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AmaranthusanatomyantioxidantsappleapplesArabidopsis thalianaarracachaautophagyautophagy-related genesautophagy.related genesbeechbeechnutcalcium oxalateCannabis sativacarotenoidsCell densityChenopodiumchitinasesCleavage polyembryonycytokinin derivativesdesiccationdevelopmentDisanthusdormancyDouglas-firDouglas firembryoembryogenesisembryogenic cultureFagus sylvaticaflavonoidsfloral iductionflow cytometryfloweringgene expressiongerminationglucanaseshemphistochemistryimage analysisimmunolabellinginductionin vitro regenerationlarchmaritime pinemicropropagationmicroscopynon-embryogenic cellsNorway spruceorganogenesisoxidative stressphenolic acidsphenolicsphenolsphotoperiodphytohormonesPicea abiespolyaminespolyphenolic compoundsproliferationProtein patternproteomePseudotsuga menziesiiputrescineResearchrootsignallingsomaclonal variationsomatic embryogenesisspermidinesperminestarchstarch grainsstereologystorage compoundsstorage proteinstissue culturestobacco cell culturetranscriptometransformationUV-B irradiationUV-B radiationVegetative propagationyaconzygotic embryoβ-1,3-glucanases

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Figure 3. Morphology of three-week-old emblings developed from embryos desiccated at different relative humidity levels (G100, G95, and G90). (A) – Overview of emblings; (B) – Length of whole shoots (dark gray columns), hypocotyls (light gray columns), and primary roots (white columns). The image of the embling inserted in graph B shows the measured parts – shoot (s), hypocotyl (h), and root (r).

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