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Citations |
Human
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Organoids
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Chip
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Mouse
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Arthropods
1.Oliveira FGL, et al. A morphofunctional study of the jumping apparatus in globular springtails. Arthropod Struct Dev (2024). http://dx.doi.org/10.1016/j.asd.2024.101333
2.Jackson JA, et al. Change in RhoGAP and RhoGEF availability drives transitions in cortical patterning and excitability in Drosophila. Curr Biol (2024). http://dx.doi.org/10.1016/j.cub.2024.04.021
3.Pan X, et al. De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. Am J Hum Genet (2024). http://dx.doi.org/10.1016/j.ajhg.2024.02.007
4.Ma M, et al. Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma. Genet Med (2024). http://dx.doi.org/10.1016/j.gim.2024.101125
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6.Dutta D et al. A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels. Nat Metab (2023). http://dx.doi.org/10.1038/s42255-023-00873-0
7.Bademosi AT et al. EndophilinA-dependent coupling between activity-induced calcium influx and synaptic autophagy is disrupted by a Parkinson-risk mutation. Neuron (2023). http://dx.doi.org/10.1016/j.neuron.2023.02.001
8.Praschberger R et al. Neuronal identity defines α-synuclein and tau toxicity. Neuron (2023). http://dx.doi.org/10.1016/j.neuron.2023.02.033
9.Diegmiller R et al. Fusome topology and inheritance during insect gametogenesis. PLoS Comput Biol (2023). http://dx.doi.org/10.1371/journal.pcbi.1010875
10.Hakes et al. Plasticity of Drosophila germ granules during germ cell development. PLoS Biol (2023). http://dx.doi.org/10.1371/journal.pbio.3002069
11.Ravenscroft TA et al. The Voltage-Gated Sodium Channel in Drosophila, Para, Localizes to Dendrites As Well As Axons in Mechanosensitive Chordotonal Neurons. eNeuro (2023). http://dx.doi.org/10.1523/ENEURO.0105-23.2023
12.Chung HL et al. Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation. Cell Metab (2023). http://dx.doi.org/10.1016/j.cmet.2023.03.022
13.Rillich B et al. On latches in biological systems: a comparative morphological and functional study of the retinaculum and the dens lock in Collembola. Front Zool (2023). http://dx.doi.org/10.1186/s12983-023-00491-2
14.Tepe B et al. Bi-allelic variants in INTS11 are associated with a complex neurological disorder. Am J Hum Genet (2023). http://dx.doi.org/10.1016/j.ajhg.2023.03.012
15.Jans K et al. Dietary lithium stimulates female fecundity in Drosophila melanogaster. Biofactors (2023). http://dx.doi.org/10.1002/biof.2007
16.Steinhoff POM et al. Comparative neuroanatomy of the central nervous system in web-building and cursorial hunting spiders. J Comp Neurol (2023). http://dx.doi.org/10.1002/cne.25554
17.Lin HH et al. A nutrient-specific gut hormone arbitrates between courtship and feeding. Nature (2022). http://dx.doi.org/10.1038/s41586-022-04408-7
18.Li S et al. Humidity response in Drosophila olfactory sensory neurons requires the mechanosensitive channel TMEM63. Nature Commun (2022). https://doi.org/10.1038/s41467-022-31253-z
19.Wang L et al. Neuronal activity induces glucosylceramide that is secreted via exosomes for lysosomal degradation in glia. Sci Adv (2022). https://doi.org/10.1126/sciadv.abn3326
20.Hernández K et al. Dscam1 overexpression impairs the function of the gut nervous system in Drosophila. Dev Dyn (2022). https://doi.org/10.1002/dvdy.554
21.Oliveira FGL. On springtails (Hexapoda: Collembola): a morphofunctional study of the jumping apparatus. Front Zool (2022). https://doi.org/10.1186/s12983-022-00463-y
22.Farnworth MS et al. An atlas of the developing Tribolium castaneum brain reveals conservation in anatomy and divergence in timing to Drosophila melanogaster. J Comp Neurol (2022). https://doi.org/10.1002/cne.25335
23.Alsous JI et al. Clonal dominance in excitable cell networks. Nature Physics (2021). https://doi.org/10.1038/s41567-021-01383-0
24.Diegmiller R et al. Size scaling in collective cell growth. Development (2021). https://doi.org/10.1242/dev.199663
25.Yang DM et al. Monitoring the Heavy Metal Lead Inside Living Drosophila with a FRET-Based Biosensor. Sensors (Basel) (2021). https://doi.org/10.3390/s20061712
26.Doherty CA et al. Coupled oscillators coordinate collective germline growth. Dev Cell (2021). http://dx.doi.org/10.1016/j.devcel.2021.02.015
27.Alsous JI et al. Dynamics of hydraulic and contractile wave-mediated fluid transport during Drosophila oogenesis. Proc Natl Acad Sci U S A (2021). http://dx.doi.org/10.1073/pnas.2019749118
28.Ravenscroft TA et al. Drosophila Voltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains. J Neurosci (2020). http://dx.doi.org/10.1523/JNEUROSCI.0142-20.2020
29.Chung HL et al. Loss- Or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron (2020). https://doi.org/10.1016/j.neuron.2020.02.021
30.Ye H et al. Retromer Subunit, VPS29, Regulates Synaptic Transmission and Is Required for Endolysosomal Function in the Aging Brain. eLife (2020). https://doi.org/10.7554/eLife.51977
31.Göpel T et al. The Circulatory System of Penaeus Vannamei Boone, 1931-Lacunar Function and a Reconsideration of the “Open vs. Closed System” Debate. J Morphol (2020). https://doi.org/10.1002/jmor.21117
32.Yang DM et al. Monitoring the Heavy Metal Lead Inside Living Drosophila with a FRET-Based Biosensor. Sensors (Basel) (2020). https://doi.org/10.3390/s20061712
33.Frase T et al. The Brain and the Corresponding Sense Organs in Calanoid Copepods – Evidence of Vestiges of Compound Eyes. Arthropod Struct Dev (2020). https://doi.org/10.1016/j.asd.2019.100902
34.Kalke P et al. From swimming towards sessility in two metamorphoses – the drastic changes in structure and function of the nervous system of the bay barnacle Amphibalanus improvisus (Crustacea, Thecostraca, Cirripedia) during development. Contributions to Zoology (2020). https://doi.org/10.1163/18759866-bja10003
35.Guo H et al. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun (2019). http://dx.doi.org/10.1038/s41467-019-12435-8
36.Kurtz P et al. Drosophila p53 directs non-apoptotic programs in postmitotic tissue. Mol Biol Cell (2019).https://doi.org/10.1091/mbc.E18-12-0791
37.Benavides LR et al. Phylogeny, evolution and systematic revision of the mite harvestman family Neogoveidae (Opiliones Cyphophthalmi). Invertebrate Systematics (2019). https://doi.org/10.1071/IS18018
38.Göpel T et al. Morphological description, character conceptualization and the reconstruction of ancestral states exemplified by the evolution of arthropod hearts. PLoS One (2018). https://doi.org/10.1371/journal.pone.0201702
39.Marcogliese PC et al. IRF2BPL Is Associated with Neurological Phenotypes. Am J Hum Genet (2018). https://doi.org/10.1016/j.ajhg.2018.07.006
40.Lin G et al. Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain. Cell Metab (2018). https://doi.org/10.1016/j.cmet.2018.05.019
41.Li-Kroeger D et al. An expanded toolkit for gene tagging based on MiMIC and scarless CRISPR tagging in Drosophila. eLife (2018). https://doi.org/10.7554/eLife.38709.001
42.Liu N et al. Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder. Hum Mol Genet (2018). https://doi.org/10.1093/hmg/ddy146
43.Lee PT et al. A gene-specific T2A-GAL4 library for Drosophila. eLife (2018). https://doi.org/10.7554/eLife.35574
44.Lee PT et al. A kinase-dependent feedforward loop affects CREBB stability and long term memory formation. eLife (2018). https://doi.org/10.7554/eLife.33007.001
45.Myers L et al. The Drosophila Ret gene functions in the stomatogastric nervous system with the Maverick TGFβ ligand and the Gfrl co-receptor. Development. (2018). http://dx.doi.org/10.1242/dev.157446
46.Frank DD et al. Early Integration of Temperature and Humidity Stimuli in the Drosophila Brain. Curr Biol (2017). http://dx.doi.org/10.1016/j.cub.2017.06.077
47.Enjin A et al. Humidity Sensing in Drosophila. Curr Biol (2017). http://dx.doi.org/10.1016/j.cub.2016.03.049
48.Osterfield M et al. Diversity of epithelial morphogenesis during eggshell formation in drosophilids. Development (2015). http://dev.biologists.org/lookup/doi/10.1242/dev.119404
49.Nagarkar-Jaiswal S et al. A library of MiMICs allows tagging of genes and reversible spatial and temporal knockdown of proteins in Drosophila. eLife (2015). http://dx.doi.org/10.7554/eLife.05338
Porcine
1.Yang H et al. Quantitative study of the microvasculature and its endothelial cells in the porcine iris. Exp Eye Res (2015). http://dx.doi.org/10.1016/j.exer.2015.02.006
2.Yang H et al. Intracellular cytoskeleton and junction proteins of endothelial cells in the porcine iris microvasculature. Exp Eye Res (2015). http://dx.doi.org/10.1016/j.exer.2015.08.025
Zebrafish
1.Iwamoto A, et al. Effect of Defective Calcium Metabolism on Otolith Formation in Zebrafish. Med Sci Innov (2024). https://petit.lib.yamaguchi-u.ac.jp/29723
2.Steventon B et al. Species-specific contribution of volumetric growth and tissue convergence to posterior body elongation in vertebrates. Development (2016). http://dev.biologists.org/lookup/doi/10.1242/dev.126375 |
| Information |
RapiClear® is a water-soluble clearing reagent that can make biological tissues transparent swiftly and easily. It can vastly enhance the visualization depth of specimen labelled with fluorescent dyes to micrometers, even millimeters. RapiClear® can be widely applied in cell morphology observation of tissues from animal, plant, and insect, as well as in portraying biomaterial scaffolds such as collagen and cellulose. The application of RapiClear® makes construction of detailed 3D images possible. |
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