(Q28210311)

English

X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP)

scientific article (publication date: February 2003)

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scholarly article

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X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP) (English)

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Wiskott-Aldrich syndrome

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thrombocytopenia

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inferred from title

author name string

Jennifer N Luthi

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Manish J Gandhi

2

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Jonathan G Drachman

3

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language of work or name

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publication date

February 2003

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Experimental Hematology

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31

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2

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150-8

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The Wiskott-Aldrich syndrome

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

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The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979).

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

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X-linked Wiskott-Aldrich syndrome in a girl

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Characterization of the Wiskott-Aldrich syndrome protein and its role in the disease

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Direct interaction of the Wiskott-Aldrich syndrome protein with the GTPase Cdc42

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

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Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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N-WASP, a novel actin-depolymerizing protein, regulates the cortical cytoskeletal rearrangement in a PIP2-dependent manner downstream of tyrosine kinases

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Wiskott-Aldrich syndrome protein induces actin clustering without direct binding to Cdc42

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Wiskott-Aldrich syndrome protein (WASp) is a binding partner for c-Src family protein-tyrosine kinases

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

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Identification of regions of the Wiskott-Aldrich syndrome protein responsible for association with selected Src homology 3 domains

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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The pleckstrin homology domain of the Wiskott-Aldrich syndrome protein is involved in the organization of actin cytoskeleton

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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EVH1/WH1 domains of VASP and WASP proteins belong to a large family including Ran-binding domains of the RanBP1 family

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

WIP, a protein associated with wiskott-aldrich syndrome protein, induces actin polymerization and redistribution in lymphoid cells

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

The Wiskott-Aldrich syndrome protein-interacting protein (WIP) binds to the adaptor protein Nck

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Thrombopoietin signal transduction: studies from cell lines and primary cells

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked thrombocytopenia caused by a novel mutation of GATA-1

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Unique and recurrent WAS gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Modulation of the phenotypic diversity of sickle cell anemia

1 reference

https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

based on heuristic

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Relationship between genotype and phenotype in monogenic diseases: Relevance to polygenic diseases

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https://api.crossref.org/works/10.1016%2FS0301-472X%2802%2901023-8

7 January 2021

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10.1016/S0301-472X(02)01023-8

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