نتایج جستجو برای: wiskott

تعداد نتایج: 1772  

Journal: :Bioorganic & medicinal chemistry letters 2011
Brenda N Goguen Galen S Loving Barbara Imperiali

Cdc42, a member of the Rho GTPase family, is a fundamental regulator of the actin cytoskeleton during cell migration. To generate a sensor for Cdc42 activation, we employed a multi-pronged approach, utilizing cysteine labeling and expressed protein ligation, to incorporate the environment sensitive fluorophore 4-N,N-dimethylamino-1,8-naphthalimide (4-DMN) into the GTPase binding domain of the W...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Daisy W Leung Chinatsu Otomo Joanne Chory Michael K Rosen

General methods to engineer genetically encoded, reversible, light-mediated control over protein function would be useful in many areas of biomedical research and technology. We describe a system that yields such photo-control over actin assembly. We fused the Rho family GTPase Cdc42 in its GDP-bound form to the photosensory domain of phytochrome B (PhyB) and fused the Cdc42 effector, the Wisko...

Journal: :The Journal of clinical investigation 1996
F S Rosen

Journal: :Blood 1980
J T Prchal A J Carroll J F Prchal W M Crist H W Skalka W J Gealy J Harley A Malluh

A family in which two male siblings were affected with Wiskott-Aldrich syndrome (WAS) was studied using G-6-PD isoenzymes as an X-linked marker in order to investigate the nature of cellular abnormalities. Isolated peripheral blood cell types from the doubly heterozygous mother of the affected males seemingly failed to express the G-6-PD allele in cis position with the WAS allele while her cult...

2012
Elad Noy Sophia Fried Omri Matalon Mira Barda-Saad

Actin polymerization is a fundamental cellular process regulating immune cell functions and the immune response. The Wiskott-Aldrich syndrome protein (WASp) is an actin nucleation promoting factor, which is exclusively expressed in hematopoietic cells, where it plays a key regulatory role in cytoskeletal dynamics. WASp interacting protein (WIP) was first discovered as the binding partner of WAS...

Journal: :Blood 1998
A Petrella I Doti V Agosti P C Giarrusso D Vitale H M Bond C Cuomo P Tassone B Franco A Ballabio S Venuta G Morrone

The recently-identified Wiskott-Aldrich syndrome protein gene (WASP) is responsible for the Wiskott-Aldrich X-linked immunodeficiency as well as for isolated X-linked thrombocytopenia (XLT). To characterize the regulatory sequences of the WASP gene, we have isolated, sequenced and functionally analyzed a 1.6-Kb DNA fragment upstream of the WASP coding sequence. Transfection experiments showed t...

Journal: :Blood 2004
Kohsuke Imai Tomohiro Morio Yi Zhu Yinzhu Jin Sukeyuki Itoh Michiko Kajiwara Jun-Ichi Yata Shuki Mizutani Hans D Ochs Shigeaki Nonoyama

Mutations of the Wiskott-Aldrich syndrome protein (WASP) gene result either in the classic Wiskott-Aldrich syndrome (WAS) or in a less severe form, X-linked thrombocytopenia (XLT). A phenotype-genotype correlation has been reported by some but not by other investigators. In this study, we characterized WASP gene mutations in 50 Japanese patients and analyzed the clinical phenotype and course of...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید