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2008, ISBN 0300105029, xxiv, 253
When Phebe Hedges, a woman in East Hampton, New York, walked into the sea in 1806, she made visible the historical experience of a family affected by the... 
Huntington Disease | New York | Public Health | Huntington’s chorea | History, 20th Century | Huntington, George, 1850–1916 | New York (State) | Eugenics | Muncey, E. B | History | 20th century | Hedges, Phebe, 1764–1806 | History, 19th Century | 19th century | Hedges, Phebe | 1764-1806 | Huntington's chorea | 1850-1916 | Huntington, George
Book
Nature Medicine, ISSN 1078-8956, 07/2009, Volume 15, Issue 7, p. 714
Journal Article
Neurodegenerative Diseases, ISSN 1660-2854, 04/2019, Volume 18, Issue 5-6, pp. 239 - 253
Journal Article
Journal Article
Nature Neuroscience, ISSN 1097-6256, 2014, Volume 17, Issue 5, pp. 694 - 703
Journal Article
Cell, ISSN 0092-8674, 08/2015, Volume 162, Issue 3, pp. 516 - 526
Journal Article
Nature Medicine, ISSN 1078-8956, 2014, Volume 20, Issue 8, pp. 881 - 885
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
Nature, ISSN 0028-0836, 06/2008, Volume 453, Issue 7197, pp. 921 - 924
Journal Article
Journal Article