| scholarly article | Q13442814 |
| P2093 | author name string | Hideki Yoshida | |
| Masamitsu Yamaguchi | |||
| Ibuki Ueoka | |||
| Kojiro Suda | |||
| Md Saheb Ali | |||
| Ryosuke Kowada | |||
| P2860 | cites work | Development and plasticity of the Drosophila larval neuromuscular junction | Q26820443 |
| Investigating the spreading and toxicity of prion-like proteins using the metazoan model organism C. elegans | Q27302907 | ||
| Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder | Q28117097 | ||
| The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteinsIntroduction | Q28185295 | ||
| The mitochondrial transporter family SLC25: identification, properties and physiopathology | Q28282100 | ||
| Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons | Q30477062 | ||
| Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy | Q30488471 | ||
| Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system. | Q33256174 | ||
| The drosophila neuromuscular junction: a model system for studying synaptic development and function | Q34399931 | ||
| Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production | Q34432596 | ||
| Mitochondrial carriers in the cytoplasmic state have a common substrate binding site | Q34479532 | ||
| Solute carriers as drug targets: current use, clinical trials and prospective. | Q34626714 | ||
| The uncoupling protein UCP: a membraneous mitochondrial ion carrier exclusively expressed in brown adipose tissue. | Q36923446 | ||
| Transport of adenine nucleotides in the mitochondria of Saccharomyces cerevisiae: interactions between the ADP/ATP carriers and the ATP-Mg/Pi carrier | Q37491431 | ||
| Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria | Q37669943 | ||
| FIG4 regulates lysosome membrane homeostasis independent of phosphatase function | Q38270487 | ||
| Etiology of Human Genetic Disease on the Fly. | Q38831628 | ||
| Identification of three conserved regions in the DREF transcription factors from Drosophila melanogaster and Drosophila virilis | Q39726769 | ||
| SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome | Q41005806 | ||
| Corrigendum: Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases | Q42542116 | ||
| Making a better RNAi vector for Drosophila: use of intron spacers | Q44948486 | ||
| Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. | Q46815739 | ||
| Identification of ter94, Drosophila VCP, as a strong modulator of motor neuron degeneration induced by knockdown of Caz, Drosophila FUS. | Q47071929 | ||
| Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice. | Q47249910 | ||
| A new Drosophila model of Ubiquilin knockdown shows the effect of impaired proteostasis on locomotive and learning abilities | Q47286660 | ||
| Imbalance of mitochondrial dynamics in Drosophila models of amyotrophic lateral sclerosis | Q48441334 | ||
| Genetic link between Cabeza, a Drosophila homologue of Fused in Sarcoma (FUS), and the EGFR signaling pathway | Q48716483 | ||
| Knockdown of the Drosophila FIG4 induces deficient locomotive behavior, shortening of motor neuron, axonal targeting aberration, reduction of life span and defects in eye development | Q49093185 | ||
| Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder. | Q50529218 | ||
| Novel Drosophila model for mitochondrial diseases by targeting of a solute carrier protein SLC25A46. | Q51730279 | ||
| SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy | Q87934269 | ||
| Reduction of Rpd3 suppresses defects in locomotive ability and neuronal morphology induced by the knockdown of Drosophila SLC25A46 via an epigenetic pathway | Q90718359 | ||
| Genetic screening of the genes interacting with Drosophila FIG4 identified a novel link between CMT-causing gene and long noncoding RNAs | Q91231494 | ||
| Insights into the genotype-phenotype correlation and molecular function of SLC25A46 | Q91279099 | ||
| Neuron-specific knockdown of Drosophila HADHB induces a shortened lifespan, deficient locomotive ability, abnormal motor neuron terminal morphology and learning disability | Q92890571 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P921 | main subject | lifetime | Q22675021 |
| learning disability | Q860740 | ||
| P304 | page(s) | 65-75 | |
| P577 | publication date | 2020-02-19 | |
| P1433 | published in | IBRO Reports | Q50812355 |
| P1476 | title | Neuron-specific knockdown of solute carrier protein SLC25A46a induces locomotive defects, an abnormal neuron terminal morphology, learning disability, and shortened lifespan | |
| P478 | volume | 8 |
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