Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
about
Comparative study of naturally occurring huntingtin fragments in Drosophila points to exon 1 as the most pathogenic species in Huntington's diseaseA potent and selective Sirtuin 1 inhibitor alleviates pathology in multiple animal and cell models of Huntington's disease.Quantitative Assessment of Eye Phenotypes for Functional Genetic Studies Using Drosophila melanogaster.A mitochondrial basis for Huntington's disease: therapeutic prospects.An automated image analysis method to measure regularity in biological patterns: a case study in a Drosophila neurodegenerative model.Rhodiola rosea Improves Lifespan, Locomotion, and Neurodegeneration in a Drosophila melanogaster Model of Huntington's Disease.The Tiny for the Biggest Answers in Huntington's Disease
P2860
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P2860
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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name
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@en
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@nl
type
label
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@en
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@nl
prefLabel
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@en
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@nl
P2093
P1476
Morphometric analysis of Huntington's disease neurodegeneration in Drosophila.
@en
P2093
Adeela Syed
Brett A Barbaro
Doug J Bornemann
J Lawrence Marsh
John Burke
Judith Purcell
Marianne R Smith
Tamas Lukacsovich
P356
10.1007/978-1-62703-438-8_3
P407
P577
2013-01-01T00:00:00Z