Drosophila as an In Vivo Model for Human Neurodegenerative Disease

L McGurk, A Berson, NM Bonini - Genetics, 2015 - academic.oup.com
With the increase in the ageing population, neurodegenerative disease is devastating to
families and poses a huge burden on society. The brain and spinal cord are extraordinarily …

Modeling Neurodegenerative Disorders in Drosophila melanogaster

H Bolus, K Crocker, G Boekhoff-Falk… - International Journal of …, 2020 - mdpi.com
Drosophila melanogaster provides a powerful genetic model system in which to investigate
the molecular mechanisms underlying neurodegenerative diseases. In this review, we …

VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis

KJ De Vos, GM Morotz, R Stoica… - Human molecular …, 2012 - academic.oup.com
A proline to serine substitution at position 56 in the gene encoding vesicle-associated
membrane protein-associated protein B (VAPB) causes some dominantly inherited familial …

Studies of neurodegenerative diseases using Drosophila and the development of novel approaches for their analysis

Y Nitta, A Sugie - Fly, 2022 - Taylor & Francis
The use of Drosophila in neurodegenerative disease research has contributed to the
identification of modifier genes for the pathology. The basis for neurodegenerative disease …

Drosophila melanogaster in the study of human neurodegeneration

F Hirth - CNS & Neurological Disorders-Drug Targets-CNS & …, 2010 - benthamdirect.com
Human neurodegenerative diseases are devastating illnesses that predominantly affect
elderly people. The majority of the diseases are associated with pathogenic oligomers from …

Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients

M Mitne-Neto, M Machado-Costa… - Human molecular …, 2011 - academic.oup.com
Amyotrophic lateral sclerosis (ALS) is an incurable neuromuscular disease that leads to a
profound loss of life quality and premature death. Around 10% of the cases are inherited and …

Flightless flies: Drosophila models of neuromuscular disease

TE Lloyd, JP Taylor - Annals of the New York Academy of …, 2010 - Wiley Online Library
The fruit fly, Drosophila melanogaster, has a long and rich history as an important model
organism for biologists. In particular, study of the fruit fly has been essential to much of our …

VAP proteins–from organelle tethers to pathogenic host interactors and their role in neuronal disease

S Kors, JL Costello, M Schrader - Frontiers in cell and developmental …, 2022 - frontiersin.org
Vesicle-associated membrane protein (VAMP)-associated proteins (VAPs) are ubiquitous
ER-resident tail-anchored membrane proteins in eukaryotic cells. Their N-terminal major …

Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis

HJ Chen, G Anagnostou, A Chai, J Withers… - Journal of Biological …, 2010 - jbc.org
Following the mutation screening of genes known to cause amyotrophic lateral sclerosis
(ALS) in index cases from 107 familial ALS (FALS) kindred, a point mutation was identified in …

[HTML][HTML] Neuromuscular junction dismantling in amyotrophic lateral sclerosis

V Cappello, M Francolini - International journal of molecular sciences, 2017 - mdpi.com
Neuromuscular junction assembly and plasticity during embryonic, postnatal, and adult life
are tightly regulated by the continuous cross-talk among motor nerve endings, muscle fibers …