Notice: Database construction is still in progress. Certain features may be incomplete, slower than usual, or temporarily unavailable while we re-ingest the knowledge graph with citation data. Thank you for your patience.
← All pathways

plant development

100566 relationships annotated with this phrase. Showing first 500 of 100566.
Source entity Relationship Target entity Species
FERONIA (FER, AT3G51550) modulates plant growth and development Arabidopsis
KAR/ (KAI2, AT4G37470) ligand (KL) signalling influences broad plant developmental processes
TCP transcription factors play important roles in diverse pathways in plants
GRAS proteins play critical and diverse roles in plant development and signaling
(HTB4, AT5G59910) interaction with specific proteins might regulate specific developmental processes Arabidopsis thaliana
maize recombinant inbred lines (RILs) were analyzed for growth patterns Zea mays L.
(BRD1, AT1G20670) pin11, rap2, and/or zcn8 genes exhibited varying activity levels throughout different growth stages Zea mays
loss of 48 genes is responsible for reduced plant height Zea mays
cbc1-1 cbc2-3 mutant noted slightly smaller growth in as previously reported Arabidopsis thaliana
NAC transcription factors are crucial throughout root development
either of the mutants may have second site mutation that exacerbates the phenotype Arabidopsis thaliana
msp1-1 plantlets were able to continue development beyond L6-growth stage only when transferred to liquid MS-medium Arabidopsis thaliana
hsc70.1 hsp70.4 double mutants develop strong phenotypes with curly/round leaves, twisted petioles, thin stems, early flowering, and short siliques Arabidopsis thaliana
mobility of HSC70.1 transcript is necessary for proper plant growth Arabidopsis thaliana
strong root system contributes to good plant growth
YABBY (YAB) transcription factors play important roles in plant development
(ARC6H, ATCDP1, CDP1, PARC6, AT3G19180) mutant does not affect plant growth Triticum turgidum
Plantago lanceolata produces epigeogenous rhizome Plantago lanceolata
(ATIRE1-1, AtIRE1b, IRE1, IRE1-1, IRE1B, AT5G24360) share overlapping roles in plant growth Arabidopsis thaliana
plastids play vital roles in plant growth
Mp glk mutants show noticeable decrease in assimilatory cell number Marchantia polymorpha
Fusarium wilt is threat to plant growth and development
double deletion of (GOM8, RHD3, AT3G13870) and (ATRL1, RL1, RSM2, AT4G39250) leads to lethality Arabidopsis thaliana
LBD genes are involved in embryo sac and leaf development in maize Zea mays
(AtC3H15, CDM1, AT1G68200) heterozygous plants showed normal development Arabidopsis thaliana
Rubisco activase (RCA, AT2G39730) plays crucial role in regulating plant growth
leaf area QTL identified one candidate gene Salix purpurea
NAC094-overexpressing plants (NAC-OE1 and NAC-OE2) exhibit stunted plant growth Lotus japonicus
presence of an individual belowground growth form (BGF) expresses certain morphological potential of a species
altering MpGLK levels causes developmental defects in Marchantia Marchantia polymorpha
Mp glk mutants exhibit developmental alterations in plant phyllotaxy Marchantia polymorpha
root morphogenesis is crucial to seedling survival
RWA proteins important for cell expansion Arabidopsis thaliana
null mutations of (ATCNGC2, CNGC2, DND1, AT5G15410) impairs plant growth Arabidopsis thaliana
homozygous phe1-1 mutants plant carrying a transposon insertion showed no difference in vegetative and reproductive development Arabidopsis thaliana
multiple lines of untargeted DAGK, N-DGD1, and tpATS1 did not show growth phenotype Arabidopsis thaliana
QK mutant showed obvious defects at 27°C including stunted growth of inflorescences Arabidopsis thaliana
over- or constitutive activation of MAPK cascade may become lethal
ov473 and ovPN59 plants showed no difference in rosette to elongation transition Nicotiana attenuata
OsHMA5 is involved in xylem loading of copper at vegetative growth stage Oryza sativa
growth phenotype depends on genotype Arabidopsis thaliana
xylan acetylation known to be important for plant development Arabidopsis thaliana
increasing GA 1 can modify vegetative and reproductive plant phenotypes
SR proteins play crucial role in plant development Arabidopsis thaliana
vital sporophytes are tightly attached to gametophore Physcomitrella patens
histone variants are involved in the regulation of various developmental processes in plants
epigeogenous rhizome production in Plantago lanceolata occurs in moist places Plantago lanceolata
ceh1 seedlings do not mature sufficiently to allow for studying PlAMV-GFP infection Arabidopsis thaliana
(TCP1, AT1G67260) participated in Arabidopsis thaliana development Arabidopsis thaliana
stem cells are vital for plant development
(RWA2, AT3G06550) (RWA3, AT2G34410) (RWA4, AT1G29890) triple mutant was much more dwarfed and stressed than (RWA1, AT5G46340) (RWA3, AT2G34410) (RWA4, AT1G29890) and (RWA2, AT3G06550) Arabidopsis thaliana
(ATCNGC4, CNGC4, DND2, HLM1, AT5G54250) mutant exhibits dwarfism Arabidopsis thaliana
brassinosteroids (BR) regulate vascular differentiation
TETRASPANIN1/TORNADO2 ( (TET1, TRN2, AT5G46700) /EKEKO) mutants show genetic interactions with (LOP1, TRN1, AT5G55540) mutants Arabidopsis thaliana
EPF/EPFL family secreted peptides play essential roles in regulating plant growth or development Arabidopsis thaliana
ZmBELL10 loss-of-function mutant results in shorter internodes Zea mays
long tap root in Plantago lanceolata occurs in dry and nutrient-poor places Plantago lanceolata
(ABA1, ATABA1, ATZEP, IBS3, LOS6, NPQ2, ZEP, AT5G67030) (TOL2, AT1G06210) /3/5/6 individuals showed no additive phenotype at vegetative and reproductive stage Arabidopsis thaliana
EILs/ (AtEIN3, EIN3, AT3G20770) family of transcription factors plays pivotal role in developmental regulation
severe developmental phenotype observed under several different growth conditions Arabidopsis thaliana
(AtMAX2, MAX2, ORE9, PPS, AT2G42620) mutants exhibit phenotypes in several developmental processes Arabidopsis thaliana
arabinogalactan proteins (AGPs) have been extensively studied and play many roles in plant growth and development
(RPL10, RPL10A, SAC52, uL16z, AT1G14320) /+ (RPL10B, uL16y, AT1G26910) (RPL10C, SAG24, uL16x, AT1G66580) triple mutant is not viable plant development Arabidopsis thaliana
number of calluses formed positively correlated to (ATHSFA2, HSFA2, AT2G26150) expression level Arabidopsis thaliana
(AtHDA7, HDA7, AT5G35600) overexpression causes delays of growth at different developmental stages Arabidopsis thaliana
dwarf males (nannandry) are unique in bryophytes among land plants
forests growing under higher vapour pressure deficit (VPD) are expected to have smaller stature
ZCN8 is candidate gene for plant development Zea mays L.
20 DAS OE plants reach plastochron 2 Marchantia polymorpha
pronounced protuberances on gemma cup rim indicate nonuniform growth Marchantia polymorpha
genotypes in managed wild blueberry fields show variation in yield
CT4:20 family showed extreme dwarf plants Solanum chacoense
(RPL10B, uL16y, AT1G26910) (RPL10C, SAG24, uL16x, AT1G66580) double mutants are indistinguishable from (RPL10B, uL16y, AT1G26910) single mutants Arabidopsis thaliana
slopes of positive correlations between blumenols and lipids decrease as plants mature Nicotiana attenuata
Lycopodiella alopecuroides exhibits relatively standard growth habit for family Lycopodiella alopecuroides
Purpureocillium lilacinum and P. lavendulum enhance plant growth and reproductive tissue development as root endophytes Gossypium hirsutum
foot of the sporophyte is wider than seta Physcomitrella patens
only graft-mobile HSC70.1 transcript is needed to restore WT growth of hsc70.1 hsp70.4 mutant Arabidopsis thaliana
HSC70.1 transcript mobility followed by HSC70.1 protein expression rescues growth phenotypes of hsc70.1 hsp70.4 mutants Arabidopsis thaliana
AtAGO7 mediates juvenile-to-adult phase transitions Arabidopsis thaliana
control lines were unaffected Arabidopsis thaliana
mutant and OE lines were examined for thallus morphology during first branching event Marchantia polymorpha
TurboID-ASK1 transgenic line appears phenotypically similar to wild-type (WT) Col-0 plants Arabidopsis thaliana
plants grown from (AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) double mutant seedlings that escaped the embryonic seedling fate exhibited pleiotropic phenotypes Arabidopsis thaliana
vascular system allowed pteridophytes to grow upright during sporophyte generation
strigolactone (SL) mixtures depend on developmental stages
OsHMGB1 positively regulates plant growth Oryza sativa
chloroplast size manipulations are unlikely to lead to higher growth Nicotiana tabacum
biomass allocation to plant organs will follow program associated with ontogenetic trajectory of plant
CRISPR/Cas9-induced suberization defects barely affect overall plant development Populus trichocarpa
rice d17 mutant exhibits severe phenotypes with respect to shoot and root architecture Oryza sativa
copper requirement is very low at vegetative stage Oryza sativa
CT4:50 and CT4:33 families showed bushy, short internode phenotype Solanum chacoense
QK mutant showed obvious defects at 27°C including aborted siliques Arabidopsis thaliana
rosette leaves of QK mutant bleached at 29°C high temperature stress Arabidopsis thaliana
(VUP1, AT3G21710) misexpression induces strong deleterious pleiotropic effects plant development Arabidopsis thaliana
ERECTA promotes axis elongation and normal morphogenesis of multiple aerial organs Arabidopsis thaliana
constitutive activation of abscisic acid (ABA) signaling reduces growth
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) single mutant is viable plant development Arabidopsis thaliana
nonphotosynthetic mutants in large seeded plants like maize grow rapidly to substantial size during period supported by seed reserves Zea mays
genes in ABA-suppressed and ZFP3-derepressed category are activated during germination and shoot regeneration Arabidopsis thaliana
ectopic expression of ZFP3-related (AtZAT6, C2H2, CZF2, ZAT6, AT5G04340) zinc finger proteins results in pleiotropic morphological abnormalities Arabidopsis thaliana
ectopic ZmSHR1 activity does not cause gross alterations in shoot anatomy Oryza sativa
brassinosteroid (BR) coordinately regulate with gibberellin (GA)
serotonin is involved in morphogenesis plants
(ATMSRA3, PMSR3, AT5G07470) is highly expressed in stamen and pollen Arabidopsis thaliana
growth defect is most pronounced during first 3–4 weeks of plant development Arabidopsis thaliana
TILLING mutant line CS92437 (#437) grown for 3 weeks in climate chamber Arabidopsis thaliana
different canopy architecture strategies deployed at different layers of the canopy affect at different plant growth stages
HSC70.1 protein mobility is not required for normal plant growth Arabidopsis thaliana
OXmiR400 plants show no obvious differences from wild-type (WT) plant seedlings under normal conditions Arabidopsis thaliana
SL-deficient mutants exhibit severe phenotypes with respect to shoot and root architecture
(MED30, AT5G63480) is essential for early plant development
atgatl5-1 mutant plants are morphologically indistinguishable from wild-type plants Arabidopsis thaliana
auxin plays crucial roles in plant development
dwarf males grow on leaves of female plants
Detlef Weigel discovered key genes of plant development
Three independent, stable YFP(s)::HSC70.1 (hsc70.1 hsp70.4) transgenic lines were selected and their root growth and flowering time were measured Arabidopsis thaliana
zmbell10-1 plants have fewer tassel branches Zea mays L.
rice (ARC6H, ATCDP1, CDP1, PARC6, AT3G19180) mutant had slight reductions in plant growth and grain weight Oryza sativa
Mp glk mutants show differences in plant morphology Marchantia polymorpha
GmHAD1-2 overexpression or suppression significantly affected shoot growth Glycine max
(RPL10C, SAG24, uL16x, AT1G66580) single mutants show phenotype indistinguishable from wild-type plants Arabidopsis thaliana
hsc70.1 hsp70.4 double-mutant lines expressing the YFP(s)::HSC70.1 fusion were analyzed for phenotypes Arabidopsis thaliana
rosettes of irAGO7 and WT plants transitioned to the elongation stage together Nicotiana attenuata
rhizosphere microbiome composition eventually stabilizes during reproductive stage Avena barbata
osmtp1 mutants show no difference in panicle number Oryza sativa
poplar mutants cultivated in hydroponics development is highly similar to wild-type (WT) development Populus × canescens
Physcomitrium patens is principal bryophyte model for studying growth and development Physcomitrium patens
axy4-1 mutant did not show visible symptoms Arabidopsis thaliana
18X-551 linkage map was utilized to map vegetative traits Salicaceae purpurea
vertical stems (peduncles) tipped with strobili die back in winter Lycopodiella alopecuroides
water availability is major determinant of plant reproduction
overaccumulation of RhNAC100 transcripts repressed elongation of hypocotyls Arabidopsis thaliana
most LBD genes studied thus far are involved in aboveground development
nitrogen (N) is essential for plant growth
discrepancy between N. benthamiana and A. thaliana IMP-ITP correlation is hypothesized to be due to different developmental context Nicotiana benthamiana; Arabidopsis thaliana
drought impairs plant growth and development Arabidopsis thaliana
expression profile of functional genes is significantly different in early developmental stage and late developmental stage Arabidopsis thaliana
knockout or overexpression of SlMPK8 did not affect plant vegetative and reproductive growth Solanum lycopersicum
soyasapogenol B is linked to rhizome development
studies on smaller bioclimatic scales investigated among-population variation (APV) at early life stages
leaf and rosette morphology in all mutants comparable to wild-type Col-0 plants Arabidopsis thaliana
plants making better use of precipitation potentially enhances plant growth
nitrogen uptake may be partially or completely inhibited during reproductive stage
seedlings were induced directly after seed germination Nicotiana tabacum
induced expression of ESCRT-III mutants caused obvious cotyledon developmental defects Arabidopsis thaliana
Blue-red discoloration in LPLA RNAi plants begins within 1 week after start of bolting Arabidopsis thaliana
hormones control proper timing of developmental transitions Arabidopsis thaliana
PHB3-GFP fusion is functional and rescues small-plant phenotype of phb3-3 loss-of-function mutant Arabidopsis thaliana
sHSPs are involved in embryogenesis
(ATSWC6, SEF, AT5G37055) mutants display similar defects during vegetative and reproductive development Arabidopsis thaliana
epigenetic mechanisms coordinate plant growth and development
highly dynamic spatial and temporal expression of these GRXs is needed for normal vegetative and reproductive plant development
expression level of alternative oxidase (AOX) is modulated by developmental stage
results confirm lethality phenotypes associated with (GAUT12, IRX8, LGT6, AT5G54690) and (GAUT8, QUA1, AT3G25140) mutants Arabidopsis thaliana
xyloglucan oligosaccharide proportions show few differences at different developmental stages Flagellaria indica
carbon (C) is essential for plant growth
perennial herbs develop new aboveground parts every year
site with highest vapour pressure deficit (VPD) is expected to have smaller stature
zm5008 mutants have fewer aboveground nodes Zea mays L.
drought affects plant development
(ATCPK32, CDPK32, CPK32, AT3G57530) participates in shoot and root development
pectins regulate cell shape and organ development
water availability is major determinant of plant growth
(TOL2, AT1G06210) /3/5/6 mutant shows no negative impact on plant growth and development Arabidopsis thaliana
double mutants lacking cytosolic O-acetylserine(thiol)lyase isoform A (OAS-TL A) are retarded in growth Arabidopsis thaliana
multiple independent tpTOC75 lines showed similar phenotypes Arabidopsis thaliana
homozygous msp1-1 plantlets develop into six-true-leaf (L6) growth stage Arabidopsis thaliana
(anac094, NAC094, AT5G39820) overexpression in WT and (NLP4, AT1G20640) mutant backgrounds results in impaired growth and reduced shoot weight in plants at 5 wpi Lotus japonicus
endoreplication is involved in several plant development pathways
(AtPPR2, EMB2750, PPR2, AT3G06430) has potential role in plant development Arabidopsis thaliana
7 DAS Mp glk mutants show air chambers either absent or just beginning to form Marchantia polymorpha
nitric oxide (NO) mediates apical dominance
RWA proteins are important determinants of plant development at the whole plant level Arabidopsis thaliana
rhd3-8 null allele causes growth defects Arabidopsis thaliana
microbial activity might lead to increased plant growth
male spores develop normally in absence of female
mutation of (ATDTX35, DTX35, FFT, AT4G25640) and OsVPE1/2 leads to accumulation of side-products which affects plant development
Plantago lanceolata produces long tap root Plantago lanceolata
maize exhibits temporal growth dynamics Zea mays L.
pin11 is candidate gene for plant development Zea mays L.
RIL haplotypes differentiate across growth stages Zea mays L.
expression of OsASTOL1 S189N with a suitable promoter achieves without compromising plant growth and yield Oryza sativa
PIN family proteins are critical for developmental processes
silencing NaAGO7 does not affect N. attenuata's development Nicotiana attenuata
Mature spike morphology in WT and hvtdf1-2 did not identify any differences in spike size Hordeum vulgare
soybean growth rates decrease with number of days after sowing Glycine max
STTM400 plants show no obvious differences from wild-type (WT) plant seedlings under normal conditions Arabidopsis thaliana
light influences plant growth and development
7 DAS marks transition to mature stage where dorsal structures initiate Marchantia polymorpha
ethylene functions in plant development as key modulator of cell expansion
(TET1, TRN2, AT5G46700) / ekeko mutants exhibit severe pleiotropic developmental defects Arabidopsis thaliana
(RPL10B, uL16y, AT1G26910) has an important role in plant development Arabidopsis thaliana
plant embryogenesis involves passage through conserved and evolutionarily old transcriptional stage Arabidopsis thaliana
plant P uptake affects subsequent plant growth
OsMTP1 knockout does not affect grain yield Oryza sativa
common quantitative trait loci (QTLs) contain candidate genes (BRD1, AT1G20670) pin11, zcn8 and rap2 Zea mays L.
higher levels of carbohydrate derivatives and fatty acyls potentially reflecting changes in developmental process
temporal and/or spatial-specific expression patterns contribute to diverse roles of (EEP1, MIR164, MIR164C, AT5G27807) during multiple developmental events
brassinosteroids (BR) regulate senescence programs
7-d-old seedlings from osfkbp20-1b and osfkbp20-1b k/d show phenotypes comparable to WT under normal conditions Oryza sativa
leucine-rich repeat receptor kinases (LRR-RKs) are crucial for plant developmental processes
absorption of water and nutrients from soil improves growth of crops
ZmBELL10 direct targets are significantly enriched in plant system development, regulation of shoot system development, and regulation of development process Zea mays L.
nitrogen (N) plays important role in plant growth and development
husk leaf width benefits maize growth and reproduction Zea mays
(AtUBP12, UBP12, AT5G06600) and (AtUBP13, UBP13, AT3G11910) have roles in developmental pathways
genotypes in managed wild blueberry fields show variation in phenology
(ECT3, AT5G61020) (YTH-domain reader protein) control morphology Arabidopsis thaliana
stem section of rwa1-1 rwa2-1 rwa3-1 rwa4-1 quadruple mutant shows drastic reduction in cell number Arabidopsis thaliana
FAR1-BINDING PROTEIN 3 (CPD45, FHY3, AT3G22170) might have additional effects on plant growth and development
expression of (IKU2, AT3G19700) under control of strong glycinin promoter may have negative effects on overall plant development, e.g. flower initiation Arabidopsis thaliana
rice line carrying mutation in IRREGULAR XYLEM10 (ATGUT1, GUT2, IRX10, AT1G27440) ortholog has smaller stature Oryza sativa
PpPINC is active in maternal tissues which will form the vaginula and the sclerotized ring structure Physcomitrella patens
inherent developmental constraints may contribute to canalization of fern physiology
qSLB 3.04 resistance allele from Mo17 confers resistance at seedling stage Zea mays
alternative splicing (AS) plays crucial role in regulating plant growth
(AtbZIP, bZIP, AT1G68880) transcription factor is involved in regulation of plant development Arabidopsis thaliana
(TOL2, AT1G06210) (TOL3, AT1G21380) (TOL5, AT5G63640) and (TOL6, AT2G38410) alone are not completely epistatic to VPS23A in development Arabidopsis thaliana
(GOM8, RHD3, AT3G13870) −/− (ATRL1, RL1, RSM2, AT4G39250) −/− genotype was not recovered in F3 seedlings Arabidopsis thaliana
OsCOI mutants were used to phenotype developmental responses Oryza sativa
total loss of enzymatic activities (e.g. clfswn) causes dramatic phenotypes Arabidopsis thaliana
(MIR400, AT1G32582) and (PPR1, AT1G06580) is required for normal seedling growth Arabidopsis
SCF-type ubiquitin ligase plays a pivotal role in upholding homeostasis for facilitating optimal plant growth and development
double deletion of (GOM8, RHD3, AT3G13870) and (ATRL1, RL1, RSM2, AT4G39250) is lethal Arabidopsis thaliana
(FIE, FIE1, FIS3, AT3G20740) cosuppression plants show severely affected plant development and organ establishment Arabidopsis thaliana
oastlAC B +/− mutant shows shorter stem by 67% compared to wild type Arabidopsis thaliana
(RPL10, RPL10A, SAC52, uL16z, AT1G14320) /+ single mutants look like wild-type Columbia (Col-0) plants Arabidopsis thaliana
(RPL10C, SAG24, uL16x, AT1G66580) single mutants look like wild-type Columbia (Col-0) plants Arabidopsis thaliana
ectopic (ATHSFA2, HSFA2, AT2G26150) expression complemented the thermotolerance defects of QK at vegetative and reproductive stages Arabidopsis thaliana
relationships between root blumenol accumulations and AMF-specific lipid accumulations changed as plants matured when grown without competitors Nicotiana attenuata
single knockout of PpPINA has no visible effect on morphology of the gametophore or phyllids Physcomitrella patens
Physcomitrella has very short life cycle of 3–6 months Physcomitrella patens
HSC70.1 mRNA mobility is required for normal plant growth Arabidopsis thaliana
OE lines exhibit normal growth pattern comparable to WT and EV plants Solanum lycopersicum
soil P availability constrains plant growth
nitrate assimilation and translocation regulation optimizes growth
phenological events are crucial in understanding plant physiological development cycles
acbp3-2 did not impact vegetative growth Arabidopsis thaliana
Citrine-TurboID transgenic line appears phenotypically similar to wild-type (WT) Col-0 plants Arabidopsis thaliana
development of true leaves is early stage of plant growth
either of the mutants may have second site mutation that reduces the severity of the phenotype Arabidopsis thaliana
tpTOC75 lines were the only ones showing growth phenotypes Arabidopsis thaliana
F-box proteins play essential roles in plant growth and development
OsGRFs are involved in different development progress Oryza sativa
OsmiR396d controls plant architecture by repressing expression of multiple target genes Oryza sativa
adult leaves are smaller than late juvenile leaves Mesembryanthemum crystallinum
nitrogen-containing compounds control proper timing of developmental transitions Arabidopsis thaliana
SlSPRH1-expressing plants showed shorter growth Arabidopsis thaliana
bzip60-1/17/28 +/− heterozygous triple mutant lost vertical growth Arabidopsis thaliana
bzip60-1/17/28 +/− heterozygous triple mutant exhibits dome-like structure Arabidopsis thaliana
bzip17-2/bzip60-1 double mutant did not present significant change in growth and development Arabidopsis thaliana
PHBs (prohibitins) in plants play positive role in development of new tissues and organs
(BADC1, BLP3, AT3G56130) (BADC3, BLP2, AT3G15690) mutant plants exhibit normal growth Arabidopsis thaliana
(AHA1, HA1, OST2, PMA, AT2G18960) and (AHA2, AtHA2, HA2, PMA2, AT4G30190) are essential for plant growth and development Arabidopsis thaliana
plant cell walls influence plant development and shape
(chr13, PIE1, SRCAP, AT3G12810) (ATSWC6, SEF, AT5G37055) (ARP6, ATARP6, ESD1, SUF3, AT3G33520) and (H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) flowers display several unfertilized or aborted ovules ovule fertility Arabidopsis thaliana
(AGL20, ATSOC1, SOC1, AT2G45660) (AGL8, FUL, AT5G60910) double mutant phenotype strongly resembles characteristics of perennial plants Arabidopsis thaliana
seedlings for TEM recordings grown on plates containing half-strength MS (Murashige and Skoog) medium Arabidopsis thaliana
structurally deficient polysaccharides impacts plant growth Arabidopsis thaliana
sporophyte survival positively correlates with vegetative growth prior to fertilization
accumulation of particular kaempferol derivatives over a certain threshold is detrimental and has a tremendous impact on plant development
over- or constitutive activation of MAPK cascade may impair growth
alternative splicing (AS) plays crucial role in regulating plant development
ZmBELL10 positively regulates internode elongation Zea mays L.
(MIR400, AT1G32582) LUC transgenic plants have phenotypes similar to OXmiR400 plants Arabidopsis thaliana
presence of an individual belowground growth form (BGF) is morphological trait that is fixed for individual species
expression of some belowground growth form (BGF) types may be environmentally determined
candidate genes (BRD1, AT1G20670) pin11, zcn8 and rap2 drive plant development Zea mays L.
soil microorganisms are pivotal in plant growth and development
plant growth in temperate regions is much higher in middle growing season than in early or late growing seasons seasonal growth dynamics
rosette leaves of wild type remained green at 29°C high temperature stress Arabidopsis thaliana
constitutive overexpression of (VUP1, AT3G21710) causes severe dwarfism Arabidopsis thaliana
virus-based microRNA silencing (VbMS) of (EAT, MIR172, MIR172B, AT5G04275) caused developmental defects Nicotiana benthamiana
plants expressing miR156-insensitive versions of (NZZ, SPL, AT4G27330) targets have bent and spoon-shaped cotyledons Arabidopsis thaliana
KinG is not essential for plant growth or cellular patterning of the root Arabidopsis thaliana
gibberellin (GA) influences cell elongation
provision of carbohydrates produced by photosynthesis is not the limiting factor for growth
plant at 6 weeks of age enters adult growth stage Mesembryanthemum crystallinum
side shoots develop above primary leaves 2 and 3 Mesembryanthemum crystallinum
bzip60-1/17/28 +/− heterozygous triple mutant exhibits stronger phenotypes than 17/28 mutant Arabidopsis thaliana
complete knockout mutant of (AHG2, ATPARN, PARN, AT1G55870) is lethal Arabidopsis thaliana
plant cell wall proteins participate in embryogenesis
MSI1–GFP plants developed normally without developmental defects of msi1-cs plants Arabidopsis thaliana
diverse modifications in FLOWERING LOCUS C (AGL25, FLC, FLF, RSB6, AT5G10140) chromatin regulate developmental processes Arabidopsis thaliana
Zingiberales is ideal for developmental studies on shoot, rhizome, and root systems
single knockout of PpPINC has no visible effect on morphology of the gametophore or phyllids Physcomitrella patens
haustorium cells of the sporophyte foot are surrounded by placenta-like space Physcomitrella patens
lumen in the vaginula is not completely filled by foot Polytrichaceae
homologous Slferl CRISPR mutants do not produce fruit during experiments Solanum lycopersicum
SET DOMAIN GROUP 2 (ATXR3, SDG2, AT4G15180) is broadly expressed during plant growth
knockdown of histone 3 variant (H3.3, HTR8, AT5G10980) leads to defects in leaf development and fertility Arabidopsis thaliana
developmental arrest after Dex induction characterizes death of entire plant Arabidopsis thaliana
(SLG1, AT5G08490) lines showed wild-type phenotype in terms of development Solanum lycopersicum
defects in RDRs can lead to developmental deficiencies
beneficial microorganisms promote plant growth
particular tetraspanin members have biological relevance in basic but vital processes in plant development Arabidopsis thaliana
kin17-1 mutant shows no obvious phenotypic abnormalities Arabidopsis thaliana
growth of nonphotosynthetic mutants is supported for several weeks by seed reserves Zea mays
mobile transcription factors function as positional signals
cuticles have been implicated in plant development
root-specific CKX gene expression combined with expression of transgenes enhancing shoot growth Arabidopsis thaliana
(BZIP17, AT2G40950) single mutant does not exhibit drastic developmental disorders
OsFBK1 knockdown lines resembled wild-type plants Oryza sativa
auxin polar transport tuned by differential membrane-localized carriers modulated Arabidopsis development Arabidopsis thaliana
phloem-mediated RNA regulatory network is involved in leaf development, tuber formation, flowering, and many other developmental processes
drought has negative effect on plant growth and development
(ARP4, ATARP4, AT1G18450) knockdown plants show rosettes with a lower number of leaves leaf number Arabidopsis thaliana
explants from pickle roots sustain somatic embryogenesis Arabidopsis thaliana
carbonylated proteins increase in abundance during Arabidopsis leaf expansion Arabidopsis thaliana
mitochondrial nicotinamide adenine dinucleotide phosphate, reduced form (NADPH)-dependent thioredoxin reductases (NTR) are not essential for plant growth
pht4;6-1 seedlings exhibited slightly more vigorous shoot and root growth Arabidopsis thaliana
atTic55-II and AtPTC52 do not appear to be vital for plant survival Arabidopsis thaliana
cytokinins (CKs) play major roles in regulation of shoot growth
ABNORMAL POLLEN TUBE GUIDANCE1 (APTG1, AT5G14850) is involved in vegetative development Arabidopsis thaliana
Ghd7 dynamically regulates morphology Oryza sativa
type VI trichomes in Solanum habrochaites have multicell stalk and four gland cells on the apex Solanum habrochaites ssp glabratum
miR156 affects tuberization and plant architecture in potato potato
(AtSIP1, RS1, SIP1, AT1G55740) is not essential for normal development Zea mays
(ZFP3, AT5G25160) and its closest C2H2-type zinc-finger protein homologs (ZFPs) influence vegetative development Arabidopsis thaliana
node structure is totally different between Arabidopsis and rice Arabidopsis thaliana; Oryza sativa
plants expressing miR156-insensitive versions of (NZZ, SPL, AT4G27330) targets have greatly reduced rate of rosette leaf initiation during vegetative growth Arabidopsis thaliana
ectopic overexpression of miR156 accelerates plastochron of rosette leaves Arabidopsis thaliana
inability to recover KinG-YFP-tagged lines when using KinG, Ub10, or 35S promoters suggests that up-regulation of KinG is either embryo or gametophyte lethal Arabidopsis thaliana
Fe deficiency treatment causes delay in growth and development Arabidopsis thaliana
ZmSHR1 -mediated induction of supernumerary stomata does not perturb general shoot morphology or overall leaf anatomy Oryza sativa
perturbations to root elongation and lateral root production do not impact shoot development Oryza sativa
auxin accumulation in the ER regulates plant development Arabidopsis thaliana
(AP2, AtAP2, FL1, FLO2, AT4G36920) transcription factors play essential roles in growth Arabidopsis thaliana
nip7;1 T-DNA mutants did not appear to exhibit drastic boron (B) developmental phenotypes in vegetative tissues Arabidopsis thaliana
(AHA1, HA1, OST2, PMA, AT2G18960) (AHA2, AtHA2, HA2, PMA2, AT4G30190) double mutant shows embryonic lethality Arabidopsis thaliana
increase in cell number and differentiation is connected to auxin metabolism Flaveria
(BIK1, AT2G39660) is necessary for normal plant growth Arabidopsis thaliana
(AR2, ATR2, AT4G30210) mutants showed reduction in dry weight of main inflorescence stem Arabidopsis thaliana
suppressor and enhancer function at two different stages of development (embryo and seedling) Arabidopsis thaliana
NbCPI-silenced plants exhibited growth inhibition phenotype with small leaves Nicotiana benthamiana
root enhancer1 (ren1-D) mutant exhibits reduced plant height Oryza sativa
supernumerary stomatal files does not cause gross alterations in shoot anatomy Oryza sativa
(AHG2, ATPARN, PARN, AT1G55870) is essential for embryogenesis Arabidopsis thaliana
(chr13, PIE1, SRCAP, AT3G12810) (ATSWC6, SEF, AT5G37055) (ARP6, ATARP6, ESD1, SUF3, AT3G33520) and (H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) mutants show dwarf and bushy phenotype Arabidopsis thaliana
(chr13, PIE1, SRCAP, AT3G12810) (ATSWC6, SEF, AT5G37055) (ARP6, ATARP6, ESD1, SUF3, AT3G33520) and (H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) flowers display altered petal number petal number Arabidopsis thaliana
plant cell wall is essential in growth and development
defect in salicylic acid (SA) accumulation in (ATPAD4, PAD4, AT3G52430) could be responsible for near wild-type plant form and leaf shape of the (BIK1, AT2G39660) (ATPAD4, PAD4, AT3G52430) double mutant Arabidopsis thaliana
(ATLFNR1, FNR1, LFNR1, AT5G66190) single mutant plants have compromised growth and development Arabidopsis thaliana
ssi2-2+SAD6 transgenic line shows wild-type-like growth phenotype Arabidopsis thaliana
(AVB1, IFL, IFL1, REV, AT5G60690) was identified as important regulator of multiple aspects of plant development Arabidopsis thaliana
C2H2-type zinc finger proteins have been implicated in the regulation of seed development
6-d-old light-grown seedlings do not show relatively high sustained growth rates observed in dark-grown plants or 1- to 2-d-old seedlings
sir1-1 mutant is retarded in growth Arabidopsis thaliana
seedlings regenerated from calli with inactivated OsGINT1 were eventually seedling lethal Oryza sativa
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) mutation results in accumulated delays during three distinct developmental phases Arabidopsis thaliana
Arabidopsis stromal CPHTC70s are essential for plant development Arabidopsis thaliana
(MIR166, MIR166G, AT5G63715) is known for development-related function Oryza sativa
boron (B) has role in plant development
heterotrimeric G-protein-based pathway plays critical roles in plant development
Δ (ATFTSZ2-1, FTSZ2-1, AT2G36250) /2–2 double mutants have gametophores that are obviously shorter than wild-type gametophores
reduction in dry weight of main inflorescence stem in (AR2, ATR2, AT4G30210) mutants showed that normal plant development was affected Arabidopsis thaliana
water availability in soils is crucial factor for plant development
C2H2-type zinc finger proteins have been implicated in the regulation of leaf organogenesis
different members of OsmiR396 deleted nontransgenic mutants may improve rice yield Oryza sativa
wild-type and (AOX1A, ATAOX1A, AtHSR3, HSR3, AT3G22370) plants are of age between 11 and 12 weeks
(GAUT13, AT3G01040) or (GAUT14, AT5G15470) have WT-like growth phenotypes
irx8-5 mutants are severely dwarfed and semi-sterile Arabidopsis thaliana
PMEI overexpression completely prevents formation of lateral organs Arabidopsis thaliana
Qua1-1 mutants are severely dwarfed and semi-sterile Arabidopsis thaliana
P (NPC3, AT3G03520) :GUS and P (AtNPC4, NPC4, AT3G03530) :GUS exhibit similar expression pattern all developmental stages Arabidopsis thaliana
dso-4 transgenic lines display stunted growth
co-suppression of (ATMST1, ATRDH1, MST1, ST1, STR1, AT1G79230) in tobacco transformed with VvHT1 shows no phenotype in vegetative growth Nicotiana tabacum
SCL6-III acts as critical transcriptional regulator of plant growth and development
anti-164bsl amiRNA plant expression line showed reduced length of rosette leaf petioles Arabidopsis thaliana
individual genes and proteins of homogalacturonan (HG) modifying enzyme classes are gradually being placed in development contexts
indole-3-acetic acid (IAA) levels and distribution supports normal plant development
overexpression of RGSV P3 gene resembled phenotype of osnrpd1 Oryza sativa
adult plants from tolQ expressing TOL6:ubq:Ven partially recovered and did not show typical tolQ dwarfed phenotype Arabidopsis thaliana
strong BR insensitivity resulted in reduced plant height Oryza sativa
(mTERF9, AT5G55580) is dispensable for growth Arabidopsis thaliana
post-transformation excision of the marker system can restore normal growth
ss1ss2ss3isa mutant is similar in appearance to ss1ss2ss3 mutant Arabidopsis thaliana
(ATLFNR2, FNR2, LFNR2, AT1G20020) single mutant plants have compromised growth and development Arabidopsis thaliana
BREVIPEDICELLUS (BP) affects pedicel angle Arabidopsis thaliana
(ARAKIN, ATMEKK1, MAPKKK8, MEKK1, AT4G08500) mutant shows dwarfism Arabidopsis thaliana
ethylene receptors have ethylene signaling-independent roles plant development and stress response Arabidopsis thaliana
depletion of GSH synthesis promoted growth of the s1c2 double mutant Arabidopsis thaliana
nutrients control proper timing of developmental transitions Arabidopsis thaliana
ap-3β mutant is similar to wild type during vegetative stage Arabidopsis thaliana
CET1-overexpressed transformants displayed shortened internodes Nicotiana sylvestris
(ATMSI1, MEE70, MSI1, AT5G58230) is required throughout plant development Arabidopsis thaliana
auxin (indole-3-acetic acid: IAA) is implicated in root initiation
carbonylated proteins are observed at high levels during seed maturation and germination Arabidopsis thaliana
(PFD3, AT5G49510) and (PFD5, AT5G23290) subunits are essential for correct development of Arabidopsis Arabidopsis thaliana
(AtTic55, Tic55, TIC55-II, AT2G24820) mutant shows no visible difference from wild-type plants under standard growth conditions
absence of FtsZ2 does not seem to impair viability Arabidopsis thaliana
(BIK1, AT2G39660) regulates normal plant growth in part by controlling salicylic acid (SA) levels Arabidopsis thaliana
trichomes are found in approximately one third of vascular land plants
(ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) mutants hemizygous for .1 display more drastic phenotypic differences morphologically and developmentally compared with (ATPDX1.1, PDX1.1, AT2G38230) mutants hemizygous for (ATPDX1, ATPDX1.3, PDX1, PDX1.3, RSR4, AT5G01410) Arabidopsis thaliana
virus-based microRNA silencing (VbMS) of (MIR165, MIR165B, AT4G00885) /166 caused developmental defects Nicotiana benthamiana
(AN3, ATGIF1, GIF, GIF1, AT5G28640) regulates leaf growth and development
br2 mutant plants express semidwarf stalks Zea mays; Sorghum bicolor; Arabidopsis thaliana
multiple C2 domains in (FTIP1, MCTP1, AT5G06850) may be cooperative to mediate MCTP function in plant development Arabidopsis thaliana
Osclf homozygous mutants have no morphological phenotypes Oryza sativa
protein complexes that modify specific histone amino acids regulate seed development
(BIK1, AT2G39660) mutants exhibited growth defect Arabidopsis thaliana
(AT-BETA-AMY, ATBETA-AMY, BAM5, BMY1, RAM1, AT4G15210) activity changes developmentally Arabidopsis thaliana
type VI trichome is found in all Solanum species Solanum species
chlorosis in transgenic Arabidopsis plants expressing ShMKS2 or both ShMKS1 and ShMKS2 abated as plants developed plant development Arabidopsis thaliana
C2H2-type zinc finger proteins have been implicated in the regulation of flower organogenesis
(ATZFP10, ZFP10, AT2G37740) overexpression results in dwarf plants with abnormal morphology Arabidopsis thaliana; Nicotiana tabacum
ESCRT-III components play important role in plant development Arabidopsis thaliana
extracellular ATP has essential extracellular roles in plant growth
phloem-mobile signaling molecules enable plants to coordinate their growth and development
cell wall modifications are integral part of plant development
biotin attachment domain-containing (BADC) proteins act during normal growth and development Arabidopsis thaliana
galactoglucomannan (GGM) may have signaling role in plant development
Strong reduction of (ATMSI1, MEE70, MSI1, AT5G58230) in transgenic co-suppression lines ( -cs) causes strong defects in vegetative and reproductive development Arabidopsis thaliana
(ARP6, ATARP6, ESD1, SUF3, AT3G33520) mutants display pleiotropic vegetative and reproductive phenotype Arabidopsis thaliana
(BIK1, AT2G39660) ein2-1 double mutant suffered same growth suppression and aberrant development as the (BIK1, AT2G39660) single mutant Arabidopsis thaliana
extracellular ATP has essential extracellular roles in plant development
plants perturbed in silique development also produce more axillary branches Arabidopsis thaliana
OsGRF4 and OsGRF6 expression enhancement may cause more spikelets Oryza sativa
disruption of the plant circadian clock can alter plant growth
disruption of the plant circadian clock can alter plant development
double mutant of (BZIP17, AT2G40950) and (BZIP28, AT3G10800) is presumed to be lethal Arabidopsis thaliana
rice E(z) genes are expressed through plant development Oryza sativa
(ATSWC6, SEF, AT5G37055) is involved in controlling Arabidopsis development Arabidopsis thaliana
(H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) mutants display pleiotropic vegetative and reproductive phenotype Arabidopsis thaliana
Arabidopsis thaliana wild-type (ecotype Columbia-ER) grown on soil Arabidopsis thaliana
Δ ftsZ3 mutants have stunted leafy gametophores Physcomitrella patens
PME activity may have indirect effect through release of oligogalacturonides (OGA) Arabidopsis thaliana
CLE putative signal peptide is required for CLE protein activity in vivo
chloroplast biogenesis is essential for plant growth and development
7-day-old seedlings from tolQ expressing TOL6:ubq:Ven exhibited variety of alterations in developmental phenotypes Arabidopsis thaliana
dwarf phenotype of (ATEXO70A1, EXO70A1, AT5G03540) was not rescued in YFP-Exo70A1(S328A)/exo70A1-1 lines Arabidopsis thaliana
OsFKBP20-1b mutant plants did not show differences in growth or development under normal conditions Oryza sativa
strong BR insensitivity resulted in reduced leaf angle Oryza sativa
TE-1-6b-L does not show obvious phenotype Arabidopsis thaliana
mutation or overexpression in (YUC, YUC1, AT4G32540) genes has interesting effects on plant development
mosses have dimorphic gametophyte
pldα1 mutants produced more rosette leaves Arabidopsis thaliana
loss of Elongator activity seems to have different effects on development depending on plant species
LBD family members are involved in secondary growth
root length exhibits a characteristic S-shape curve during the transition from vegetative to reproductive phase Cicer arietinum
axs1-1/+ axs2-1 mutants exhibit more pronounced morphological phenotype with severely small and chlorotic plants that eventually die Arabidopsis thaliana
NbCPI silencing results in growth inhibition phenotype with small leaves Nicotiana benthamiana
distinct SNP variants in PtREV gene underscores importance of (AVB1, IFL, IFL1, REV, AT5G60690) transcription factor in regulating expression of different developmental processes Populus trichocarpa
seed germination is crucial developmental stage of the plant
(ZFP3, AT5G25160) mutant phenotype is similar to wild-type Arabidopsis thaliana
boron (B) is essential for plant growth and development
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ProSNBE lines have many characteristics similar to (ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) Arabidopsis thaliana
transgenic approaches may be used in a combinatorial manner for growth promotion of belowground and aboveground organs
transgenic (OHP, OHP1, PDE335, AT5G02120) plants rescued with -HA developed normal phenotype Arabidopsis thaliana
paralogs of cytosolic ribosomal proteins (RPs) apparently have specific developmental roles
Arabidopsis SWR1 complex is required for normal growth and development Arabidopsis thaliana
T 1 plants from all eight pUbi–HTA1 lines compared to wild-type and pTF101.1 transgenic plants Oryza sativa
leaf senescence is ultimate stage of leaf development
lack of conductive tissues in bryophytes has limited physical stature of bryophytes
full knockout of (AR2, ATR2, AT4G30210) would have revealed stronger phenotypes Arabidopsis thaliana
variegation suppression in imgi2 is development-dependent developmental stage Arabidopsis thaliana
(AtSEC24A, ERMO2, SEC24A, AT3G07100) has roles in multiple different developmental pathways Arabidopsis thaliana
miR156 overexpression plants caused drastic phenotype Solanum tuberosum
Transformed and nontransformed plants showed no significant differences in seed development Arabidopsis thaliana
TRV-GFP RNA was detected in infected plants undergoing vegetative to reproductive growth
tobacco (Nicotiana benthamiana) RH58 / VDL mutant is defective in plant morphogenesis Nicotiana benthamiana
mature miR156 gradually decreases in abundance as the plant ages Arabidopsis thaliana
Plants constitutively expressing the IPS1-based MIM156 transgene have exaggerated adult growth traits such as serrated leaf margins Arabidopsis thaliana
removal of immature siliques results in outgrowth of more secondary inflorescences Arabidopsis thaliana
root-defective mutants in maize have strong, semidwarf stalks Zea mays
GA2oxA9 was expressed in bread wheat during early stages of stem elongation
plants analyzed 44 days after sowing (DAS) followed photosynthetic parameter assessments Arabidopsis thaliana
second metabolomics analysis set was performed at 70 DAS when all plant lines were still in vegetative growth Arabidopsis thaliana
(AtHDA7, HDA7, AT5G35600) silencing causes delays of growth at different developmental stages Arabidopsis thaliana
histone (H2B, HTB2, AT5G22880) monoubiquitination (H2Bub) affects root growth Arabidopsis thaliana
(AR2, ATR2, AT4G30210) mutants did not display stronger morphological defects Arabidopsis thaliana
(ATMES17, MES17, AT3G10870) (ILL2, AT5G56660) (IAR3, JR3, AT1G51760) mutant does not have any adult phenotypes compared with their parental lines Arabidopsis thaliana
brassinosteroid (BR) influences cell elongation
brassinosteroid (BR) are distinct from gibberellin (GA)
17/28 mutant presented drastic developmental disorders without any external stimulus Arabidopsis thaliana
4-week growth measurement in phenomics facility covers almost entire vegetative life span from young seedlings to mature plants Arabidopsis thaliana
secondary cell walls provide mechanical support for plant growing bodies
β-estradiol-inducible system did not produce mature plants Brachypodium distachyon
(chr13, PIE1, SRCAP, AT3G12810) (ATSWC6, SEF, AT5G37055) (ARP6, ATARP6, ESD1, SUF3, AT3G33520) and (H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) mutants show loss of apical dominance Arabidopsis thaliana
nucleosome assembly proteins mediate normal plant growth
nucleosome assembly proteins mediate normal plant growth and development
SAP family members show slightly fluctuating transcript levels during development from seedling to fully developed plant with mature fruits Arabidopsis thaliana
hydrogen peroxide exerts great influence on plant development
(AtDPE1, DPE1, AT5G64860) (MEX1, RCP1, AT5G17520) double mutant failed to grow to maturity in 12-h photoperiod
NO overproducer1 (ARAPPT, CUE1, NOX1, PPT, AT5G33320) chlorophyll a/b binding protein underexpressed1 mutant linked to plant development Arabidopsis thaliana
microRNA156 (miR156) affects plant architecture Solanum tuberosum
ZINC FINGER PROTEIN3 (ZFP3, AT5G25160) overexpression causes defects in fertility Arabidopsis thaliana
reduced sink strength in young shoot tissues inhibits growth of young shoot tissues
(ATMES17, MES17, AT3G10870) (IBR3, AT3G06810) mutant does not have any adult phenotypes compared with their parental lines Arabidopsis thaliana
s1c2 double mutant shows improved growth compared to sir1-1 mutant Arabidopsis thaliana
sir1-1 cad2-1 double mutant (s1c2) is viable Arabidopsis thaliana
miR156 negatively regulates adult-to-reproductive state transition Arabidopsis thaliana
osfdml1 mutants display no visible differences during vegetative development Oryza sativa
(BZIP17, AT2G40950) and (BZIP28, AT3G10800) play essential roles in growth and development Arabidopsis thaliana
cell wall-degrading enzyme catalyzes cell wall modifications
temperature fluctuations adversely affect vegetative stages Oryza sativa
drought stress affects plant growth and development
knockdown of (ARP4, ATARP4, AT1G18450) transcript levels causes pleiotropic phenotype similar to (chr13, PIE1, SRCAP, AT3G12810) (ATSWC6, SEF, AT5G37055) (ARP6, ATARP6, ESD1, SUF3, AT3G33520) and (H2A.Z, HTA9, AT1G52740) (H2A.Z, HTA11, AT3G54560) mutants Arabidopsis thaliana