TGF beta pathway deregulation and abnormal phospho-SMAD2/3 staining in hereditary cerebral hemorrhage with amyloidosis-Dutch type

Author(s):
Moursel, L.G.; Munting, L.P. (0000-0002-2352-4451); Graaf, L.M. van der; Duinen, S.G. van; Goumans, M.J.T.H. (0000-0001-9344-6746); Ueberham, U.; Natte, R.; Buchem, M.A. van (0000-0003-1881-1998); Roon-Mom, W.M.C. van; Weerd, L. van der (0000-0002-5997-2125)
Published
2018
Publication type
Article / Letter to editor
hereditary cerebral hemorrhage with amyloidosis-Dutch typecerebral amyloid angiopathyamyloid beta mutation E22Qphospho-SMAD23 granulesTGF betapostmortem human brain tissue
Date issued
2018-07-31
Language
English
Is part of
Brain Pathology (2018), Vol. 28, no. 4, p. 495-506
hdl
1887/86394
doi
10.1111/bpa.12533