Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita (Q43105030)

14 November 2017

Nonrandom X-chromosome inactivation in hemopoietic cells from carriers of dyskeratosis congenita (English)

1 reference

14 November 2017

Nonrandom X-Chromosome Inactivation in Hemopoietic Cells from Carriers of Dyskeratosis Congenita (English)

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

17 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

17 November 2024

author name string

A. M. Ferraris

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

17 November 2024

G. L. Forni

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

17 November 2024

R. Mangerini

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

17 November 2024

G. F. Gaetani

4

1 reference

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17 November 2024

language of work or name

English

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publication date

1 August 1997

1 reference

14 November 2017

August 1997

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9311754

full work available at URL

17 November 2024

https://doi.org/10.1016/s0002-9297(07)64075-0

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

https://europepmc.org/articles/PMC1715903

17 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9311754

https://europepmc.org/articles/PMC1715903?pdf=render

17 November 2024

1 reference

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https://api.elsevier.com/content/article/PII:S0002929707640750?httpAccept=text/xml

17 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

https://api.elsevier.com/content/article/PII:S0002929707640750?httpAccept=text/plain

17 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

American Journal of Human Genetics

17 November 2024

published in

1 reference

14 November 2017

61

1 reference

14 November 2017

2

1 reference

14 November 2017

458-461

1 reference

Skewed X-chromosome inactivation in female carriers of dyskeratosis congenita

14 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Fine mapping of the dyskeratosis congenita locus in Xq28.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Dyskeratosis congenita: an inherited bone marrow failure syndrome

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Dyskeratosis congenita: three additional families show linkage to a locus in Xq28.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease.

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Carrier detection in X-linked severe combined immunodeficiency based on patterns of X chromosome inactivation

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

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

25 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715903

Expression of the gene defect in X-linked agammaglobulinemia

15 August 2018

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

Assignment of the gene for dyskeratosis congenita to Xq28

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

Polyclonal origin of medullary carcinoma of the thyroid in multiple endocrine neoplasia type 2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

Dyskeratosis congenita: unusual presenting features within a kindred

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0002-9297(07)64075-0

"Stem cell" origin of the hematopoietic defect in dyskeratosis congenita

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9311754

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

1 reference

14 November 2017

1 reference

14 November 2017

1 reference