| P2093 | author name string | Hiroshi Takashima | |
| | Hideki Yoshida | |
| | Masamitsu Yamaguchi | |
| | Yasushi Okada | |
| | Jialin Li | |
| | Ryo Tanaka | |
| | Yuji Okamoto | |
| | Ibuki Ueoka | |
| | Yu Hiramatsu | |
| | Kojiro Suda | |
| P2860 | cites work | Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein | Q24308776 |
| | Degradation of aromatics and chloroaromatics by Pseudomonas sp. strain B13: cloning, characterization, and analysis of sequences encoding 3-oxoadipate:succinyl-coenzyme A (CoA) transferase and 3-oxoadipyl-CoA thiolase | Q24538758 |
| | Development and plasticity of the Drosophila larval neuromuscular junction | Q26820443 |
| | Methods to assay Drosophila behavior | Q30452184 |
| | Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons | Q30477062 |
| | A model of toxic neuropathy in Drosophila reveals a role for MORN4 in promoting axonal degeneration | Q33112264 |
| | The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients | Q37125579 |
| | Peripheral neuropathy associated with mitochondrial disease in children | Q37995703 |
| | The clinical and biochemical spectrum of human pyruvate dehydrogenase complex deficiency | Q38244968 |
| | The DNA replication-related element (DRE)/DRE-binding factor system is a transcriptional regulator of the Drosophila E2F gene | Q38333101 |
| | Molecular pathogenesis of peripheral neuropathies: insights from Drosophila models | Q38755995 |
| | Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease | Q39541685 |
| | Identification of three conserved regions in the DREF transcription factors from Drosophila melanogaster and Drosophila virilis | Q39726769 |
| | Fuel selection in animals | Q39748853 |
| | Properties and subunit structure of pig heart pyruvate dehydrogenase | Q43987947 |
| | A new Drosophila model of Ubiquilin knockdown shows the effect of impaired proteostasis on locomotive and learning abilities | Q47286660 |
| | Neuron-specific knockdown of the Drosophila fat induces reduction of life span, deficient locomotive ability, shortening of motoneuron terminal branches and defects in axonal targeting. | Q47727633 |
| | Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein. | Q51532431 |
| | Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46. | Q51730279 |
| | Neuron-specific knockdown of Drosophila PDHB induces reduction of lifespan, deficient locomotive ability, abnormal morphology of motor neuron terminals and photoreceptor axon targeting. | Q51736444 |
| | Hippo, Drosophila MST, is a novel modifier of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS | Q57462896 |
| | Mitochondrial neuropathy | Q81638264 |
| | Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs | Q91231494 |
| P433 | issue | 2 | |
| P921 | main subject | lifetime | Q22675021 |
| | learning disability | Q860740 |
| P304 | page(s) | 150-158 | |
| P577 | publication date | 2019-04-03 | |
| P1433 | published in | Experimental Cell Research | Q1524289 |
| P1476 | title | Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability | |
| P478 | volume | 379 | |