(Q42533826)

English

Perforin polymorphism A91V and susceptibility to B-precursor childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group

scientific article published on 22 June 2006

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

Perforin polymorphism A91V and susceptibility to B-precursor childhood acute lymphoblastic leukemia: a report from the Children's Oncology Group (English)

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

lymphoblastic leukemia

1 reference

based on heuristic

inferred from title

author name string

P A Mehta

1

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

S M Davies

2

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

A Kumar

3

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

M Devidas

4

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

S Lee

5

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

T Zamzow

6

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

J Elliott

7

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

J Villanueva

8

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

J Pullen

9

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

Y Zewge

10

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

A Filipovich

11

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

Children's Oncology Group

12

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

22 June 2006

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

20

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

9

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

1539-1541

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

https://scigraph.springernature.com/pub.10.1038/sj.leu.2404299

0 references

Aberrant maturation of mutant perforin underlies the clinical diversity of hemophagocytic lymphohistiocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

Functional significance of the perforin/granzyme cell death pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

Perforin-mediated cytotoxicity is critical for surveillance of spontaneous lymphoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

The ninth component of complement and the pore-forming protein (perforin 1) from cytotoxic T cells: structural, immunological, and functional similarities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

Isolation and biochemical and functional characterization of perforin 1 from cytolytic T-cell granules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

28 May 2018

A proportion of patients with lymphoma may harbor mutations of the perforin gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

16 August 2018

A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

16 August 2018

Characterisation of diverse PRF1 mutations leading to decreased natural killer cell activity in North American families with haemophagocytic lymphohistiocytosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

16 August 2018

Atypical features of familial hemophagocytic lymphohistiocytosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

16 August 2018

Cytolysis by H-2-specific T killer cells. Assembly of tubular complexes on target membranes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2922049

16 August 2018

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404299

21 January 2018

A single amino acid change, A91V, leads to conformational changes that can impair processing to the active form of perforin

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404299

21 January 2018

Inherited Perforin andFasMutations in a Patient with Autoimmune Lymphoproliferative Syndrome and Lymphoma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404299

21 January 2018

Assembly of two types of tubules with putative cytolytic function by cloned natural killer cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404299

21 January 2018

Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16791263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of a lytic, pore-forming protein (perforin) from cytolytic T-lymphocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16791263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A single amino acid change A91V in perforin: a novel, frequent predisposing factor to childhood acute lymphoblastic leukemia?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16791263

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/SJ.LEU.2404299

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 November 2017

ResearchGate publication ID

0 references

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