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leaf development

62209 relationships annotated with this phrase. Showing first 500 of 62209.
Source entity Relationship Target entity Species
self-shaded leaves are mainly leaves exposed to sun in past and subsequently shaded by newly developed leaves
mutation of TaSPL8 causes loss of the lamina joint connecting the leaf blade to the leaf sheath Triticum aestivum
ectopic expression of the Arabidopsis cytokinin synthesis gene (ATIPT7, IPT7, AT3G23630) in tomato results in more complex leaves Solanum lycopersicum
successive leaves initiate in distichous phyllotaxy
long leaf allele is associated with longer, but less dense, stomata Triticum aestivum
FLL5A locus typically increases length in 2–3 topmost leaves
(H3.3, HTR8, AT5G10980) K27A variant plays important role in leaf morphology Arabidopsis thaliana
(H3.3, HTR8, AT5G10980) K27A lines display leaf morphology defects Arabidopsis thaliana
leaf senescence is final stage of leaf development
variation in leaf mass per area (LMA) was largest across years Vaccinium angustifolium; Vaccinium myrtilloides
Brassica rapa had similar maximum photosynthesis capacity, leaf thickness and leaf dry mass per area Brassica rapa; Arabidopsis thaliana
developmental and physiological processes in leaves could lead to apparent 12C/13C fractionation between leaf biomass and direct photosynthetic products
partial embryonic class seedlings produced true leaves from the apex Arabidopsis thaliana
wheat orthologues of the (PRS, PRS1, WOX3, AT2G28610) gene control leaf size
relationship between A and gs is not coordinated across leaf development
most proximal domains of the maize sheath do not emerge from shoot until the leaf is the fourth primordium from the SAM Zea mays
LS of 2019 and 2020 were not related across genotypes of two species Vaccinium angustifolium; Vaccinium myrtilloides
axillary meristem undergoes expansion and production of a few leaves and/or leaf primordia
sc35-scl quintuple mutant shows serrated leaves Arabidopsis thaliana
WUSCHEL-related homoeobox 3 (PRS, PRS1, WOX3, AT2G28610) genes underlie leaf size mutants in rice (narrow leaf2 (nl2) and nl3) Oryza sativa
TCP proteins regulate leaf size
(AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) (AS2, AT1G65620) complex inhibits expression of (BP, BP1, KNAT1, AT4G08150) (KNOX1)
(ATNS1, NS1, OVA8, AT4G17300) transcripts are detected in growing margins of the newly emerged Leaf 1 Zea mays
epidermal overexpression of (FUS3, AT3G26790) induces formation of cotyledonlike leaves Arabidopsis thaliana
(AtNPF1.2, NPF1.2, NRT1.11, AT1G52190) and (NRT1.12, AT3G16180) expression levels are more abundant in larger expanded leaves Arabidopsis thaliana
narrow and curly leaf (nal7) mutant includes smaller bulliform cells Oryza sativa
scl28-3 mutant produced leaves with 33% increase in estimated number of palisade parenchyma cells Arabidopsis thaliana
rough sheath2 mutant exhibits aberrant proliferation of sheath-like tissue at base of blade Zea mays
afila (af) mutation causes replacement of leaflets by branched tendrils Pisum sativum
rainfall was associated and positively related to leaf structural traits (LMA, LS) Vaccinium angustifolium; Vaccinium myrtilloides
plants grown from (AGD1, VAL1, AT5G61980) (HSI2-L1, HSL1, VAL2, AT4G32010) double mutant seedlings exhibited variegated leaves Arabidopsis thaliana
increased flag leaf length is associated with longer epidermal pavement cell size Triticum aestivum
TCP transcription factor can interact with ASYMMETRIC LEAVES 2 (AS2, AT1G65620) Arabidopsis thaliana
FPF1-Like expression extends internally from leaf margin toward the middle domain Zea mays
leaf tip in (ATNS1, NS1, OVA8, AT4G17300) (ATNS2, NS2, SYNC2, SYNC2_ARATH, AT3G07420) double mutants resembles WT siblings Zea mays
δ13C value of leaves integrates 13C abundance from leaf's own photosynthesis during autotrophic stage
bulk leaf matter δ13C decreases during leaf ontogeny
overexpression of (bHLH, AT5G51780) genes can result in large leaf angle Oryza sativa
SlAS2-like interacts with SlTCP29 Solanum lycopersicum
(AS2, AT1G65620) (AtLHP1, LHP1, TFL2, AT5G17690) and (ASL19, JLO, LBD30, AT4G00220) complex represses KNOX genes
day 23 of leaf development plants commenced to bolt and leaves reached state of full expansion Arabidopsis thaliana
leaf primordia develop at periphery of the shoot apical meristem Triticum aestivum
SlTCP24 may play important role in leaf development Solanum lycopersicum
SlAS2 interacts with SlTCP29 Solanum lycopersicum
seasonal shifts in WUE may be driven by ontogenetic processes
(ATNS1, NS1, OVA8, AT4G17300) expression density at Stage 1 is high in leaf Zea mays
(NZZ, SPL, AT4G27330) overexpression in the -D line in Col-0 resulted in curly-leaf phenotype Arabidopsis thaliana
trait-trait relationships suggest common principles in leaf trait development
G8 genotype showed highest leaf mass per area (LMA) Vaccinium angustifolium; Vaccinium myrtilloides
(AGL9, SEP3, AT1G24260) mutations suppress leaf curling Arabidopsis thaliana
MtBP gene expression in shoot buds in 21- and 70-d-old mtphan mutants is up-regulated compared to wild-type plants Medicago truncatula
more than 30% of tomato plants infected with TRV-STTM319 showed range of leaf simplification with reduced or no leaflets Solanum lycopersicum
shoot growth reduction in high salt in Thellungiella occurs at the level of leaf expansion Thellungiella salsuginea
disruption of expression of CIN-like TCPs can cause abnormal leaf morphology Arabidopsis thaliana; Solanum lycopersicum
(AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) (AS2, AT1G65620) complex directly inhibits expression of KNOTTED1-like homeobox I (KNOX I) gene Arabidopsis thaliana
strong positive relationship between seasonal phenology and LMA is also observed in similar deciduous forests located in northeastern United States
Wavy auricle in blade1 mutant exhibits aberrant proximal-distal patterning of maize leaves Zea mays
FPF1-Like expression requires (ATNS1, NS1, OVA8, AT4G17300) /2 function Zea mays
magnitude of delta BL (ΔBL) increased with leaf developmental stage/age
CT1:13 family showed small leaf phenotype Solanum chacoense
taller trees could have greater leaf area index Populus tremuloides
SlAS2 interacts with SlTCP24 Solanum lycopersicum
grass leaf comprises distal blade fused to a proximal sheath
SlTCP29 may play important role in leaf development Solanum lycopersicum
SlTCP24 and SlTCP29 can act in same pathway Solanum lycopersicum
Arabidopsis (MIR319, MIR319B, AT5G41663) controls leaf morphogenesis Arabidopsis thaliana
maize embryo typically initiates four additional leaf primordia before seed quiescence Zea mays subsp. mays
LMA and VD increased with irradiance
Nps1 mutant leaflets showed reduced serration of the leaf margin Solanum lycopersicum
several KNOX genes varied significantly in SlTCP24/29-KO lines Solanum lycopersicum
transgenic RHW1 OE lines exhibited enlarged sheath width Zea mays
CT41 family showed small and inward-curling leaf phenotype Solanum chacoense
ProSCL28:SCL28-VENUS construct fully complements increased cell number phenotype in scl28-3 Arabidopsis thaliana
(BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) is involved in leaf cell differentiation Arabidopsis thaliana
(H3.3, HTR8, AT5G10980) K27A lines correlates positively with leaf morphology defects Arabidopsis thaliana
developmental aberrations in (H3.3, HTR8, AT5G10980) K27A include leaf morphology defects Arabidopsis thaliana
overexpression of CLAUSA causes simpler leaves with fewer leaflets Solanum lycopersicum
vein architecture can often be influenced by environmental signals during leaf development
(EEP1, MIR164, MIR164C, AT5G27807) ASYMMETRIC LEAVES1, and (IAA3, SHY2, AT1G04240) /SHORT HYPOCOTYL2 cooperatively repress accumulation of CUC gene transcripts Arabidopsis thaliana
study of Hakea prostrata analyzed changes in lipid profiles and levels of transcripts encoding lipid remodeling enzymes during leaf development Hakea prostrata
StSPLs might control leaf size and shape Solanum tuberosum
rachises and petioles of leaves on apical nodes 1 to 4 in mtphan are much longer and shorter, respectively, compared to wild-type plants Medicago truncatula
proximal leaf margin of mtphan mtpin10 double mutant remains curled like that in mtphan single mutant Medicago truncatula
MtPHAN promotes stipule development Medicago truncatula
35S::mHWS transgene did not induce hyl1-like and ago1-like leaf phenotypes Arabidopsis thaliana
polarized cell divisions result in clonal cell lineages Zea mays
FLL5A+ allele conferred more erect leaf angle Triticum aestivum
OsbHLH92 knockout lines showed erect leaves Oryza sativa
CLAUSA narrows morphogenetic window at the leaf margin Solanum lycopersicum
SlTCP29 interacts with itself Solanum lycopersicum
all leaves are asymmetrical from their inception
variation in leaf size (LS) was largest across years Vaccinium angustifolium; Vaccinium myrtilloides
Begonia luxurians develops ectopic leaves from trichomes Begonia luxurians
OsBU1 overexpression results in larger leaf angle Oryza sativa
marginal leaf-domain deletion in (ATNS1, NS1, OVA8, AT4G17300) (ATNS2, NS2, SYNC2, SYNC2_ARATH, AT3G07420) double mutants affects proximal region of the leaf blade Zea mays
Hirschfeldia incana has thick leaf thick leaf Hirschfeldia incana
basipetal transport in the attached bundles declines prior to the expansion of the first leaf expansion of the first leaf Cucumis sativus
(RCA, AT2G39730) gene expression is developmentally regulated by leaf age
FLL5A mediates longer leaf length
(AS2, AT1G65620) forms protein complex with TCP proteins Arabidopsis thaliana
(AS2, AT1G65620) interacts with JAGGED LATERAL ORGAN (ASL19, JLO, LBD30, AT4G00220)
relationship between stomatal density and Rdark.25 suggests that these changes are both associated with leaf ontogeny
Gnarley1 mutant exhibits aberrant proximal-distal patterning of maize leaves Zea mays
Gnarley1 mutation is dominant mutation in KNOX4 homeobox gene Zea mays
transgenic RHW1 OE lines did not alter blade width in foliar leaves Zea mays
LS of 2018 and 2020 were not related across genotypes of two species Vaccinium angustifolium; Vaccinium myrtilloides
cell division rate in wild-type leaves decreased until cell division ceased in 12-d-old plants Arabidopsis thaliana
TCP proteins regulate leaf morphology
study studied leaf thickness (LMA)
study studied other structural and functional traits that influence leaf economic spectrum traits
G13 and G16 genotypes showed highest leaf mass per area (LMA) Vaccinium angustifolium; Vaccinium myrtilloides
FLL5A NIL pair found no difference in leaf emergence rate under glasshouse conditions
SlTCP24 is expressed at higher level in leaves Solanum lycopersicum
FLOWERING PROMOTING FACTOR1-Like (FPF1-Like) is co-expressed with NS1 at primordial leaf margins Zea mays
five Arabidopsis long-PIN paralogs are required for phyllotaxis Arabidopsis thaliana
SlTCP29 is expressed at higher level in leaves Solanum lycopersicum
Rough sheath1 mutant exhibits aberrant proximal-distal patterning of maize leaves Zea mays
teosinte-branched mutant has lengthy husk leaf blades Zea mays
RHW1 acts as MYB-like transcriptional repressor to mediate husk leaf width Zea mays
artificial mutant of TaSPL8 results in erect leaves Triticum aestivum
leaf longevity influences leaf function
SlTCP29 interacts with SlTCP24 Solanum lycopersicum
SlTCP24 and SlTCP29 form heterodimer SlTCP24-SlTCP29 heterodimer Solanum lycopersicum
Arabidopsis thaliana had thinner leaf with similar Sm,v Arabidopsis thaliana
Brassica nigra achieved similar high photosynthesis rate with significantly thinner leaf Brassica nigra
canopy phenology describes timing of leafing
simple leaves is leaf morphology type
LA is expressed earlier and more widely than CLAUSA Solanum lycopersicum
leaf asymmetries are established following leaf initiation
developmental stages of leaf primordia govern final leaf size Triticum aestivum
leaf traits vary among leaf phenological stage
OsBUL1, OsBC1, and LO9-711 heterotrimer influences leaf angle Oryza sativa
TCP transcription factor LANCEOLATE (LA) is involved in leaf-shape formation Solanum lycopersicum
SlTCP29 is expressed at all stages of leaf development Solanum lycopersicum
SlAS2 interacts with SlTCP29 Solanum lycopersicum
SlAS2 interacts with SlTCP24 Solanum lycopersicum
SlTCP24 and SlTCP29 interact with each other Solanum lycopersicum
SlTCP24 belongs to CIN-like TCP transcription factors Solanum lycopersicum
LA belongs to CIN-like TCP transcription factors Solanum lycopersicum
leaf optical properties are defined by tissue morphology
leaves attain their shape early during development
leaf developmental genes are identified in coleoptile Zea mays subsp. mays
precipitation in early growing season combined with temperature plays a crucial role in controlling leaf expansion
youngest rosette leaf and cauline leaves of (AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) mutants curl tightly in an upward direction leaf morphology Arabidopsis thaliana
leaf curling in (AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) and (AGL20, ATSOC1, SOC1, AT2G45660) mutants shows temporal and spatial pattern Arabidopsis thaliana
miR156 OE lines (miR156 OE 5.1 and 6.2) exhibit drastic change in leaf phenotype potato
rachises and petioles on the fourth and fifth nodes from the top in 4-week-old mtphan mutant are longer and shorter, respectively, compared to wild-type plants Medicago truncatula
MtPHAN and (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) are functional orthologs Medicago truncatula; Arabidopsis thaliana
SlPHAN down-regulation results in change of pinnate compound leaves to peltately palmate compound leaves Solanum lycopersicum
transgenic plants have slightly thicker leaf blades Solanum tuberosum
(HIRA, AT3G44530) co-suppression in transgenic plants resulted in phenotype similar to (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) mutant phenotype
CIN clade genes control transition of leaf development from cell division to cell expansion phase
CLAUSA has unique role in compound leaf species to promote exit from the morphogenetic stage Solanum lycopersicum
LA determines developmental context of CLAUSA activity Solanum lycopersicum
milkweed (POD1, AT1G67960) mutation encodes KANADI protein Zea mays
(ATNS1, NS1, OVA8, AT4G17300) and WOX3a paralogs are both detected in first leaf primordium at Stage 1 Zea mays
leaf architecture of miR156 OE lines is dramatically affected by miR156 overexpression potato
newly emerging leaves from axillary shoots on heterograft stocks have more prominent but fewer trichomes and exhibit small and thick lamina along with reduced numbers of leaflets potato
SHOOT MERISTEMLESS (STM) acts to exclude ASYMMETRIC LEAVES1 (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) expression in the SAM Arabidopsis thaliana
(ADO3, FKF1, AT1G68050) decoy increases rosette leaf number Arabidopsis thaliana
(PSB29, THF1, AT2G20890) leaf variegation is attributed to a low level of (FTSH2, VAR2, AT2G30950) Arabidopsis thaliana
wild-type leaf cells possess approximately rectangular shape
leaf primordia develop into flat leaves after tissue differentiation along several planes Triticum aestivum
Vcmax.25 peak occurs at period of full leaf expansion
(MIR319, MIR319B, AT5G41663) targeting of ApTCP2 controls leaf morphogenesis Arabidopsis thaliana
denser leaves (in contrast to thicker leaves) would result in higher leaf mass per unit area (LMA)
(VUP1, AT3G21710) promoter drives expression in leaf meristematic regions Arabidopsis thaliana
young leaves of RNAi mutants were still expanding at the time of induction
(ATXTH27, EXGT-A3, XTH27, AT2G01850) is essential for tertiary vein development Arabidopsis thaliana
Lotus japonicus contains LjPHAN1 and LjPHAN2 Lotus japonicus
FUSED COMPOUND LEAF1 (FCL1) is similarly expressed in mtbp and wild-type plants Medicago truncatula
AN3-GS yellow overexpression line results in increased leaf size Arabidopsis thaliana
TCP transcription factors are known to regulate leaf curvature Arabidopsis thaliana
moderate increase in phosphate supply does not affect leaf size Hakea prostrata
petiole length on apical nodes 5 to 7 in mtphan is still largely reduced compared to wild-type Medicago truncatula
reduced cell size and altered cell morphology of petioles of mature mtphan plants are restored in the double mutant to that of wild-type and (ELP1, AT5G48090) mutant Medicago truncatula
down-regulation of SlPHAN results in peltately palmate compound leaves Solanum lycopersicum
wild-type plants hemizygous for RPL27aC : rpl27ac-1d have pointed, serrated leaves Arabidopsis thaliana
(ABI3, AtABI3, SIS10, AT3G24650) plants exhibit leaf primordia
(AGL7, AP1, AtAP1, AT1G69120) cal (AGL8, FUL, AT5G60910) triple mutants generate cauline leaf-like structures Arabidopsis thaliana
Δ (ATFTSZ2-1, FTSZ2-1, AT2G36250) /2–2 double mutants display altered leaf morphology
first true leaves which were less than 1 cm long and strongly expanding at the time of the measurements Nicotiana tabacum
first pair of true leaves of p35S::ShMKS2 plants initiated but were not capable of expanding fully to maturity leaf expansion Arabidopsis thaliana
ASYMMETRIC LEAVES1 (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) and lateral organ boundary (LOB) domain transcription factor, (AS2, AT1G65620) exclude expression of KNOXI genes in incipient leaf primordia Arabidopsis thaliana
morphological modifications of petiole epidermal cells in mtphan resemble those of pulvini Medicago truncatula
strong LeT6 overexpression leads to SlPHAN down-regulation phenotypes Solanum lycopersicum
pea cri mutant exhibits ectopic stipules on adaxial leaf surface Pisum sativum
wild-type and transgenic lines show no significant differences in leaf width, leaf length, total number of longitudinal veins, bundle sheath cell size, cell number, and distance between veins Oryza sativa
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) rosette leaves are significantly thinner in midrib and lamina regions Arabidopsis thaliana
(AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) mutants show position-dependent changes in leaf morphology Arabidopsis thaliana
miR156 overexpression in potato subspecies andigena 7540 exhibits suppression of leaf complexity Solanum tuberosum
MtPHAN is (ARP, AT2G41460) gene Medicago truncatula
KNOXI plays a similar role to SGL1 in lateral leaflet initiation Solanum lycopersicum; Capsella hirsuta
virus-based microRNA silencing (VbMS) successfully silenced (MIR319, MIR319B, AT5G41663) Solanum lycopersicum
rpl27ac-2 / + rpl27ab-2 / + transheterozygote has pointed and serrated leaves Arabidopsis thaliana
reduced number of cell layers must have been compensated for by subtle differences in cell size, cell number, and orientation Oryza sativa
effect on mesophyll cell layers could be a direct consequence of ectopic (EAL1, SGR7, SHR, AT4G37650) activity Oryza sativa
(VUP1, AT3G21710) OX seedlings exhibit smaller, round-shaped, and darker green cotyledons and leaves Arabidopsis thaliana
imgi2 leaves are filled with many tightly packed cells Arabidopsis thaliana
young Hakea prostrata leaves are able to develop on plants with very low phosphorus (P) status Hakea prostrata
rao6 mutant has mutation in (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) (ASYMMETRIC LEAVES 1) at position 96 Arabidopsis thaliana
rolled leaves are seen in other mutants with altered auxin levels Arabidopsis thaliana
Rice Os- (ASL39, LBD37, AT5G67420) FOX Arabidopsis line K16331 and K19624 plants with hyponastic cotyledons and SH13 plants with hyponastic cotyledons show lowest rice Os- (ASL39, LBD37, AT5G67420) expression Arabidopsis thaliana
ASYMMETRIC LEAVES2 (AS2, AT1G65620) LBD6 overexpression produces hyponastic leaf morphology Arabidopsis thaliana
Os- (ASL39, LBD37, AT5G67420) expression and/or nitrogen content of the cell may regulate leaf curling phenotype Arabidopsis thaliana
VIGS-NbCesA8-infected plants have small and curled fourth pair of leaves Nicotiana benthamiana
MIR171c-overexpressing plants manifest altered leaf shape and patterning
polarity character conversion results in macrohair patches on abaxial leaf side Zea mays
(ATDET2, DET2, DWF6, AT2G38050) mutant has lower cell number per leaf blade than wild-type Arabidopsis thaliana
cell division, expansion, and differentiation determine final leaf size
CIN-like TCP genes control cell division arrest at leaf margins in early stages of leaf development Arabidopsis thaliana
OsMED14_1 RNAi transgenic plants have narrower leaves compared with wild-type plants Oryza sativa
OsMED14_1 physically interacted with rice YABBY5 showed involvement of OsMED14_1 in lateral organ development such as leaf lamina expansion Oryza sativa
AS2-YFP construct rescues as2-1 mutation Arabidopsis thaliana
SlLAM1 mRNA encompasses single cell layer in middle domain of inner leaf tissues Solanum lycopersicum
(WOX1, AT3G18010) (PRS, PRS1, WOX3, AT2G28610) activity plays a minimal role in proximal-distal growth Arabidopsis thaliana
(AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) plants do not show leaf curling Arabidopsis thaliana
(AVB1, IFL, IFL1, REV, AT5G60690) mutants exhibit fewer stem leaves Arabidopsis thaliana
epidermal cells of the adaxial surface of fully expanded leaves in 70-d-old mtphan mutant are smooth and appear to be less differentiated compared to jigsaw puzzle-like leaf pavement cells of corresponding wild-type plants Medicago truncatula
mtphan mutant phenotypes were rescued in stable transgenic plants by MtPHAN genomic sequence including its promoter and the coding sequence fused to the GFP Medicago truncatula
mtphan mutant exhibits less differentiated leaf epidermal cells on adaxial surface Medicago truncatula
iamt1-D dominant mutant causes curled leaves Arabidopsis thaliana
reduced ABA levels in (ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) mutants explains altered leaf structure and organization Arabidopsis thaliana
reil2-1 mutant phenotype is characterized by delayed appearance of the first rosette leaves at 10°C and spoon-shaped leaves Arabidopsis thaliana
(AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) (AGL20, ATSOC1, SOC1, AT2G45660) mutant shows only mild leaf curling Arabidopsis thaliana
imgi2 leaves are morphologically similar to gi2 leaves Arabidopsis thaliana
(ATPDX1.1, PDX1.1, AT2G38230) mutant does not show curled leaves Arabidopsis thaliana
lines 207_30 and 207_31 have significant difference in number of cell layers between abaxial and adaxial epidermal layers Oryza sativa
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) ferulic acid, and ROS coordinate cell proliferation exit for leaf development Arabidopsis thaliana
miROE8 exhibited largest leaf angle Oryza sativa
endopolyploidy in M. crystallinum is seemingly in line with cotyledon/leaf expansion Mesembryanthemum crystallinum
short-day (SD) conditions suppress leaf curl Arabidopsis thaliana
kn1 misexpressed along veins of blade causes knots Zea mays
recruitment of leaf founder cells to incipient leaf primordia involves down-regulation of KNOXI gene expression
Tnt1 retrotransposon insertion mutants of M. truncatula PHAN and BP genes were isolated and characterized M. truncatula PHAN and BP genes Medicago truncatula
curling of the proximal leaf margin in mtphan mutant does not occur when laminae are only a few millimeters in length early leaf development Medicago truncatula
MtPHAN has a novel role in maintenance of petiole identity through preventing ectopic acquisition of motor organ characteristics in petioles Medicago truncatula
petiole length in mtphan sgl1 double mutant is further reduced compared to single mutants Medicago truncatula
shoot growth reduction in high salt in Thellungiella occurs at the level of leaf initiation Thellungiella salsuginea
expanded leaves usually do not contain proliferating cells
wild-type leaves have cells that are regularly arranged in parallel to midrib
mRNA accumulation of the psbB-psbT-psbH-petB-petD operon does not change during leaf ontogenesis in tobacco Nicotiana tabacum
youngest rosette leaf and cauline leaves are specifically affected because they are only organs in a relatively immature state when SEPALLATA 3 (AGL9, SEP3, AT1G24260) levels reach the critical threshold Arabidopsis thaliana
gain-of-function (AVB1, IFL, IFL1, REV, AT5G60690) mutants show severe anatomical phenotypes related to leaf architecture Populus trichocarpa
miR156 overexpression in potato results in higher number of leaves with reduced leaflets potato
PHANTASTICA (PHAN) is ortholog of ASYMMETRIC LEAVES1 (AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) Antirrhinum species
rachises and petioles on apical nodes 1 to 3 in 4-week-old plants are not different between wild-type and mtphan mutant Medicago truncatula
MtBP transcripts are excluded from incipient and subsequent leaf primordia Medicago truncatula
pea COCHLEATA (COCH) plays a role in stipule and nodule development Pisum sativum
rolled leaves phenotype may be directly caused by altered IAA levels or buildup of IAA conjugates or IBA in the leaf Arabidopsis thaliana
OsMIR396d overexpression results in increased leaf angle Oryza sativa
GUN1-GFP protein cannot be detected in expanding or mature leaves Arabidopsis thaliana
Beyma leaf size is 10–20% smaller than MG-20 leaf size
(MEX1, RCP1, AT5G17520) leaves are thinner than wild-type leaves
genes related to adaxial leaf curling have been identified adaxial leaf curling Oryza sativa; Zea mays
abaxialization/adaxialization of the leaf often manifests as leaf curling
ACL1 and ACL2 expressions increased as development progressed leaf development
as2-∆LZL-NLS-YFP construct produces Type IV phenotype Arabidopsis thaliana
leaflet initiation potential is influenced by blade expansion
mutants lacking (ATCIPK23, CIPK23, LKS1, PKS17, SnRK3.23, AT1G30270) are not altered in leaf flattening Arabidopsis thaliana
WT and cur1 produce similar number of leaves Oryza sativa
leaf senescence is last stage of leaf development
complex interaction network of biological pathways contributes to leaf development Zea mays
morphological injuries is usually expressed as leaf senescence
(AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) and auxin promote leaf fate Arabidopsis thaliana
MtPHAN is involved in suppression of petiolule development in wild-type plants Medicago truncatula
overexpression of knox genes may lead to different developmental consequences
msi1-cs plants exhibit abnormal late leaf development Arabidopsis thaliana
intermediate phenotype plants develop curved rosette leaves rosette leaf morphology Arabidopsis thaliana
floral programs initiated in organs retaining vegetative identity results in leaf curling Arabidopsis thaliana
inorganic phosphate (Pi) supply resulted in slight increase in production of new leaves Hakea prostrata
miR156 OE lines exhibit altered venation pattern in leaves Solanum tuberosum; Nicotiana tabacum
LG1 is involved in controlling ligule and auricle development Zea mays
LG1 has function in leaf development in rice Oryza sativa
petioles of mtphan plants contain enlarged central vascular bundle Medicago truncatula
MtBP transcripts in mtphan mutant are detected in shoot apical meristem (SAM) and similarly excluded from leaf primordia as in wild-type plants Medicago truncatula
SGL1 acts as indeterminate factor in the control of lateral leaflet initiation Medicago truncatula
TRV-STTM165/166 plants did not observe obvious changes in leaf abaxial-adaxial polarity Nicotiana benthamiana
GUN1-GFP protein is already largely undetectable in tip region of newly emerging leaves Arabidopsis thaliana
curled cauline leaves maintain leaf identity Arabidopsis thaliana
rachis length on apical nodes 5 to 7 is not much different between wild-type and mtphan mutant Medicago truncatula
mtphan mtpin10 double mutants exhibit compound leaves with smooth leaf margins, resembling those of the mtpin10 single mutant Medicago truncatula
double (EMB2279, EMB88, SOT5, AT1G30610) (AS2, AT1G65620) mutants displayed many narrow or needle-like leaves Arabidopsis thaliana
(GUN1, AT2G31400) mRNA is substantially lower in seedlings and mature leaves Arabidopsis thaliana
epidermal cells of stipule lamina and digitation in mtphan are less curving compared to wild-type plants Medicago truncatula
MtBP is not responsible for development of ectopic tissues in mtphan mutant Medicago truncatula
rolled leaves phenotype is a result of changes in auxin levels in the plant Arabidopsis thaliana
leaf growth in Arabidopsis has been linked to increased endopolyploidy Arabidopsis thaliana
(AS2, AT1G65620) mutant results in undifferentiated meristem characters in leaves
(VUP1, AT3G21710) OX plants exhibit drastically reduced rosette size Arabidopsis thaliana
agl24-3 (AGL22, FAQ1, SVP, AT2G22540) plants show inconsistent leaf curling Arabidopsis thaliana
soc1-2 mutations were tested for effect on leaf curling phenotype Arabidopsis thaliana
MYB domain protein (ARP) specifies leaf adaxial identity
mtphan mutant plants develop asymmetric lateral leaflets on petioles in 82% of plants (107 out of 131) Medicago truncatula
Vitis spp. leaves vary in surface contour Vitis spp.
some Vitis spp. cultivars exhibit profound heteroblasty Vitis spp.
VbMS of (MIR319, MIR319B, AT5G41663) reduced complexity of tomato compound leaves Solanum lycopersicum
low auxin phenotypes include smaller leaves Arabidopsis thaliana
cell proliferation is inhibited in (EMB2279, EMB88, SOT5, AT1G30610) leaves Arabidopsis thaliana
Δ (FTSZ2-2, AT3G52750) mutant leaf cells possess approximately rectangular shape
(AGL15, AT5G13790) (AGL18, AT3G57390) (AGL22, FAQ1, SVP, AT2G22540) plants show inconsistent leaf curling Arabidopsis thaliana
miR156 OE plants exhibit suppression of leaf complexity Solanum tuberosum
SPLs have role in leaf development in Arabidopsis Arabidopsis thaliana
recruitment of leaf founder cells to incipient leaf primordia involves expression of the MYB domain transcription factor gene, (ARP, AT2G41460)
ectopic petiolule phenotype in mtphan compound leaf is variable among plants but is much pronounced in 70-d-old plants Medicago truncatula
MtPHAN maintains proper leaf margin development Medicago truncatula
TRV-MIM319 plants showed similar phenotype to La mutant lines Solanum lycopersicum
histological examination of leaf sections demonstrated normal patterning of subepidermal layers Oryza sativa
leaf epidermal morphogenesis may influence leaf morphology
miROE lines exhibited increased top three leaves angles Oryza sativa
(EMB2279, EMB88, SOT5, AT1G30610) has a role in promoting leaf adaxial identity formation Arabidopsis thaliana
(FTSH2, VAR2, AT2G30950) (EMB2279, EMB88, SOT5, AT1G30610) double mutants displayed a similar phenotype to (EMB2279, EMB88, SOT5, AT1G30610) mutants Arabidopsis thaliana
altered expression levels of TCP genes in msi1-cs may partially account for bulged leaf phenotype Arabidopsis thaliana
threshold model incorporates photosynthetic cell differentiation Zea mays
chloroplast degradation phenotype of (AtDPE1, DPE1, AT5G64860) (MEX1, RCP1, AT5G17520) double mutant appeared to be triggered earlier in leaf development than in (MEX1, RCP1, AT5G17520) single mutant
(AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) (AGL20, ATSOC1, SOC1, AT2G45660) mutant does not show leaf curling Arabidopsis thaliana
youngest rosette leaf and cauline leaves curl in (AGL15, AT5G13790) (AGL18, AT3G57390) (AGL24, AT4G24540) (AGL22, FAQ1, SVP, AT2G22540) and (AGL20, ATSOC1, SOC1, AT2G45660) mutants Arabidopsis thaliana
(AS1, ATMYB91, ATPHAN, LL2, MYB91, AT2G37630) negatively regulates (BP, BP1, KNAT1, AT4G08150) Arabidopsis thaliana
MtPHAN and SGL1 act independently in compound leaf patterning and polarity development Medicago truncatula
adaxial cell identity was reduced in (EMB2279, EMB88, SOT5, AT1G30610) mutant Arabidopsis thaliana
ectopic expression of MADS-domain proteins involved in floral development is associated with leaf curling Arabidopsis thaliana
LG3 is expressed in proximal part of developing leaves Zea mays
mtphan mutant exhibits petioles acquiring motor organ characteristics Medicago truncatula
leaf primordia development is not different between mtphan mutant and wild-type plants Medicago truncatula
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) plants exhibited delay in development of rosette leaves Arabidopsis thaliana
(AGL20, ATSOC1, SOC1, AT2G45660) mutations enhance leaf curling Arabidopsis thaliana
MtPIN10 is not involved in MtPHAN-dependent proximal leaf margin development Medicago truncatula
extra tissues in mature mtbp mtphan double mutant plants develop similarly to mtphan single mutant on the adaxial leaf surface Medicago truncatula
SlPHAN down-regulation leads to LeT6 overexpression phenotypes Solanum lycopersicum
mtphan mutant may represent partially reduced function mutant Medicago truncatula
growth in leaves occurs primarily through mitotic cell division Arabidopsis thaliana
Rice Os- (ASL39, LBD37, AT5G67420) FOX Arabidopsis retransformant line SH13 produces 10.3 rosette leaves on MS medium Arabidopsis thaliana
mock-treated P (NPC3, AT3G03520) :GUS and P (AtNPC4, NPC4, AT3G03530) :GUS show scattered GUS expression in leaf margins Arabidopsis thaliana
BY240 mutant shows no difference in leaf length and width of top three leaves Oryza sativa
transgenic expression of cellulase increased size of leaves Arabidopsis thaliana
leaf serration is independent of (APRR5, PRR5, AT5G24470) Arabidopsis thaliana
TE-2-6b plants at even later stages show extreme folding of leaves Arabidopsis thaliana
TE-2-6b Arabidopsis plants show striking resemblance to jaw-D mutants Arabidopsis thaliana
decreased TCP levels lead to abnormal continuation of cell division at the leaf edge Arabidopsis thaliana
as2-1 mutant plants have leaf margin that curls downward Arabidopsis thaliana
second leaf is small Oryza sativa
P1 primordium corresponds to 15th leaf at late stage Oryza sativa
OsELP3 knockout phenotype is similar to cur1 mutant phenotype Oryza sativa
osnam-1 mutant shows abnormal boundary formation between consecutive leaves Oryza sativa
MtSTM and MtKNOX6 transcripts are up-regulated in shoot buds in mtphan mutant but remain extremely low in leaves of both mtphan mutant and wild-type plants different developmental stages Medicago truncatula
Vitis spp. leaves vary in dentation Vitis spp.
rpl27ac-2 homozygous mutant has rosette leaves that are pointed and serrated Arabidopsis thaliana
rpl27ac-1d / + plants hemizygous for RPL27aC : rpl27ac-1d have most severe leaf shape change Arabidopsis thaliana
leaf epidermis tissue effects of ROS1/DEL induction on morphology could not be observed in leaf epidermis tissue Solanum lycopersicum
(ATNS1, NS1, OVA8, AT4G17300) transcripts are detected in two foci in the SAM periphery corresponding to the leaf and right margins of the incipient Leaf 2 primordium Zea mays
Abaxially Curled Leaf 1 (ACL1) overexpression results in abaxial leaf curling Oryza sativa
ACL1 overexpression could induce abaxial leaf curling Oryza sativa
differential expression of different members of class I KNOX genes could be due to phenotypic difference between (FAS1, FUGU2, NFB2, AT1G65470) and (AtCYP71, CYP71, AT3G44600) leaves
Nicotiana benthamiana plants expressing SAP11 AYWB have wrinkled leaves Nicotiana benthamiana
(ATNUC-L1, NUC-L1, NUC1, PARL1, AT1G48920) is suggested to have a role in development of flat, symmetric leaves Arabidopsis thaliana
individual plastids harboured 8–35 plastome copies in 2–6 nucleoids per organelle in meristematic material
sllam1-1 has defective blade expansion and significantly reduced leaf width Solanum lycopersicum
miR396-GRF/ (AN3, ATGIF1, GIF, GIF1, AT5G28640) module plays antagonistic roles in determining proximal-distal maturation gradient
tomato provides an excellent system to address whether the leaflet initiation potential is influenced by blade expansion Solanum lycopersicum
sllam1 mutants in extreme cases become strip-like overall leaf Solanum lycopersicum
leaflet initiation does not depend on blade expansion
first to third leaves are formed during embryogenesis Oryza sativa
CUR1 is expressed in leaf primordia Oryza sativa
DcLCYB1-expressing transgenic tobacco lines show increased leaf area Nicotiana tabacum
(OSH1, AT5G01580) showed a similar fused and twisted leaf structure to osnam-1 Oryza sativa
vesicular traffic controllers play a role in leaf growth Zea mays
(AGL20, ATSOC1, SOC1, AT2G45660) mutant results in production of more rosette leaves Arabidopsis thaliana
regulatory network with a small number of central hubs underpins extensive phospholipid replacement Hakea prostrata
kn1 misexpressed at margin of leaf blade causes ectopic sheath/auricle prongs grow out Zea mays
leaf founder cells are developed at periphery of the shoot apical meristem (SAM)
(ELP1, AT5G48090) expression in petioles of 35S:: overexpression line is ectopic as reported previously (ELP1, AT5G48090) overexpression line Medicago truncatula
AS1-AS2 nuclear complex represses transcription of KNOX genes Arabidopsis thaliana
PHAN plays a role in leaf adaxial-abaxial polarity Capsella hirsuta; Solanum lycopersicum; Pisum sativum
chromatin modification, cell proliferation, ribosomal proteins, and trans-acting small interfering RNA biogenesis are involved in regulating leaf development Arabidopsis thaliana
Antirrhinum phan mutant exhibits first leaves that are usually broader and heart shaped Antirrhinum majus
TRV-STTM165/166 plants showed ectopic leaf outgrowths on leaf middle vein Nicotiana benthamiana
rpl27ac-3 homozygous mutant has rosette leaves that are pointed and serrated Arabidopsis thaliana
anatomical identity of palisade and spongy cells disappeared in (EMB2279, EMB88, SOT5, AT1G30610) leaves Arabidopsis thaliana
leaf curling is sensitive to dosage of (AGL9, SEP3, AT1G24260) Arabidopsis thaliana
FT mutations suppress leaf curl Arabidopsis thaliana
mtphan mutant exhibits shortened petioles Medicago truncatula
MtBP transcripts are strongly detected in shoot apical meristem (SAM) Medicago truncatula
hws-1 mutant shows partial fusion of cauline leaves to the inflorescence stem Arabidopsis thaliana
wild-type and transgenic lines show no significant difference in mesophyll cell size, mesophyll cell number between veins, or leaf thickness Oryza sativa
ectopic expression of APETALA 3 (AP3, ATAP3, AT3G54340) is mainly responsible for curled leaf phenotype of (CLF, ICU1, SDG1, SET1, AT2G23380) and (AtLHP1, LHP1, TFL2, AT5G17690) mutants Arabidopsis thaliana
Abaxially Curled Leaf 2 (ACL2) overexpression induces abaxial leaf curling Oryza sativa
ACL1 and ACL2 function was proved to be similar and related to leaf development Oryza sativa
early P5 stage is characterized by leaf blade begins to emerge from previous leaf sheath
BR-perceptional mutants exhibit increased stomata number Arabidopsis thaliana
crinkly leaves and siliques phenotype in SAP11 AYWB Arabidopsis is similar to phenotype in jaw-D mutants Arabidopsis thaliana
as2-∆ICG 25–80 -YFP construct does not rescue as2-1 mutation Arabidopsis thaliana
(MIR156H, AT5G55835) is expressed in leaf primordia Arabidopsis thaliana
lateral leaflet primordium generation occurs during P3 stage Solanum lycopersicum
BY240 mutant exhibits Leaf-rolling Index (LRI) of 100 in top three leaves at later reproductive stages Oryza sativa
overexpression of ACL2 could induce abaxial leaf curling
loss/gain of function mutants of HD-ZIPIII genes result in leaf curling
(BP, BP1, KNAT1, AT4G08150) is not expressed in 14-day-old (FAS1, FUGU2, NFB2, AT1G65470) leaves
Arabidopsis plants expressing rGRF2 developed larger leaves harbouring more cells Arabidopsis thaliana
NARROW AND ROLLED LEAF 2 (NRL2; (AtPIF4, PIF4, SRL2, AT2G43010) ) remains unaffected in OsMED14_1 RNAi plants Oryza sativa
SlLAM1 expression pattern in leaf margins was not affected by e or e slmp mutation Solanum lycopersicum
leaflet initiation and blade expansion are regulated by independent mechanisms Solanum lycopersicum
leaf of garden pea contains two pairs of leaflets, one pair of large stipules, two pairs of tendrils, and one terminal tendril Pisum sativum
first leaf has indistinguishable leaf blade and leaf sheath Oryza sativa
ADAXIALIZED LEAF1 (ADL1) is essential for restricting differentiation of bulliform cells to adaxial side Oryza sativa
original cry1-104 mutant produces leaves without trichomes Arabidopsis thaliana
DREB/CBF play roles in leaf development
VIGS-NbCOBRA-infected plants have small, flat, and lumpy fourth pair of leaves Nicotiana benthamiana
single leaf development from founder cells requires integration of development of leaf ligules Oryza sativa
ACL1 might function in leaf development Oryza sativa
F2 individuals without T-DNA displayed wild-type leaf shape
late P4 stage is characterized by leaf blade totally elongated but still enwrapped
OSHB3 is mainly expressed on adaxial side of the leaf primordia and young leaf Oryza sativa
transgenic aspen plants had small leaves relative to wild-type
sllam1-1 observed similar trend in leaflet initiation across successive leaves Solanum lycopersicum
SlLAM1 only confers the activity of blade expansion rather than leaflet initiation Solanum lycopersicum
Zea mays ortholog of (PPR30, AT3G23020) shows strongest expression near base of the maize leaf Zea mays
(FAS1, FUGU2, NFB2, AT1G65470) mutant plants show serrated leaves Arabidopsis thaliana
TW (3-week-old seedlings) had smallest midrib Phyllostachys edulis
osnam-1 mutant has considerably shorter seventh leaf blade than sixth Oryza sativa
leaf size and shape are determined by coordinated regulation of cell division and expansion
NIL Lin387 has cell width of 27.03 μm Zea mays
WUSCHEL-like homeobox genes ( (ATNS1, NS1, OVA8, AT4G17300) and (ATNS2, NS2, SYNC2, SYNC2_ARATH, AT3G07420) ) affects leaf width (LW) Zea mays
viable double mutant ubp12w/ (AtUBP13, UBP13, AT3G11910) displays short petioles Arabidopsis thaliana
(PG45, PGA4, AT1G02790) mutant exhibits abnormal leaf curvature Arabidopsis thaliana
(PG45, PGA4, AT1G02790) OE#5-5 leaves have 5.3-fold the number of round adaxial mesophyll cells found in Col Arabidopsis thaliana
ectopic expression of OsNF-YB7 results in developmental abnormalities of the leaves Oryza sativa
wild-type plants continued to produce rosette leaves Arabidopsis thaliana
leaf 4 lacks meristematic activity within the epidermis Pisum sativum
leaf 4 had emerged in most plants at 20 DAP when salt stress was applied Hordeum vulgare
leaf width is expression of development
leaf width, length, and angle collectively define canopy architecture
scl6-II scl6-III (ATHAM3, HAM3, LOM3, SCL6-IV, AT4G00150) mutant plants exhibit abnormal leaf patterning Arabidopsis thaliana
BRI1–GFP overexpression line exhibits opposite phenotypes to BR-related mutants Arabidopsis thaliana
somatic endopolyploidization results in relatively large cells with higher chloroplast numbers Beta vulgaris; Arabidopsis thaliana; Nicotiana tabacum; Zea mays
sllam1 mutants make fewer or more primary and intercalary leaflets Solanum lycopersicum
Elongator has evolved to play a unique role in rice development Oryza sativa
bulliform cells keep leaf blade flat by absorbing water Oryza sativa
cur1 mutant produces leaves with reduced leaf width Oryza sativa
transient meristem is associated with heteroblastic change in cur1 Oryza sativa
AtGCN5 (BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) and (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) -dependent histone acetylation may control adult leaf trait Arabidopsis thaliana
bulliform cells may participate in expansion of very young leaves Oryza sativa
bulliform cells have been suggested to determine curling and stretching movement of the leaf
ACL1 expressed in leaf primordium
BY240 demonstrates characteristic of leaf margins curled abaxially Oryza sativa
siR109944 overexpression displayed increased flag leaf angles Oryza sativa
cellular ptDNA levels increased to 2550–3150 in maize Zea mays
sllam1 mutants with reduced blade expansion form fewer leaflets in early produced leaves (L1 to L5) Solanum lycopersicum
blade expansion in both stipules and leaflets in pea lath mutants is reduced in pea lath mutants Pisum sativum
plants with heterozygous genotypes or same genotype as EMS-9311 at Os07g0102300 site exhibited normal leaves similar to wild type Oryza sativa
curled later1 (cur1) mutant produced narrow and adaxially curled leaf blades at late adult stage Oryza sativa
flag leaf emerged soon after production of C-type leaves Oryza sativa
cur1 phenotype is distinct from fishbone mutant phenotype Oryza sativa
(ARK3, AtKINUa, PAK, AT1G12430) choi hybrid H111 present with greater specific leaf weight (SLW) Brassica rapa subsp. chinensis
trichomes on leaf edges were small and densely distributed in TW and OY Phyllostachys edulis
rice Os- (ASL39, LBD37, AT5G67420) FOX Arabidopsis lines exhibit hyponastic leaf phenotypes Arabidopsis thaliana
metabolite profiles of rice Os- (ASL39, LBD37, AT5G67420) FOX Arabidopsis lines with hyponastic leaf morphology are not derived from secondary effects of hyponastic leaf curling Arabidopsis thaliana
ACLs (Abaxially Curled Leaf genes) show non-tissue-specific expression in young leaf Oryza sativa
increased number and exaggeration of bulliform cells causes developmental discoordination of abaxial and adaxial sides Oryza sativa
(KNAT6, KNAT6L, KNAT6S, AT1G23380) is not expressed in (FAS1, FUGU2, NFB2, AT1G65470) 25-day-old serrated leaves
Col-0 TE-2-6b plants strikingly resemble Arabidopsis Col-0 jaw-D mutants Arabidopsis thaliana
OsMED14_1 transcripts are present in whole leaf Oryza sativa
ROLLING-LEAF 14 (RL14) remains unaffected in OsMED14_1 RNAi plants Oryza sativa
formation of (AS2, AT1G65620) bodies is correlated with functions of (AS2, AT1G65620) in development Arabidopsis thaliana
SlLAM1 is largely epistatic to E and SlMP in regulating blade expansion and final leaf forms Solanum lycopersicum
reduced number of secondary leaflets in later produced leaves in sllam1 results in altered overall leaf shape Solanum lycopersicum
Os07g0102300 was the gene underlying the semi-rolled leaves Oryza sativa
hyponastic leaf phenotypes positively correlates with rice Os- (ASL39, LBD37, AT5G67420) expression levels Arabidopsis thaliana
ACL1 overexpression causes abaxial leaf curling Oryza sativa
overexpression of ACL1 could induce abaxial leaf curling
bul-1 mutant exhibits increased stomata number Arabidopsis thaliana
direct regulation of (BP, BP1, KNAT1, AT4G08150) by (FAS1, FUGU2, NFB2, AT1G65470) depended on the leaf developmental stage
(ATGRP8, CCR1, GR-RBP8, GRP8, RBGA6, AT4G39260) mutant has more but smaller cells Arabidopsis thaliana
TE-2-6b plants at later stages form finger-like outgrowths along leaf edges Arabidopsis thaliana
SlLAM1 expression reduction starts as early as in P4 primordia Solanum lycopersicum
ACLs (Abaxially Curled Leaf genes) show non-tissue-specific expression in shoot apical meristem Oryza sativa
bes1-D mutant exhibits opposite phenotypes to BR-related mutants Arabidopsis thaliana
leaves formed on older transgenic aspen plants were of normal size normal leaf size
SLENDER LEAF 1 (SLE1) remains unaffected in OsMED14_1 RNAi plants Oryza sativa
cell proliferation in the boundary region between adaxial and abaxial domains might result in balanced expansion of leaf primordia along the medial–lateral axis Arabidopsis thaliana
(ARF3, ETT, AT2G33860) gene is expressed and functions only at early stages of leaf development Arabidopsis thaliana
ptDNA is present during all stages of leaf development Arabidopsis thaliana; Beta vulgaris; Nicotiana tabacum; Zea mays
knotty closely spaced beads-on-a-string structures found in all four species studied, practically at all stages of leaf development Arabidopsis thaliana; Beta vulgaris; Nicotiana tabacum; Zea mays
cellular ptDNA levels increased to 2620–3080 in Arabidopsis Arabidopsis thaliana
adult leaves in Arabidopsis gradually become larger and more serrated in leaf margins compared with juvenile leaves Arabidopsis thaliana
leaflet initiation in tomato may occur more than one time in each tomato leaf Solanum lycopersicum
OsNAM influences leaf length Oryza sativa
(ATNS1, NS1, OVA8, AT4G17300) (Narrow Sheath1) and (ATNS2, NS2, SYNC2, SYNC2_ARATH, AT3G07420) (Narrow Sheath2) have redundant functions in maize leaf development Zea mays
F1 plant (PH6WC × Lin387) has leaf width (LW) of ear leaf higher than wide leaf parent Zea mays
BC5F2-1 population (P/P genotype) has leaf width of 8.62 cm Zea mays
−3CAG genotype has leaf width of 7.09 cm Zea mays
upregulation of (AtGRF9, GRF9, AT2G45480) in CR-1 was consistent with phenotype of the narrow leaf with decreased cell numbers Zea mays
MYB HYPOCOTYL ELONGATION-RELATED controls cell expansion during leaf development Arabidopsis thaliana
gibberellin (GA) has role in leaf differentiation
small RNA-based regulatory steps facilitates delimitation of cell types comprising the upper versus lower parts of the leaf
periclinal divisions in subepidermal cells precede outgrowth of leaf primordia
leaves arise at the flanks of shoot apical meristem (SAM)
adaxial tissue needs to be present for leaves to develop a lamina shape Arabidopsis thaliana
TAS3-derived tasiARF serves as morphogen-like signal
down-regulation of secondary wall CesA may affect leaf development Nicotiana benthamiana
scl6-II scl6-III (ATHAM3, HAM3, LOM3, SCL6-IV, AT4G00150) triple mutant plants manifest altered leaf shape and patterning