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Novel approach to quantitative spatial gene expression uncovers genetic stochasticity in the developing Drosophila eye

https://doi.org/10.1101/175711
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inferredcites →https://doi.org/10.1002/jez.b.21299openalex-snapshot
Association of orthodenticle with natural variation for early embryonic patterning in Drosophila melanogaster
inferredcites →https://doi.org/10.1007/978-1-4614-8232-1_3openalex-snapshot
Catching the Next Wave: Patterning of the Drosophila Eye by the Morphogenetic Furrow
inferredcites →https://doi.org/10.1007/bf01435042openalex-snapshot
Measuring fitness and intergenic interactions: The evolution of resistance to diazinon inLucilia cuprina
inferredcites →https://doi.org/10.1016/0092-8674(93)90535-xopenalex-snapshot
The TGFβ homolog dpp and the segment polarity gene hedgehog are required for propagation of a morphogenetic wave in the Drosophila retina
inferredcites →https://doi.org/10.1016/0092-8674(93)90536-yopenalex-snapshot
The segment polarity gene hedgehog is required for progression of the morphogenetic furrow in the developing Drosophila eye
inferredcites →https://doi.org/10.1016/0092-8674(95)90291-0openalex-snapshot
Hairy and Emc negatively regulate morphogenetic furrow progression in the drosophila eye
inferredcites →https://doi.org/10.1016/0092-8674(95)90508-1openalex-snapshot
cAMP-dependent protein kinase and hedgehog act antagonistically in regulating decapentaplegic transcription in drosophila imaginal discs
inferredcites →https://doi.org/10.1016/0092-8674(95)90509-xopenalex-snapshot
Function of protein kinase A in hedgehog signal transduction and Drosophila imaginal disc development
inferredcites →https://doi.org/10.1016/0165-1684(94)90060-4openalex-snapshot
Topographic distance and watershed lines
inferredcites →https://doi.org/10.1016/j.cell.2008.01.014openalex-snapshot
The Evolution of Gene Regulation Underlies a Morphological Difference between Two Drosophila Sister Species
inferredcites →https://doi.org/10.1016/j.cell.2011.05.003openalex-snapshot
Interlocked Feedforward Loops Control Cell-Type-Specific Rhodopsin Expression in the Drosophila Eye
inferredcites →https://doi.org/10.1016/j.cell.2016.05.025openalex-snapshot
Enhancer Control of Transcriptional Bursting
inferredcites →https://doi.org/10.1016/j.cub.2013.08.053openalex-snapshot
Live Imaging of Bicoid-Dependent Transcription in Drosophila Embryos
inferredcites →https://doi.org/10.1016/j.cub.2016.07.034openalex-snapshot
Genetic Convergence in the Evolution of Male-Specific Color Patterns in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2005.01.017openalex-snapshot
Extracellular Signals Responsible for Spatially Regulated Proliferation in the Differentiating Drosophila Eye
inferredcites →https://doi.org/10.1016/j.resmic.2004.01.019openalex-snapshot
Adaptation to the deleterious effects of antimicrobial drug resistance mutations by compensatory evolution
inferredcites →https://doi.org/10.1016/j.ydbio.2008.11.037openalex-snapshot
The HLH protein Extramacrochaetae is required for R7 cell and cone cell fates in the Drosophila eye
inferredcites →https://doi.org/10.1016/s0012-1606(74)80016-3openalex-snapshot
Sequential gene activation by ecdysone in polytene chromosomes of Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0092-8674(01)00266-5openalex-snapshot
The EGF Receptor Defines Domains of Cell Cycle Progression and Survival to Regulate Cell Number in the Developing Drosophila Eye
inferredcites →https://doi.org/10.1016/s0960-9822(01)00093-8openalex-snapshot
Proneural enhancement by Notch overcomes Suppressor-of-Hairless repressor function in the developing Drosophila eye
inferredcites →https://doi.org/10.1016/s0960-9822(06)00056-xopenalex-snapshot
Proneural function of neurogenic genes in the developing Drosophila eye
inferredcites →https://doi.org/10.1016/s0960-9822(98)70441-5openalex-snapshot
Multiple functions of the EGF receptor in Drosophila eye development
inferredcites →https://doi.org/10.1016/s1534-5807(03)00156-4openalex-snapshot
Distinction between Color Photoreceptor Cell Fates Is Controlled by Prospero in Drosophila
inferredcites →https://doi.org/10.1021/nn405717popenalex-snapshot
Next-Generation in Situ Hybridization Chain Reaction: Higher Gain, Lower Cost, Greater Durability
inferredcites →https://doi.org/10.1038/35046017openalex-snapshot
Genetic control and evolution of sexually dimorphic characters in Drosophila
inferredcites →https://doi.org/10.1038/369398a0openalex-snapshot
atonal is the proneural gene for Drosophila photoreceptors
inferredcites →https://doi.org/10.1038/hdy.1982.60openalex-snapshot
The effect of genetic background on the fitness of diazinon resistance genotypes of the Australian sheep blowfly, Lucilia cuprina
inferredcites →https://doi.org/10.1038/msb.2012.11openalex-snapshot
Comparative transcriptomics of pathogenic and non‐pathogenic Listeria species
inferredcites →https://doi.org/10.1038/nature04615openalex-snapshot
Stochastic spineless expression creates the retinal mosaic for colour vision
inferredcites →https://doi.org/10.1038/nature10811openalex-snapshot
The Drosophila melanogaster Genetic Reference Panel
inferredcites →https://doi.org/10.1038/ncomms10461openalex-snapshot
Periodic patterning of the Drosophila eye is stabilized by the diffusible activator Scabrous
inferredcites →https://doi.org/10.1038/ncomms12248openalex-snapshot
A single-molecule view of transcription reveals convoys of RNA polymerases and multi-scale bursting
inferredcites →https://doi.org/10.1038/nmeth.1253openalex-snapshot
Imaging individual mRNA molecules using multiple singly labeled probes
inferredcites →https://doi.org/10.1038/nrg3949openalex-snapshot
Pervasive robustness in biological systems
inferredcites →https://doi.org/10.1073/pnas.0911042107openalex-snapshot
Molecular and functional basis of phenotypic convergence in white lizards at White Sands
inferredcites →https://doi.org/10.1073/pnas.1220912110openalex-snapshot
Dynamic interpretation of maternal inputs by the Drosophila segmentation gene network
inferredcites →https://doi.org/10.1073/pnas.1410022111openalex-snapshot
Dynamic regulation of eve stripe 2 expression reveals transcriptional bursts in living Drosophila embryos
inferredcites →https://doi.org/10.1093/gbe/evx262openalex-snapshot
A Large Panel of Drosophila simulans Reveals an Abundance of Common Variants
inferredcites →https://doi.org/10.1093/genetics/120.1.213openalex-snapshot
Diazinon resistance, fluctuating asymmetry and fitness in the Australian sheep blowfly, lucilia cuprina.
inferredcites →https://doi.org/10.1093/genetics/151.3.921openalex-snapshot
Evolution by Small Steps and Rugged Landscapes in the RNA Virus ϕ6
inferredcites →https://doi.org/10.1093/molbev/msq160openalex-snapshot
Compensatory Mutations Restore Fitness during the Evolution of Dihydrofolate Reductase
inferredcites →https://doi.org/10.1098/rspb.2000.1030openalex-snapshot
Pervasive compensatory adaptation inEscherichia coli
inferredcites →https://doi.org/10.1101/gad.11.23.3254openalex-snapshot
Hedgehog directly controls initiation and propagation of retinal differentiation in the Drosophila eye
inferredcites →https://doi.org/10.1101/gr.191635.115openalex-snapshot
Noise in gene expression is coupled to growth rate
inferredcites →https://doi.org/10.1109/83.217222openalex-snapshot
Morphological grayscale reconstruction in image analysis: applications and efficient algorithms
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00313.xopenalex-snapshot
RAPID FITNESS RECOVERY IN MUTATIONALLY DEGRADED LINES OF CAENORHABDITIS ELEGANS
inferredcites →https://doi.org/10.1111/j.1558-5646.2011.01276.xopenalex-snapshot
FITNESS RECOVERY AND COMPENSATORY EVOLUTION IN NATURAL MUTANT LINES OF C. ELEGANS
inferredcites →https://doi.org/10.1126/science.1208227openalex-snapshot
optix Drives the Repeated Convergent Evolution of Butterfly Wing Pattern Mimicry
inferredcites →https://doi.org/10.1126/science.1243039openalex-snapshot
Interchromosomal Communication Coordinates Intrinsically Stochastic Expression Between Alleles
inferredcites →https://doi.org/10.1142/s0219720017500081openalex-snapshot
Quantitative analysis of the heterogeneous population of endocytic vesicles
inferredcites →https://doi.org/10.1186/1471-213x-10-28openalex-snapshot
Cell cycle arrest by a gradient of Dpp signaling during Drosophila eye development
inferredcites →https://doi.org/10.1186/1471-213x-7-13openalex-snapshot
Mechanism of G1 arrest in the Drosophilaeye imaginal disc
inferredcites →https://doi.org/10.1242/dev.113.4.1245openalex-snapshot
hairy gene function in the Drosophila eye: normal expression is dispensable but ectopic expression alters cell fates
inferredcites →https://doi.org/10.1242/dev.121.8.2279openalex-snapshot
wingless and patched are negative regulators of the morphogenetic furrow and can affect tissue polarity in the developing Drosophila compound eye
inferredcites →https://doi.org/10.1242/dev.124.17.3233openalex-snapshot
Hedgehog is an indirect regulator of morphogenetic furrow progression in the Drosophila eye disc
inferredcites →https://doi.org/10.1242/dev.124.7.1393openalex-snapshot
Drosophila embryonic pattern repair: how embryos respond to bicoid dosage alteration
inferredcites →https://doi.org/10.1242/dev.125.18.3731openalex-snapshot
Transcriptional regulation of atonal during development of the Drosophila peripheral nervous system
inferredcites →https://doi.org/10.1242/dev.125.23.4777openalex-snapshot
Regulation of EGF receptor signaling establishes pattern across the developing Drosophila retina
inferredcites →https://doi.org/10.1242/dev.126.24.5795openalex-snapshot
Progression of the morphogenetic furrow in the Drosophila eye: the roles of Hedgehog, Decapentaplegic and the Raf pathway
inferredcites →https://doi.org/10.1242/dev.128.20.3889openalex-snapshot
Notch signalling and the initiation of neural development in theDrosophilaeye
inferredcites →https://doi.org/10.1242/dev.138560openalex-snapshot
Single-molecule RNA detection at depth by hybridization chain reaction and tissue hydrogel embedding and clearing
inferredcites →https://doi.org/10.1371/journal.pbio.1001935openalex-snapshot
The Genomic Landscape of Compensatory Evolution
inferredcites →https://doi.org/10.1371/journal.pgen.1000671openalex-snapshot
Compensatory Evolution of Gene Regulation in Response to Stress by Escherichia coli Lacking RpoS
inferredcites →https://doi.org/10.1371/journal.pgen.1001186openalex-snapshot
Genetic Basis of Growth Adaptation of Escherichia coli after Deletion of pgi, a Major Metabolic Gene
inferredcites →https://doi.org/10.1371/journal.pgen.1002240openalex-snapshot
Evidence for Hitchhiking of Deleterious Mutations within the Human Genome
inferredcites →https://doi.org/10.1371/journal.pgen.1002346openalex-snapshot
A Conserved Developmental Patterning Network Produces Quantitatively Different Output in Multiple Species of Drosophila
inferredcites →https://doi.org/10.1371/journal.pgen.1003731openalex-snapshot
Dynamic Rewiring of the Drosophila Retinal Determination Network Switches Its Function from Selector to Differentiation
inferredcites →https://doi.org/10.1371/journal.pone.0047503openalex-snapshot
The Role of the bHLH Protein Hairy in Morphogenetic Furrow Progression in the Developing Drosophila Eye
inferredcites →https://doi.org/10.1387/ijdb.072483jropenalex-snapshot
Pattern formation in the Drosophila eye disc
inferredcites →https://doi.org/10.3390/biology5020028openalex-snapshot
Cryptic Genetic Variation in Evolutionary Developmental Genetics
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