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inflorescence development

13095 relationships annotated with this phrase. Showing first 500 of 13095.
Source entity Relationship Target entity Species
capitula mimic solitary flowers
loss-of-function mutation in ERECTA results in compact and firm inflorescence appearance Arabidopsis thaliana
spikelet density and number of branches showed statistically significant decrease associated with loss of one copy of (AtSIP1, RS1, SIP1, AT1G55740) in kn1 homozygotes Zea mays
OsROXY1 is expressed in young leaf primordia Oryza sativa
OsROXY2 signal is strongly detectable in middle of the main inflorescence Oryza sativa
(CLL2, EPFL4, AT4G14723) and (AtEPFL6, CHAL, EPFL6, AT2G30370) expressed in endodermis of inflorescence stems are perceived by ERECTA to induce cortex cell proliferation Arabidopsis thaliana
OsROXY2 is weakly detectable throughout primary branch primordia Oryza sativa
(SMAX1, AT5G57710) did not affect primary inflorescence height Arabidopsis thaliana
Mp (ATPIN1, PIN1, AT1G73590) can partially rescue At (ATPIN1, PIN1, AT1G73590) inflorescence phenotype Arabidopsis thaliana; Marchantia polymorpha
(CLL2, EPFL4, AT4G14723) (also called CHALLAH-LIKE2 ) is expressed in endodermis of inflorescence stems Arabidopsis thaliana
Asteraceae possess capitula
(AtEPFL6, CHAL, EPFL6, AT2G30370) (also called CHALLAH) is expressed in endodermis of inflorescence stems Arabidopsis thaliana
At pin1-3 plants produce pin-like bare stems Arabidopsis thaliana
ERECTA family members including ERECTA ERECTA-LIKE1 (ERL1, AT5G62230) and (ERL2, AT5G07180) have been extensively studied given the impact of the erecta ( er ) mutation Arabidopsis thaliana
ribosomal protein mutants may have distinct developmental defects affecting inflorescence development Arabidopsis thaliana
kn1 single mutant has tassel phenotype Zea mays
OsROXY1 transcript accumulates at high levels in roots Oryza sativa
OsROXY2 is expressed in roots Oryza sativa
OsROXY1 transcript is detectable at lower levels in stems Oryza sativa
OsROXY2 is expressed in spikelets Oryza sativa
OsROXY1 transcript is detectable at lower levels in leaves Oryza sativa
overexpression of mutated VvGRF4 alleles resulted in longer inflorescences and pedicels Arabidopsis thaliana
primary branch primordia differentiate into secondary inflorescence branches and spikelets Oryza sativa
OsROXY1 is expressed in roots Oryza sativa
KN1 and (AtSIP1, RS1, SIP1, AT1G55740) are expressed at similar levels in tassel primordia Zea mays
secondary inflorescences are called spikelets Oryza sativa
osfdml1 mutants show statistically decreased numbers of secondary branches Oryza sativa
OsROXY1 is expressed in flag leaf primordia Oryza sativa
35S:CLE7 transgenic plants shows pin-formed inflorescence shoots Arabidopsis thaliana
both loose cluster clones (M171 and 1-86) show similar inflorescence phenotypes Vitis vinifera
OsMED14_1 knockdown plants show reduced panicle branching Oryza sativa
HvFT3 accelerates early inflorescence development Hordeum vulgare
Cluster architecture variability can be explained by rachis length, berry number, berry volume Vitis vinifera
osnam-1 mutant panicle indicates inflorescence meristem (IM) terminated early Oryza sativa
Increase in rachis length and pedicel length can be easily correlated with loose cluster phenotype Vitis vinifera
multi-flower phenotype exhibited by MtSUP mutants share similarities with mutants in chickpea and pea Medicago truncatula; Cicer arietinum; Pisum sativum
inflorescence genes affect lateral branch meristems
number of branches (meristems) defines final number of flowers
model incorporating multiple phenotypes included tassel branch number Zea mays
Latent bud contains shoot apical meristem, young leaves and two premature inflorescences Vitis vinifera
VvGRF4 mRNA in loose cluster clones (LCCs) was kept at high levels in stage 2 and stage 3 Vitis vinifera
osnam-1 mutant has significantly fewer lateral organs on primary branches Oryza sativa
35S:CLE1 transgenic plants shows pin-formed inflorescence shoots Arabidopsis thaliana
loose cluster architecture is correlated with elongated rachis Vitis vinifera
Stage 2 (when miR396 is moderately expressed) had mutated alleles and compact cluster allele equally represented heterozygous situation Vitis vinifera
FM develops from the axil of each bract results in no spike is generated, instead the I2 meristem terminates as a flower meristem Medicago truncatula
MtSUP seems to restrict MtPIM expression to FM Medicago truncatula
MtSUP controls number of flowers produced Medicago truncatula
osnam-1 mutant panicle has hardly any secondary branches Oryza sativa
SG-64 exhibits spreading panicle Oryza sativa
Spr3(t) is associated with spreading panicle Oryza sativa
Spr3(t) may be the same locus as Spr3 Oryza sativa
Spr3(t) may be the same locus as Spr3 Oryza sativa
increases in PBNP, SBNP, GNP, FGNP, UGNP, and GD did not lead to increase in grain yield per plant Oryza sativa
EVE1-overexpressing transgenic plants did not produce inflorescence stem Arabidopsis thaliana
FD regulates meristem maintenance Arabidopsis thaliana
SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) functions with FLOWERING LOCUS T (FT)–FD complex Arabidopsis thaliana
a small proportion of ae4-1 rev-6 plants had day 4 inflorescence that generated very few flowers but many primordia Arabidopsis thaliana
mRNA pools of loose cluster clones contain predominantly mRNAs derived from mutated VvGRF4 alleles Vitis vinifera
OsMED14_1 knockdown produces pleiotropic effects such as reduced panicle branching Oryza sativa
Stage 1 inflorescence samples contained inflorescences from latent buds Vitis vinifera
(AtLHP1, LHP1, TFL2, AT5G17690) mutation causes formation of a terminating flower at the shoot apex Arabidopsis thaliana
Pinot noir (PN) clones show variation in inflorescence architecture Vitis vinifera
inflorescence meristem (IM) remains open and fails to produce a terminal flower
botryoids form only first order flowers
maize RAMOSA pathway is regulated inflorescence branching Zea mays
variation in activity of central florigens alters inflorescence development and architecture
too weak or absent florigen signal during later stages results in extra spikelets displaying reduced fertility
low expression of Hd3a and RFT1 is accompanied by delay in early inflorescence development Oryza sativa
osnam-1 mutant panicle has significantly fewer primary branches than WT Oryza sativa
differential effects on apical meristem versus lateral branch meristems permits morphological differentiation
branch meristems (BM) produces spikelet pair meristems (SPM) Zea mays; Sorghum bicolor
paired spikelets in wheat are reminiscent of spikelet pairs in maize Triticum aestivum; Zea mays
invasion of MtPIM to I2 is produced in mtsup-1 apices Medicago truncatula
spikelet meristems (SM) form one floret Hordeum vulgare
OsROXY1 is expressed in leaves Oryza sativa
I2 meristems in mtsup-1 produce spike instead of flower Medicago truncatula
genetic control of inflorescence architecture in grasses has been linked to reproductive success
functional alleles of (ATHD1, ATHDA19, HD1, HDA1, HDA19, HDAC19, RPD3A, AT4G38130) (HEADING DATE 1) and (ATEHD1, EHD1, AT3G20290) (EARLY ) that express Hd3a and RFT highly reduce primary branching and spikelet number on rice panicles Oryza sativa
TEOSINTE BRANCHED1 antagonises FT1-dependent activation of spikelet meristem identity genes
Wuyujing-7 control produces compact panicle at caryopsis ripening stage Oryza sativa
negative effectors of growth influence inflorescence architecture
florigens influence branch/spikelet architecture
modulating the expression of flowering-time genes can modify progression of inflorescence development
increased dosage of TEOSINTE BRANCHED1 promotes formation of paired spikelets in wheat Triticum aestivum
orthologue of SUP in eudicots has novel function in I2 meristem determinacy
meristem activity during early ontogeny indicates involvement of highly similar processes at distinct hierarchical levels
cephalioids have main axis lacking elongation
MtPI expression expanded towards indeterminate I2 meristem Medicago truncatula
I2 meristems lose vegetative nature and acquire floral identity Medicago truncatula
FT2 influences branch number
missense FT-A2 allele significantly increased spikelet number durum wheat
PENNYWISE (BLH9, BLR, HB-6, LSN, PNY, RPL, VAN, AT5G02030) and POUND-FOOLISH (BLH8, PNF, AT2G27990) are essential for specification of axillary meristems (AMs) during inflorescence development Arabidopsis thaliana
secondary inflorescence specification differs between pea and Arabidopsis Pisum sativum; Arabidopsis thaliana
Medicago truncatula SUPERMAN (MtSUP) regulates activity of secondary inflorescence meristem Medicago truncatula
syncephalia have development that recapitulates that of a capitulum, except heads replace single flowers on receptacle
(AtCYP71, CYP71, AT3G44600) mutant affects inflorescence development
(AtCYP71, CYP71, AT3G44600) and (AtLHP1, LHP1, TFL2, AT5G17690) have synergistic functions in regulating inflorescence architecture Arabidopsis thaliana
Main inflorescence length was compared between heterozygous plants and null segregants Arabidopsis thaliana
MtFULc transcript occupies wider area in mtsup-1 than in wild type Medicago truncatula
wheat and barley plants expressing null alleles of APETALA1 (AGL7, AP1, AtAP1, AT1G69120) -like genes including VERNALIZATION 1 (REM39, VRN1, AT3G18990) form longer inflorescences with more spikelets Triticum aestivum; Hordeum vulgare
MtSUP is controlling activity of I2 meristems Medicago truncatula
conventional inflorescence meristems (IM) elongate and develop lateral flower meristems (FMs)
Eps-A m 1 locus showed the most significant F values and P values for number of spikelets per spike
MtSUP and MtWUS expression patterns show spatial overlap in I2 and FM Medicago truncatula
wheat plants that over-express (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) flower while regenerating from callus and bear rudimentary inflorescences with few infertile spikelets Triticum aestivum
spatial and temporal expression pattern of SUP-like genes could be correlated with differences in inflorescence architecture among plant species
MtFRUITFULLc (MtFULc) is inflorescence marker Medicago truncatula
Menyanthaceae develop branched inflorescences with racemose branching pattern on main axis
florigen-dependent pathway influences inflorescence architecture
FT-LIKE 1 (FT-L1) and PANICLE PHYTOMER2 (IAA27, PAP2, AT4G29080) perform similar roles in rice inflorescence development Oryza sativa
increased dosage of TEOSINTE BRANCHED1 delays specific stages of inflorescence development Triticum aestivum
wild-type inflorescence development follows acropetal succession Medicago truncatula
sparse inflorescence1 (spi1) gene is associated with reduced number of branches and spikelets in inflorescence Zea mays
knockout alleles of an1 have been shown to reduce or abolish tassel branching Zea mays
Stage 3 (when miR396 is highly expressed) had mRNA pools dominated by VvGRF4-m1 and VvGRF4-m2 forms Vitis vinifera
defect in branch meristem initiation leads to development of fewer branches Zea mays
NIL(Spr3) produces spreading panicle at caryopsis ripening stage Oryza sativa
eve1-D plants failed to produce axillary and lateral inflorescences Arabidopsis thaliana
MADS-box transcription factors that control I2 and FM identity are repressed in MtSUP mutants Medicago truncatula
Arabidopsis exhibits racemose branching pattern
activity of I2 meristems defines number of flowers produced Medicago truncatula
genetic networks established between meristem identity genes during inflorescence development share significant similarities between eudicot species Arabidopsis and M. truncatula Arabidopsis thaliana; Medicago truncatula
RA1 promotes meristematic determinacy in inflorescence Zea mays
Triticeae COMPOSITUM pathway is regulated spike architecture Triticum aestivum
inflorescence meristem (IM) elongates inflorescence meristem structure
spikelet meristems (SM) form multiple florets Triticum aestivum
missense allele of CO-like5 (ATCOL5, BBX6, COL5, AT5G57660) produces more spikelets wheat
(AtbZIP, bZIP, AT1G68880) transcription factor bZIPC1 increases spikelet number wheat
Wuyujing-7 exhibits erect compact panicle Oryza sativa
chromosome segment substitution line (CSSL) SG-64 shows spreading panicle phenotype Oryza sativa
formation of spreading panicle is accompanied by decrease in 100-grain weight Oryza sativa
eve1-D mutant could not generate axillary and lateral inflorescences Arabidopsis thaliana
outgrowth (exsertion) direction of primary branches during inflorescence development is important factor influencing inflorescence structure Oryza sativa
NIL(Spr3) exhibits spreading panicle with primary branches nearly perpendicular to inflorescence rachis Oryza sativa
eve1-D plants did not display axillary or lateral inflorescences Arabidopsis thaliana
MtSUP might control balance of cell proliferation in I2 Medicago truncatula
transcriptional differences of MtSUP orthologues could correlate with higher levels of inflorescence complexity
capitula may occupy flower positions in branched inflorescences
flowering genes perform enduring role during inflorescence development
delayed progression between double-ridge and lemma primordium stages facilitates formation of more spikelets Triticum aestivum
in situ hybridization experiments provides data for detailed, solid understanding of inflorescence development Petunia hybrida
(EVE1, AT4G03350) may regulate growth during inflorescence stem development Arabidopsis thaliana
ramosa 1 (ra1) mutant exhibits increased number of long primary branches Zea mays
mutation in specific regulatory gene functioning in inflorescence development pathways leads to changes in the length of primary branches or panicle Oryza sativa; Zea mays
spreading panicle of NIL(Spr3) contains several basipetal primary branches formed in a cluster Oryza sativa
detailed description of inflorescence development in petunia is used to discuss and clear up persistent confusion and controversy concerning classification of inflorescence architectures Petunia hybrida
some ae4-1 rev-6 double mutant plants were arrested after producing one or several flowers Arabidopsis thaliana
plants with racemose type of inflorescence have bracts that replace vegetative leaves
MtPIM expression similarly expands towards indeterminate I2 meristem Medicago truncatula
number of fractionation steps may vary development of compound heads
Helianthus annuus develops racemose main axis that terminates into a radiate head Helianthus annuus
I2 meristem in MtSUP mutants terminates in flower instead of spike Medicago truncatula
Goodeniaceae develop branched inflorescences with racemose branching pattern on main axis and cymose pattern on basal lateral branches
rice genotypes expressing Hd3a and RFT1 at higher levels produce fewer spikelets per panicle Oryza sativa
wheat and barley plants expressing null alleles of FLOWERING LOCUS T2 (FT2) form longer inflorescences with more spikelets Triticum aestivum; Hordeum vulgare
strong alleles of FT-like12 (FTL12) promote formation of dense and highly branched inflorescences Oryza sativa; Triticum aestivum; Zea mays
ABERRANT PANICLE ORGANIZATION 1 (APO1) is temporal regulator of meristem identity Oryza sativa
'10_11' shoot apical meristem (SAM) progressed to stamen primordium stage
spreading panicle is accompanied by undesirable traits Oryza sativa; Oryza glaberrima
barren inflorescence2 (bif2) plays a key role in lateral primordia initiation Zea mays
(APO1, AT1G64810) mutant exhibits abnormal panicle phyllotaxy (distichous phyllotaxy) Oryza sativa
NIL(Spr3) in Wuyujing-7 genetic background shows increased FGNP Oryza sativa
maintenance of putative stem-cells in the central zone (CZ) of the inflorescence meristem (IM) results in open inflorescences
weak Ppd-1 alleles facilitate development of paired spikelets Triticum aestivum
overexpression of FT causes determinate inflorescence structure
pANT::TFL1 transgenic line increased number of cauline leaves Arabidopsis thaliana
pAP1:: (TFL-1, TFL1, AT5G03840) transgenic line in background did not restore cauline leaf numbers to wild-type Arabidopsis thaliana
eudicot species show different inflorescence architectures according to complexity of branching
MtSUP participates in process by which I2 meristems acquire determinate fate Medicago truncatula
rice genotypes with low expression of Hd3a and RFT1 produce more spikelets per panicle Oryza sativa
genes that act downstream to control branch and spikelet development could be targeted to boost floret number
manipulation of the flowering pathway provides a means to generate more elaborately branched cereal inflorescences cereal crops
rice inflorescence architecture depends primarily on number of rachis-branches Oryza sativa
ABERRANT PANICLE ORGANIZATION 1 (APO1) plays a role in preventing precocious conversion of inflorescence meristems to spikelet meristems Oryza sativa
NIL(Spr3) in Wuyujing-7 genetic background shows increased UGNP Oryza sativa
'Karl' SAM development is at triple mound stage at 35 d while '10_11' SAM development is at stamen primordium stage Hordeum vulgare
floral transition and development to 'triple mound' stage occurred simultaneously in 'Karl' and '10_11' shoot apical meristem (SAM)
Ionopsidium acaule showed abundant expression of (LFY, LFY3, AT5G61850) mRNA and protein in inflorescence meristem Ionopsidium acaule
AGAMOUS-LIKE 24 (AGL24, AT4G24540) –SUPPRESSOR OF OVEREXPRESSION OF CONTANS1 (AGL20, ATSOC1, SOC1, AT2G45660) complex up-regulates flower meristem identity genes Arabidopsis thaliana
ft-2 stm-10 double mutant produced Class I inflorescence phenotype Arabidopsis thaliana
modelling is a helpful aid to follow consequences of meristem decisions for inflorescence development
primary inflorescences of rev-6 single mutant plants usually produced several branches Arabidopsis thaliana
(KAT2, AT4G18290) (KAT5, PKT1, PKT2, AT5G48880) double mutant phenotypes are strikingly similar to (AIM1, AT4G29010) phenotypes Arabidopsis thaliana
pAP1:: (TFL-1, TFL1, AT5G03840) transgenic line in background had significantly increased cauline leaf numbers in strongest lines compared with (TFL-1, TFL1, AT5G03840) mutant Arabidopsis thaliana
Spr3 is unknown genetic factor in controlling the outspreading of the primary branches in rice inflorescence Oryza sativa; Oryza glaberrima
truncation of inflorescences may have had common ontogenetic pathway
modulating the expression of flowering-time genes provides opportunity to change number and arrangement of grain-producing florets
weak flowering signal facilitates production of extra branches or spikelets
small panicles formed few primary branches and spikelets Oryza sativa
mutation in specific regulatory gene functioning in inflorescence development pathways leads to alteration of the inflorescence architecture Oryza sativa; Zea mays
inflorescence initiation at the SAM occurs between 15 d and 21 d after planting in both 'Karl' and '10_11' Hordeum vulgare
wild-type plants displayed inflorescence meristem (IM), flowers, axillary shoot apical meristems (SAMs), and floral meristems (FMs) Arabidopsis thaliana
OCL1 overexpression line K3 had shorter and more upright lateral branches with aborted flowers Zea mays
rice ABERRANT PANICLE ORGANIZATION pathway underlies inflorescence type Oryza sativa
Triticeae COMPOSITUM pathway underlies inflorescence type Triticum aestivum
spikelet meristem (SM) forms floret meristem (FM) Oryza sativa
reduced (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) expression decelerates inflorescence meristem (IM) development Triticum aestivum; Hordeum vulgare
Brachypodium spikelets often have awned lemmas Brachypodium distachyon
spikelet of wheat is regular arrangement of five florets Triticum aestivum
P3 plants produce numerous shortened inflorescences Arabidopsis thaliana
production of far fewer secondary branches on the panicles is undesirable trait in Oryza glaberrima Steud. Oryza glaberrima
common ontogenetic pathway for truncation would require every open inflorescence sharing common structure
OCL1 overexpression line K6 had shorter and more upright lateral branches with aborted flowers Zea mays
female stage of skunk cabbage inflorescence is characterized by petals open slightly and stigmas become exserted Symplocarpus foetidus; Symplocarpus renifolius
NIL(Spr3) in Wuyujing-7 genetic background shows increased SBNP Oryza sativa
(BP, BP1, KNAT1, AT4G08150) loss-of-function mutation results in reduced floral internodes Arabidopsis thaliana
Brachypodium inflorescence matures basipetal maturation Brachypodium distachyon
FLOWERING LOCUS T (FT)–FD complex up-regulates flower meristem identity genes Arabidopsis thaliana
ectopic FT can induce AM formation Arabidopsis thaliana
inflorescence structure in tomato remains unchanged in self pruning mutants Solanum lycopersicum
inflorescence genes affect apical meristem of the inflorescence
genetic control of inflorescence architecture in grasses might present process to improve seed yield in cereal crops
strong alleles of TERMINAL FLOWER 1 (TFL-1, TFL1, AT5G03840) CENTRORADIALIS (CN) promote formation of dense and highly branched inflorescences Oryza sativa; Triticum aestivum; Zea mays
lack of internode elongation is analogous to compressed inflorescence axis in Ionopsidium acaule Ionopsidium acaule
AGAMOUS-LIKE 24 (AGL24, AT4G24540) –SUPPRESSOR OF OVEREXPRESSION OF CONTANS1 (AGL20, ATSOC1, SOC1, AT2G45660) complex functions with SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) Arabidopsis thaliana
rpn9a-1 rev-6 inflorescences also produced filamentous structures Arabidopsis thaliana
NILs carrying early and late alleles at Eps-A m 1 locus showed highly significant differences in number of spikelets per spike
MtSUP has role in secondary inflorescence meristem and common primordia determinacy Medicago truncatula
Overexpression of (Plsp2B, TPP, AT2G30440) resulted in less branched inflorescences Arabidopsis thaliana
ramosa3 mutant of Zea mays has excessive branching Zea mays
RAMOSA 2 (Ra2) mutant exhibits increased number of long primary branches Zea mays
cyme of petunia is distinct body plan compared with racemes of Arabidopsis and Antirrhinum Petunia hybrida; Arabidopsis thaliana; Antirrhinum
eve1-D plants did not generate primary inflorescence Arabidopsis thaliana
OCL1 overexpression affects timing of ear and tassel initiation Zea mays
introgression line harboring the cultivated allele of LIGULELESS1 (OsLG1) exhibits long awns, especially on lower florets Oryza rufipogon
(BP, BP1, KNAT1, AT4G08150) plays a key role in development of the inflorescence stem Arabidopsis thaliana
VatpC alleles show non-significant differences in spikelet number
nullisomic-tetrasomic lines lacking chromosome 1B showed non-significant differences in number of spikelets per spike
TERMINAL FLOWER1 (TFL-1, TFL1, AT5G03840) and CENTRORADIALIS (CEN) control inflorescence architecture Arabidopsis thaliana; Antirrhinum majus
thermogenesis might be required for efficient development of reproductive organs Symplocarpus foetidus; Symplocarpus renifolius
SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) combined activities required for specification of coflorescence meristems Arabidopsis thaliana
35S:FT inflorescences produced floral nodes Arabidopsis thaliana
differences in expression patterns may account for different types of inflorescence architectures Solanaceae
FZP mutation results in formation of axillary meristems in rudimentary glume axils Oryza sativa
spreading panicle of NIL(Spr3) is formed in late panicle development Oryza sativa
carbon content of inflorescence/bunch increased slowly between stages 53 and 57 then stabilized Vitis vinifera L. cv. Chardonnay
strong ectopic transcriptomic activity at LP stage contributes to formation of extra spikelets in flo.a Hordeum vulgare
wheat PHOTOPERIOD-1 controls initiation of additional spikelets Triticum aestivum
bisexual stage of skunk cabbage inflorescence is characterized by stamens at the base of each stigma start emerging from the surface of the spadix Symplocarpus foetidus; Symplocarpus renifolius
temperature and Eps-Am1 alleles interaction does not affect spikelet number Triticum monococcum
capitulum inflorescence undergoes profound changes in SAM development Helianthus annuus
ALOG transcription factors have regulatory signaling roles during development of reproductive meristems in cereal inflorescences Hordeum vulgare L.
three separate SMs differentiate into individual spikelets Hordeum vulgare
extra spikelets in flo.a formed on abaxial side of CS at rachis node Hordeum vulgare
(LFY, LFY3, AT5G61850) is not expressed in indeterminate inflorescence apex Arabidopsis
ft-2 stm-10 and fd-3 stm-10 double mutants produced Class III umbrella phenotype Arabidopsis thaliana
meristem decisions on flower and shoot production specify inflorescence development
Brachypodium spikelets contain several diminished and underdeveloped florets at the apex Brachypodium distachyon
stm-10 mutant produced cauline leaves Arabidopsis thaliana
increasing the level of extensins results in obviously shorter inflorescences Arabidopsis
thermogenesis is weak at bisexual stage
heat production is virtually undetectable at immature or male stages
ae4-2 rev-6 plants occasionally produced inflorescence that only contained filamentous structures Arabidopsis thaliana
J (JOINTLESS) loss-of-function mutant results in loss of inflorescence determinacy Solanum lycopersicum
shoots with terminal flowers undergo profound changes in SAM development Datura stramonium
recessive mutations in (TFL-1, TFL1, AT5G03840) and CEN result in conversion of indeterminate shoot into determinate flower Arabidopsis thaliana; Antirrhinum majus
immature stage of skunk cabbage inflorescence is characterized by inflorescence just emerging and heat production has not occurred yet Symplocarpus foetidus; Symplocarpus renifolius
total mass of the spadix increases progressively during inflorescence development
first inflorescence phase involves making cauline leaves with secondary shoots in their axils on an elongated stem Arabidopsis thaliana
pLFY:: (TFL-1, TFL1, AT5G03840) transgenic line in background had cauline leaf numbers similar to wild-type Arabidopsis thaliana
thermogenesis in skunk cabbage is closely associated with stages of inflorescence development
pith increases its mass progressively during inflorescence development
pANT:: (TFL-1, TFL1, AT5G03840) transgenic line in background had cauline leaf numbers similar to wild-type Arabidopsis thaliana
SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) up-regulates flower meristem identity genes Arabidopsis thaliana
primary inflorescences of wild-type plants usually produced several branches Arabidopsis thaliana
JOINTLESS suppresses sympodial identity in inflorescence meristems Solanum lycopersicum
inflorescence generation involves dramatic alterations between vegetative and reproductive stages within apical meristems
(SKU6, SPR1, AT2G03680) confers spreading panicle phenotype Oryza sativa
florigen expressed at normal or strong levels results in timely branch or spikelet formation
milder and delayed (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) expression causes longer inflorescences bearing more spikelets Triticum aestivum; Hordeum vulgare
rice plants that over-express (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) flower while regenerating from callus and bear rudimentary inflorescences with few infertile spikelets Oryza sativa
processes that act downstream of florigens control inflorescence development
RA1 acts downstream of ra2 Zea mays
(EVE1, AT4G03350) controls inflorescence stem development related to APETALA 1 (AGL7, AP1, AtAP1, AT1G69120) and APETALA 2 (AP2, AtAP2, FL1, FLO2, AT4G36920) regulation Arabidopsis thaliana
SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) combined activities required for specification of flower meristems Arabidopsis thaliana
spatial constraints at the inflorescence meristem (IM) could play a role at the time when terminal flower production determination
SHOOT MERISTEMLESS (SHM1, SHMT1, STM, AT4G37930) and FLOWERING LOCUS T (FT)–FD complex are required for specification of floral meristems Arabidopsis thaliana
FT and FD function with STM to maintain meristem integrity Arabidopsis thaliana
RAMOSA3 (RA3) gene controls inflorescence architecture Zea mays
massive heat production in spadices occurs only during female stage
rice OsPTB1 and OsPTB2 regulate panicle development Oryza sativa
repeated touch stimulation of Arabidopsis seedlings causes short inflorescences Arabidopsis thaliana
loss of HvALOG1 might be compensated for by other ALOG proteins in more basal spike parts Hordeum vulgare
ft-2 stm-10 Class I inflorescences produced cauline leaves Arabidopsis thaliana
cortex cell proliferation induced by (CLL2, EPFL4, AT4G14723) and (AtEPFL6, CHAL, EPFL6, AT2G30370) promotes inflorescence growth Arabidopsis thaliana
OsMADS34 expression in emf2b mutants occurs in stages In7 to SP8 Oryza sativa
cl7(t) mutant has altered morphology of panicle Oryza sativa
ant-4 ail6-2/+ ail7-1 plants show several inflorescence meristem defects
fd-3 stm-10 double mutant produced Class I inflorescence phenotype Arabidopsis thaliana
petunia PFG plays crucial role in transition from vegetative growth to inflorescence identity Petunia hybrida
barley ALOG1 (HvALOG1) predominantly governs floral organ development Hordeum vulgare L.
spike development results in emergence of new SMs Hordeum vulgare
defects in flo.a omit basal section Hordeum vulgare
HvALOG1 plays dominant role in specifying SM determinacy and maintaining boundary formation Hordeum vulgare
(ATGPAT4, GPAT4, AT1G01610) RNAi lines exhibit abnormal inflorescence development Brassica napus
triple SM (TSM) originates from upper axillary spikelet primordium of double ridge Hordeum vulgare
DEGs in group C4 were enriched with functions related to shoot system development, plant organ formation, floral whorl development, auxin homeostasis Hordeum vulgare
mutations in HvALOG1 result in production of extra spikelets sharing the same rachis node with regular spikelet triplet Hordeum vulgare
shoot apical meristem (SAM) maturation determines compound inflorescence production Solanum lycopersicum
production of extra spikelets is controlled by multiple genes
HvALOG1 plays a crucial role in maintaining inflorescence architecture in barley Hordeum vulgare
pLFY::TFL1 transgenic line increased number of cauline leaves Arabidopsis thaliana
aqcfl1 plants exhibited shorter central inflorescences with fewer nodes and flowers Aquilegia coerulea
reduced SHOOT MERISTEMLESS (STM) function ectopic FT and FD promote formation of axillary meristems Arabidopsis thaliana
temperature and Eps-A m 1 alleles show non-significant interaction for spikelet number
RAMOSA3 isoform of (Plsp2B, TPP, AT2G30440) loss of leads to abnormal inflorescence branching Zea mays
Overexpression of TPS gave rise to highly branched inflorescences Arabidopsis thaliana
OsROXY1 is strongly expressed in tips of primary branch primordia Oryza sativa
barley ALOG1 (HvALOG1) exhibits boundary-specific expression pattern Hordeum vulgare L.
DEFORMED ROOTS AND LEAVES1 (DRL1, TKPR1, AT4G35420) mutant cause disorganized inflorescence growth Arabidopsis thaliana
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpressing plants show bolting delayed by almost 3 weeks relative to wild-type plants
rice inflorescence comprises secondary inflorescences Oryza sativa
ft-10 tsf-1 double mutant phenocopies 35S::TFL1 plants Arabidopsis thaliana
35S::TFL1 plants shows I1* phase Arabidopsis thaliana
tfl1-20 mutant produces approximately four solitary flowers before terminal flower formation Arabidopsis thaliana
hyper-vegetative shoot is observed in TFL1-overexpressing plants Arabidopsis thaliana
TAWAWA1 (TAW1) gain-of-function mutant exhibits prolonged florescence meristem activity Oryza sativa
RICE CENTRORADIALIS 2 (RCN2) overexpression exhibits denser-panicled phenotype Oryza sativa
spikelet meristems (SMs) develop into spikelets Triticum ssp.; Hordeum vulgare L.
1,326 and 973 genes differentially expressed between LP-basal and AP-basal indicates HvALOG1 may also participate in other pathways regulating spike development Hordeum vulgare
(OSH1, AT5G01580) mutant regenerated from callus exhibits inflorescence defect Oryza sativa
serk1-1 −/− /serk2-1 −/+ /bak1-5 −/− mutant phenocopies er105 mutant in pedicel length Arabidopsis thaliana
recessive alleles of barley ALOG1 (HvALOG1) produce non-canonical extra spikelets Hordeum vulgare L.
wheat FLOWERING LOCUS T1 controls initiation of additional spikelets Triticum aestivum
halted TSM differentiation in double knockouts resulted in loss of ability to produce spikelets Hordeum vulgare
Aquilegia coerulea 'Origami' produces one or occasionally two main inflorescence axes Aquilegia coerulea
double knockouts alog1 CR/alog2 CR had development of upper glume of LSs inhibited Hordeum vulgare
genetic modifications of canonical spikelet arrangements lead to formation of non-canonical extra spikelets per rachis node Triticum ssp.; Hordeum vulgare L.
extra floret-a (flo.a) mutant produced extra spikelets Hordeum vulgare L.
barley ALOG protein family might work synergistically to regulate inflorescence shape Hordeum vulgare
positional effect of mutant phenotypes along spike emphasizes unequal spatiotemporal redundancies among ALOG members Hordeum vulgare
clusters C4 and C6 showed specific differential expression patterns in upper middle and base parts of spikes at LP stage Hordeum vulgare
ALOG family members in tomato have been shown to act synergistically in precisely control SAM maturation, synchronized flowering, compound inflorescence production Solanum lycopersicum
TfUFO-overexpressing torenias did not show change in inflorescence architecture Torenia
TfUFO activity is necessary but insufficient for termination of inflorescence Torenia
new SMs align until spike reaches maximum spikelet count Hordeum vulgare
ALOG-1 influenced by PHOTOPERIOD-1 is expressed in developing inflorescence Triticum aestivum
Virus-induced gene silencing of AqcFL1 loci results in plants with shorter inflorescences with fewer flowers Aquilegia coerulea
miR172-targeted suppression of SUPERNUMERARY BRACT (SNB), OsINDETERMINATE SPIKELET 1 (OsIDS1) and OsTOE1 decreases number of branches and spikelets Oryza sativa
post-transcriptional manipulation of protein turnover plays an important role in controlling inflorescence branching Oryza sativa
ft-10 tsf-1 double mutant shows aerial rosette-like structures Arabidopsis thaliana
presence of (TFL-1, TFL1, AT5G03840) is important for generation of normal inflorescence
inflorescence transition meristem size is altered in Zmfcp1 Zmcle7 double mutant Zea mays
presence or absence of the awn greatly affects apparent architecture of grass inflorescences
Brachypodium spikelets are highly variable for number of fertile florets that develop (4–20) Brachypodium distachyon
FT plays a role in coflorescence specification Arabidopsis thaliana
P4 plants differ in height of inflorescence Arabidopsis thaliana
presence of extra spikelets affects connection of developing organs to rachis node Hordeum vulgare
findings on ALOG function in inflorescence development may contribute to understanding of molecular mechanisms underlying inflorescence development
barley ALOG1 (HvALOG1) predominantly governs meristem maintenance Hordeum vulgare L.
inflorescence meristem (IM) activity duration is primary factor defining inflorescence architecture
spatial arrangement of meristems is primary factor defining inflorescence architecture
barley has spikelet triplets originating from same rachis node Hordeum vulgare L.
nine flo-like mutants from different genetic backgrounds display extra spikelets in upper-mid part of spike Hordeum vulgare
all reproductive meristems (IM, TSM, SM, FM) were devoid of HvALOG1 signals Hordeum vulgare
miR172-targeted suppression of SUPERNUMERARY BRACT (SNB), OsINDETERMINATE SPIKELET 1 (OsIDS1) and OsTOE1 further delays transition to floral meristem Oryza sativa
serk1-1 −/− /serk2-1 −/+ /bak1-5 −/− mutant phenocopies er105 mutant in inflorescence architecture Arabidopsis thaliana
triple SM (TSM) bifurcates into three separate SMs Hordeum vulgare
unequal spatiotemporal redundancies among ALOG members regulate spikelet development Hordeum vulgare
differentiation in the individual tissues and their intracellular structure during inflorescence development of skunk cabbage is examined in detail in this work Symplocarpus foetidus; Symplocarpus renifolius
connection of developing organs to rachis node affects development of CSs Hordeum vulgare
limited space at nodal complex constrains complete development of spikelet quartets Hordeum vulgare
transcriptomes of BW and flo.a samples were separated at LP and AP stages Hordeum vulgare
Hvalog2 single knockout transgenic plants (ALOG1/alog2 CR) had spike and spikelet phenotypes not significantly altered compared to null transgenic control lines Hordeum vulgare
VvGRF4 is upregulated in loose cluster clones Vitis vinifera
VvGRF4 mutated variants expression promotes pedicel elongation Arabidopsis thaliana
clustered inflorescences in serk1-1 −/− /serk2-1 −/+ /bak1-5 −/− and er105 mutants are associated with shortened pedicels of these mutants Arabidopsis thaliana
capitula are aggregates of multiple florets
cell elongation had ceased in inflorescences of 8-week-old plants (8WAI) Arabidopsis thaliana
OsROXY1 is expressed in inflorescence meristem Oryza sativa
Ghd8 is highly expressed in inflorescence meristem
osnam-1 /+ oscuc3-1 double mutant has normal panicle architecture Oryza sativa
(EEP1, MIR164, MIR164C, AT5G27807) (ANAC098, ATCUC2, CUC2, AT5G53950) module is also considered to influence cell elongation in internodes during inflorescence development Arabidopsis thaliana
homozygous mutant plants having alleles that removed portions of peak-3 alone (e.g., slwox9 pro-Reg2-5) or in combination with peak-2 (e.g., slwox9 pro-Reg2-4) were not more severely branched than plants with alleles that partially or completely removed peak-2 Solanum lycopersicum
pLFY::WOX9-RNAi transgenic lines produce ectopic flowers Arabidopsis thaliana
development from apical meristems results in racemes
inflorescence meristem (IM) develops in different ways depending on species
DOT expression overlaps with ALF expression
EVG promotes DOT expression
genetic interaction between MADS-box genes and (TFL-1, TFL1, AT5G03840) is conserved for determining inflorescence architecture in flowering plants
interaction between AqcFL1A and AqcAGL24.1 is consistent with phenotype in aqcfl1 plants Aquilegia
HA–TWD1-Ct shows more equal distribution of inflorescence lengths at nodes Arabidopsis thaliana
SWR1-mediated incorporation of (H2A.Z, HTA11, AT3G54560) histone variant regulates inflorescence architecture Arabidopsis thaliana
five Arabidopsis long-PIN paralogs are required for patterning inflorescence primordia Arabidopsis thaliana
barley ALOG family members synergistically modulate inflorescence morphology Hordeum vulgare L.
defects in flo.a are restricted to upper-middle section of spike Hordeum vulgare
CS glumes transformed into organs with varying degrees of development ranged from leaf-like state to complete florets featuring lemma, palea, stamens, ovary Hordeum vulgare
wheat DUO-B1 controls initiation of additional spikelets Triticum aestivum
loss of one copy of (AtSIP1, RS1, SIP1, AT1G55740) reduced tassel branches further in kn1 homozygotes Zea mays
At pin1-4 plants produce pin-like bare stems Arabidopsis thaliana
miR164-mediated cleavage of (ANAC098, ATCUC2, CUC2, AT5G53950) transcripts in internode cells enables rapid growth of the internode at later stages of inflorescence development Arabidopsis thaliana
transgenic ZCN4 OE plants produce bushy tassel with increased branches and spikelet density Zea mays
EVERGREEN (EVG) is fully redundant in exp or her mutant background Petunia hybrida
AP1-like genes in rice are involved in specifying inflorescence meristems Oryza sativa
specific expression of gt1 in the nodal plexus in maize suppresses initiation of multiple ears Zea mays ssp. mays
altered tassel traits of ZCN4 OE plants were not apparent in transgenic RHW1 OE lines Zea mays
TERMINAL FLOWER1 (TFL-1, TFL1, AT5G03840) maintains indeterminate state of inflorescences Arabidopsis thaliana
Landsberg erecta- 0 (Ler-0) harbors loss-of-function mutation in ERECTA gene Arabidopsis thaliana
only vascular plant PIN proteins could restore At (ATPIN1, PIN1, AT1G73590) inflorescences Arabidopsis thaliana
SWR1 and ER signaling pathway regulates inflorescence architecture
EVG expression is separated in space from DOT expression
evg mutants in a mixed W115/W138 genetic background display solitary flower phenotype Petunia hybrida
evg phenotype in mixed W115/W138 genetic background gets stronger in mixed W115/W138 genetic background Petunia hybrida
35S:miR156a plants have axillary inflorescences that bolt prior to outgrowth of the primary inflorescence Arabidopsis thaliana
(IMB4, AT4G27640) mutants show delayed emergence of primary inflorescence stems Arabidopsis thaliana
Four different Pinot noir cluster types can be distinguished as compact, loose, upright growing and mixed berry size clusters Vitis vinifera
Loose cluster clones (LCCs) M171 and 1-86 show significantly increased rachis length, pedicel length and berry size Vitis vinifera
VvGRF4 mRNA levels of compact cluster clones (CCCs) were highest at stage 1 with RPKM values around 90, dropping to around 10 at stage 3 developmental stages Vitis vinifera
extra floral bracts accompanied by extra pair of glumes Hordeum vulgare
GFP signals at AP stage were limited to rachis and boundary domain of floret organs Hordeum vulgare
secondary spikelets of alog-1 in wheat are mainly formed in central region of inflorescence Triticum aestivum
spike development results in gradient of spikelet developmental stages along spike length Hordeum vulgare
HvALOG1 coordinates gene expression related to cell division activity, spikelet identity/determinacy, boundary formation, organ growth, hormone signaling Hordeum vulgare
aqcfl1 plants consistently showed reduced inflorescence height Aquilegia coerulea
gcn5-1/hag1-1 mutants display overproliferation of young buds Arabidopsis thaliana
maize ramosa3 (ra3) mutant produces highly branched male and female inflorescences Zea mays
ft-10 tsf-1 / ft-10 tsf-1 (scion/rootstock) plants produces hyper-vegetative shoots Arabidopsis thaliana
extrapetals (exp) mutant transforms cymose inflorescence into solitary flower Petunia hybrida
extrapetals (exp) mutant results in solitary flower
rice orthologs of (AGL20, ATSOC1, SOC1, AT2G45660) (AGL22, FAQ1, SVP, AT2G22540) (AGL24, AT4G24540) and (AGL3, SEP4, AT2G03710) determine panicle branching Oryza sativa
pp2-a13-1 mutant shows altered inflorescence morphology Arabidopsis thaliana
differentially regulated genes in (ATSPL7, SPL7, AT5G18830) (ATSPL14, FBR6, SPL14, SPL1R2, AT1G20980) spl17 and nl1 mutants globally indicate persistence of vegetative program during panicle development rice
variation in the regulatory region of FZP causes increases in secondary inflorescence branching Oryza sativa
combination of (TFL-1, TFL1, AT5G03840) overexpression and loss of function of FT and (TSF, AT4G20370) does not produce additive effect Arabidopsis thaliana
(HB-3, STIP, WOX9, WOX9A, AT2G33880) mutant shows weak inflorescence branching Oryza sativa
branched inflorescence phenotype was tightly associated with deletions in the second ATAC-seq peak region (peak-2, 350 bp) in the distal portion of the promoter Solanum lycopersicum
pinoid (ABR, PID, AT2G34650) mutant strikingly resembles (ATPIN1, PIN1, AT1G73590) mutant phenotypes
identification of non-cell-autonomous signal preventing phase reversion would contribute to better understanding of how inflorescence shape is determined rice
continued formation of flower buds leads to retardation of inflorescence termination Torenia
aqcfl1 inflorescences resulted in open flowers at the level of the rosette leaves Aquilegia coerulea
gcn5-5/hag1-5 mutants display overproliferation of young buds Arabidopsis thaliana
promoter dissection by chromatin accessibility and CRISPR-Cas9 in vivo analysis mapped distinct SlWOX9 functions controlling early SAM growth or inflorescence branching Solanum lycopersicum
(ATSPL7, SPL7, AT5G18830) (ATSPL14, FBR6, SPL14, SPL1R2, AT1G20980) spl17 mutant is reminiscent of osmads14, 15, 18, 34 quadruple mutant rice
barley ALOG1 (HvALOG1) is orthologous to Oryza G1 Hordeum vulgare L.; Oryza sativa
HvALOG1 being only expressed ALOG gene at LP and AP stages suggests key role in regulating SM activity and boundary establishment Hordeum vulgare
genetic redundancy among ALOG proteins is particularly important during early spike development Hordeum vulgare
genes controlling number of flowers per I2 have not been identified in legumes
pseudanthia combine hundreds of individual flowers
Asteraceae inflorescences contain hundreds of morphologically and functionally distinct flowers
genes that regulate (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) /Hd3a/RFT1/ZCN8 could be targeted to boost floret number
I2 transient meristem terminates as FM Medicago truncatula
barley plants that over-express (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) flower while regenerating from callus and bear rudimentary inflorescences with few infertile spikelets Hordeum vulgare
ZmBAD1/WAB1 regulates inflorescence or flower organ development Zea mays
meristem activity needs to be weakened to establish normal spike morphology Hordeum vulgare
primary rachis branches are initiated in spiral arrangement Oryza sativa
higher FZP expression led to lower NSB, GSB and GN Oryza sativa
OsROXY2 is expressed in leaves Oryza sativa
reduction in tassel branch numbers is enhanced with loss of one copy of (AtSIP1, RS1, SIP1, AT1G55740) Zea mays
inflorescence reversion leads back to formation of leaves and vegetative shoots Arabidopsis thaliana
OsROXY1 is expressed in stems Oryza sativa
OsROXY2 is expressed in inflorescence meristem Oryza sativa
sor1-d mutation did not restore inflorescence height phenotypes of (AtMAX2, MAX2, ORE9, PPS, AT2G42620) Arabidopsis thaliana
loose cluster architecture is correlated with elongated pedicels Vitis vinifera
photoperiod-insensitive alleles exhibit normal spike development
CArG-box mutations within the promoter region of (REM39, VRN1, AT3G18990) result in subsequent slower growth of the spikelet in short days compared with long days
F-box-domain-containing protein ABERRANT PANICLE ORGANIZATION1 (HORVU7Hr1G108970) showed reduced expression in transgenic line Hordeum vulgare
ABERRANT PANICLE ORGANIZATION1 homolog suppresses precocious conversion of inflorescence meristems to spikelet meristems Oryza sativa
pin-formed1 (ATPIN1, PIN1, AT1G73590) mutant develops pin-like inflorescences Arabidopsis thaliana
loss of a single copy of (AtSIP1, RS1, SIP1, AT1G55740) enhances tassel branch reduction phenotype Zea mays
grass (Poaceae) species have spikelet as basic unit of inflorescence
vascular bundle will form in middle of the main inflorescence Oryza sativa
Ib-TFL1 appears to be involved in maintenance of inflorescence state in axillary meristems Impatiens balsamina
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) overexpressing plants as they grew older inflorescence stalks lost apical dominance and produced numerous lateral branches with short internodes
OsROXY2 is expressed in flag leaf primordia Oryza sativa
reproductive rachis meristem produces axillary meristems until abortion Oryza sativa
rate of meristem fate transition determines whether an axillary meristem grows into higher-order branch Oryza sativa
characterization of the molecular function of the candidate genes would continue to drive understanding of the process of inflorescence development in rice Oryza sativa
indeterminate spikelets results in branched inflorescence Hordeum vulgare
branched inflorescence meristems of vrs4 spikes initiated directly from spikelet meristem Hordeum vulgare
BDI1 controls outgrowth of spikelet meristems Hordeum vulgare
(ATCOM1, ATGR1, COM1, GR1, AT3G52115) (BDI1) contributes to specification of spike inflorescence shape Hordeum vulgare
T6P has regulatory role in inflorescence architecture Zea mays
primary inflorescence meristem (IM) gives rise to primary branches Oryza sativa
impairment of MtSUP function leads to production of additional flowers Medicago truncatula
weak florigen signal results in extra spikelets or branches forming during early stages
I2 meristem marker MtFULc was detected in MtSUP mutants Medicago truncatula
inflorescence meristem (IM) gives rise to various meristems with increasing determinacy
increased branching is associated with delayed expression of genes that coordinate inflorescence development and spikelet meristem identity
early flowering photoperiod insensitive Ppd-1 alleles with high (ATFT1, ATFUT1, FT1, FUT1, MUR2, AT2G03220) expression reduce spikelet number in wheat Triticum aestivum
reduced florigen levels help increase inflorescence branching
KN1 and (AtSIP1, RS1, SIP1, AT1G55740) have similar expression patterns in tassel primordia Zea mays
OsROXY1 signal is localized in cell layers near the apex surface Oryza sativa
RICE CENTRORADIALIS 1 (RCN1) overexpression causes delayed phase transition from branch to floral meristem Oryza sativa
(STPL, WOX8, WOX9B, AT5G45980) null mutant plants did not show reproductive branching or inflorescence phenotypes Arabidopsis thaliana
loss of (CDS5, AT3G60620) reduces panicle length Oryza sativa
(TFL-1, TFL1, AT5G03840) predominance over FT results in shoot apex does not develop a normal inflorescence
s-n5568 allele suggested sequences beyond peak-2 also contribute to the control of inflorescence branching Solanum lycopersicum
evg mutants in W115 background display solitary flower phenotype
kn1 tassels have fewer branches and reduced spikelet density tassel morphology Zea mays
OsROXY1 is expressed in spikelets Oryza sativa
35S::TFL1 plants shows aerial rosette-like structures Arabidopsis thaliana
vasculature-specific expression of FT causes different phenotypic rescue responses in main inflorescence Arabidopsis thaliana
grafting 35S::FT rootstock plants to ft-10 tsf-1 tfl1-20 scion plants had different effects on inflorescence morphology in the scion plants
mutations of FZP orthologs affect inflorescence architecture Zea mays; Hordeum vulgare; Triticum aestivum; Brachypodium distachyon
tobacco FD genes overexpression results in bushy, bunch-like architecture of inflorescences Nicotiana tabacum
ft-10 soc1-2 double mutant produces normal inflorescence Arabidopsis thaliana
plants of either At (ATPIN1, PIN1, AT1G73590) allele co-expressing Mp produced near wild-type inflorescences Arabidopsis thaliana
(HB-3, STIP, WOX9, WOX9A, AT2G33880) pleiotropic vegetative and reproductive roles are conserved in Solanaceae
EVERGREEN (EVG) is WOX homeodomain protein Petunia