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Kendal Broadie
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Journal Articles

Glycosphingolipids are linked to elevated neurotransmission and neurodegeneration in a Drosophila model of Niemann Pick type C

In collection:
Drosophila as a Disease Model , Neurodegenerative Disorders
Anna E. Eberwein, Swarat S. Kulkarni, Emma Rushton, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2023) 16 (10): dmm050206.
https://doi.org/10.1242/dmm.050206
Published: 12 October 2023
View article titled, Glycosphingolipids are linked to elevated neurotransmission and neurodegeneration in a Drosophila model of Niemann Pick type C
Open the PDF for Glycosphingolipids are linked to elevated neurotransmission and neurodegeneration in a Drosophila model of Niemann Pick type C in another window
Includes: Supplementary data
Journal Articles

Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease model

In collection:
Drosophila as a Disease Model
William M. Parkinson, Michelle Dookwah, Mary Lynn Dear, Cheryl L. Gatto, Kazuhiro Aoki, Michael Tiemeyer, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2016) 9 (5): 513–527.
https://doi.org/10.1242/dmm.022939
Published: 1 May 2016
View article titled, Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease model
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Journal Articles

Overelaborated synaptic architecture and reduced synaptomatrix glycosylation in a Drosophila classic galactosemia disease model

Patricia Jumbo-Lucioni, William Parkinson, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2014) 7 (12): 1365–1378.
https://doi.org/10.1242/dmm.017137
Published: 1 December 2014
View article titled, Overelaborated synaptic architecture and reduced synaptomatrix glycosylation in a Drosophila classic galactosemia disease model
Open the PDF for Overelaborated synaptic architecture and reduced synaptomatrix glycosylation in a Drosophila classic galactosemia disease model in another window
Journal Articles

Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila

Samuel H. Friedman, Neil Dani, Emma Rushton, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2013) 6 (6): 1400–1413.
https://doi.org/10.1242/dmm.012229
Published: 1 November 2013
View article titled, Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila
Open the PDF for Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila in another window
Includes: Supplementary data
Journal Articles

Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase

Saul S. Siller, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2011) 4 (5): 673–685.
https://doi.org/10.1242/dmm.008045
Published: 1 September 2011
View article titled, Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase
Open the PDF for Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase in another window
Includes: Supplementary data
Journal Articles

Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P

R. Lane Coffee, Jr, Charles R. Tessier, Elvin A. Woodruff, III, Kendal Broadie
Journal: Disease Models & Mechanisms
Dis Model Mech (2010) 3 (7-8): 471–485.
https://doi.org/10.1242/dmm.004598
Published: 7 July 2010
View article titled, Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P
Open the PDF for Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P in another window
Includes: Supplementary data