<p>(A,B) Knock-down of Aop (3166R-1) suppresses the climbing (A) and wing inflation phenotype (B) caused by pan-neuronal knock-down of Surf1 with <i>nSyb-Gal4</i>. (C,D) Heterozygosity for <i>pnt</i> (<i>pnt</i><sup><i>Δ88</i></sup>) suppresses the climbing (C) and wing inflation phenotype (D) caused by knock-down of Surf1 with <i>nSyb-Gal4</i>. (E,F) Heterozygosity for <i>Ras85D</i> (<i>Ras85D</i><sup><i>ΔC40B</i></sup>) suppresses the climbing (E) and wing inflation phenotype (F) caused by knock-down of Surf1 with <i>nSyb-Gal4</i>. Controls are <i>nSyb-Gal4</i> hemizygotes. (G,H) Heterozygosity for <i>pnt</i> (G), or <i>Ras85D</i> (H) suppresses the climbing phenotype in <i>park</i><sup><i>25</i></sup> homozygous flies. Controls are <i>w<...
The G2019S mutation within the LRRK2 gene, is the most common genetic cause of Parkinson’s, being re...
<p>(A) Inhibition of Dl and Notch in the dopaminergic neurons during adulthood shortens and extends ...
Drosophila is a well-established model to study the molecular basis of neurodegenerative diseases. W...
Mitochondrial dysfunction activates the mitochondrial retrograde signaling pathway, resulting in lar...
<div><p>Mitochondrial dysfunction activates the mitochondrial retrograde signaling pathway, resultin...
<p>(A,B) Knock-down of Aop (3166R-1) suppresses the climbing (A) and wing inflation phenotype (B) ca...
Abstract Background The identification of a DNA variant in pyridoxal kinase (Pdxk) associated with i...
Although the pathogenesis of Parkinsonâ s disease (PD) remains unclear, mutations in leucine-rich r...
Neurological diseases are devastating illnesses that affect over one billion people worldwide. Droso...
<p>Like PQ-exposed <i>TH-Gal4>UAS-hsp70</i> flies, exposed <i>TH-Gal4>UAS-HSPA1L</i> flies also exhi...
<p>(A) Numbers of genes that are mis-regulated by Pnt and Aop knock-down versus control. (B) Correla...
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder. Despite recent adva...
(A) Representative confocal images of cortical Kenyon neurons of the Drosophila brain sections show ...
Introduction: Mitochondrial defects have been implicated in Parkinson's disease (PD) since complex I...
Many neurodegenerative disorders, such as Alzheimer's, Parkinson's and polyglutamine disea...
The G2019S mutation within the LRRK2 gene, is the most common genetic cause of Parkinson’s, being re...
<p>(A) Inhibition of Dl and Notch in the dopaminergic neurons during adulthood shortens and extends ...
Drosophila is a well-established model to study the molecular basis of neurodegenerative diseases. W...
Mitochondrial dysfunction activates the mitochondrial retrograde signaling pathway, resulting in lar...
<div><p>Mitochondrial dysfunction activates the mitochondrial retrograde signaling pathway, resultin...
<p>(A,B) Knock-down of Aop (3166R-1) suppresses the climbing (A) and wing inflation phenotype (B) ca...
Abstract Background The identification of a DNA variant in pyridoxal kinase (Pdxk) associated with i...
Although the pathogenesis of Parkinsonâ s disease (PD) remains unclear, mutations in leucine-rich r...
Neurological diseases are devastating illnesses that affect over one billion people worldwide. Droso...
<p>Like PQ-exposed <i>TH-Gal4>UAS-hsp70</i> flies, exposed <i>TH-Gal4>UAS-HSPA1L</i> flies also exhi...
<p>(A) Numbers of genes that are mis-regulated by Pnt and Aop knock-down versus control. (B) Correla...
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder. Despite recent adva...
(A) Representative confocal images of cortical Kenyon neurons of the Drosophila brain sections show ...
Introduction: Mitochondrial defects have been implicated in Parkinson's disease (PD) since complex I...
Many neurodegenerative disorders, such as Alzheimer's, Parkinson's and polyglutamine disea...
The G2019S mutation within the LRRK2 gene, is the most common genetic cause of Parkinson’s, being re...
<p>(A) Inhibition of Dl and Notch in the dopaminergic neurons during adulthood shortens and extends ...
Drosophila is a well-established model to study the molecular basis of neurodegenerative diseases. W...