X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2710) 2710
Publication (642) 642
Book Review (619) 619
Book Chapter (174) 174
Conference Proceeding (57) 57
Dissertation (34) 34
Book / eBook (5) 5
Government Document (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1970) 1970
protein misfolding (1407) 1407
humans (1280) 1280
biochemistry & molecular biology (1212) 1212
protein folding (1026) 1026
animals (913) 913
proteins (611) 611
misfolding (506) 506
aggregation (486) 486
protein aggregation (451) 451
alzheimers-disease (442) 442
amyloid (410) 410
mutation (345) 345
protein conformation (333) 333
cell biology (330) 330
mice (327) 327
protein (325) 325
amyloid - chemistry (321) 321
misfolding diseases (320) 320
biophysics (319) 319
in-vitro (301) 301
models, molecular (291) 291
nervous system diseases (282) 282
neurodegeneration (282) 282
alpha-synuclein (271) 271
alzheimer's disease (262) 262
neurodegenerative diseases (259) 259
article (256) 256
neurosciences (256) 256
amyloid - metabolism (250) 250
analysis (247) 247
oligomers (234) 234
protein structure, secondary (229) 229
amino acid sequence (220) 220
kinetics (219) 219
protein binding (219) 219
prions (216) 216
fibril formation (215) 215
prion protein (212) 212
disease (197) 197
multidisciplinary sciences (194) 194
prion (194) 194
toxicity (183) 183
research (175) 175
protein misfolding diseases (170) 170
animal diseases (158) 158
amyloidosis (155) 155
biology (153) 153
molecular chaperones (152) 152
molecular sequence data (152) 152
mechanism (151) 151
parkinsons-disease (150) 150
amyloid fibrils (148) 148
prions - metabolism (146) 146
transgenic mice (143) 143
common mechanism (142) 142
protein structure, tertiary (141) 141
biological sciences (140) 140
physiological aspects (139) 139
oxidative stress (138) 138
prions - chemistry (137) 137
peptides (136) 136
binding (135) 135
amyotrophic-lateral-sclerosis (134) 134
circular dichroism (134) 134
scrapie (132) 132
fibrils (128) 128
protein denaturation (128) 128
amyotrophic lateral sclerosis (127) 127
biochemistry (126) 126
protein stability (124) 124
thermodynamics (124) 124
creutzfeldt-jakob-disease (119) 119
parkinson's disease (119) 119
fluorescence (113) 113
in-vivo (110) 110
protein multimerization (109) 109
mutations (107) 107
endoplasmic-reticulum (104) 104
brain - metabolism (103) 103
amyloid beta-peptides - chemistry (102) 102
amyloid beta-peptides - metabolism (102) 102
proteins - chemistry (102) 102
unfolded protein response (101) 101
medicine, research & experimental (100) 100
models, biological (100) 100
cell line (99) 99
protein-misfolding diseases (99) 99
apoptosis (98) 98
genetic aspects (98) 98
pathology (98) 98
stability (96) 96
a-beta (95) 95
neurodegenerative disease (95) 95
brain (94) 94
peptide (92) 92
misfolding cyclic amplification (91) 91
hydrogen-ion concentration (90) 90
proteins - metabolism (90) 90
alzheimer disease - metabolism (89) 89
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2857) 2857
Japanese (12) 12
Chinese (6) 6
French (6) 6
German (4) 4
Korean (4) 4
Spanish (3) 3
Portuguese (2) 2
Swedish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2010, 1. Aufl., Wiley series on protein and peptide science, ISBN 0471799289, xxx, 1045
An increasingly aging population will add to the number of individuals suffering from amyloid. Protein Misfolding Diseasesprovides a systematic overview of the... 
Proteins | Protein folding | therapy | Disorders | diagnosis | Senile Plaques | Amyloidosis | Metabolism | etiology | Science | Chemistry | Industrial & Technical
Book
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2006, Volume 103, Issue 29, pp. 11045 - 11050
Journal Article
Neuroscience Letters, ISSN 0304-3940, 09/2019, Volume 709, p. 134316
Over 20 years ago, the synaptic protein α-synuclein was identified as the primary component of the Lewy bodies (LBs) that are a of Parkinson’s disease (PD).... 
Prion-like | Misfolding | Neurodegeneration | Transmission | Lewy body
Journal Article
Human Mutation, ISSN 1059-7794, 10/2012, Volume 33, Issue 10, pp. 1464 - 1473
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2015, Volume 112, Issue 16, pp. E1994 - E2003
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 03/2012, Volume 109, Issue 12, pp. 4467 - 4472
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 02/2010, Volume 396, Issue 2, pp. 375 - 383
The serpinopathies encompass a large number of diseases caused by inappropriate conformational change and self-association (polymerization) of a serpin (serine... 
Aggregation | Polymerization | Serpin | Misfolding | Metastability
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 08/2005, Volume 351, Issue 4, pp. 850 - 864
Despite its importance in biological phenomena, a comprehensive understanding of the mechanism of amyloid formation remains elusive. Here, we use atomic force... 
Protein misfolding | Atomic-force microscopy | Amyloid fibril | Protofibril | Templated growth
Journal Article
Journal Article
BMB Reports, ISSN 1976-6696, 2017, Volume 50, Issue 1, p. 37
The tubby protein (Tub), a putative transcription factor, plays important roles in the maintenance and function of neuronal cells. A splicing defect-causing... 
Aggresome | Obesity | Mutation | Misfolding | Tubby
Journal Article
Acta Pharmacologica Sinica, ISSN 1671-4083, 07/2018, Volume 39, Issue 7, pp. 1133 - 1141
Journal Article
Journal Article
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, ISSN 0027-8424, 06/2013, Volume 110, Issue 24, pp. 9758 - 9763
The generation of toxic oligomers during the aggregation of the amyloid-beta (A beta) peptide A beta 42 into amyloid fibrils and plaques has emerged as a... 
IMPLIES | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | neurodegeneration | COMMON MECHANISM | POLYMERIZATION | OLIGOMERS | FORMS | molecular mechanisms | chemical kinetics | protein misfolding | CONFORMATIONAL CONVERSION | KINETICS | PROTEINS | Naturvetenskap | Kemi | Physical Chemistry | Fysikalisk kemi | Natural Sciences | Chemical Sciences
Journal Article
03/2014
TAR DNA binding protein of 43 kDa (TDP-43) has been implicated in the pathogenesis of amyotrophic lateral sclerosis and frontotemporal lobar degeneration.... 
0487 | native state stabilization | TDP-43 | protein aggregation | protein misfolding | FTLD | ALS | aggregation inhibition
Dissertation
ACS Chemical Neuroscience, ISSN 1948-7193, 05/2019, Volume 10, Issue 5, pp. 2374 - 2384
Aggregation of the amyloid-β (Aβ) peptide into plaques is believed to play a crucial role in Alzheimer's disease. Amyloid plaques consist of fibrils of full... 
toxicity | aggregation mechanism | coaggregation | Misfolding | Alzheimer | BACE
Journal Article
Neuroscientist, ISSN 1073-8584, 2019, pp. 1073858418822993 - 1073858418822993
Polyglutamine (polyQ) diseases are a group of hereditary neurodegenerative disorders caused by expansion of unstable polyQ repeats in their associated disease... 
neurodegeneration | protein misfolding | muscle | peripheral pathology | CAG repeat expansion
Journal Article
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.