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Journal of the American College of Cardiology, ISSN 0735-1097, 07/2016, Volume 68, Issue 1, p. 25
Journal Article
Amyloid, ISSN 1350-6129, 03/2019, Volume 26, Issue sup1, pp. 27 - 28
Journal Article
Kidney International, ISSN 0085-2538, 09/2019, Volume 96, Issue 3, pp. 628 - 641
Amyloidoses are rare life-threatening diseases caused by protein misfolding of normally soluble proteins. The fatal outcome is predominantly due to renal... 
mouse model | glomerular amyloid deposits | hereditary systemic amyloidosis | Life Sciences | Human health and pathology
Journal Article
Journal Article
JOURNAL OF BIOLOGICAL CHEMISTRY, ISSN 0021-9258, 04/2019, Volume 294, Issue 15, pp. 6130 - 6141
The tetrameric protein transthyretin is a transporter of retinol and thyroxine in blood, cerebrospinal fluid, and the eye, and is secreted by the liver,... 
inhibition mechanism | peptide | POLYNEUROPATHY | amyloidosis | PROTEIN | SAFETY | transthyretin | BIOCHEMISTRY & MOLECULAR BIOLOGY | peptides | inhibition | DIFLUNISAL | POTENT | amyloid | drug discovery | DEPOSITS | seeding | TAFAMIDIS | protein aggregation | aging | AGGREGATION
Journal Article
Proceedings of the National Academy of Sciences of the United States, ISSN 0027-8424, 07/2018, Volume 115, Issue 29, p. 7463
Journal Article
Amyloid, ISSN 1350-6129, 10/2018, Volume 25, Issue 4, pp. 215 - 219
The nomenclature committee of the International Society of Amyloidosis (ISA) meets every second year to discuss and formulate recommendations. The conclusions... 
nomenclature | aggregation | Amyloid | amyloidosis | misfolding | MEDICINE, RESEARCH & EXPERIMENTAL | MEDICINE, GENERAL & INTERNAL | PROTEIN | DEPOSITS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Terminology as Topic | Amyloidosis - classification | International Agencies | Humans | Societies, Scientific | Amyloid - classification
Journal Article
Journal Article
Neurodegenerative disease management, 02/2019, Volume 9, Issue 1, pp. 25 - 30
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 07/2000, Volume 300, Issue 5, pp. 1033 - 1039
Tissue deposition of normally soluble proteins, or their fragments, as insoluble amyloid fibrils causes the usually fatal, acquired and hereditary systemic... 
electron microscopy | protofilaments | amyloid | image analysis | fibrils | Protofilaments | Image analysis | Amyloid | Electron microscopy | Fibrils | VISUALIZATION | TRANSTHYRETIN | VARIANTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | X-RAY-DIFFRACTION | HUMAN LYSOZYME | FIBRILLOGENESIS | MICROSCOPY | FRAGMENTS | BETA-PROTEIN | APOLIPOPROTEIN-A-I | Immunoglobulin lambda-Chains - ultrastructure | Humans | Plaque, Amyloid - chemistry | Apolipoprotein A-I - genetics | Prealbumin - ultrastructure | Protein Structure, Quaternary | Apolipoprotein A-I - ultrastructure | Serum Amyloid A Protein - ultrastructure | Prealbumin - chemistry | Apolipoprotein A-I - chemistry | Immunoglobulin lambda-Chains - chemistry | Peptide Fragments - ultrastructure | Peptide Fragments - metabolism | Serum Amyloid A Protein - metabolism | Protein Structure, Secondary | Muramidase - chemistry | Muramidase - genetics | Muramidase - metabolism | Apolipoprotein A-I - metabolism | Microscopy, Electron | Mutation - genetics | Muramidase - ultrastructure | Immunoglobulin lambda-Chains - metabolism | Peptide Fragments - chemistry | Serum Amyloid A Protein - chemistry | Image Processing, Computer-Assisted | Prealbumin - metabolism | Amino Acid Substitution - genetics | Plaque, Amyloid - metabolism | Amyloid Neuropathies - metabolism | Plaque, Amyloid - ultrastructure | Index Medicus
Journal Article
Neurodegenerative disease management, 12/2018
Hereditary  transthyretin amyloidosis (ATTR) is a fatal systemic disease that results from deposition of the misfolded protein transthyretin (TTR) in tissues.... 
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 07/2018, Volume 379, Issue 1, pp. 22 - 31
Journal Article
Amyloid, ISSN 1350-6129, 10/2016, Volume 23, Issue 4, pp. 209 - 213
The Nomenclature Committee of the International Society of Amyloidosis (ISA) met during the XVth Symposium of the Society, 3 July-7 July 2016, Uppsala, Sweden,... 
inclusion body | nomenclature | amyloidosis | Amyloid fibril | amyloid protein | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSTHYRETIN AMYLOIDOSIS | MEDICINE, GENERAL & INTERNAL | TRANSMISSION | SEMEN | DISEASE | SENILE SYSTEMIC AMYLOIDOSIS | Staining and Labeling - methods | Prealbumin - genetics | Guidelines as Topic | Apolipoprotein C-III - chemistry | Protein Precursors - chemistry | Humans | Apolipoprotein C-III - metabolism | tau Proteins - metabolism | Amyloidosis - diagnosis | Amyloidogenic Proteins - chemistry | Apolipoprotein C-III - genetics | Apolipoprotein C-II - genetics | tau Proteins - chemistry | Sequence Analysis, Protein | tau Proteins - genetics | Amyloidosis - genetics | Amyloidosis - classification | Prealbumin - chemistry | alpha-Synuclein - genetics | Apolipoprotein C-II - chemistry | Amyloidogenic Proteins - genetics | Biomarkers - metabolism | Gene Expression | Protein Precursors - genetics | Amyloidosis - pathology | Terminology as Topic | Protein Precursors - metabolism | alpha-Synuclein - chemistry | Amyloidogenic Proteins - metabolism | Prealbumin - metabolism | Apolipoprotein C-II - metabolism | Birefringence | Congo Red - chemistry | alpha-Synuclein - metabolism | Coloring Agents - chemistry | Index Medicus | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Cell- och molekylärbiologi
Journal Article
Amyloid, ISSN 1350-6129, 6/2012, Volume 19, Issue S1, pp. 14 - 15
Current dogma for transthyretin (TTR) pathogenesis is that mutations in TTR alter its structure such that the tetramer becomes unstable and prone to release of... 
wild-type | Transthyretin | Wild-type | MEDICINE, RESEARCH & EXPERIMENTAL | MEDICINE, GENERAL & INTERNAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | PREALBUMIN | Prealbumin - genetics | Amyloidosis - pathology | Prealbumin - metabolism | Amyloidosis - genetics | Humans | Protein Multimerization | Amyloidosis - metabolism | Index Medicus
Journal Article
Kidney International, ISSN 0085-2538, 05/2010, Volume 77, Issue 9, pp. 757 - 759
LECT2 amyloidosis is the latest systemic type of amyloidosis to be described. It was discovered in patients with nephrotic syndrome and renal failure and is... 
AMINO-ACID-SEQUENCE | PROTEIN | PURIFICATION | LIVER | UROLOGY & NEPHROLOGY | MICE | EXPRESSION | Amyloidosis - pathology | Kidney - pathology | Renal Insufficiency - pathology | Humans | Nephrotic Syndrome - pathology | Amyloidosis - drug therapy | Kidney Glomerulus - pathology | Index Medicus
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 68, Issue 1, pp. 25 - 28
  Other tests including serum and urine electrophoresis with immunofixation, serum free light-chain concentrations, echocardiography with strain, cardiac... 
Cardiovascular | Internal Medicine | endomyocardial biopsy | light-chain amyloid | amyloidosis | immunohistochemistry | transthyretin | survival | STATEMENT | CARDIAC & CARDIOVASCULAR SYSTEMS | THERAPY | DISEASE | Cardiomyopathies | Amyloid | Amyloidosis | Biopsy | Humans | Prealbumin | Proteins | Immunoglobulins | Apolipoproteins | Cardiomyopathy | Light | Index Medicus | Abridged Index Medicus
Journal Article