Oculocerebrorenal syndrome of Lowe protein controls cytoskeletal reorganisation during human platelet spreading-Reference-Cited by-同舟云学术

Oculocerebrorenal syndrome of Lowe protein controls cytoskeletal reorganisation during human platelet spreading

Published:2022-09-29 Issue:1 Volume:200 Page:87-99
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Bura Ana¹,de Matteis Maria Antonietta²³,Bender Markus⁴^ORCID,Swinkels Maurice⁵^ORCID,Versluis Jurjen⁵,Jansen A. J. Gerard⁵^ORCID,Jurak Begonja Antonija¹^ORCID

Affiliation:

1. Department of Biotechnology University of Rijeka Rijeka Croatia

2. Telethon Institute of Genetics and Medicine, TIGEM Pozzuoli Naples Italy

3. Department of Molecular Medicine and Medical Biotechnology University of Naples Federico II Naples Italy

4. Institute of Experimental Biomedicine University Hospital Wuerzburg, Rudolf Virchow Center Wuerzburg Germany

5. Erasmus MC University Medical Center Rotterdam the Netherlands

Funder

American Society of Hematology

Associazione Italiana per la Ricerca sul Cancro

Deutsche Forschungsgemeinschaft

Fondazione Telethon

H2020 European Research Council

Hrvatska Zaklada za Znanost

International Centre for Genetic Engineering and Biotechnology

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.18478

Reference56 articles.

1. Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms.

2. Cloning and expression of human 75-kDa inositol polyphosphate-5-phosphatase.

3. AttreeO OlivosIM OkabeI BaileyLC NelsonDL LewisRAet al.The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate‐5‐phosphatase.1992.

4. The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase.