivella

series ordinal

2

object named as

S. Rivella

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

Ornella Parolini

series ordinal

7

object named as

O. Parolini

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

author name string

E. Maestrini

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

C. Tribioli

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

M. Rocchi

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

G. Camerino

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

S. Santachiara-Benerecetti

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

L. D. Notarangelo

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

D. Toniolo

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

language of work or name

English

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publication date

1 January 1992

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stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1346076/?tool=EBI

file format

HTML

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1346076/pdf/?tool=EBI

file format

Portable Document Format

online access status

open access

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

https://europepmc.org/articles/PMC1682517

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

https://europepmc.org/articles/PMC1682517?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1346076

retrieved

16 September 2022

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

volume

50

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

page(s)

156-163

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

cites work

Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Specific methylation pattern at the 3′ end of the human housekeeping gene for glucose 6-phosphate dehydrogenase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

X-chromosome inactivation and developmental patterns in mammals

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Carrier detection in the Wiskott Aldrich syndrome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

CpG islands of the X chromosome are gene associated

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Definition of the gene loci in X-linked immunodeficiencies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

retrieved

13 July 2018

Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase

1 reference

stated in

PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

Probes for CpG islands on the distal long arm of the human X chromosome are clustered in Xq24 and Xq28.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

The nucleotide sequence of a CpG island demonstrates the presence of the first exon of the gene encoding the human lysosomal membrane protein lamp2 and assigns the gene to Xq24.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1682517

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13 July 2018

Allelic exclusion of glucose-6-phosphate dehydrogenase in platelets and T lymphocytes from a Wiskott-Aldrich syndrome carrier

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glucose-6-phosphate dehydrogenase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome inactivation in the Wiskott-Aldrich syndrome: a marker for detection of the carrier state and identification of cell lineages expressing the gene defect

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1346076

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1682517

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

PubMed publication ID

1346076

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1346076

retrieved

7 August 2017

 

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