(Q45365700)

English

Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis

scientific article published on 14 June 2011

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scholarly article

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Europe PubMed Central

PubMed publication ID

13 December 2017

Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Epstein–Barr virus

0 references

author name string

Huang Zhizhuo

1

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Xu Junmei

2

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Shen Yuelin

3

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Qin Qiang

4

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Liu Chunyan

5

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Xie Zhengde

6

1 reference

Europe PubMed Central

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13 December 2017

Shen Kunling

7

1 reference

Europe PubMed Central

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13 December 2017

publication date

14 June 2011

1 reference

Europe PubMed Central

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13 December 2017

Pediatric Blood & Cancer

1 reference

Europe PubMed Central

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13 December 2017

58

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Europe PubMed Central

PubMed publication ID

13 December 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

410-414

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Familial and acquired hemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

EBV-elicited familial hemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Clonal change of infiltrating T-cells in children with familial hemophagocytic lymphohistiocytosis: possible association with Epstein-Barr virus infection

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Clinical features and treatment strategies of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Identification of the homologous beige and Chediak-Higashi syndrome genes

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Cytophagic histiocytic panniculitis with fatal haemophagocytic lymphohistiocytosis in a paediatric patient with perforin gene mutation

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

A spectrum of mutations in SH2D1A that causes X-linked lymphoproliferative disease and other Epstein-Barr virus-associated illnesses

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

HLA class I polymorphisms are associated with development of infectious mononucleosis upon primary EBV infection

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Susceptibility to primary Epstein-Barr virus infection is associated with interleukin-10 gene promoter polymorphism

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Tumor necrosis factor alpha promoter polymorphism associated with increased susceptibility to secondary hemophagocytic lymphohistiocytosis in the Korean population

1 reference

https://api.crossref.org/works/10.1002%2FPBC.23216

21 January 2018

Identifiers

10.1002/PBC.23216

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

release_5gqca2d3obcqfowug5ycbn3rlq

1 reference

https://api.fatcat.wiki/v0/release/5gqca2d3obcqfowug5ycbn3rlq

24 November 2022

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

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