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1970, Emily Chamberlain Cook contest, Volume 1969-1970, [3] leaves.
Book
2006, Methods in enzymology, ISBN 9780121828189, Volume 413., xxxvi, 375
The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a... 
Amyloid | Prions | Amyloid beta-protein | Amyloid beta-Peptides
Book
2006, Methods in enzymology, ISBN 0121828174, Volume 412., xl, 403
The ability of polypeptides to form alternatively folded, polymeric structures such as amyloids and related aggregates is being increasingly recognized as a... 
Amyloid | Prions | Amyloid beta-protein | Amyloid beta-Peptides
Book
Nature Structural & Molecular Biology, ISSN 1545-9993, 04/2009, Volume 16, Issue 4, pp. 380 - 389
Journal Article
1999, Methods in enzymology ; 309., ISBN 0121822109, Volume 309, xix, 820 p. : ill. ; 24 cm.
This volume includes a core of methodologies to attack the unique experimental problems presented by protein misassembly. Emphasis is on human biology... 
Amyloid | Protein folding | Prions | Cell aggregation | Proteins | Amyloid beta-protein
Book
2006, Methods in enzymology, ISBN 9780080468976, Volume 413.
Web Resource
1997, Advances in protein chemistry, ISBN 0120342502, Volume 50., xx, 282
Book
Journal of Biological Chemistry, ISSN 0021-9258, 01/2006, Volume 281, Issue 2, pp. 993 - 1000
We describe here the use of cysteine substitution mutants in the Alzheimer disease amyloid plaque peptide A beta -(1-40) to probe amyloid fibril structure and... 
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 01/2016, Volume 428, Issue 2, pp. 274 - 291
Journal Article
Neuron, ISSN 0896-6273, 12/2009, Volume 64, Issue 6, pp. 828 - 840
The N-terminal 17 amino acids of huntingtin (NT17) can be phosphorylated on serines 13 and 16; however, the significance of these modifications in Huntington's... 
humdisease | molneuro | NEURONAL INTRANUCLEAR INCLUSIONS | NUCLEAR | PHOSPHORYLATION | EXPANSION | NEURODEGENERATION | TOXICITY | PATHOLOGY | TRANSGENIC MOUSE MODEL | NEUROSCIENCES | AGGREGATION | TRINUCLEOTIDE REPEAT | Molecular Weight | Humans | Nerve Degeneration - physiopathology | Nerve Degeneration - genetics | Alanine - chemistry | Amino Acid Sequence - genetics | Nerve Degeneration - metabolism | Aspartic Acid - genetics | Nerve Tissue Proteins - chemistry | Alanine - genetics | Amyloid - metabolism | Nuclear Proteins - genetics | Huntington Disease - physiopathology | Disease Models, Animal | Amyloid - genetics | Genetic Predisposition to Disease - genetics | Gene Expression Regulation - genetics | Serine - genetics | Alanine - metabolism | Mice, Transgenic | Protein Structure, Tertiary - genetics | Mutation - genetics | Nuclear Proteins - chemistry | Serine - chemistry | Huntington Disease - metabolism | Nerve Tissue Proteins - genetics | Serine - metabolism | Huntingtin Protein | Phenotype | Animals | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Amino Acid Substitution - genetics | Aspartic Acid - metabolism | Mice | Aspartic Acid - chemistry | Proteins | Medical colleges | Alanine | Nervous system diseases | Neurosciences | Huntington's chorea | Neurons | Physiological aspects | Aspartate | Huntingtons disease | Phosphorylation | Neurodegeneration | Pathogenesis | Neuropathology | Rodents | Mutation | Index Medicus
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2015, Volume 1345, pp. 67 - 87
Journal Article
International Journal of Refrigeration, ISSN 0140-7007, 02/2019, Volume 98, pp. 211 - 221
Journal Article