Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
about
Actin cytoskeletal defects in immunodeficiencyMultiple WASP-interacting protein recognition motifs are required for a functional interaction with N-WASPA high-throughput chemically induced inflammation assay in zebrafish.Ubiquitylation-dependent negative regulation of WASp is essential for actin cytoskeleton dynamicsDisease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration.Platelet actin nodules are podosome-like structures dependent on Wiskott-Aldrich syndrome protein and ARP2/3 complex.WASP localizes to the membrane skeleton of platelets.Evolution of highly polymorphic T cell populations in siblings with the Wiskott-Aldrich Syndrome.Clinical and molecular characteristics of 35 Chinese children with Wiskott-Aldrich syndrome.Platelet-associated IgAs and impaired GPVI responses in platelets lacking WIP.Wiskott-Aldrich syndrome: a comprehensive review.Intermittent X-linked thrombocytopenia with a novel WAS gene mutation.Current and emerging treatment options for Wiskott-Aldrich syndrome.Sclerosing cholangitis and intracranial lymphoma in a child with classical Wiskott-Aldrich syndrome.IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function.WIP is a chaperone for Wiskott-Aldrich syndrome protein (WASP).IL-2 in the tumor microenvironment is necessary for Wiskott-Aldrich syndrome protein deficient NK cells to respond to tumors in vivo.A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disordersDiversity of polyproline recognition by EVH1 domains.The Wiskott-Aldrich syndrome: from genotype-phenotype correlation to treatment.Cytokinesis, ploidy and aneuploidy.Wiskott-Aldrich syndrome protein--dynamic regulation of actin homeostasis: from activation through function and signal termination in T lymphocytes.Prolonged survival after splenectomy in Wiskott-Aldrich syndrome: a case reportUnregulated actin polymerization by WASp causes defects of mitosis and cytokinesis in X-linked neutropenia.Wiskott-Aldrich syndrome caused by a new mutation associated with multifocal dermal juvenile xanthogranulomas.Current understanding of the Wiskott-Aldrich syndrome and prospects for gene therapy.Childhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene.Possible application of flow cytometry for evaluation of the structure and functional status of WASP in peripheral blood mononuclear cells.Development of lentiviral gene therapy for Wiskott Aldrich syndrome
P2860
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P2860
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
description
2005 nî lūn-bûn
@nan
2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@ast
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@en
type
label
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@ast
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@en
prefLabel
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@ast
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@en
P2093
P1476
Genotype-proteotype linkage in the Wiskott-Aldrich syndrome.
@en
P2093
Eileen Remold-O'Donnell
Fred S Rosen
Maxim I Lutskiy
P304
P356
10.4049/JIMMUNOL.175.2.1329
P407
P577
2005-07-01T00:00:00Z