Literature DB >> 23571384

De novo splice mutation in the versican gene in a family with Wagner syndrome.

Pierre-Raphaël Rothschild, Isabelle Audo, Brigitte Nedelec, Tiffany Ghiotti, Antoine P Brézin, Claire Monin, Sophie Valleix.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2013        PMID： 23571384     DOI： 10.1001/jamaophthalmol.2013.681

Source DB:  PubMed          Journal:  JAMA Ophthalmol        ISSN： 2168-6165            Impact factor:   7.389


× No keyword cloud information.
  4 in total

1.  Multimodal Imaging in Wagner Syndrome.

Authors:  Akshay S Thomas; Kari Branham; Russell N Van Gelder; Stephen P Daiger; Lori S Sullivan; Sara J Bowne; John R Heckenlively; Mark E Pennesi
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2016-06-01       Impact factor: 1.300

2.  The versican-hyaluronan complex provides an essential extracellular matrix niche for Flk1+ hematoendothelial progenitors.

Authors:  Sumeda Nandadasa; Anna O'Donnell; Ayako Murao; Yu Yamaguchi; Ronald J Midura; Lorin Olson; Suneel S Apte
Journal:  Matrix Biol       Date:  2021-01-14       Impact factor: 11.583

3.  A family with Wagner syndrome with uveitis and a new versican mutation.

Authors:  Pierre-Raphaël Rothschild; Antoine P Brézin; Brigitte Nedelec; Cyril Burin des Roziers; Tiffany Ghiotti; Lucie Orhant; Mathieu Boimard; Sophie Valleix
Journal:  Mol Vis       Date:  2013-09-26       Impact factor: 2.367

4.  Identification of Novel Copy Number Variations of VCAN Gene in Three Chinese Families with Wagner Disease.

Authors:  Songshan Li; Mengke Li; Limei Sun; Xiujuan Zhao; Ting Zhang; Li Huang; Sijian Huang; Chonglin Chen; Zhirong Wang; Xiaoyan Ding
Journal:  Genes (Basel)       Date:  2020-08-25       Impact factor: 4.096
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.