B. Staveley

发表

Identifying potential PARIS homologs in D. melanogaster.

E. Merzetti, B. E. Staveley, B. Staveley, 2016, Genetics and molecular research : GMR.

CHARACTERIZATION OF FBXO9 IN DROSOPHILA MELANOGASTER by Poly Talukdar, B.Sc. A Thesis submitted to the School of Graduate Studies in partial fulfillment of the requirements for the degree of Master of Science

B. E. Staveley, D. Bignell, D. Marshall, 2016 .

Arm-Gal4 inheritance influences development and lifespan in Drosophila melanogaster.

B. E. Staveley, F. A. Slade, B. Staveley, 2015, Genetics and molecular research : GMR.

The FBXO7 homologue nutcracker and binding partner PI31 in Drosophila melanogaster models of Parkinson's disease.

E. Merzetti, B. E. Staveley, Lindsay A. Dolomount, 2017, Genome.

Altered expression of CG 5961 , a putative Drosophila melanogaster homologue of FBXO 9 , provides a new model of Parkinson disease

E. Merzetti, B. E. Staveley, B. Staveley, 2016 .

Thinking Inside the Box: Drosophila F-Box Protein Models of Human Disease

E. Merzetti, B. E. Staveley, Colleen Connors, 2013 .

Genetic analysis of protein kinase B (AKT) in Drosophila

J. Woodgett, P. Heitzler, V. Stambolic, 1998, Current Biology.

Knockdown of the putative Lifeguard homologue CG3814 in neurons of Drosophila melanogaster.

P. G. M'Angale, B. E. Staveley, B. Staveley, 2016, Genetics and molecular research : GMR.

Pink1 Rescues Gal4-Induced Developmental Defects in the Drosophila Eye

A. M. Todd, B. Staveley, Amy M. Todd, 2015 .

Pink1 and parkin demonstrate multifaceted roles when co-expressed with Foxo

B. E. Staveley, A. M. Todd, B. Staveley, 2013 .

Bax-inhibitor-1 knockdown phenotypes are suppressed by Buffy and exacerbate degeneration in a Drosophila model of Parkinson disease

P. G. M'Angale, B. E. Staveley, B. Staveley, 2017, PeerJ.

The inhibition of Cg2076, the GHITM homologue in neurons of Drosophila Melanogaster can be rescued by Buffy

B. E. Staveley, P. G. M. Angale, B. Staveley, 2016 .

Genetic evidence that heparin-like glycosaminoglycans are involved in wingless signaling.

W. A. Johnson, R. Binari, A. Manoukian, 1997, Development.

Expression of Drosophila FOXO regulates growth and can phenocopy starvation

J. Kramer, B. E. Staveley, Jason Davidge, 2003, BMC Developmental Biology.

GAL4 causes developmental defects and apoptosis when expressed in the developing eye of Drosophila melanogaster.

J. Kramer, B. E. Staveley, B. Staveley, 2003, Genetics and molecular research : GMR.

Protected P-element termini suggest a role for inverted-repeat-binding protein in transposase-induced gap repair in Drosophila melanogaster.

R. Hodgetts, B. E. Staveley, T. Heslip, 1995, Genetics.

Compensatory growth in novel Drosophila Akt1 mutants

J. D. Slade, B. Staveley, 2015, BMC Research Notes.

Enhanced survival of Drosophila Akt1 hypomorphs during amino-acid starvation requires foxo.

J. D. Slade, B. Staveley, 2016, Genome.

Draft Enhanced survival of Drosophila Akt 1 hypomorphs during amino-acid starvation requires foxo

B. Staveley, 2015 .

Bcl-2 homologue Debcl enhances α-synuclein-induced phenotypes in Drosophila

P. G. M'Angale, B. E. Staveley, B. Staveley, 2016, PeerJ.

Mutant α-synuclein-induced degeneration is reduced by parkin in a fly model of Parkinson's disease

B. E. Staveley, A. Haywood, Annika F.M. Haywood, 2006 .

Alteration of Drp1 Expression in Drosophila Models of Parkinson Disease

B. E. Staveley, A. Hasan, B. Staveley, 2020 .

Mitochondrial dynamics in degenerative disease and disease models

E. Merzetti, B. E. Staveley, B. Staveley, 2013 .

A loss of Pdxk model of Parkinson disease in Drosophila can be suppressed by Buffy

P. G. M'Angale, B. E. Staveley, B. Staveley, 2017, BMC Research Notes.

Overexpression of Buffy enhances the loss of parkin and suppresses the loss of Pink1 phenotypes in Drosophila.

P. G. M'Angale, B. E. Staveley, B. Staveley, 2017, Genome.

Pink1 suppresses alpha-synuclein-induced phenotypes in a Drosophila model of Parkinson's disease.

B. Staveley, Amy M. Todd, 2008, Genome.

Expression of Pink1 with α-synuclein in the dopaminergic neurons of Drosophila leads to increases in both lifespan and healthspan.

B. Staveley, Amy M. Todd, 2012, Genetics and molecular research : GMR.

Targeting of an enhancer trap to vestigial.

R. Hodgetts, J. Bell, S. O'Keefe, 1994, Developmental biology.

Inhibition of foxo and minibrain in Dopaminergic Neurons Can Model Aspects of Parkinson Disease in Drosophila melanogaster

B. E. Staveley, Mahin S. Chavoshi, B. Staveley, 2016 .

Extended longevity and survivorship during amino-acid starvation in a Drosophila Sir2 mutant heterozygote.

B. E. Staveley, J. D. Slade, B. Staveley, 2016, Genome.

parkin counteracts symptoms in a Drosophila model of Parkinson's disease

B. Staveley, A. F. Haywood, 2004, BMC Neuroscience.

Manipulation of components that control feeding behavior in Drosophila melanogaster increases sensitivity to amino acid starvation.

B. E. Staveley, J. D. Slade, B. Staveley, 2016, Genetics and molecular research : GMR.

foxo is required for resistance to amino acid starvation in Drosophila.

J. Kramer, B. E. Staveley, J. D. Slade, 2008, Genome.

Bmc Developmental Biology Expression of Drosophila Foxo Regulates Growth and Can Phenocopy Starvation

J. Kramer, Jason Davidge, Joseph M Lockyer, 2022 .

Inhibition of mitochondrial calcium uptake 1 in Drosophila neurons.

P. G. M'Angale, B. Staveley, 2017, Genetics and molecular research : GMR.

Phenotypic consequences of copper-zinc superoxide dismutase overexpression in Drosophila melanogaster.

A. Hilliker, B. E. Staveley, J. Phillips, 1990, Genome.

parkin counteracts symptoms in a Drosophila model of Parkinson's disease

B. Staveley, A. F. Haywood, 2004, BMC Neuroscience.

Inhibition of Ref(2)P, the Drosophila homologue of the p62/SQSTM1 gene, increases lifespan and leads to a decline in motor function

B. E. Staveley, E. Hurley, B. Staveley, 2021, BMC research notes.

Inhibition of Ref(2)P, the Drosophila homologue of p62/SQSTM1, increases lifespan and leads to motor function decline

B. E. Staveley, E. Hurley, B. Staveley, 2020 .

spargel, the PGC-1α homologue, in models of Parkinson disease in Drosophila melanogaster

E. Merzetti, B. E. Staveley, B. Staveley, 2015, BMC Neuroscience.

The Bcl-2 homologue Buffy rescues α-synuclein-induced Parkinson disease-like phenotypes in Drosophila

P. G. M'Angale, B. E. Staveley, B. Staveley, 2016, BMC Neuroscience.

Successes of Modelling Parkinson Disease in Drosophila

B. E. Staveley, B. Staveley, 2012 .

12 Successes of Modelling Parkinson Disease in Drosophila

B. E. Staveley, B. Staveley, 2017 .

Drosophila Models of Parkinson Disease

B. E. Staveley, B. Staveley, 2015 .

Successes of Modelling Parkinson Disease in Drosophila 235 2 . The Drosophila approach to model human disease

B. E. Staveley, B. Staveley, 2012 .

A Blueberry Extract Supplemented Diet Partially Restores α-Synuclein-Dependent Lifespan Loss and Developmental Defects in Drosophila

D. B. Lipsett, B. Staveley, 2014 .

Bcl-2 Orthologues, Buffy and Debcl, Can Suppress Drp1-Dependent Age-Related Phenotypes in Drosophila

B. Staveley, A. Hasan, 2024, Biomolecules.

TER94 , the Drosophila Homologue of the ALS-related VCP gene, Influences Lifespan and Leads to a Decline in Motor Function

B. E. Staveley, E. Hurley, B. Staveley, 2020 .

Huntingtin interacting protein 1 can regulate neurogenesis in Drosophila

D. Nicholson, Sophie Roy, J. N. Moores, 2008, The European journal of neuroscience.

Altered expression of CG5961, a putative Drosophila melanogaster homologue of FBXO9, provides a new model of Parkinson disease.

E. Merzetti, B. Staveley, 2016, Genetics and molecular research : GMR.

The HtrA2 Drosophila model of Parkinson's disease is suppressed by the pro-survival Bcl-2 Buffy.

P. G. M'Angale, B. E. Staveley, B. Staveley, 2017, Genome.