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seedling development

13449 relationships annotated with this phrase. Showing first 500 of 13449.
Source entity Relationship Target entity Species
developmental changes could easily cause heterogeneity in phloem transport in seedlings depending on phloem connectivity
seedling phenotypes classified into three types: embryonic, partial embryonic, and normal Arabidopsis thaliana
KAR pathway controls mesocotyl elongation in the dark Arabidopsis thaliana; Oryza sativa; Lotus japonicus; Brachypodium distachyon
young leaves begin to act as sources and supplement seedling growth during second week of development
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) ∆CTH mutant exhibits longer hypocotyls under white light growth conditions Arabidopsis thaliana
coleoptilar nodes appear between 4 to 6 days after germination Zea mays
carbohydrate supply, energy sensing, and phytohormone signaling are mechanistically linked during seedling emergence Arabidopsis thaliana
(ANAC037, VND1, AT2G18060) (ANAC076, NAC076, VND2, AT4G36160) and (ANAC105, NAC105, VND3, AT5G66300) have physiological roles in the regulation of seedling development Arabidopsis thaliana
mutants with reduced oil storage often suffer reduced establishment
Arabidopsis lines mutated in lipases that catalyze the initial step of TAG breakdown arrested before their cotyledons opened fully cotyledon opening Arabidopsis thaliana
(PFD3, AT5G49510) mutant showed slightly darker color Arabidopsis thaliana
addition of a new sink (the first leaf) marks the beginning of the transition from a simple one-sink system to a more complex two-sink system
QK mutant seedlings have abnormal cotyledons Arabidopsis thaliana
cost associated with leaf development accrues before leaf expansion
(KAI2, AT4G37470) and (D14, AT3G03990) can affect seedling growth Arabidopsis thaliana
opening of cotyledons and petioles in Nps1 seedlings after 120 h of light exposure showed reduced curvature compared with wild-type and (FLA, FRI, RSB7, AT4G00650) mutant seedlings Solanum lycopersicum
μ2-YFP fully complemented μ2-1 mutant phenotype of dark-grown hypocotyls Arabidopsis thaliana
pUBQ:MAX2 D693K mutant exhibits longer hypocotyls under white light growth conditions Arabidopsis thaliana
(ASG6, CRK2, AT1G70520) seedlings did not survive beyond three-leaf stage Zea mays
Nps1 showed slightly reduced cotyledon expansion under white light Solanum lycopersicum
increased lipid mobilization largely recovers seedling establishment Arabidopsis thaliana
m123-2 mutant showed differences compared to wild-type in response to ABA at later stages on seedling growth characterized by formation of true leaves Arabidopsis thaliana
(SMAX1, AT5G57710) expression is consistent with (SMAX1, AT5G57710) function at early stages Arabidopsis thaliana
development of leaves occurred in series
gradual transition of new leaves from sink to source tissue can be visualized by tracking the movement of CF from cotyledons into developing leaves
sink-source transition occurred between day 9 and day 11
first leaf transition to carbon source causes increase in seedling growth rate Cucumis sativus
Karrikins (KARs) have neutral or positive effects on cotyledon expansion Arabidopsis thaliana
young leaves begin to act as sources and supplement seedling growth
carbon assimilation in cotyledons remained stable during first week of development
average translocation area in each seedling did not change during first 2 weeks of development
timing of this transition is consistent with sink manipulation experiments
seedling physiology is critical to plant establishment
ethylene-induced formation of the apical hook in etiolated seedlings requires GA and auxin Arabidopsis thaliana
candidate genes are acting through pathways that contribute to variation in early-life seedling performance in common gardens Picea rubens
DG2 and PD1a with higher MGDG and DGDG produce healthy cotyledons
nicotinamide treatment has less severe effect on plant growth Arabidopsis thaliana
Mustard seedlings (Sinapis alba, L., var. Albatros) were grown under continuous illumination at 20°C and 60% humidity Sinapis alba
growth in the second true leaf is not initiated until after day 10
apparent stability of transport after day 9 is not surprising considering that cucumber seedlings increase carbon fixation as they mature and become sink-limited adults Cucumis sativus
Karrikins (KARs) have positive effects on seedling vigor
(ILL2, AT5G56660) (IAR3, JR3, AT1G51760) (IBR3, AT3G06810) mutant has decreased apical hook curvature Arabidopsis thaliana
HFA or some derived degradation product may reduce establishment success for HFA-accumulating lines
DG2 and PD1a are more successful in establishing new plants than (cL37, PSRP5, AT3G56910)
reduced rate of HFA-TAG mobilization in (cL37, PSRP5, AT3G56910) can only further compound resource starvation under conditions where 51% of all TAG molecules were HFA-TAG
m123-2 mutant showed differences compared to wild-type in response to ABA at later stages on seedling growth characterized by expansion and greening of cotyledons Arabidopsis thaliana
time-lapse imaging of seedlings grown under white light revealed opening of both cotyledons and petiole was extremely delayed in the Nps1 seedlings Solanum lycopersicum
(ABI4, ATABI4, GIN6, ISI3, SAN5, SIS5, SUN6, AT2G40220) loss-of-function mutant displays insensitivity to ABA in seedling development
(cL37, PSRP5, AT3G56910) contained 4 μg seed⁻¹ oil and 40% of the seeds attained opened cotyledons
(AtSAMS3, MAT4, MTO3, SAMS3, AT3G17390) seedlings were smaller than L119 seedlings Arabidopsis thaliana
seedlings were grown at 22°C temperature
seedlings subjected to oryzalin followed their developing program by cotyledon greening and opening Medicago truncatula
(PFD5, AT5G23290) mutant showed shorter hypocotyls Arabidopsis thaliana
(VQ29, AT4G37710) and (PIF1, PIL5, AT2G20180) activity occurs during early seedling development Arabidopsis thaliana
post-germination growth and seedling establishment involves further increase in water uptake
Arabidopsis PROTEOLYSIS6 controls seedling establishment Arabidopsis thaliana
PD1a seedlings show fully opened cotyledons of 61.3% ± 1.82% Arabidopsis thaliana
defect in seedling establishment can be rescued by exogenous sugars Arabidopsis thaliana
Col-0 was stratified and transferred as 7-day-old seedlings Arabidopsis thaliana
ref8* cotyledons are less than half of wild-type cotyledon size Arabidopsis thaliana
overexpression of ZmDREB4.1 repressed hypocotyl elongation Nicotiana tabacum
max2-1 / abi3-8 double mutant displayed longer hypocotyls at young seedling stage and multiple branches at adult stage compared with wild type and abi3-8 and abi5-7 single mutants Arabidopsis thaliana
(ATMES17, MES17, AT3G10870) (IBR3, AT3G06810) mutant shows apical hook curvature Arabidopsis thaliana
(ATTPS1, TPS1, AT1G78580) loss-of-function mutants cause seedling developmental arrest Arabidopsis thaliana
weak light condition causes retarded growth in wild-type and (ANAC037, VND1, AT2G18060) (ANAC076, NAC076, VND2, AT4G36160) (ANAC105, NAC105, VND3, AT5G66300) seedlings Arabidopsis thaliana
m123-1 mutant showed differences compared to wild-type in response to ABA at later stages on seedling growth characterized by formation of true leaves Arabidopsis thaliana
disparity between seed oil content and successful cotyledon opening in (cL37, PSRP5, AT3G56910) and DG2 is evident in (cL37, PSRP5, AT3G56910) and DG2
(ATZFP1, ZFP1, AT1G80730) overexpression reduces hypocotyl length of germinated seedlings Arabidopsis thaliana
(ABI3, AtABI3, SIS10, AT3G24650) plants exhibit premature expression of seedling traits
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) knockout plants exhibit hyponastic petioles
RING E3 ligase RING-H2 protein (RHA2A, AT1G15100) regulates early seedling development Arabidopsis thaliana
m123-2 mutant showed differences compared to wild-type in response to ABA at later stages on seedling growth characterized by root growth Arabidopsis thaliana
transgenic Arabidopsis plants repressing both PNC genes led to arrested seedling growth Arabidopsis thaliana
phytochrome-interacting factors (PIFs) act as positive regulators of abscisic acid (ABA) signaling
AtNAP1-mediated chromatin remodeling appears to play more important roles in post-germination growth of seedlings Arabidopsis thaliana
(CER9, SUD1, AT4G34100) mutant shows suppressed cotyledon greenness Arabidopsis thaliana
seedlings germinated on noninducing medium then transferred to DEX containing medium after 5 d no growth retardation upon (AtROS1, DML1, ROS1, AT2G36490) and DEL activation Solanum lycopersicum
DG2 seedlings show fully opened cotyledons of 76% ± 1.49% Arabidopsis thaliana
(cL37, PSRP5, AT3G56910) hypocotyls show 5.6-fold less length than (FAE1, KCS18, AT4G34520) Arabidopsis thaliana
(ABX45, AS11, ATDGAT, AtDGAT1, DGAT1, RDS1, TAG1, AT2G19450) Arabidopsis mutant has 25% reduction in establishment Arabidopsis thaliana
Brachypodium distachyon shoots regenerated from transformed calli overexpressing BdTHX1 showed seedling-lethal phenotypes Brachypodium distachyon
seedlings grown for 13 days
seeds soaked on water continued to develop normally normal seedling development Medicago truncatula
mutants with defective FA utilization through β-oxidation show arrested development before cotyledon opening Arabidopsis thaliana
IAA derived by (ATMES17, MES17, AT3G10870) is less important for apical hook development Arabidopsis thaliana
lower total oil likely plays a part in poor seedling development
m123-2 mutant seedlings are more resistant compared to wild-type seedlings to inhibition of expansion and greening of cotyledons Arabidopsis thaliana
(ZFP3, AT5G25160) ectopic expression in Col-0 background produces seedlings with short hypocotyls Arabidopsis thaliana
prunasin content is insignificant in young 1-week-old seedlings Eucalyptus cladocalyx
pectic arabinose levels decline sharply during germination Hordeum vulgare
μ2-1 seedlings had etiolated hypocotyls Arabidopsis thaliana
(ATPDX1.1, PDX1.1, AT2G38230) mutant does not show epinastic cotyledons Arabidopsis thaliana
(cL37, PSRP5, AT3G56910) seedlings show 2.8-fold decrease in seedlings with two true leaves compared to (FAE1, KCS18, AT4G34520) Arabidopsis thaliana
seedlings grown in darkness
further increases in acyltransferase expression may affect establishment success of DG2 and PD1a
(cL37, PSRP5, AT3G56910) line atrophies during transition to photoautotrophic growth Arabidopsis thaliana
seedlings grown under continuous white light
TE-2-6b plantlets at early stages have epinastic primary leaves Arabidopsis thaliana
reserved nutrients would last until true leaves emerged during postembryonic development Arabidopsis thaliana
rate of TAG mobilization can play a more important role in establishment
seed-to-seedling transition is driven by hypocotyl cell elongation
conclusions from this study predict that gains in establishment would slow or even be reversed as HFA proportions increase
seedlings subjected to oryzalin followed their developing program by hypocotyl rising Medicago truncatula
loss of function of (AtbZIP1, bZIP1, AT5G49450) causes changes in rates of early seedling establishment Arabidopsis thaliana
seedlings grown on inhibitor-soaked petriplates grown under white light Lycopersicon esculentum
ethylene regulates seedling morphology
(ATMBAC1, BAC1, MBAC1, AT2G33820) is highly abundant during early seedling growth Arabidopsis
wild-type tomato seedlings grown at temperature of 25 ± 2°C Lycopersicon esculentum
transient pale cotyledon phenotype was ameliorated by day 10 after sowing Arabidopsis thaliana
(IBR1, SDRA, AT4G05530) (IBR3, AT3G06810) (ATECI2, ECHIB, ECI2, IBR10, PEC12, AT4G14430) (ATECH2, ECH2, AT1G76150) and higher-order combinations of these mutants illuminates diverse roles for IBA-derived IAA in seedling development Arabidopsis thaliana
(PG45, PGA4, AT1G02790) plants have reduced hypocotyl length Arabidopsis thaliana
35Spro–MIR171c mutant plants have greener cotyledons and stems Arabidopsis thaliana
mutant collection opens the door to global analysis of photosynthesis and early seedling development Setaria viridis
(ATFD1, FD1, AT1G10960) mutants show gradual chlorosis at two-leaf stage Oryza sativa
pPLA inhibitors suppressed elongation in etiolated seedlings Arabidopsis thaliana
atfh8-1 mutant used in plant growth and seedling development experiments Arabidopsis thaliana
TE-2-6b plantlets at early stages are smaller than Col-0 plants Arabidopsis thaliana
(ATFD1, FD1, AT1G10960) plants treated with 2% glucose grew to four-leaf stage Oryza sativa
upregulation of (AtETR1, EIN1, ETR, ETR1, RDO3, AT1G66340) along with other ETRs may have bearing on ethylene-regulated seedling development Solanum lycopersicum
seedlings grown in growth cabinet Triticum aestivum
Mutation of OsCUC3 in osnam-1 resulted in abnormal leaf phenotype appearing in three-leaf seedling stage Oryza sativa
sucrose synthase activity is less dependent on than root length and hypocotyl length Arabidopsis thaliana
atfh8-2 mutant used in plant growth and seedling development experiments Arabidopsis thaliana
(ABCD1, ACN2, AtABCD1, CTS, PED3, PXA1, AT4G39850) mutants require exogenous fixed carbon to fuel seedling growth prior to establishment of photosynthesis
tissues and cell types become seedling
induction of (AtDGAT2, DGAT2, AT3G51520) in seedling tissues is first time reported in seedling tissues Olea europaea
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) knockout plants exhibit epinastic cotyledons
sucrose is in high demand after germination Arabidopsis thaliana
brassinosteroids (BRs) regulate hypocotyl elongation
ref8* gir1-1 cotyledons are initially similar to wild-type cotyledon size Arabidopsis thaliana
osnam oscuc3 line leaf appeared in three early leaves Oryza sativa
AtplaIVC-1 mutants had longer hypocotyls than wild-type plants Arabidopsis thaliana
(ATCAND1, CAND1, ETA2, HVE, TIP120, AT2G02560) mutants at seedling stage grow normally compared to wild-type plants Arabidopsis thaliana
Sv-cfm1 mutant plants dies 10–12 days after planting Setaria italica
(APTG1, AT5G14850) is required for seedling growth Arabidopsis thaliana
phenotypes of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) single mutant are similar to phenotypes of max2-1/abi3-8 and max2-1/abi5-7 double mutants under continuous white light Arabidopsis thaliana
(ZFP6, AT1G67030) overexpression results in shorter hypocotyls Arabidopsis thaliana
auxin is required for apical hook initiation and maintenance in etiolated seedlings Arabidopsis thaliana
oil levels do not synchronize with proportion of fully opened cotyledons
examination of possible translational regulation of (OBP3, AT3G55370) would be of interest during early post-embryonic developmental stages Arabidopsis thaliana
plant models are used to investigate seedling development defects
BR (brassinosteroid) has role in apical hook formation Arabidopsis thaliana
transgenic lines were germinated on synthetic medium (1/2 MS plus 1% sucrose) supplemented with 2 μM BRZ Arabidopsis thaliana
soluble sugars are utilized as carbon and energy sources for shoot and root apical meristems Oryza sativa
No (WT) seedlings were grown in 0.5 MS liquid medium supplemented with 1% saccharose Arabidopsis thaliana
Sv-cfm1 mutant is seedling-lethal Setaria italica
strigolactones (SLs) inhibit hypocotyl elongation
S-CN-deb is less active than GR24 5DS regarding hypocotyl inhibition Arabidopsis thaliana
differentially regulated proteins are linked to seedling architecture Arabidopsis thaliana
(ATHKL1, HKL1, AT1G50460) affects seedling growth responses to glucose (glc) and auxin Arabidopsis thaliana
(ATR4, CYP83B1, RED1, RNT1, SUR2, AT4G31500) knockout plants exhibit extended hypocotyls
decrease in lipid levels, notably TGs, with seedling growth corroborates observations in previous studies reporting rapid reduction in TG levels and total lipids during seedling growth Arabidopsis thaliana
flooding inhibits seedling establishment
pOp-ipt transgenic lines 11 and 13 show dose-dependent inhibition of hypocotyl elongation Arabidopsis thaliana
DEX concentration of 0.25 μM produces maximal reduction in hypocotyl length in line 11 seedlings Arabidopsis thaliana
coronatine (COR) (10 nM and 100 nM) induces severe reduction in hypocotyl and root growth Solanum lycopersicum
switch to photoautotrophic growth depends on available lipid reserves, light conditions, and chloroplast development Arabidopsis thaliana
syd-5 brm-3 double mutant have defects on cotyledon separation Arabidopsis thaliana
cotyledons of 24-kDa oleosin knockdown plant do not re-green and abscise normal post-germination development Glycine max
timing of germination contributes to successful seedling establishment
AgNO3 significantly decreases BRP effects on apical hook Arabidopsis thaliana
both DGAT genes were expressed in all seedling organs examined Olea europaea
seedlings exposed to compound during entire growth period
BL (brassinolactone) partially suppresses enhanced apical hook phenotype of BRP-treated plants Arabidopsis thaliana
(SPT, AT4G36930) expression occurs in hypocotyl of germinating seedling
(ATFD1, FD1, AT1G10960) mutants begin to rapidly desiccate and die at three-leaf stage Oryza sativa
BR-deficient plants show lack of apical hook formation Arabidopsis thaliana
1 μM BRZ and 5 μM ACC combination yields similar phenotypes as 40 μM BRP treatment Arabidopsis thaliana
sueN mutants were able to continue to grow after cotyledon stage on sulphur-free medium Arabidopsis thaliana
(EFO2, RUP2, AT5G23730) overexpression results in enhanced hypocotyl elongation Arabidopsis thaliana
expression present in underlying cells of the rib zone and peripheral zone Medicago truncatula
severe deficiency in chlorophylls and carotenoids causes premature lethality Solanum lycopersicum
isobutanol treatment does not visibly affect broccoli seedling growth and development Brassica oleracea var. alboglabra
(SGB1, AT1G79820) mutant exhibited open hooks Arabidopsis thaliana
(EFO2, RUP2, AT5G23730) overexpression promotes hypocotyl elongation Arabidopsis thaliana
bes1-D single mutant were less sensitive to ACC (1-aminocyclopropane-1-carboxylic acid) in hypocotyl inhibition Arabidopsis thaliana
cross-talk between ethylene and auxin is important for hypocotyls elongation
(SGB1, AT1G79820) mutant exhibited shorter hypocotyls Arabidopsis thaliana
both genes were down-regulated in actively dividing cells like shoot tips and young seedling roots Olea europaea
seed storage proteins (SSPs) provide carbon resources for seedling development
partially closed cotyledons response was dependent on PIF activity
BR and ethylene have complex interaction seedling development Arabidopsis thaliana
ct-2, ct-5 and ct-9 knockout mutants show similar phenotypes to wild type Col-0 Arabidopsis thaliana
(HCC1, AT3G08950) promoter-gus fusion shows expression in root and shoot apical meristems, cotyledon tips, and nascent secondary roots Arabidopsis thaliana
AgNO3 partially reverses BRP inhibition of hypocotyl length Arabidopsis thaliana
BRZ treatment causes lack of apical hook formation Arabidopsis thaliana
ein2-1 mutant has little effect on hypocotyl length on BRZ Arabidopsis thaliana
immunocytochemical studies were performed separately in hooks, epicotyls, and roots Cicer arietinum
brassinosteroid (BR) and glucose (Glc) have been shown to modulate hypocotyl directional growth Arabidopsis thaliana
transcriptional analysis in Arabidopsis seedlings revealed high mRNA levels of type-1 DGAT during post-embryonic stages in cotyledons and hypocotyls Arabidopsis thaliana
seedlings grown at 24°C in complete darkness Arabidopsis thaliana
BRP causes exaggerated apical hooks
cotyledons of emerging seedling of 24-kDa oleosin knockdown open as in control wild-type Glycine max
sueN mutants showed emergence of two to three pairs of true leaves Arabidopsis thaliana
(EFO1, RUP1, AT5G52250) overexpression promotes hypocotyl elongation Arabidopsis thaliana
ltp5-1 seedlings had hypocotyls significantly shorter than wild-type and ltp5-1/+ seedlings in dark conditions Arabidopsis thaliana
(AGB1, ATAGB1, ELK4, AT4G34460) mutant exhibited shorter hypocotyls Arabidopsis thaliana
Pro35S:CaUBP12 plants show enhanced ABA sensitivity as measured by seedling establishment Arabidopsis thaliana
flu mutants expressing truncated FLU derivatives grew at rates similar to WT and flu seedlings under constant light conditions
ACC treatment (1 μM) in dark reduces hypocotyl elongation Arabidopsis thaliana
Atscp2-1 plants are dependent on exogenous carbon source to avoid delayed seedling establishment Arabidopsis thaliana
brassinosteroid (BR) and ethylene have overlapping functions in hypocotyl elongation
ectopic (SPT, AT4G36930) expression results in smaller cotyledons Arabidopsis thaliana
Arabidopsis double mutant (ATMEK4, ATMKK4, MKK4, AT1G51660) (ATMAP2K_ALPHA, ATMEK5, ATMKK5, MAP2K_A, MEK5, MKK5, AT3G21220) is seedling lethal Arabidopsis thaliana
symbiosis with mycorrhizal fungi is linked to successful seedling development
wild-type seedlings show no significant effect on hypocotyl length when treated with DEX at highest concentrations Arabidopsis thaliana
salt gradient screen is limited to young seedling stages of wheat and other grain cereals
extracellular invertase LIN6 provides carbohydrates to sustain heterotrophic growth Nicotiana tabacum
brassinopride (BRP) causes exaggerated apical hooks Arabidopsis thaliana
bzr1-1D;bes1-D double mutant were less sensitive to ACC (1-aminocyclopropane-1-carboxylic acid) in hypocotyl inhibition Arabidopsis thaliana
hkl1-1 seedlings had 40% increase in hypocotyl length relative to Col-0 seedlings Arabidopsis thaliana
pOsNAM::GUS transgenic plants show GUS signal in seedlings Oryza sativa
(PGX1, AT3G26610) and (PGX2, AT1G78400) overexpression lines have excess growth of hypocotyls Arabidopsis thaliana
Ccrboh expression in roots shows 7-fold induction in older seedlings Citrullus colocynthis
seed storage proteins (SSPs) provide sulphur resources for seedling development
BRZ (brassinazole) and ACC (1-aminocyclopropane-1-carboxylic acid) have additive effects on hypocotyl elongation Arabidopsis thaliana
wild-type seeds after 7 days of growth have started to extend hypocotyl and apical axis to form primary leaves Glycine max
cotyledons of wild-type seed re-green and remain attached to seedling for more than 2 weeks Glycine max
seedling shoots were harvested at four-leaf stage Oryza sativa
ethylene causes enhanced apical hook formation Arabidopsis thaliana
GhADF8 gene is at relatively high levels in cotyledons Gossypium hirsutum
hhp1-1 mutant shows reduced cotyledon greening compared to wild-type (WT) and complemented-hhp1-1 (c-hhp1-1) Arabidopsis thaliana
repression of invertase at the seedling stage interferes with development Nicotiana tabacum
double mutants combining (AVB1, IFL, IFL1, REV, AT5G60690) with 26S proteasome mutant (AE3, ATHMOV34, RPN8A, AT5G05780) resulted in almost all plants arresting at the seedling stages Arabidopsis thaliana
hsc70-2 (ATHSP70, HSC70-4, HSP70, HSP70-4, AT3G12580) double mutant is seedling lethal Arabidopsis thaliana
low night temperature treatments reduce hypocotyl length Cucumis sativus
(EAT, MIR172, MIR172B, AT5G04275) in shoot apex was present at nearly constant level from 6 to 12 days after planting Arabidopsis thaliana
abscisic acid (ABA) response appears to be required for etiolated development
cotyledons showed strong GUS staining throughout the vascular tissue Medicago truncatula
seedling growth was monitored over 21 d Arabidopsis thaliana
prSERK1::GUS expression visualized through seedling development
(ATRBX1, HRT1, RBX1, ROC1, AT5G20570) -1D and partial loss-of-function alleles show opposite effects for cotyledon expansion Arabidopsis thaliana
developing seedlings devote nutritional reserves almost exclusively to hypocotyl extension
tissue 1–2 mm behind the root apical meristem showed GUS expression in the cortical and epidermal cells Medicago truncatula
developmental delay observed in (GUN1, AT2G31400) seedlings at 54 h was transient Arabidopsis thaliana
TaSnRK2.7 transgenic Arabidopsis showed no evident difference in seedling size Arabidopsis thaliana
Mn deficiency phenotype is evident at seedling stage
GUS was also strong in vascular tissue immediately below the shoot apical meristem (SAM) Medicago truncatula
transient increase in LHCB1 and RBCS transcripts is similar to transient increase in early development of dark-grown Arabidopsis seedlings Arabidopsis thaliana
rack1 single and double mutants could germinate and develop into green seedlings Arabidopsis thaliana
bzr1-1D;bes1-D double mutant were not only insensitive to BRP Arabidopsis thaliana
fft-1 mutant seedlings grew and matured more quickly than WT seedlings Arabidopsis thaliana
GUS staining only observed in vascular tissue Medicago truncatula
gin2-1 seedlings average hypocotyl length was about 45% less than Ler seedlings Arabidopsis thaliana
sucrose is known to inhibit early seedling development in Arabidopsis Arabidopsis thaliana
pSAG:GUS transgenic plants show weak GUS staining in 4- to 7-d-old seedlings Arabidopsis thaliana
Starch stored in the endosperm fulfils this role energy source during seedling establishment Hordeum vulgare
SAM-defective ae4-1 rev-6 plants included those where SAM was terminated and whole seedling was arrested Arabidopsis thaliana
lincomycin enhances cotyledon expansion in (GUN1, AT2G31400) seedlings Arabidopsis thaliana
absence of functional (GUN1, AT2G31400) results in alterations in early seedling development and altered sensitivity to sucrose and ABA Arabidopsis thaliana
(GUN1, AT2G31400) seedlings grown in presence of sucrose for 54 h had only 54% at hypocotyl and cotyledon emergence stage (0.7) Arabidopsis thaliana
sucrose perturbed (GUN1, AT2G31400) seedling development at each growth stage Arabidopsis thaliana
SD-grown green seedlings exposed to an EOD-FRp might experience partial reversal to the etiolated state
(AtPLT1, PLT1, AT3G20840) (PLT2, AT1G51190) /+ (AIL6, PLT3, AT5G10510) (BBM, PLT4, AT5G17430) mutant sometimes lacks hypocotyl Arabidopsis thaliana
kaempferol addition did not affect hypocotyl length Arabidopsis thaliana
quercetin addition did not affect hypocotyl length Arabidopsis thaliana
35S::KAT5.2 transgene rescued seedling establishment in absence of exogenous sucrose Arabidopsis thaliana
AtSAG is important negative regulator of ABA signalling Arabidopsis thaliana
sugar sensitivity of (GUN1, AT2G31400) seedlings changes during development Arabidopsis thaliana
triple response of dark-grown seedlings to ethylene is defined by inhibition of hypocotyl elongation
ethylene reduction of BR action inhibits hypocotyl elongation
ethylene causes triple response phenotype Arabidopsis thaliana
transgenic lines were grown under 16-h light/8-h dark long day growth condition at 22°C for 2 weeks Arabidopsis thaliana
24-kDa oleosin knockdown seedling growth proceeds with embryo continuing to slowly elongate and differentiate while cotyledon appears to be static and unchanging Glycine max
bm2-bm3-bm4 seedlings combination of mutations appears to arrest growth prior to seedling emergence
specific XTHs involvement in meristematic tissue differentiation and vascular development points to involvement of XTHs in seedling growth
HcAlkIN1 and HcSUS1 have important roles in establishment of seedlings of Hymenaea courbaril Hymenaea courbaril
(AtTT8, BHLH42, TT8, AT4G09820) mutant seedlings had longer petioles petiole length Arabidopsis thaliana
seedlings of Hymenaea courbaril are usually quite large 30–40 cm tall Hymenaea courbaril
misexpression of embryonic characteristics results in arrested seedling development
progesterone (pregn-4-ene-3,20-dione; PO) influences hypocotyl elongation
wild-type and (REM11, VAL, AT5G60140) single mutant seedlings rescued early in seed development (7–10 DAF) observed nongreen and abnormal growth phenotypes Arabidopsis thaliana
(FAR1, AT5G22500) mutant is hyposensitive to ABA-mediated seedling greening
AtSAG overexpression line (OX2) exhibits decreased sensitivity to abscisic acid (ABA) Arabidopsis thaliana
best haplotype of glutamine synthetase gene conferred superior seedling growth Triticum aestivum
bilateral symmetry in just germinated seedlings is evidenced by two symmetrically located cotyledons and shoot apical meristem (SAM) between cotyledons
germinated seedlings treated with 3,4-DHP display various defects in cotyledons
abi3-12 mutation suppresses (AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) seedling phenotype
(AtHDA7, HDA7, AT5G35600) up-regulation leads to delay of growth in postgermination Arabidopsis thaliana
(AtCLE6, CLE6, AT2G31085) transcript accumulates at highest level during early seedling stage Arabidopsis thaliana
epidermal cell fate specification is critical for post-germination survival
(ATSIZ1, SIZ1, AT5G60410) loss-of-function mutants show significantly reduced cotyledon growth rate Arabidopsis thaliana
peroxisome dysfunction confers seedling growth defects plants
wild type oil bodies are rapidly consumed following germination Arabidopsis thaliana
(ATMIN7, BEN1, BIG5, MIN7, AT3G43300) mutant hypocotyls were shorter than wild-type hypocotyls Arabidopsis thaliana
gibberellins (GA) growth promotion was limited primarily to early time points before cotyledons fully open
Z-carlactone (Z-CL) inhibited hypocotyl elongation in wild-type seedlings Arabidopsis thaliana
changes in phloem physiology impact growth and allocation Cucumis sativus
(SMAX1, AT5G57710) (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings suppressed increased length and upward orientation of cotyledonary petioles in (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings Arabidopsis thaliana
cotyledonary petiole growth was restored to wild-type phenotypes in (SMAX1, AT5G57710) (AtMAX2, MAX2, ORE9, PPS, AT2G42620) seedlings Arabidopsis thaliana
weak (112A-2A, EMB30, GN, GNOM, MIZ2, VAN7, AT1G13980) mutants produce viable seedlings Arabidopsis thaliana
ABA-dependent proline accumulation occurs during post-germinative growth Medicago truncatula
(ATFLS2, FLS2, AT5G63580) promoter exhibits expression in vascular tissue of cotyledons Arabidopsis thaliana
(HB-3, STIP, WOX9, WOX9A, AT2G33880) seedlings without sucrose show growth arrest apparent 2 days after germination
Ccrboh gene reaches high mRNA transcript levels at 3 days after germination Citrullus colocynthis
wild-type seedlings had 80% at stage of cotyledon emergence in 9-d-old seedlings grown on 0.5 μM ABA Arabidopsis thaliana
SD-grown wild-type (WT) seedlings exposed to an EOD-FRp displayed partially closed cotyledons typical of etiolated seedlings
hydrolytic cleavage of sucrose provides substrate to sustain heterotrophic growth
cell elongation is one of main events taking place in hypocotyl Hymenaea courbaril
bak1-4 bkk1-1 double mutant showed seedling-lethality phenotype Arabidopsis thaliana
35S::miR164b lines show occasional cotyledon separation defects Arabidopsis thaliana
SPATULA (SPT, AT4G36930) acts as regulator of cotyledon expansion Arabidopsis thaliana
plants must respond to light and nutrients
effect of sucrose on seedling development was greater with (GUN1, AT2G31400) than with wild-type seedlings Arabidopsis thaliana
cotyledon expansion and anthocyanin accumulation are co-ordinately regulated Arabidopsis thaliana
seed germination and early seedling development are hypersensitive to sucrose Arabidopsis thaliana
sucrose rescue of (HB-3, STIP, WOX9, WOX9A, AT2G33880) seedlings but not (PGA6, WUS, WUS1, AT2G17950) seedling rescue
(EAT, MIR172, MIR172B, AT5G04275) increased approximately 2-fold from 1 to 3 weeks after planting under SD conditions Arabidopsis thaliana
germinating seedlings determine timing of development
CaMV35S::PapsFIL seedlings showed different seedling phenotypes Arabidopsis thaliana
shared transcriptional network drives common downstream facets of morphogenesis such as hypocotyl growth
growth arrest in (HB-3, STIP, WOX9, WOX9A, AT2G33880) seedlings results in early seedling lethality
sag mutant exhibits increased sensitivity to abscisic acid (ABA) Arabidopsis thaliana
protein hydrolysis plays important role during post-germination seedling establishment Arabidopsis thaliana
(ATRING1A, RING1A, AT5G44280) −/− (AtBMI1B, ATDRIP1, AtRING1B, DRIP1, AT1G06770) −/− (AtLHP1, LHP1, TFL2, AT5G17690) −/− triple mutant has tiny and sessile cotyledons Arabidopsis thaliana
Dunghan Shali cultivar is known to have strong seedling vigor compared with Hitomebore Oryza sativa
brassinosteroids (BRs) promoted hypocotyl growth
(FRO1, NDUFS4, AT5G67590) mutants show sugar-sensitive establishment Arabidopsis thaliana
(SHM1, SHMT1, STM, AT4G37930) mutant displays lack of SAM activity Arabidopsis thaliana
lack of SAM activity prevents growth Arabidopsis thaliana
Z-carlactone (Z-CL) was inactive in all genotypes at 1 μm concentration Arabidopsis thaliana
GR24 inhibited hypocotyl elongation in Atd14 and (KAI2, AT4G37470) seedlings Arabidopsis thaliana
SlJMJ23-OE transgenic Arabidopsis plants have sensitivity during post-germination stage Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) mutant shows promoter activity of GATA-NOS101 similar to wild-type in blue light and dark grown seedlings Arabidopsis thaliana
(APEM9, DAU, DAYU, PEX26, AT3G10572) mutants display defects in growth Arabidopsis thaliana
orchid seedlings are entirely dependent on fungi
(ATHKL1, HKL1, AT1G50460) was negative regulator of seedling growth when expressed in WT background Arabidopsis thaliana
increased temperature strongly influenced seedling growth Pinus sylvestris
cts-1 mutant is impaired in seedling establishment Arabidopsis thaliana
(ATFLS2, FLS2, AT5G63580) promoter exhibits expression in developing cotyledons Arabidopsis thaliana
hypocotyl of young seedlings might be embedded almost entirely underground when cotyledons first perceive light at the soil surface
hypocotyl of older seedlings might be self-shaded by cotyledons
DG2 contained 7 μg seed⁻¹ oil and opened 76% of their cotyledons seed oil content and cotyledon opening
diphenyl methylphosphonate treatment preventing oil body breakdown resulted in TAG retained in seedlings that became chlorotic and only partially opened cotyledons
higher rate of mobilization for DG2 and PD1a would greatly augment resources for the developing seedling
DG2 and PD1a with greater mobilization of HFA-TAG providing them with even greater resources
(ATTPS1, TPS1, AT1G78580) knockout mutants undergo seedling developmental arrest Arabidopsis thaliana
seedlings that produce fully opened cotyledons almost uniformly produce two true leaves Arabidopsis thaliana
GUN1-GFP protein is hardly detectable in cotyledons at 120 and 144 h Arabidopsis thaliana
m123-1 mutant showed differences compared to wild-type in response to ABA at later stages on seedling growth characterized by expansion and greening of cotyledons Arabidopsis thaliana
PD1a hypocotyls were significantly longer than those of (cL37, PSRP5, AT3G56910) Arabidopsis thaliana
RpoA:HA is detected as early as 3rd day after imbibition Nicotiana tabacum
seedling morphogenesis in Arabidopsis operates predominantly through (KAI2, AT4G37470) rather than AtD14 Arabidopsis thaliana
N-lauroylethanolamine (NAE 12:0) induce morphological alterations in seedlings Arabidopsis thaliana
ZMK1 is involved in coleoptile growth Zea mays
germinating seedlings control reproductive success
(EAT, MIR172, MIR172B, AT5G04275) declined very slightly with much greater variation from week 1 to week 7 Arabidopsis thaliana
leaf is only acting as a carbon source on day 11
(CPD45, FHY3, AT3G22170) is strongly expressed in whole seedling during establishment Arabidopsis thaliana
Class 1 shohai1 (shai1) seeds produced slightly smaller seedlings than normal Zea mays
(EDA23, GSO2, AT5G44700) has strong expression at 3 days after germination Arabidopsis thaliana
C-glycosylated and O-glycosylated flavonoids significantly increase in seedlings during the first 10 days after germination
seedlings were grown in total darkness Arabidopsis thaliana
(ZFP7, AT1G24625) overexpression reduces hypocotyl length of germinated seedlings Arabidopsis thaliana
(SMXL3, AT3G52490) /4/5 deficiency results in seedling lethality Arabidopsis thaliana
plants expressing an artificial microRNA (amiRNA) targeting three members of the SAUR19–24 subfamily exhibit reductions in hypocotyl elongation Arabidopsis thaliana
AtPORA is transiently expressed in early seedling development Arabidopsis thaliana
germinating seedlings perceive light and nutrients
stabilized SAUR fusion proteins expression causes defective apical hook maintenance Arabidopsis thaliana
water-deficit-induced endogenous NO accumulation was accompanied by decrease in elongation of embryo axes Medicago truncatula
(AtcathB3, AT4G01610) gene is expressed during post-germination in cotyledons Arabidopsis thaliana
apical hook formation in etiolated seedlings is considered essential for protection of the shoot apical meristem during germination
(AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) (VAL3, AT4G21550) triple mutant show growth arrest Arabidopsis thaliana
(AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) (VAL3, AT4G21550) triple mutant develop a variety of embryonic phenotypes during their growth and development Arabidopsis thaliana
gd1 mutant exhibits shorter shoots and roots Oryza sativa
other double mutant seedlings have mis-shapen, only partially green cotyledons Arabidopsis thaliana
pex6-2 mutant grew relatively well without sucrose Arabidopsis thaliana
TRICHOME BIREFRINGENCE (TB) is causal mutation in dez Arabidopsis thaliana
seedling emergence causes differential growth leading to apical hook formation
(AtCLE6, CLE6, AT2G31085) over-expression caused hypocotyl elongation Arabidopsis thaliana
(AtEIN3, EIN3, AT3G20770) (AtEIL1, EIL1, AT2G27050) (ETHYLENE INSENSITIVE 3 -LIKE 1) inhibits root enlargement
development of rescued double mutant seedlings is delayed compared to rescued bio1.1 or bio2.1 seedlings Arabidopsis thaliana
ABSCISIC ACID-INSENSITIVE 5 (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) plays important role in post-germinative growth Arabidopsis thaliana
self-seed from pdf2-2 mutant plants additionally heterozygous for atml1-3 produced high proportion of abnormal but viable seedlings (62%, n = 312)
ZMK1 is involved in gravitropism Zea mays
inhibition of extensin peroxidase activity promotes hypocotyl height at higher concentration tomato
hypocotyl length (dark grown) is measured using Fiji Arabidopsis thaliana
84461-2 mutant shows reduced cotyledon area under long days Arabidopsis thaliana
seedling vigor is important agronomic trait Oryza sativa
OsOFP19 overexpression line shows barely any coleoptile elongation Oryza sativa
miR156 levels are highest in young seedlings Arabidopsis thaliana
osacbp2 mutants are reduced in shoot elongation rates Oryza sativa
sufficient Pi supply delays greening Arabidopsis thaliana
(CKRC1, SAV3, TAA1, TIR2, WEI8, AT1G70560) (AtTAR2, TAR2, AT4G24670) double mutant develop normally up to day 3 post germination
ethylene is involved in formation of apical hooks
seeds are plated on half-strength Linsmaier and Skoog media without sucrose containing indicated concentrations of epibrassinolide (eBL), propiconazole (PPZ), or mock Arabidopsis thaliana
plants grown in the dark for seven days have hypocotyl lengths measured using Fiji Arabidopsis thaliana
aleurone functions are crucial for seedling establishment after germination Arabidopsis thaliana
different temporal patterns of anthocyanin and LHCB1 transcript accumulation in (GUN1, AT2G31400) seedlings may be consequence of differences in early seedling development Arabidopsis thaliana
(GUN1, AT2G31400) and wild-type seedlings after 96 h had open expanded cotyledons whether grown in presence or absence of sucrose Arabidopsis thaliana
NR-dependent NO accumulation by ABA leads to axis elongation Medicago truncatula
soil-grown seedlings are grown under continuous light at 22°C Arabidopsis thaliana
hypocotyl is critical for morphological establishment of the seedling
rif18 mutant seedlings showed improved seedling establishment in presence of (AtDWF4, CLM, CYP90B1, DWF4, PSC1, SAV1, SNP2, AT3G50660) Arabidopsis thaliana
npc4-1 seedlings were grown on 0.5 MS liquid medium supplemented with 2% sucrose Arabidopsis thaliana
svr4-2 T-DNA insertion allele is seedling-lethal
seedlings were grown at 23°C under 18 h light/6 h dark and 40–50 μmol m−2 s−1 light intensity Arabidopsis thaliana
cell division is not of profound importance to hypocotyl elongation Arabidopsis thaliana
IAA conjugates and IBA play a role in apical hook development Arabidopsis thaliana
higher level of HFA-TAG mobilization in DG2 and PD1a may be an additional contributor to successful establishment
35S::GFP::MYB62 transgenic line demonstrates identical phenotype to (AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpressing plants
(KAI2, AT4G37470) mutant shows elongated hypocotyls Arabidopsis thaliana
(VQ18, AT2G44340) and (VQ26, AT3G60090) were also expressed in roots and cotyledons of early seedlings Arabidopsis thaliana
YLG cannot effectively regulate hypocotyl growth Arabidopsis thaliana
(AtPHR1, PHR1, AT4G28610) (PHOSPHATE STARVATION RESPONSE 1) inhibits hypocotyl elongation
(GSO1, SGN3, AT4G20140) is required for seedling establishment Arabidopsis thaliana
epinastic cotyledons were present in more than 80% of T1 plants
FLOWERING LOCUS C (AGL25, FLC, FLF, RSB6, AT5G10140) expression is reduced in seedlings after 5 days Arabidopsis thaliana
imb4-1 fra1-5 double mutant shows growth and developmental defects indistinguishable from imb4-1 single mutant in seedlings Arabidopsis thaliana
(ATMYC2, JAI1, JIN1, MYC2, RD22BP1, ZBF1, AT1G32640) regulates GATA-box containing promoter Arabidopsis thaliana
GR24 inhibits cotyledon expansion Arabidopsis thaliana
(ATHSFA2, HSFA2, AT2G26150) expression restored at least partially cotyledon morphology Arabidopsis thaliana
hypocotyl elongation is regulated by ERFVIIs acting as NO sensors through the Cys-Arg/N-end rule pathway
(EAT, MIR172, MIR172B, AT5G04275) increased 8–10 fold in whole shoots during first two weeks after planting under LD conditions Arabidopsis thaliana
similar observations were made in cotyledons Arabidopsis thaliana
(OSH1, AT5G01580) osh15 double mutants initiate coleoptile Oryza sativa
DG2 and PD1a with 50% and 38% more 0-HFA-TAG than (cL37, PSRP5, AT3G56910) had less acute resource starvation compared to (cL37, PSRP5, AT3G56910)
establishment of DG2 and PD1a is clearly improved over (cL37, PSRP5, AT3G56910)
T2 seedlings were grown for 12–15 days
hypocotyl and root lengths were similar under air or 1-MCP treatment in both erf.c1 and ERF.C1-OE lines Solanum lycopersicum
early seedling development is critical stage Cucumis sativus
seedlings were grown on rotary shaker Arabidopsis thaliana
pea seedlings are grown in soil in growth chamber Pisum sativum
osnam-1 showed abnormal leaves in three-leaf seedling stage Oryza sativa
(ASG6, CRK2, AT1G70520) seedlings could not survive beyond three-leaf stage Zea mays
FLOWERING LOCUS C (AGL25, FLC, FLF, RSB6, AT5G10140) protein expression is slightly reduced in aerial part without leaves after 3 days Arabidopsis thaliana
endosperm-deprived embryos produce nonviable seedlings Arabidopsis thaliana
ethylene signaling regulates soil emergence
rol1-2 mutant provokes aberrant morphology in cotyledons Arabidopsis thaliana
difference between peas and cucumbers is possibly explained by structure of their cotyledons Pisum sativum; Cucumis sativus
tip of the leaf is no longer importing dye on day 9
day 7 is the date when the first leaf blade became visible
transport stabilization at adult-like velocities in cucumber seedlings may coincide with transition from being source to sink limited Cucumis sativus
(CPD45, FHY3, AT3G22170) mutant is hyposensitive to ABA-mediated seedling greening
vYFP-labeled Hc-L fusion protein overexpression causes growth-retarded seedling phenotype Arabidopsis thaliana
(ATSYP132, SYP132, AT5G08080) single mutant dies as abnormal seedlings
MG132 treatment should not enhance cotyledon expansion in (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutant
(BES1, BZR2, AT1G19350) and (BZR1, AT1G75080) mutations show non-additive effects cotyledon expansion
prolonged induction of OPL2m-VENUS is seedling lethal Arabidopsis thaliana
penta della mutant had longer hypocotyls Arabidopsis thaliana
(AP-3 beta, PAT2, WAT1, AT3G55480) loss-of-function mutant has increased percentage of arrested plants in medium lacking sucrose Arabidopsis thaliana
GR24 did not inhibit hypocotyl elongation in max2-1 seedlings Arabidopsis thaliana
Double ale1-4 pdf2-2 mutant plants showed post-germination growth indistinguishable from wild-type
malondialdehyde (MDA) accumulation correlates with growth reduction Arabidopsis thaliana
(AtCPK21, CPK21, AT4G04720) mutant was stratified and transferred as 7-day-old seedlings Arabidopsis thaliana
(EAL1, SGR7, SHR, AT4G37650) mutant seedlings grown under continuous white fluorescent light Lycopersicon esculentum
GA signaling pathway is pivotal in hypocotyl elongation
(AtGSH2, GSH2, GSHB, AT5G27380) (glutathione synthase) loss-of-function mutant shows seedling-lethal phenotype Arabidopsis thaliana
(SMAX1, AT5G57710) single mutant has short hypocotyls Arabidopsis thaliana
cotyledonary petiole growth was not significantly affected in (SMAX1, AT5G57710) seedlings Arabidopsis thaliana
(AtPSKR2, PSKR2, AT5G53890) overexpression promotes hypocotyl elongation Arabidopsis thaliana
1-butanol induce morphological alterations in seedlings Arabidopsis thaliana
cop1-4/EIN3ox plants developed long hypocotyls in darkness Arabidopsis thaliana
pex6-3 35S:PEX5 lacked persistent oil bodies and resembled wild type when grown without sucrose Arabidopsis thaliana
ERF.B3-SRDX seedlings have hypocotyl length 50% lower than wild-type Solanum lycopersicum
1-butanol induce defects in Arabidopsis seedling development Arabidopsis thaliana
seedling growth is subject to analysis of effects of 1-butanol and N-lauroylethanolamine (NAE 12:0) Arabidopsis thaliana
1-aminocyclopropane-1-carboxylic acid (ACC) suppresses hypocotyl elongation Arabidopsis thaliana
acyl CoA oxidase mutant stops growing at establishment stage post-germination Arabidopsis thaliana
Z-carlactone (Z-CL) at 10 μm concentration required for significant but relatively weak response in hypocotyl elongation Arabidopsis thaliana
seedlings of ale1-4 pdf2-2 mutants were rarely normal
tri-galacturonate restores skotomorphogenesis in dark-grown dez mutants Arabidopsis thaliana
apical hook development is crucial to survival and establishment of germinating seedlings
germinated seeds from 4n × 2n cross abort at early stage of seedling growth Oryza sativa
Arabidopsis RAD homolog (ATRL2, MEE3, RSM1, AT2G21650) overexpression resulted in reduction in hypocotyl length Arabidopsis thaliana
(AtEIN3, EIN3, AT3G20770) (AtEIL1, EIL1, AT2G27050) (ETHYLENE INSENSITIVE 3 -LIKE 1) inhibits root elongation
germination-defective1 (gd1) mutant is defective in seedling development Oryza sativa
(ATPSKR1, PSKR1, AT2G02220) expression in epidermis is sufficient to promote hypocotyl growth Arabidopsis thaliana
bou-2 seedlings growth may resume with added sugar Arabidopsis thaliana
(M3Kdelta6, SIS8, AT1G73660) overexpression lines exhibit significantly lower rates of cotyledon expansion Arabidopsis thaliana
MtCIR1 negatively regulates salt stress response during seedling growth Medicago truncatula; Arabidopsis thaliana
pex6-1 35S:PEX5 lacked persistent oil bodies and resembled wild type when grown without sucrose Arabidopsis thaliana
accumulation of glycerol-3-phosphate causes arrested development Arabidopsis thaliana
abh1-8 ago1-38 double mutant exhibits fused cotyledons Arabidopsis thaliana
(ARF6, AT1G30330) supports hypocotyl elongation Arabidopsis
(ARF6, AT1G30330) support of hypocotyl elongation promotes cell expansion Arabidopsis
(ATP1, RAF2, SDIRIP1, AT5G51110) is induced very early during seedling development Arabidopsis thaliana
osacbp2-P05815 mutant does not possess elongated coleoptiles Oryza sativa
cotyledon provides nutrients for seedling establishment
BFA treatment of (AGC1-1, D6PK, AT5G55910) overexpressor seedlings largely normalizes growth of etiolated (AGC1-1, D6PK, AT5G55910) overexpressor seedlings
endosperm governs viable seedling formation
negative role of (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) in root hair development and positive role of in hypocotyl elongation may be coordinated to provide evolutionary advantage for seedling fitness Arabidopsis thaliana
growth on no-sucrose treatments increased etiolated hypocotyl length Arabidopsis thaliana
seedlings germinated from (BIO1, BIO3, AT5G57590) (ATSUC5, SUC5, AT1G71890) and (BIO2, BIOB, EMB49, AT2G43360) seeds exhibited strong deformations of their cotyledons Arabidopsis thaliana
CONSTITUTIVE PHOTOMORPHOGENIC 1 (ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) loss of function is associated with post-germination growth arrest Arabidopsis thaliana
Arabidopsis seedlings use lipids and proteins stored in embryo cells Arabidopsis thaliana
post-translational modifications of major chloroplast RNA-binding proteins may help elucidate roles in seedling development Arabidopsis thaliana
carlactone (CL) and/or CL-derived strigolactones are poor regulators of seedling morphogenesis Arabidopsis thaliana
pex6-1 mutant was sucrose dependent seedling growth Arabidopsis thaliana
PSKR1ox2 seedlings display significantly longer hypocotyls Arabidopsis thaliana
ped mutant stops growing at establishment stage post-germination Arabidopsis thaliana
storage molecule utilization mutants may be restored by externally added sugar Arabidopsis thaliana
Arabidopsis mutants with non-photosynthetic cotyledons require externally added sugar Arabidopsis thaliana
lack of SAM activity prevents leaf formation Arabidopsis thaliana
accumulation of methylglyoxal causes arrested development Arabidopsis thaliana
(MIR159, MIR159A, AT1G73687) overexpression shows no cotyledon epinasty phenotype
(MIR159, MIR159B, AT1G18075) overexpression shows no cotyledon epinasty phenotype
(MIR159C, AT2G46255) overexpression shows no cotyledon epinasty phenotype
(ATCOP1, COP1, DET340, EMB168, FUS1, AT2G32950) mutation does not affect cotyledon expansion under control conditions
(ATCESA2, ATH-A, CESA2, AT4G39350) mutant in Arabidopsis exhibits stunted growth of hypocotyls Arabidopsis thaliana