Literature DB >> 8961624

WASPbase: a database of WAS- and XLT-causing mutations.

K Schwarz.   

Abstract

Mesh：

Year:  1996        PMID： 8961624     DOI： 10.1016/0167-5699(96)30061-3

Source DB:  PubMed          Journal:  Immunol Today        ISSN： 0167-5699


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  7 in total

Review 1.  The Wiskott-Aldrich syndrome.

Authors:  A J Thrasher; C Kinnon
Journal:  Clin Exp Immunol       Date:  2000-04       Impact factor: 4.330

Review 2.  X-linked agammaglobulinemia: lack of mature B lineage cells caused by mutations in the Btk kinase.

Authors:  C I Smith; C M Bäckesjö; A Berglöf; L J Brandén; T Islam; P T Mattsson; A J Mohamed; S Müller; B Nore; M Vihinen
Journal:  Springer Semin Immunopathol       Date:  1998

Review 3.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Springer Semin Immunopathol       Date:  1998

Review 4.  Wiskott-Aldrich syndrome.

Authors:  S Nonoyama; H D Ochs
Journal:  Curr Allergy Asthma Rep       Date:  2001-09       Impact factor: 4.806

5.  Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing.

Authors:  Baolei Yuan; Xuan Zhou; Keiichiro Suzuki; Gerardo Ramos-Mandujano; Mengge Wang; Muhammad Tehseen; Lorena V Cortés-Medina; James J Moresco; Sarah Dunn; Reyna Hernandez-Benitez; Tomoaki Hishida; Na Young Kim; Manal M Andijani; Chongwei Bi; Manching Ku; Yuta Takahashi; Jinna Xu; Jinsong Qiu; Ling Huang; Christopher Benner; Emi Aizawa; Jing Qu; Guang-Hui Liu; Zhongwei Li; Fei Yi; Yanal Ghosheh; Changwei Shao; Maxim Shokhirev; Patrizia Comoli; Francesco Frassoni; John R Yates; Xiang-Dong Fu; Concepcion Rodriguez Esteban; Samir Hamdan; Juan Carlos Izpisua Belmonte; Mo Li
Journal:  Nat Commun       Date:  2022-06-25       Impact factor: 17.694

6.  WIP regulates signaling via the high affinity receptor for immunoglobulin E in mast cells.

Authors:  Alexander Kettner; Lalit Kumar; Inés M Antón; Yoji Sasahara; Miguel de la Fuente; Vadim I Pivniouk; Hervé Falet; John H Hartwig; Raif S Geha
Journal:  J Exp Med       Date:  2004-02-02       Impact factor: 14.307

7.  A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.

Authors:  Sook Kyung Park; Chun Soo Kim; Dae Kyu Song; Joo Young Kim; In Jang Choi; Dae Kwang Kim
Journal:  J Korean Med Sci       Date:  2007-12       Impact factor: 2.153
  7 in total

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