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Drosophila as an In Vivo Model for Human Neurodegenerative Disease
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 …
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 …
the molecular mechanisms underlying neurodegenerative diseases. In this review, we …
VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis
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 …
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
The use of Drosophila in neurodegenerative disease research has contributed to the
identification of modifier genes for the pathology. The basis for neurodegenerative disease …
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 …
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 …
profound loss of life quality and premature death. Around 10% of the cases are inherited and …
Flightless flies: Drosophila models of neuromuscular disease
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 …
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
Vesicle-associated membrane protein (VAMP)-associated proteins (VAPs) are ubiquitous
ER-resident tail-anchored membrane proteins in eukaryotic cells. Their N-terminal major …
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 …
(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 …
are tightly regulated by the continuous cross-talk among motor nerve endings, muscle fibers …