|
| 37491400 | Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. | Nat Rev Genet | 2024 |
| 37491400 | Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans. | Nat Rev Genet | 2024 |
| 35218524 | Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development. | Cerebellum | 2023 |
| 36255738 | The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. | Hum Mol Genet | 2023 |
| 37607236 | Daam2 phosphorylation by CK2α negatively regulates Wnt activity during white matter development and injury. | Proc Natl Acad Sci U S A | 2023 |
| 37653044 | A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels. | Nat Metab | 2023 |
| 37556359 | Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases. | G3 (Bethesda) | 2023 |
| 36718090 | SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia. | Brain | 2023 |
| 37090554 | CK2α-dependent regulation of Wnt activity governs white matter development and repair. | bioRxiv | 2023 |
| 37084732 | Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. | Cell Metab | 2023 |
| 37328295 | The Voltage-Gated Sodium Channel in <i>Drosophila</i>, Para, Localizes to Dendrites As Well As Axons in Mechanosensitive Chordotonal Neurons. | eNeuro | 2023 |
| 37013900 | De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. | Genet Med | 2023 |
| 36567227 | Drosophila as a diet discovery tool for treating amino acid disorders. | Trends Endocrinol Metab | 2023 |
| 36946697 | Glia-neuron coupling via a bipartite sialylation pathway promotes neural transmission and stress tolerance in <i>Drosophila</i>. | Elife | 2023 |
| 36875645 | Sphingolipids in neurodegenerative diseases. | Front Neurosci | 2023 |
| 37319212 | Aging Fly Cell Atlas identifies exhaustive aging features at cellular resolution. | Science | 2023 |
| 37502976 | Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assays. | medRxiv | 2023 |
| 37036445 | Autolysosomal exocytosis of lipids protect neurons from ferroptosis. | J Cell Biol | 2023 |
| 35218524 | Loss of Neuron Navigator 2 Impairs Brain and Cerebellar Development. | Cerebellum | 2023 |
| 37556359 | Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases. | G3 (Bethesda) | 2023 |
| 37653044 | A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels. | Nat Metab | 2023 |
| 37502976 | Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assays. | medRxiv | 2023 |
| 37607236 | Daam2 phosphorylation by CK2α negatively regulates Wnt activity during white matter development and injury. | Proc Natl Acad Sci U S A | 2023 |
| 37090554 | CK2α-dependent regulation of Wnt activity governs white matter development and repair. | bioRxiv | 2023 |
| 37319212 | Aging Fly Cell Atlas identifies exhaustive aging features at cellular resolution. | Science | 2023 |
| 37084732 | Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. | Cell Metab | 2023 |
| 36946697 | Glia-neuron coupling via a bipartite sialylation pathway promotes neural transmission and stress tolerance in <i>Drosophila</i>. | Elife | 2023 |
| 37013900 | De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. | Genet Med | 2023 |
| 37036445 | Autolysosomal exocytosis of lipids protect neurons from ferroptosis. | J Cell Biol | 2023 |
| 37328295 | The Voltage-Gated Sodium Channel in <i>Drosophila</i>, Para, Localizes to Dendrites As Well As Axons in Mechanosensitive Chordotonal Neurons. | eNeuro | 2023 |
| 36718090 | SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia. | Brain | 2023 |
| 36875645 | Sphingolipids in neurodegenerative diseases. | Front Neurosci | 2023 |
| 36567227 | Drosophila as a diet discovery tool for treating amino acid disorders. | Trends Endocrinol Metab | 2023 |
| 36255738 | The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival. | Hum Mol Genet | 2023 |
| 34418791 | Recent insights into the role of glia and oxidative stress in Alzheimer's disease gained from Drosophila. | Curr Opin Neurobiol | 2022 |
| 35502740 | Systematic expression profiling of Dpr and DIP genes reveals cell surface codes in Drosophila larval motor and sensory neurons. | Development | 2022 |
| 36346220 | Two neuronal peptides encoded from a single transcript regulate mitochondrial complex III in <i>Drosophila</i>. | Elife | 2022 |
| 35880044 | Regulation of <i>Drosophila</i> oviduct muscle contractility by octopamine. | iScience | 2022 |
| 36206744 | De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. | Am J Hum Genet | 2022 |
| 35871307 | ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infection. | Ann Clin Transl Neurol | 2022 |
| 35484057 | 'Fly-ing' from rare to common neurodegenerative disease mechanisms. | Trends Genet | 2022 |
| 36332614 | The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. | Am J Hum Genet | 2022 |
| 36067766 | The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. | Am J Hum Genet | 2022 |
| 36125045 | Promoting validation and cross-phylogenetic integration in model organism research. | Dis Model Mech | 2022 |
| 35857503 | Neuronal activity induces glucosylceramide that is secreted via exosomes for lysosomal degradation in glia. | Sci Adv | 2022 |
| 35723254 | An expanded toolkit for <i>Drosophila</i> gene tagging using synthesized homology donor constructs for CRISPR-mediated homologous recombination. | Elife | 2022 |
| 35405010 | The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. | Hum Mol Genet | 2022 |
| 36476864 | Mechanisms of IRF2BPL-related disorders and identification of a potential therapeutic strategy. | Cell Rep | 2022 |
| 35302163 | Lord of the fruit flies: an interview with Hugo Bellen. | Dis Model Mech | 2022 |
| 35044823 | Loss of IRF2BPL impairs neuronal maintenance through excess Wnt signaling. | Sci Adv | 2022 |