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Biochemical and Biophysical Research Communications, ISSN 0006-291X, 10/2019, Volume 518, Issue 1, pp. 94 - 99
The second domain of gelsolin (G2) hosts mutations responsible for a hereditary form of amyloidosis. The active form of gelsolin is Ca -bound; it is also a... 
X-ray crystallography | Pathogenic mutations | Gelsolin | Calcium | AGel amyloidosis | Physiological aspects | Amyloidosis | Structure | Crystals | Index Medicus
Journal Article
Molecular Imaging and Biology, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, pp. 887 - 897
Gelsolin amyloidosis (AGel), also known as familial amyloidosis, Finnish type (FAF), is an autosomal, dominant, incurable disease caused by a point mutation... 
Nanobody | AGel | Medicine & Public Health | VHH | Gelsolin | Imaging / Radiology | SPECT | Index Medicus
Journal Article
Composites: Mechanics, Computations, Applications, ISSN 2152-2057, 2018, Volume 9, Issue 4, pp. 311 - 329
Journal Article
1999, Springer laboratory., ISBN 3540656359, xiv, 234
Book
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 07/2019, Volume 116, Issue 28, pp. 13958 - 13963
Journal Article
Amyloid, ISSN 1350-6129, 07/2019, Volume 26, Issue 3, pp. 118 - 124
Objectives: Previous clinical studies have shown frequent cardiac symptoms in patients with hereditary gelsolin (AGel) amyloidosis, possibly related to amyloid... 
hereditary amyloidosis | AGel | Meretoja disease | Gelsolin | heart | MEDICINE, RESEARCH & EXPERIMENTAL | TRANSTHYRETIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | INVOLVEMENT | BIOPSY | FEATURES | MEDICINE, GENERAL & INTERNAL | FINNISH-TYPE | FAMILIAL AMYLOIDOSIS | DYSTROPHY | MUTATION | Index Medicus
Journal Article
MOLECULAR IMAGING AND BIOLOGY, ISSN 1536-1632, 12/2016, Volume 18, Issue 6, pp. 887 - 897
Gelsolin amyloidosis (AGel), also known as familial amyloidosis, Finnish type (FAF), is an autosomal, dominant, incurable disease caused by a point mutation... 
Nanobody | BREAST-CARCINOMA | GELSOLIN AMYLOIDOSIS | SINGLE-DOMAIN ANTIBODY | BLOOD-BRAIN-BARRIER | SPECT | ANTI-HER2 NANOBODY | HEAVY-CHAIN | IN-VITRO | FRAGMENTS | AGel | FAMILIAL AMYLOIDOSIS | VHH | FINNISH TYPE | Gelsolin | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Journal Article
1990, 2nd ed., Practical approach series., ISBN 9780199630837, xix, 311
Book
Fortschritte der Neurologie · Psychiatrie, ISSN 0720-4299, 04/2011, Volume 79, Issue 4, pp. 238 - 241
Zusammenfassung Die AGel-Amyloidose ist eine autosomal dominant vererbte systemische Amyloidose, die bisher überwiegend in Finnland nachgewiesen wurde. Diese... 
Kasuistik | facial palsy | hereditary amyloidosis | gelsolin | polyneuropathy | AGel amyloidosis
Journal Article
Design and Culture, ISSN 1754-7075, 03/2014, Volume 6, Issue 1, pp. 85 - 109
Adam Michaels, cofounder of Project Projects and editor/designer of the Inventory Books series, and Jeffrey Schnapp, Professor and founder of Harvard's... 
media theory | new media | Quentin Fiore | paperback book | Jeffrey Schnapp | Adam Michaels | Jerome Agel | Marshall McLuhan | Marshall mcluhan | Adam michaels | Jeffrey schnapp | New media | Paperback book | Quentin fiore | Media theory | Jerome agel | ART
Journal Article
Amyloid, ISSN 1350-6129, 12/2009, Volume 16, Issue 4, pp. 246 - 246
Hereditary gelsolin amyloidosis (AGel amyloidosis) is a systemic disorder caused by a G654A or G654T gelsolin mutation, reported from Europe, North America,... 
posterior column degeneration | amyloid | ataxia | gelsolin | complement | peripheral neuropathy | AGel amyloidosis
Journal Article
Proceedings - 2018 4th International Conference on Science and Technology, ICST 2018, 11/2018
Conference Proceeding
Amyloid, ISSN 1350-6129, 3/2013, Volume 20, Issue 1, pp. 39 - 44
Journal Article
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