(Q57075425)

Geneviève de Saint Basile

18

object named as

Hans D. Ochs

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4

object named as

Geneviève de Saint Basile

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Luigi D Notarangelo

15

object named as

Luigi D. Notarangelo

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author name string

Klaus Schwarz

1

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Shigeaki Nonoyama

2

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Manuel C. Peitsch

3

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Teresa Espanol

5

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Anders Fasth

6

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Alain Fischer

7

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Kristina Freitag

8

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Wilhelm Friedrich

9

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Sebastian Fugmann

10

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Hans-Peter Hossle

11

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Alison Jones

12

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Christine Kinnon

13

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Andreas Wechsler

16

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Michael Weiss

A multiinstitutional survey of the Wiskott-Aldrich syndrome.

17

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publication date

November 1996

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published in

Trends in Immunology

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volume

17

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issue

11

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page(s)

496-502

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Wiskott-Aldrich syndrome. An immunologic deficiency disease involving the afferent limb of immunity

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Sex-linked hereditary thrombocytopenia as a variant of Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Hereditary thrombocytopenia: relation to Wiskott-Aldrich syndrome with special reference to splenectomy. Report of a family and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Scanning of the Wiskott-Aldrich syndrome (WAS) gene: identification of 18 novel alterations including a possible mutation hotspot at Arg86 resulting in thrombocytopenia, a mild WAS phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Wiskott-Aldrich syndrome: no strict genotype-phenotype correlations but clustering of missense mutations in the amino-terminal part of the WASP gene product

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Studies of the expression of the Wiskott-Aldrich syndrome protein

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Regulation of the polarization of T cells toward antigen-presenting cells by Ras-related GTPase CDC42

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Wiskott-Aldrich syndrome protein physically associates with Nck through Src homology 3 domains

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

Structural basis for the binding of proline-rich peptides to SH3 domains

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021

The structure and function of proline-rich regions in proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0167-5699%2896%2980901-7

7 January 2021