On the public citation graph
Maternal Co-ordinate Gene Regulation and Axis Polarity in the Scuttle Fly Megaselia abdita
0 signed · 107 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1985.tb04030.xopenalex-snapshot
Isolation of caudal, a Drosophila homeo box‐containing gene with maternal expression, whose transcripts form a concentration gradient at the pre‐blastoderm stage
inferredcites →https://doi.org/10.1002/j.1460-2075.1988.tb02801.xopenalex-snapshot
Gap genes define the limits of antennapedia and bithorax gene expression during early development in Drosophila.
inferredcites →https://doi.org/10.1006/tpbi.2000.1460openalex-snapshot
Phenogenetic Drift and the Evolution of Genotype–Phenotype Relationships
inferredcites →https://doi.org/10.1007/bf00585968openalex-snapshot
Der Entwicklungsgang der Mi�bildung ?Doppelabdomen? im partiell UV-bestrahlten Ei von Smittia parthenogenetica (Dipt., Chironomidae)
inferredcites →https://doi.org/10.1007/s00427-008-0204-5openalex-snapshot
Expression and regulation of caudal in the lower cyclorrhaphan fly Megaselia
inferredcites →https://doi.org/10.1007/s004270050238openalex-snapshot
Segmentation gene expression in the mothmidge Clogmia albipunctata (Diptera, Psychodidae) and other primitive dipterans
inferredcites →https://doi.org/10.1007/s10709-006-0032-3openalex-snapshot
Compensatory vs. pseudocompensatory evolution in molecular and developmental interactions
inferredcites →https://doi.org/10.1016/0092-8674(87)90124-3openalex-snapshot
Pole region-dependent repression of the Drosophila gap gene Krüppel by maternal gene products
inferredcites →https://doi.org/10.1016/0092-8674(87)90197-8openalex-snapshot
Expression of the caudal gene in the germ line of Drosophila: Formation of an RNA and protein gradient during early embryogenesis
inferredcites →https://doi.org/10.1016/0092-8674(88)90183-3openalex-snapshot
The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner
inferredcites →https://doi.org/10.1016/0092-8674(89)90062-7openalex-snapshot
The gradient morphogen bicoid is a concentration-dependent transcriptional activator
inferredcites →https://doi.org/10.1016/0092-8674(91)90110-kopenalex-snapshot
Nanos is the localized posterior determinant in Drosophila
inferredcites →https://doi.org/10.1016/0092-8674(92)90466-popenalex-snapshot
The origin of pattern and polarity in the Drosophila embryo
inferredcites →https://doi.org/10.1016/0925-4773(96)00504-7openalex-snapshot
orthodenticle regulation during embryonic head development in Drosophila
inferredcites →https://doi.org/10.1016/j.cell.2007.05.025openalex-snapshot
Probing the Limits to Positional Information
inferredcites →https://doi.org/10.1016/j.cell.2007.05.026openalex-snapshot
Stability and Nuclear Dynamics of the Bicoid Morphogen Gradient
inferredcites →https://doi.org/10.1016/j.cub.2009.06.061openalex-snapshot
hunchback Functions as a Segmentation Gene in the Spider Achaearanea tepidariorum
inferredcites →https://doi.org/10.1016/j.tree.2012.01.016openalex-snapshot
A model of developmental evolution: selection, pleiotropy and compensation
inferredcites →https://doi.org/10.1016/j.ydbio.2007.10.037openalex-snapshot
Characterization of the Drosophila segment determination morphome
inferredcites →https://doi.org/10.1016/j.ydbio.2010.07.010openalex-snapshot
Mutual regulatory interactions of the trunk gap genes during blastoderm patterning in the hemipteran Oncopeltus fasciatus
inferredcites →https://doi.org/10.1016/j.ydbio.2013.01.008openalex-snapshot
Quantitative dynamics and increased variability of segmentation gene expression in the Drosophila Krüppel and knirps mutants
inferredcites →https://doi.org/10.1016/j.ydbio.2013.04.001openalex-snapshot
Erratum to “Quantitative dynamics and increased variability of segmentation gene expression in the Drosophila Krüppel and knirps mutants” [Dev. Biol. 376 (2013) 99–112]
inferredcites →https://doi.org/10.1016/s0092-8674(94)90622-xopenalex-snapshot
Synergy between the hunchback and bicoid morphogens is required for anterior patterning in Drosophila
inferredcites →https://doi.org/10.1016/s0925-4773(97)00100-7openalex-snapshot
Comparison of bicoid-dependent regulation of hunchback between Musca domestica and Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0925-4773(98)00014-8openalex-snapshot
Activation of posterior pair-rule stripe expression in response to maternal caudal and zygotic knirps activities
inferredcites →https://doi.org/10.1016/s0960-9822(03)00451-2openalex-snapshot
Live Imaging of Endogenous RNA Reveals a Diffusion and Entrapment Mechanism for nanos mRNA Localization in Drosophila
inferredcites →https://doi.org/10.1038/23709openalex-snapshot
Caudal is the Hox gene that specifies the most posterior Drosophile segment
inferredcites →https://doi.org/10.1038/287795a0openalex-snapshot
Mutations affecting segment number and polarity in Drosophila
inferredcites →https://doi.org/10.1038/324537a0openalex-snapshot
A molecular gradient in early Drosophila embryos and its role in specifying the body pattern
inferredcites →https://doi.org/10.1038/324668a0openalex-snapshot
Cross-regulatory interactions among the gap genes of Drosophila
inferredcites →https://doi.org/10.1038/332281a0openalex-snapshot
Regulation of the Drosophila segmentation gene hunchback by two maternal morphogenetic centres
inferredcites →https://doi.org/10.1038/335025a0openalex-snapshot
The molecular genetics of embryonic pattern formation in Drosophila
inferredcites →https://doi.org/10.1038/337138a0openalex-snapshot
The bicoid protein is a positive regulator of hunchback transcription in the early Drosophila embryo
inferredcites →https://doi.org/10.1038/338646a0openalex-snapshot
The Drosophila posterior-group gene nanos functions by repressing hunchback activity
inferredcites →https://doi.org/10.1038/338741a0openalex-snapshot
Differing strategies for organizing anterior and posterior body pattern in Drosophila embryos
inferredcites →https://doi.org/10.1038/340363a0openalex-snapshot
Determination of spatial domains of zygotic gene expression in the Drosophila embryo by the affinity of binding sites for the bicoid morphogen
inferredcites →https://doi.org/10.1038/341340a0openalex-snapshot
The caudal gene product is a direct activator of fushi tarazu transcription during Drosophila embryogenesis
inferredcites →https://doi.org/10.1038/346577a0openalex-snapshot
A morphogenetic gradient of hunchback protein organizes the expression of the gap genes Krüppel and knirps in the early Drosophila embryo
inferredcites →https://doi.org/10.1038/376253a0openalex-snapshot
Activation of posterior gap gene expression in the Drosophila blastoderm
inferredcites →https://doi.org/10.1038/sdata.2015.5openalex-snapshot
High-resolution gene expression data from blastoderm embryos of the scuttle fly Megaselia abdita
inferredcites →https://doi.org/10.1046/j.1525-142x.2001.003002109.xopenalex-snapshot
Developmental system drift and flexibility in evolutionary trajectories
inferredcites →https://doi.org/10.1046/j.1525-142x.2001.003004251.xopenalex-snapshot
Divergent structure and function of the bicoid gene in Muscoidea fly species
inferredcites →https://doi.org/10.1046/j.1525-142x.2001.01043.xopenalex-snapshot
Rapid restructuring of bicoid‐dependent hunchback promoters within and between Dipteran species: implications for molecular coevolution
inferredcites →https://doi.org/10.1046/j.1525-142x.2002.02016.xopenalex-snapshot
Coevolution in bicoid‐dependent promoters and the inception of regulatory incompatibilities among species of higher Diptera
inferredcites →https://doi.org/10.1073/pnas.012292899openalex-snapshot
A single Hox3 gene with composite bicoid and zerknüllt expression characteristics in non-Cyclorrhaphan flies
inferredcites →https://doi.org/10.1073/pnas.0500373102openalex-snapshot
The role of binding site cluster strength in Bicoid-dependent patterning in Drosophila
inferredcites →https://doi.org/10.1073/pnas.1012675108openalex-snapshot
Episodic radiations in the fly tree of life
inferredcites →https://doi.org/10.1073/pnas.190095397openalex-snapshot
Function of bicoid and hunchback homologs in the basal cyclorrhaphan fly Megaselia (Phoridae)
inferredcites →https://doi.org/10.1073/pnas.96.7.3786openalex-snapshot
The anterior determinant bicoid of Drosophila is a derived Hox class 3 gene
inferredcites →https://doi.org/10.1093/emboj/16.14.4403openalex-snapshot
Mechanism and Bicoid‐dependent control of hairy stripe 7 expression in the posterior region of the Drosophila embryo
inferredcites →https://doi.org/10.1093/nar/gku1142openalex-snapshot
SuperFly: a comparative database for quantified spatio-temporal gene expression patterns in early dipteran embryos
inferredcites →https://doi.org/10.1101/pdb.emo143openalex-snapshot
The Scuttle Fly Megaselia abdita (Phoridae): A Link between Drosophila and Mosquito Development
inferredcites →https://doi.org/10.1101/pdb.prot5600openalex-snapshot
Megaselia abdita: Culturing and Egg Collection
inferredcites →https://doi.org/10.1101/pdb.prot5602openalex-snapshot
Megaselia abdita: Fixing and Devitellinizing Embryos: Figure 1.
inferredcites →https://doi.org/10.1111/j.1440-169x.2006.00881.xopenalex-snapshot
Role of hunchback in segment patterning of Locusta migratoria manilensis revealed by parental RNAi
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00252.xopenalex-snapshot
bicoid occurrence and Bicoid‐dependent hunchback regulation in lower cyclorrhaphan flies
inferredcites →https://doi.org/10.1186/1471-2164-14-123openalex-snapshot
Comparative transcriptomics of early dipteran development
inferredcites →https://doi.org/10.1242/dev.01046openalex-snapshot
hunchbackis required for suppression of abdominal identity, and for proper germband growth and segmentation in the intermediate germband insectOncopeltus fasciatus
inferredcites →https://doi.org/10.1242/dev.01289openalex-snapshot
Differential cytoplasmic mRNA localisation adjusts pair-rule transcription factor activity to cytoarchitecture in dipteran evolution
inferredcites →https://doi.org/10.1242/dev.01784openalex-snapshot
Non-canonical functions ofhunchbackin segment patterning of the intermediate germ cricketGryllus bimaculatus
inferredcites →https://doi.org/10.1242/dev.018317openalex-snapshot
Delimiting the conserved features of hunchback function for the trunk organization of insects
inferredcites →https://doi.org/10.1242/dev.01939openalex-snapshot
A major role for zygotichunchbackin patterning theNasoniaembryo
inferredcites →https://doi.org/10.1242/dev.02576openalex-snapshot
AcaudalmRNA gradient controls posterior development in the waspNasonia
inferredcites →https://doi.org/10.1242/dev.030270openalex-snapshot
Evidence for a composite anterior determinant in the hover flyEpisyrphus balteatus(Syrphidae), a cyclorrhaphan fly with an anterodorsal serosa anlage
inferredcites →https://doi.org/10.1242/dev.046649openalex-snapshot
Maternal activation of gap genes in the hover fly Episyrphus
inferredcites →https://doi.org/10.1242/dev.067926openalex-snapshot
Diversity in insect axis formation: two orthodenticle genes and hunchback act in anterior patterning and influence dorsoventral organization in the honeybee (Apis mellifera)
inferredcites →https://doi.org/10.1242/dev.101.1.1openalex-snapshot
The molecular basis for metameric pattern in the Drosophila embryo
inferredcites →https://doi.org/10.1242/dev.101.3.421openalex-snapshot
Hierarchy of the genetic interactions that specify the anteroposterior segmentation pattern of the Drosophila embryo as monitored by caudal protein expression
inferredcites →https://doi.org/10.1242/dev.109.2.271openalex-snapshot
Effects of ectopic expression of caudal during Drosophila development
inferredcites →https://doi.org/10.1242/dev.111.2.367openalex-snapshot
Interactions of the Drosophila gap gene giant with maternal and zygotic pattern-forming genes
inferredcites →https://doi.org/10.1242/dev.111.2.601openalex-snapshot
Spatial regulation of the gap gene giant during Drosophila development
inferredcites →https://doi.org/10.1242/dev.111.2.611openalex-snapshot
Mutually repressive interactions between the gap genes giant and Krüppel define middle body regions of the Drosophila embryo
inferredcites →https://doi.org/10.1242/dev.112.3.679openalex-snapshot
The maternal gene nanos has a central role in posterior pattern formation of the Drosophila embryo
inferredcites →https://doi.org/10.1242/dev.12.1.89openalex-snapshot
Studies on embryonic determination of the harlequin-fly, Chironomus dorsalis. II. Effects of partial irradiation of the egg by ultra-violet light
inferredcites →https://doi.org/10.1242/dev.120.10.3043openalex-snapshot
Autonomous concentration-dependent activation and repression of Krüppel by hunchback in the Drosophila embryo
inferredcites →https://doi.org/10.1242/dev.121.12.4227openalex-snapshot
Conserved and divergent expression aspects of the Drosophila segmentation gene hunchback in the short germ band embryo of the flour beetle Tribolium
inferredcites →https://doi.org/10.1242/dev.121.4.1023openalex-snapshot
Zygotic caudal regulation by hunchback and its role in abdominal segment formation of the Drosophila embryo
inferredcites →https://doi.org/10.1242/dev.128.18.3459openalex-snapshot
Grasshopperhunchbackexpression reveals conserved and novel aspects of axis formation and segmentation
inferredcites →https://doi.org/10.1242/dev.31.2.329openalex-snapshot
Embryonic defects in Drosophila eggs after partial u.v. irradiation at different wavelengths
inferredcites →https://doi.org/10.1242/dev.97.1.169openalex-snapshot
Histochemical and autoradiographic study of the cultured rat visceral yolk sac
inferredcites →https://doi.org/10.1242/jcs.29.1.1openalex-snapshot
Pattern formation in early insect embryogenesis-data calling for modification of a recent model
inferredcites →https://doi.org/10.1371/journal.pbio.1000596openalex-snapshot
The Formation of the Bicoid Morphogen Gradient Requires Protein Movement from Anteriorly Localized mRNA
inferredcites →https://doi.org/10.1371/journal.pcbi.1002589openalex-snapshot
Efficient Reverse-Engineering of a Developmental Gene Regulatory Network
inferredcites →https://doi.org/10.1371/journal.pone.0046658openalex-snapshot
Medium-Throughput Processing of Whole Mount In Situ Hybridisation Experiments into Gene Expression Domains
inferredcites →https://doi.org/10.1371/journal.pone.0084421openalex-snapshot
A Staging Scheme for the Development of the Scuttle Fly Megaselia abdita
inferredcites →https://doi.org/10.4161/fly.5864openalex-snapshot
Data Pushing: A Fly-Centric Guide to Bioinformatics Tools
inferredcites →https://doi.org/10.4161/fly.6060openalex-snapshot
Pipeline for acquisition of quantitative data on segmentation gene expression from confocal images
inferredcites →https://doi.org/10.7554/elife.04785.001openalex-snapshot
Quantitative system drift compensates for altered maternal inputs to the gap gene network of the scuttle fly Megaselia abdita
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1007/978-3-030-71737-7_4openalex-snapshot
Life’s Attractors Continued: Progress in Understanding Developmental Systems Through Reverse Engineering and In Silico Evolution
inferred← citeshttps://doi.org/10.1007/978-3-319-60855-6_20openalex-snapshot
The Origin and Evolution of Maternal Genes
inferred← citeshttps://doi.org/10.1016/j.coisb.2018.08.004openalex-snapshot
Shift happens: The developmental and evolutionary dynamics of the gap gene system
inferred← citeshttps://doi.org/10.1016/j.gde.2016.06.004openalex-snapshot
Emerging developmental genetic model systems in holometabolous insects
inferred← citeshttps://doi.org/10.1016/j.scib.2022.06.014openalex-snapshot
Scaling Dictates the Decoder Structure
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.04.015openalex-snapshot
Speeding up anterior-posterior patterning of insects by differential initialization of the gap gene cascade
inferred← citeshttps://doi.org/10.1038/sdata.2015.5openalex-snapshot
High-resolution gene expression data from blastoderm embryos of the scuttle fly Megaselia abdita
inferred← citeshttps://doi.org/10.1093/molbev/msw013openalex-snapshot
Gap Gene Regulatory Dynamics Evolve along a Genotype Network
inferred← citeshttps://doi.org/10.1101/2025.01.13.632851openalex-snapshot
Breaking anterior-posterior symmetry in the moth fly Clogmia albipunctata
inferred← citeshttps://doi.org/10.1134/s1062360416040093openalex-snapshot
Morphogenetic networks which determine the spatial expression of zygotic genes in early Drosophila embryo
inferred← citeshttps://doi.org/10.1142/s0219720024500112openalex-snapshot
Body plan evolvability: The role of variability in gene regulatory networks
inferred← citeshttps://doi.org/10.1186/s13227-017-0082-xopenalex-snapshot
Formation and subdivision of the head field in the centipede Strigamia maritima, as revealed by the expression of head gap gene orthologues and hedgehog dynamics
inferred← citeshttps://doi.org/10.1186/s13227-017-0083-9openalex-snapshot
Non-canonical dorsoventral patterning in the moth midge Clogmia albipunctata
inferred← citeshttps://doi.org/10.1242/dev.204732openalex-snapshot
Genomic resources for the scuttle fly Megaselia abdita : a model organism for comparative developmental studies in flies
inferred← citeshttps://doi.org/10.1371/journal.pbio.2003174openalex-snapshot
A damped oscillator imposes temporal order on posterior gap gene expression in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003896openalex-snapshot
Asymmetric chromatin accessibility underlies anterior-posterior axis specification in moth fly embryos
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.