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

Moursel, L.G.; Munting, L.P.; Graaf, L.M. van der; Duinen, S.G. van; Goumans, M.J.T.H.; Ueberham, U.; ... ; Weerd, L. van der (2018)

Article / Letter to editor

• hereditary cerebral hemorrhage with amyloidosis-Dutch type
• cerebral amyloid angiopathy
• amyloid beta mutation E22Q
• phospho-SMAD2
• 3 granules
• TGF beta
• postmortem human brain tissue

• All authors: Moursel, L.G.; Munting, L.P.; Graaf, L.M. van der; Duinen, S.G. van; Goumans, M.J.T.H.; Ueberham, U.; Natte, R.; Buchem, M.A. van; Roon-Mom, W.M.C. van; Weerd, L. van der
• Date: 2018-07-31
• Journal: Brain Pathology
• Volume: 28
• Issue: 4
• Pages: 495 - 506
• DOI: doi:10.1111/bpa.12533