(Q73083022)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Enhanced frequency of a PTPRC (CD45) exon A mutation (77C-->G) in systemic sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

Schwinzer R

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Witte T

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Hundrieser J

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Ehlers S

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Momot T

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Hunzelmann N

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Krieg T

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Schmidt RE

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

Wonigeit K

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

publication date

1 March 2003

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

168-169

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12618866%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.gene.6363894

1 November 2019

exact match

0 references

cites work

CD45: new jobs for an old acquaintance

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Genetically determined lack of CD45R- T cells in healthy individuals. Evidence for a regulatory polymorphism of CD45R antigen expression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

A point mutation in the human CD45 gene associated with defective splicing of exon A.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

A point mutation in PTPRC is associated with the development of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Does 77C-->G in PTPRC modify autoimmune disorders linked to the major histocompatibility locus?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

An inactivating point mutation in the inhibitory wedge of CD45 causes lymphoproliferation and autoimmunity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Phenotypical and biochemical characterization of a variant CD45R expression pattern in human leukocytes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

The exon A (C77G) mutation is a common cause of abnormal CD45 splicing in humans.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

A point mutation in CD45 may be associated with an increased risk of HIV-1 infection

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

A prospective study of CD45 isoform expression in haemophagocytic lymphohistiocytosis; an abnormal inherited immunophenotype in one family

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Abnormal T-cell phenotype in familial erythrophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021

Genetic factors in the etiology of systemic sclerosis and Raynaud phenomenon

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6363894

7 January 2021