| scholarly article | Q13442814 |
| P50 | author | Barry Ganetzky | Q57191850 |
| P2093 | author name string | Michael J Palladino | |
| Tricia J Hadley | |||
| P2860 | cites work | Temperature-sensitive paralytic mutations demonstrate that synaptic exocytosis requires SNARE complex assembly and disassembly | Q28281473 |
| Absence epilepsy in tottering mutant mice is associated with calcium channel defects | Q28587452 | ||
| Mechanisms of neurotransmitter release | Q33602444 | ||
| Modeling human neurodegenerative diseases in Drosophila: on a wing and a prayer. | Q33870792 | ||
| Insights from mouse models into the molecular basis of neurodegeneration | Q33938799 | ||
| Studying human neurodegenerative diseases in flies and worms | Q34083380 | ||
| The significance of tau and alpha-synuclein inclusions in neurodegenerative diseases | Q34264641 | ||
| The molecular bases of Alzheimer's disease and other neurodegenerative disorders | Q34386085 | ||
| The swiss cheese mutant causes glial hyperwrapping and brain degeneration in Drosophila. | Q34439060 | ||
| A Drosophila mutation that eliminates a calcium-dependent potassium current | Q37406521 | ||
| A Drosophila mutant with a temperature-sensitive block in nerve conduction | Q37593423 | ||
| Spongecake and eggroll: two hereditary diseases in Drosophila resemble patterns of human brain degeneration | Q38554951 | ||
| Preventing neurodegeneration in the Drosophila mutant bubblegum | Q41673343 | ||
| Seizures and failures in the giant fiber pathway of Drosophila bang- sensitive paralytic mutants | Q41680198 | ||
| Modifications of seizure susceptibility in Drosophila | Q41718887 | ||
| Genetic suppression of polyglutamine toxicity in Drosophila | Q41724127 | ||
| Apoptosis, excitotoxicity, and neuropathology | Q41729276 | ||
| Tauopathy in Drosophila: neurodegeneration without neurofibrillary tangles | Q43642001 | ||
| Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons. | Q45296540 | ||
| Defective glia in the Drosophila brain degeneration mutant drop-dead | Q46099342 | ||
| Genetic suppression of seizure susceptibility in Drosophila | Q46160513 | ||
| A-to-I pre-mRNA editing in Drosophila is primarily involved in adult nervous system function and integrity | Q47070866 | ||
| Expanded polyglutamine protein forms nuclear inclusions and causes neural degeneration in Drosophila | Q47945602 | ||
| Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene | Q48045866 | ||
| The Drosophila erg K+ channel polypeptide is encoded by the seizure locus | Q48054809 | ||
| A Component of Calcium-activated Potassium Channels Encoded by the Drosophila slo Locus | Q48215777 | ||
| Molecular analysis of the para locus, a sodium channel gene in Drosophila | Q48287063 | ||
| The structural brain mutant Vacuolar medulla of Drosophila melanogaster with specific behavioral defects and cell degeneration in the adult | Q48349708 | ||
| Neural disease: Drosophila degenerates for a good cause | Q48352728 | ||
| Genetic dissection of behavior / Seymour Benzer. - (1973) | Q52470662 | ||
| Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70. | Q52574703 | ||
| Abnormal Electroretinograms in Visual Mutants of Drosophila | Q59059939 | ||
| Nonphototactic Mutants in a Study of Vision of Drosophila | Q59071581 | ||
| Neuropathology of degenerative cell death in Caenorhabditis elegans | Q71971010 | ||
| Increased proteolytic activity of the granule neurons may contribute to neuronal death in the weaver mouse cerebellum | Q72189408 | ||
| The lurcher gene induces apoptotic death in cerebellar Purkinje cells | Q72221078 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Drosophila | Q312154 |
| neurodegeneration | Q1755122 | ||
| P1104 | number of pages | 12 | |
| P304 | page(s) | 1197-1208 | |
| P577 | publication date | 2002-07-01 | |
| P1433 | published in | Genetics | Q3100575 |
| P1476 | title | Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila | |
| P478 | volume | 161 |
| Q36858585 | A Drosophila model for Angelman syndrome |
| Q47597551 | A Presynaptic Function of Shank Protein in Drosophila. |
| Q33374520 | A functional misexpression screen uncovers a role for enabled in progressive neurodegeneration. |
| Q41140839 | A mutation in Drosophila Aldolase causes temperature-sensitive paralysis, shortened lifespan, and neurodegeneration |
| Q35050903 | A neuroprotective function of NSF1 sustains autophagy and lysosomal trafficking in Drosophila |
| Q36206004 | A novel Drosophila SOD2 mutant demonstrates a role for mitochondrial ROS in neurodevelopment and disease |
| Q44893473 | Acute induction of conserved synaptic signaling pathways in Drosophila melanogaster. |
| Q91890102 | Aging and the clock: Perspective from flies to humans |
| Q55420913 | Bone marrow transplantation corrects haemolytic anaemia in a novel ENU mutagenesis mouse model of TPI deficiency. |
| Q93025387 | CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum |
| Q57652395 | Characterization of Drosophila ATPsynC mutants as a new model of mitochondrial ATP synthase disorders |
| Q35227177 | Death following traumatic brain injury in Drosophila is associated with intestinal barrier dysfunction. |
| Q36724350 | Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology |
| Q36669350 | Demonstrating the temperature sensitivity of synaptic transmission in a Drosophila mutant. |
| Q24676326 | Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy |
| Q37012024 | Evidence of a triosephosphate isomerase non-catalytic function crucial to behavior and longevity |
| Q30576721 | Female contact modulates male aggression via a sexually dimorphic GABAergic circuit in Drosophila |
| Q52691945 | Flubendiamide affects visual and locomotory activities of Drosophila melanogaster for three successive generations (P, F1 and F2). |
| Q28394202 | Genetically encoded redox sensor identifies the role of ROS in degenerative and mitochondrial disease pathogenesis |
| Q41726164 | Genome-wide screen for modifiers of Na (+) /K (+) ATPase alleles identifies critical genetic loci |
| Q34204041 | Hsp70- and Hsp90-mediated proteasomal degradation underlies TPIsugarkill pathogenesis in Drosophila |
| Q36104670 | Intramyocellular fatty-acid metabolism plays a critical role in mediating responses to dietary restriction in Drosophila melanogaster |
| Q50868181 | Lithium chloride alleviates neurodegeneration partly by inhibiting activity of GSK3β in a SCA3 Drosophila model. |
| Q33647726 | Maintaining the brain: insight into human neurodegeneration from Drosophila melanogaster mutants |
| Q39694673 | Mislocalization of mitochondria and compromised renal function and oxidative stress resistance in Drosophila SesB mutants. |
| Q47257087 | Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila. |
| Q51736760 | Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a Drosophila Model of Leigh Syndrome. |
| Q47072041 | Mitochondrial encephalomyopathy in Drosophila. |
| Q37351787 | Mitochondrial superoxide radicals differentially affect muscle activity and neural function |
| Q27317174 | Modes of metabolic compensation during mitochondrial disease using the Drosophila model of ATP6 dysfunction |
| Q21563602 | Modification of a hydrophobic layer by a point mutation in syntaxin 1A regulates the rate of synaptic vesicle fusion |
| Q35846393 | Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila |
| Q47071329 | Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants. |
| Q64861600 | Neurodegeneration and locomotor dysfunction in Drosophila scarlet mutants |
| Q36856014 | Neurodegeneration in a Drosophila model of adrenoleukodystrophy: the roles of the Bubblegum and Double bubble acyl-CoA synthetases |
| Q36269243 | Neurodegenerative mutants in Drosophila: a means to identify genes and mechanisms involved in human diseases? |
| Q34587578 | Neuropathology in Drosophila membrane excitability mutants |
| Q36470506 | Neuropathology in Drosophila mutants with increased seizure susceptibility |
| Q37470011 | Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity |
| Q33859513 | Pantethine rescues a Drosophila model for pantothenate kinase-associated neurodegeneration |
| Q36873362 | Probing mechanisms that underlie human neurodegenerative diseases in Drosophila |
| Q34645131 | Profile of Barry Ganetzky |
| Q40778134 | Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders |
| Q42024986 | Sialyltransferase regulates nervous system function in Drosophila |
| Q34575681 | Sodium valproate alleviates neurodegeneration in SCA3/MJD via suppressing apoptosis and rescuing the hypoacetylation levels of histone H3 and H4 |
| Q27309025 | Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics |
| Q37365327 | Swiss cheese et allii, some of the first neurodegenerative mutants isolated in Drosophila. |
| Q34610836 | The genetic analysis of functional connectomics in Drosophila |
| Q34714976 | Triosephosphate isomerase I170V alters catalytic site, enhances stability and induces pathology in a Drosophila model of TPI deficiency |
| Q51699373 | Wiser (tsl): a recessive X-linked temperature-sensitive lethal mutation that affects the wings and the eyes in Drosophila melanogaster. |
| Q35056697 | wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death |
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