(Q33404650)

26 July 2017

title

The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome (English)

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26 July 2017

main subject

Wiskott-Aldrich syndrome

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author name string

Lyon MF

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26 July 2017

Peters J

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26 July 2017

Glenister PH

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26 July 2017

Ball S

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26 July 2017

Wright E

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26 July 2017

language of work or name

English

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publication date

1 April 1990

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

26 July 2017

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inferred from page(s)

published in

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

2433-2437

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EXCEPTIONAL INHERITANCE OF A SEX-LINKED GENE IN THE MOUSE EXPLAINED ON THE BASIS THAT THE X/O SEX-CHROMOSOME CONSTITUTION IS FEMALE

26 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Wiskott-Aldrich syndrome: new perspectives in pathogenesis and management.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

The William Allan memorial award address: X-chromosome inactivation and the location and expression of X-linked genes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Multilocus molecular mapping of the mouse X chromosome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Hereditary X-linked thrombocytopenia maps to the same chromosomal region as the Wiskott-Aldrich syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Chromosome maps of man and mouse. IV.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53703

Expression on blood cells of sialophorin, the surface glycoprotein that is defective in Wiskott-Aldrich syndrome

21 June 2018

1 reference

12 December 2020

Report of the committee on the genetic constitution of the X chromosome

1 reference

12 December 2020

Conservation and reorganization of loci on the mammalian X chromosome: a molecular framework for the identification of homologous subchromosomal regions in man and mouse

1 reference

12 December 2020

Genetic control over the inactivation of autosomal genes attached to the X-chromosome

1 reference

12 December 2020

Enzyme-activity mutations detected in mice after paternal fractionated irradiation

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.87.7.2433

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release_6j44fchvhzawxk7z64ln6332ji

26 July 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6j44fchvhzawxk7z64ln6332ji

24 November 2022

mapped directly with Wikidata item

PMC publication ID

53703

1 reference

26 July 2017

1 reference