The molecular basis of X-linked immunodeficiency disease (Q35848833)

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scientific article published on January 1, 1992

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Language	Label	Description	Also known as
English	The molecular basis of X-linked immunodeficiency disease	scientific article published on January 1, 1992

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

The molecular basis of X-linked immunodeficiency disease (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

author name string

C. Kinnon

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1528025

retrieved

5 October 2022

R. Levinsky

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1528025

retrieved

5 October 2022

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

1528025

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1528025

retrieved

5 October 2022

publication date

1 January 1992

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

published in

Journal of Inherited Metabolic Disease

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

volume

15

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

page(s)

674-682

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

cites work

Localization of the properdin structural locus to Xp11.23-Xp21.1.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X chromosome inactivation patterns in obligate carriers of X-linked lymphoproliferative syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of mutations in two families with X-linked chronic granulomatous disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intact

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of the cDNA coding for properdin, a positive regulator of the alternative pathway of human complement

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

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/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determination

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

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/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of chronic granulomatous disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

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/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Partial Xq25 deletion in a family with the X-linked lymphoproliferative disease (XLP)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phorbol myristate acetate stimulated NBT test: a simple method suitable for antenatal diagnosis of chronic granulomatous disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of PGK1 to X-linked severe combined immunodeficiency (IMD4) allows predictive testing in families with no surviving male

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1528025

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF01799623

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

PubMed publication ID

1528025

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1528025

retrieved

10 August 2017

 

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