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Literature DB >> 15654814

Wiskott-Aldrich syndrome: another piece in the puzzle.

L D Notarangelo, L Mori.

Abstract

Entities: Disease

Mesh：

Substances：

Year: 2005 PMID： 15654814 PMCID： PMC1809300 DOI： 10.1111/j.1365-2249.2005.02707.x

Source DB: PubMed Journal: Clin Exp Immunol ISSN： 0009-9104 Impact factor: 4.330

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31 in total

1. The spleen in the Wiskott-Aldrich syndrome: histopathologic abnormalities of the white pulp correlate with the clinical phenotype of the disease.

Authors: W Vermi; L Blanzuoli; M D Kraus; P Grigolato; F Donato; G Loffredo; C E Marino; D Alberti; L D Notarangelo; F Facchetti
Journal: Am J Surg Pathol Date: 1999-02 Impact factor: 6.394

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

Authors: M D Cooper; H P Chae; J T Lowman; W Krivit; R A Good
Journal: Am J Med Date: 1968-04 Impact factor: 4.965

3. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

Authors: J M Derry; H D Ochs; U Francke
Journal: Cell Date: 1994-08-26 Impact factor: 41.582

4. Wiskott-Aldrich syndrome protein regulates podosomes in primary human macrophages.

Authors: S Linder; D Nelson; M Weiss; M Aepfelbacher
Journal: Proc Natl Acad Sci U S A Date: 1999-08-17 Impact factor: 11.205

5. Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect.

Authors: Angela Gismondi; Loredana Cifaldi; Cinzia Mazza; Silvia Giliani; Silvia Parolini; Stefania Morrone; Jordan Jacobelli; Elisabetta Bandiera; Luigi Notarangelo; Angela Santoni
Journal: Blood Date: 2004-03-04 Impact factor: 22.113

6. Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5.

Authors: Christopher D C Allen; K Mark Ansel; Caroline Low; Robin Lesley; Hirokazu Tamamura; Nobutaka Fujii; Jason G Cyster
Journal: Nat Immunol Date: 2004-08-01 Impact factor: 25.606

7. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.

Authors: Anna Virginia Gulino; Daniele Moratto; Silvano Sozzani; Patrizia Cavadini; Karel Otero; Laura Tassone; Luisa Imberti; Silvia Pirovano; Lucia D Notarangelo; Roberta Soresina; Evelina Mazzolari; David L Nelson; Luigi D Notarangelo; Raffaele Badolato
Journal: Blood Date: 2004-03-16 Impact factor: 22.113

Wiskott-Aldrich syndrome: another piece in the puzzle.

1. The spleen in the Wiskott-Aldrich syndrome: histopathologic abnormalities of the white pulp correlate with the clinical phenotype of the disease.

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

3. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

4. Wiskott-Aldrich syndrome protein regulates podosomes in primary human macrophages.

5. Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect.

6. Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5.

7. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.

8. Maturation of DC is associated with changes in motile characteristics and adherence.

9. Early deficit of lymphocytes in Wiskott-Aldrich syndrome: possible role of WASP in human lymphocyte maturation.

10. T cell lines characterize events in the pathogenesis of the Wiskott-Aldrich syndrome.

1. [Associated diseases and differential diagnostic considerations in childhood atopic eczema].

Review 2. Diversity of polyproline recognition by EVH1 domains.