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Retroactive Maintains Cuticle Integrity by Promoting the Trafficking of Knickkopf into the Procuticle of Tribolium castaneum

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/dvdy.20389openalex-snapshot
Retroactive, a membrane‐anchored extracellular protein related to vertebrate snake neurotoxin‐like proteins, is required for cuticle organization in the larva of Drosophila melanogaster
inferredcites →https://doi.org/10.1007/s00360-005-0005-3openalex-snapshot
Insect chitin synthases: a review
inferredcites →https://doi.org/10.1016/j.asd.2006.05.003openalex-snapshot
Cuticle differentiation during Drosophila embryogenesis
inferredcites →https://doi.org/10.1016/j.ibmb.2007.06.011openalex-snapshot
Characterization of recombinant chitinase-like proteins of Drosophila melanogaster and Tribolium castaneum
inferredcites →https://doi.org/10.1016/j.ibmb.2009.02.002openalex-snapshot
Analysis of functions of the chitin deacetylase gene family in Tribolium castaneum
inferredcites →https://doi.org/10.1016/j.ibmb.2010.01.011openalex-snapshot
Genes encoding proteins with peritrophin A-type chitin-binding domains in Tribolium castaneum are grouped into three distinct families based on phylogeny, expression and function
inferredcites →https://doi.org/10.1016/j.ibmb.2010.03.003openalex-snapshot
Recent advances in understanding mechanisms of insect cuticle differentiation
inferredcites →https://doi.org/10.1016/j.ibmb.2010.09.011openalex-snapshot
Both UDP N-acetylglucosamine pyrophosphorylases of Tribolium castaneum are critical for molting, survival and fecundity
inferredcites →https://doi.org/10.1016/s0022-1910(00)00123-2openalex-snapshot
The Wigglesworth Lecture: Insects for studying fundamental problems in biology
inferredcites →https://doi.org/10.1016/s0065-2806(08)60031-4openalex-snapshot
Physiology and Biochemistry of Insect Moulting Fluid
inferredcites →https://doi.org/10.1073/pnas.0800739105openalex-snapshot
Functional specialization among insect chitinase family genes revealed by RNA interference
inferredcites →https://doi.org/10.1073/pnas.1112288108openalex-snapshot
Knickkopf protein protects and organizes chitin in the newly synthesized insect exoskeleton
inferredcites →https://doi.org/10.1093/genetics/161.1.171openalex-snapshot
Genetic Control of Cuticle Formation During Embryonic Development ofDrosophila melanogaster
inferredcites →https://doi.org/10.1093/jee/83.5.1745openalex-snapshot
A Gene for Lindane + Cyclodiene Resistance in the Red Flour Beetle (Coleoptera: Tenebrionidae)
inferredcites →https://doi.org/10.1093/molbev/msm092openalex-snapshot
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0
inferredcites →https://doi.org/10.1111/j.1365-2583.2005.00576.xopenalex-snapshot
The Tribolium chitin synthase genes TcCHS1 and TcCHS2 are specialized for synthesis of epidermal cuticle and midgut peritrophic matrix
inferredcites →https://doi.org/10.1242/dev.02177openalex-snapshot
DrosophilaKnickkopf and Retroactive are needed for epithelial tube growth and cuticle differentiation through their specific requirement for chitin filament organization
inferredcites →https://doi.org/10.1242/dev.033845openalex-snapshot
boudin is required for septate junction organisation in Drosophila and codes for a diffusible protein of the Ly6 superfamily
inferredcites →https://doi.org/10.1242/jcs.s3-104.67.369openalex-snapshot
The cuticle and associated structures of Podura aquatica at the moult
inferredcites →https://doi.org/10.1242/jeb.00709openalex-snapshot
Chitin metabolism in insects: structure, function and regulation of chitin synthases and chitinases

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4598524openalex-extracted
inferred← citeshttps://doi.org/10.1002/arch.21165openalex-snapshot
THE KNICKKOPF DOMON DOMAIN IS ESSENTIAL FOR CUTICLE DIFFERENTIATION IN Drosophila melanogaster
inferred← citeshttps://doi.org/10.1002/ps.5879openalex-snapshot
Effect of RNAi ‐mediated silencing of two Knickkopf family genes ( LmKnk2 and LmKnk3 ) on cuticle formation and insecticide susceptibility in Locusta migratoria
inferred← citeshttps://doi.org/10.1002/ps.70749openalex-snapshot
PcCPR12 participates in coordinating chitin and lipid metabolism to maintain cuticle structural stability in Panonychus citri
inferred← citeshttps://doi.org/10.1002/ps.7156openalex-snapshot
Mutation of a lepidopteran‐specific PMP ‐like protein, BmLSPMP ‐like, induces a stick body shape in silkworm, Bombyx mori
inferred← citeshttps://doi.org/10.1007/978-3-030-12919-4_1openalex-snapshot
Chito-Protein Matrices in Arthropod Exoskeletons and Peritrophic Matrices
inferred← citeshttps://doi.org/10.1007/978-3-642-36160-9_8openalex-snapshot
The Arthropod Cuticle
inferred← citeshttps://doi.org/10.1007/s00792-015-0792-8openalex-snapshot
Chitinase from Thermomyces lanuginosus SSBP and its biotechnological applications
inferred← citeshttps://doi.org/10.1007/s10493-025-01031-9openalex-snapshot
Knockdown of farnesyl pyrophosphate synthetase gene TuFPPS by RNAi extends quiescent period and halts molting of the spider mite, Tetranychus urticae
inferred← citeshttps://doi.org/10.1007/s13592-014-0292-3openalex-snapshot
Putative orthologues of genetically identified Drosophila melanogaster chitin producing and organising genes in Apis mellifera
inferred← citeshttps://doi.org/10.1016/b978-0-323-85619-5.00010-9openalex-snapshot
The insect cuticle
inferred← citeshttps://doi.org/10.1016/j.actbio.2025.05.046openalex-snapshot
Exoskeletal cuticle proteins enable Drosophila locomotion
inferred← citeshttps://doi.org/10.1016/j.colcom.2025.100818openalex-snapshot
Insect cuticle: A source of inspiration for biomimetic Interface material design
inferred← citeshttps://doi.org/10.1016/j.exppara.2015.01.011openalex-snapshot
Molecular characterisation and functional analysis of LsChi2, a chitinase found in the salmon louse (Lepeophtheirus salmonis salmonis, Krøyer 1838)
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.02.013openalex-snapshot
Knickkopf and retroactive proteins are required for formation of laminar serosal procuticle during embryonic development of Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.ibmb.2015.02.014openalex-snapshot
Elucidation of the serosal cuticle machinery in the beetle Tribolium by RNA sequencing and functional analysis of Knickkopf1, Retroactive and Laccase2
inferred← citeshttps://doi.org/10.1016/j.ibmb.2017.08.003openalex-snapshot
Timed Knickkopf function is essential for wing cuticle formation in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.ibmb.2022.103783openalex-snapshot
SERCA interacts with chitin synthase and participates in cuticular chitin biogenesis in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ibmb.2022.103845openalex-snapshot
Fatty acid binding protein is required for chitin biosynthesis in the wing of Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.ibmb.2023.104058openalex-snapshot
Advances in understanding insect chitin biosynthesis
inferred← citeshttps://doi.org/10.1016/j.ibmb.2024.104112openalex-snapshot
Dynamics of cuticle-associated transcript profiles during moulting of the bed bug Cimex lectularius
inferred← citeshttps://doi.org/10.1016/j.ibmb.2024.104113openalex-snapshot
An optimized artificial blood feeding assay to study tick cuticle biology
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131704openalex-snapshot
Roles of a newly lethal cuticular structural protein, AaCPR100A, and its upstream interaction protein, G12-like, in Aedes aegypti
inferred← citeshttps://doi.org/10.1074/jbc.m114.599597openalex-snapshot
Functional Analysis of Insect Molting Fluid Proteins on the Protection and Regulation of Ecdysis
inferred← citeshttps://doi.org/10.1074/jbc.m114.614933openalex-snapshot
Obstructor A Organizes Matrix Assembly at the Apical Cell Surface to Promote Enzymatic Cuticle Maturation in Drosophila
inferred← citeshttps://doi.org/10.1093/jee/toag145openalex-snapshot
Essential roles of LmKnk and LmRtv in chitin formation during locust pro-nymphal cuticle development
inferred← citeshttps://doi.org/10.1093/molbev/msv052openalex-snapshot
Multispecies Analysis of Expression Pattern Diversification in the Recently Expanded Insect Ly6 Gene Family
inferred← citeshttps://doi.org/10.1093/molbev/msx237openalex-snapshot
Diverse Cis-Regulatory Mechanisms Contribute to Expression Evolution of Tandem Gene Duplicates
inferred← citeshttps://doi.org/10.1111/1744-7917.13313openalex-snapshot
Knickkopf ( LmKnk ) is required for chitin organization in the foregut of Locusta migratoria
inferred← citeshttps://doi.org/10.1111/imb.12308openalex-snapshot
Studies on the chitin/chitosan binding properties of six cuticular proteins analogous to peritrophin 3 from Bombyx mori
inferred← citeshttps://doi.org/10.11606/t.17.2017.tde-30032017-144620openalex-snapshot
Abordagem comparativa da maturação cuticular em abelhas sociais e solitárias utilizando-se RNA-seq, quantificação de hidrocarbonetos e microscopia eletrônica
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004537openalex-snapshot
Functional Specialization Among Members Of Knickkopf Family Of Proteins In Insect Cuticle Organization
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006100openalex-snapshot
The Gene Expression Program for the Formation of Wing Cuticle in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006257openalex-snapshot
miR-71 and miR-263 Jointly Regulate Target Genes Chitin synthase and Chitinase to Control Locust Molting
inferred← citeshttps://doi.org/10.1371/journal.pone.0134824openalex-snapshot
Transcriptome Analysis of the Emerald Ash Borer (EAB), Agrilus planipennis: De Novo Assembly, Functional Annotation and Comparative Analysis
inferred← citeshttps://doi.org/10.1371/journal.pone.0213796openalex-snapshot
Exploring integument transcriptomes, cuticle ultrastructure, and cuticular hydrocarbons profiles in eusocial and solitary bee species displaying heterochronic adult cuticle maturation
inferred← citeshttps://doi.org/10.1534/genetics.113.158766openalex-snapshot
Mutation of a Cuticular Protein, BmorCPR2 , Alters Larval Body Shape and Adaptability in Silkworm, Bombyx mori
inferred← citeshttps://doi.org/10.1534/genetics.117.300300openalex-snapshot
Body Shape and Coloration of Silkworm Larvae Are Influenced by a Novel Cuticular Protein
inferred← citeshttps://doi.org/10.2174/1381612826666200721002354openalex-snapshot
Drosophila, Chitin and Insect Pest Management
inferred← citeshttps://doi.org/10.3390/biology12060866openalex-snapshot
Dusky-like Is Critical for Morphogenesis of the Cellular Protuberances and Formation of the Cuticle in Henosepilachna vigintioctopunctata
inferred← citeshttps://doi.org/10.3390/ijms21051904openalex-snapshot
Identification and Functional Study of Chitin Metabolism and Detoxification-Related Genes in Glyphodes pyloalis Walker (Lepidoptera: Pyralidae) Based on Transcriptome Analysis
inferred← citeshttps://doi.org/10.3390/insects15080623openalex-snapshot
Identification and Functional Insights of Knickkopf Genes in the Larval Cuticle of Leptinotarsa decemlineata
inferred← citeshttps://doi.org/10.3390/insects17080849openalex-snapshot
BmMBNL Knockout Disrupts Molting of Silkworm, Bombyx mori, Through Inhibiting Expressions of Chitin Synthetase and Chitinase
inferred← citeshttps://doi.org/10.3390/ma15031041openalex-snapshot
Improving Polysaccharide-Based Chitin/Chitosan-Aerogel Materials by Learning from Genetics and Molecular Biology
inferred← citeshttps://doi.org/10.64898/2026.01.15.699689openalex-snapshot
Moulting in Pancrustacea is characterised by both deeply conserved and recently evolved gene modules
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