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cell growth

9607 relationships annotated with this phrase. Showing first 500 of 9607.
Source entity Relationship Target entity Species
double mutants had similar growth rates to m8-2 single mutant Phaeodactylum tricornutum
CCMP1379 shows growth rate continued to increase up to 27°C without reaching a plateau Synechococcus spp.
growth rate exhibits incremental response to changing temperature Synechococcus spp.
secreted AGPs participate in cell expansion
CAR14569 mutants showed defect in root hair growth Arabidopsis thaliana
cortical MT defects probably account for slow cell growth of mutant roots Zea mays
HSF3- overexpression lines carrying additional mutations in (MED8, AT2G03070) had significantly lower growth rates than WT and HSF3- overexpression line Phaeodactylum tricornutum
diverse arrays support different cell growth modes
ZmPME is downregulated in zmbell10-1 Zea mays L.
epidermal cell length decreased in basipetal gradient Brassica rapa
ZmAN3 might directly regulate cell expansion Zea mays
(ATEXP15, ATEXPA15, ATHEXP ALPHA 1.3, EXP15, EXPA15, AT2G03090) is downstream of (BZIP17, AT2G40950) and (BZIP28, AT3G10800)
turgor pressure and cell wall stiffness of (ATPTS, PANC, PTS, AT5G48840) offer powerful explanatory principles to explain cellular growth Arabidopsis thaliana
replenishing the media extended exponential growth phase Arabidopsis thaliana
crumpled kernel mutant (crk2) exhibits reductions in endosperm cell size Zea mays
(MED8, AT2G03070) mutants have significantly lower cell concentrations Phaeodactylum tricornutum
Atbuzz insertion line in kinase domain stimulates epidermal cell length Arabidopsis thaliana
PCC 7002 shows growth rate continued to increase up to 27°C without reaching a plateau Synechococcus spp.
microtubules are required for plant cell growth
(TGS1, AT1G45231) mutations produce reduced cell growth in mammals Mammalia
Phaeodactylum tricornutum WT had no significant differences in growth rate compared with (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) mutants Phaeodactylum tricornutum
ptATS2b knockout led to reduced growth rate Phaeodactylum tricornutum
SMT15 mRNA abundance shows nonlinear correlation with growth rate Chlamydomonas reinhardtii
cell with larger exocytic zones could grow more quickly than cell with a smaller exocytic zone if both cells had the same steady-state vesicle concentrations Physcomitrella patens
5-ml cultures grown in loosely-capped 60-ml cylindrical beakers exhibits fresh weight increase exponentially from 0 to 5 days fresh weight increase (0 to 5 days) Zea mays
(CAR9, AT1G70790) overexpression in fer-4 background partly rescued root hair growth defect Arabidopsis thaliana
(PLA2-BETA, AT2G19690) and (AT4G17140) play roles in cell elongation and division Arabidopsis thaliana
apical actin cluster predicts cell growth directions
filament length and morphology do not require (ATBARD1, BARD1, ROW1, AT1G04020) Ustilago maydis
(ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) overexpression could not compensate for growth deficits associated with (MED8, AT2G03070) mutation Phaeodactylum tricornutum
(EMB2804, TFCB, AT3G10220) is required for plant cell growth
(FER, AT3G51550) is involved in cell growth
CCMP2606 shows growth rate continued to increase up to 27°C without reaching a plateau Synechococcus spp.
defective endocytosis in RADIAL SWELLING9 (ADL1, ADL1A, AG68, DL1, DRP1A, RSW9, AT5G42080) plants results in defects in cell elongation Arabidopsis thaliana
Cell size in zmbell10-1 is smaller than in WT Zea mays L.
extent of filament bundling might correlate with cell expansion Arabidopsis thaliana
double mutants had significantly lower growth rates than WT and (ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) mutants Phaeodactylum tricornutum
ZmXYB is downregulated in zmbell10-1 Zea mays L.
membrane-bound AGPs participate in cell expansion
both ptATS2s play an essential role in algal cell growth Phaeodactylum tricornutum
ion transport is involved in cell expansion
smt15-1 pSMT15.1 line 62 shows restoration of growth to various degrees Chlamydomonas reinhardtii
larger exocytic zones could support cell growth at lower vesicle concentrations than smaller exocytic zones Physcomitrella patens
Δ (ATBARD1, BARD1, ROW1, AT1G04020) mutant strain shows no differences in cell morphology and length Ustilago maydis
(MED8, AT2G03070) mutants replicated more slowly than Phaeodactylum tricornutum WT Phaeodactylum tricornutum
T411 cells had retarded growth Chlamydomonas reinhardtii
(PARP1, AT2G31320) transcripts increased progressively during exponential growth phase Arabidopsis thaliana
areal strain rates of individual pavement cells ranged from 5.2% to 9.6% per hour Arabidopsis thaliana
C. reinhardtii cc124 (wild type) displayed reduced growth in photoautotrophic conditions Chlamydomonas reinhardtii
Synechocystis hliD/scpE single-deletion mutant affected neither cell growth Synechocystis
up-regulation of AtVRLK1 enhances cell elongation Arabidopsis thaliana
wild-type and (BADC1, BLP3, AT3G56130) (BADC3, BLP2, AT3G15690) cell cultures grew at similar rates in absence and presence of Tween 80 Arabidopsis thaliana
predicted vesicle concentrations at the shank range between ∼125 and 477 vesicles μm −3 Physcomitrella patens
specific requirement for active transport to sustain cell growth is dependent on size of the exocytic zone Physcomitrella patens
T411 line showed significantly decreased cell numbers Chlamydomonas reinhardtii
smt15-1 pSMT15.1 line 57 shows restoration of growth to various degrees Chlamydomonas reinhardtii
(BZIP17, AT2G40950) and (BZIP28, AT3G10800) double mutant exhibits impaired gene expression involved in cell growth
nuclear volume is expected to increase accordingly with increased polyploidy
GRMZM2G445169 (expansin (ATEXP4, ATEXPA4, ATHEXP ALPHA 1.6, EXPA4, XPA4, AT2G39700) ) is involved in cell expansion Zea mays
PI(3,5)P2 is required for polarized cell growth Physcomitrella patens
cerulenin treatment leads to progressive enlargement of cells Chlamydomonas
cell wall maintains outer radius R 0 and thickness d Physcomitrella patens
(ATVPS34, PI3K, VPS34, AT1G60490) KD mutants had reduced growth particularly in photoautotrophic conditions Chlamydomonas reinhardtii
VLCFA biosynthesis significantly affects cell elongation in Arabidopsis Arabidopsis thaliana
metaxylem in maize roots shows positive relationship between cell size, nuclear size, and ploidy level Zea mays
cells in long G1 phase can grow manyfold in size Chlamydomonas reinhardtii
plant cell walls control turgor-driven water uptake and cell growth
ascorbate is high and constant during period of highest relative growth rates Arabidopsis thaliana
type I ROPs mediate localized accumulation of F-actin associated with localized expansion of cell surface
smaller exocytic regions at experimentally relevant vesicle concentrations produced growth rates slower than 1 nm s −1 Physcomitrella patens
diluting the cultures resulted in large increase in exponential growth compared to normal growth cycle Arabidopsis thaliana
cell wall elongates at a rate of growth rate Physcomitrella patens
Areal strain rates were comparable to previously reported rates for pavement cells at early growth stages Arabidopsis thaliana
Al toxicity primarily affects cell elongation
actin and ROPs have roles in polarized cell growth
balance between AI cell growth and progression toward aposporous female gametophyte formation needs to be linked to turgor driven cell wall extension Hieracium spp.
AtSAUR19 promotes cell expansion
growth curves were the same whether cells were grown in dark or light light and dark growth conditions Arabidopsis thaliana
(ADF9, AT4G34970) exhibit strongest expression in fast-growing tissues Arabidopsis thaliana
pavement cells with higher ploidy had increased cell size Phaseolus vulgaris
diffusion cannot sustain cell growth at estimated lower bound vesicle concentrations Physcomitrella patens
analytical model predicts growth at 5 ± 2.9 nm s −1 Physcomitrella patens
large exocytic regions and experimentally measured vesicle concentrations diffusion alone could lead to cell growth rates slightly slower than 2 nm s −1 Physcomitrella patens
upper limit of exocytosis zone size illustrates that without F-actin, diffusion-based cell growth could never achieve growth rates greater than 2 nm s −1 Physcomitrella patens
largest EBC located on flower bud had nuclei diameter of close to 136 μm Mesembryanthemum crystallinum
(BZIP17, AT2G40950) and (BZIP28, AT3G10800) function together to mediate noninducible expression of multiple genes involved in cell growth Arabidopsis thaliana
optical density at 595 nm is used to determine growth cycle of cultures
root bending, waving or coiling results from asymmetric cell elongation Arabidopsis thaliana
predicted growth rate at measured vesicle concentrations is similar to normal growth Physcomitrella patens
ZmBELL10 has critical roles in regulating cell division and cell elongation Zea mays L.
plasma membrane (PM) H+-ATPase plays regulatory roles in cell expansion Arabidopsis thaliana
T1B3 and T411 lines showed altered growth patterns Chlamydomonas reinhardtii
apex or apical dome is growth region
introduction of Pro residue at position 119 in (ATTPS1, TPS1, AT1G78580) did not compromise yeast growth Saccharomyces cerevisiae
G2/M arrest is associated with size expansion Arabidopsis thaliana
CrRLK1L mutants revealed role during polarized growth Arabidopsis thaliana
turgor-driven wall extension increases cell volume
primary cell wall allows expansion growth
overexpression of xyloglucanase enhanced growth by increasing cell size Populus
growing apices of these cells are often at significant distance from nucleus
downstream targets of PHYTOCHROME INTERACTING FACTOR 4 (AtPIF4, PIF4, SRL2, AT2G43010) trigger cellular growth Arabidopsis thaliana
brassinolide (BL) promotes cell expansion
mRNA level of Lhcb is associated with cell size Arabidopsis thaliana
cell wall biogenesis is involved in cell expansion
cellulose deficient mutants exhibit reduced cell division
(AtXTH22, TCH4, XTH22, AT5G57560) plays key role in cell elongation
cell turgor drives cell expansion Arabidopsis thaliana
FERONIA is required for cell elongation Arabidopsis thaliana
antibiotic treatment did not affect culture growth Arabidopsis thaliana
higher trans-zeatin concentrations in actively growing fruits promotes cell expansion Solanum lycopersicum
restoration of plant size in heterologously expressed plants is due to corresponding increase in cell size Arabidopsis thaliana
final length of the style depends on cell wall properties Petunia
epidermal cell length in 4KOR-XI-2pro plants is approximately 1.7-fold greater than epidermal cell length in 4KO Arabidopsis thaliana
(ARK3, AtKINUa, PAK, AT1G12430) choi reciprocal F1 hybrids (WQ, WTC × 2Q and QW, 2Q × WTC) have increased cell size Brassica rapa subsp. chinensis
AMPK is implicated in regulation of genes involved in cell growth Mammalia
reactive oxygen species (ROS) could affect cell elongation
H12 cell walls present a strong reduction in cellulose (more than 60%) during active growing phase Zea mays
cell size in OsMED14_1 RNAi culms is reduced to 63% compared with wild-type Oryza sativa
knockout lines have inhibited cell elongation in gametophore stems Physcomitrella patens
final length of the style depends on growth rate Petunia
(APD1, AT4G13040) has been implicated in cell expansion
azidohomoalanine (Aha) causes greater inhibition of cell growth rate Arabidopsis thaliana
endoreduplication permits cell enlargement
(PPAN, SNAIL1, AT5G61770) SKO lines have significantly shorter cell length Physcomitrella patens
habituated cells showed growing in clumps
FERONIA regulates cell expansion Arabidopsis thaliana
actively growing cells in elongation region are those in which newly formed cells are quickly expanding and accelerate maturation of organelles
50 mutant genes are involved in cell growth Arabidopsis thaliana
ES7 (endosidin 7) did not provoke inhibition of yeast cell growth Saccharomyces cerevisiae
(ATEXP8, ATEXPA8, ATHEXP ALPHA 1.11, EXP8, EXPA8, AT2G40610) is downstream of (BZIP17, AT2G40950) and (BZIP28, AT3G10800)
water uptake results in cell volume increase
variable cellular growth rates combined with imprecision of cell divisions would be expected to increase variability in cell sizes
geometric structure and constraint have large influence on ability of individual cell to grow
cell wall elasticity contributes to growth heterogeneity Arabidopsis thaliana
cortical array has important role in determining direction of cell and organ growth
71 GO terms overrepresented in unique-to-GPWAS gene set included cell growth Zea mays
cellulose microfibrils are determinants of growth anisotropy
plant cell growth is diffuse growth or tip growth
passive microfibril reorientation in the direction of growth anisotropy may help to determine final cell size
lower PG content in oxPAP cells might inhibit cellular growth under LC Synechocystis
female gametophyte provides traceable model system to study mechanisms controlling cell growth, cell division, cell fate, pattern formation Arabidopsis thaliana
ROS may regulate cell elongation
cell growth influenced by cell's context within organ and tissue Arabidopsis thaliana
phosphoinositide and phospholipid signals regulate growth
thaxtomin A inhibits normal cell elongation Nicotiana tabacum
polyamine oxidase (PAO) activity formerly related to cell elongation in roots and hypocotyls Glycine max
reduced phosphatidylglycerol (PG) content in oxPAP cells under ambient air (LC) causes retarded cellular growth Synechocystis sp. PCC 6803
reactive oxygen species (ROS) accumulation in (SCR, SGR1, AT3G54220) mutant results in reduced mitotic activity and shorter cells
CsubMADS1 OX cultures grow more slowly than WT cultures Coccomyxa subellipsoidea
HPG-treated cells showed less severe decrease in growth rate Arabidopsis thaliana
Sll0545 is essential for growth Synechocystis
inactivation of Dw3 reduces cell elongation Sorghum bicolor
5-ml cultures grown in loosely-capped 60-ml cylindrical beakers exhibits fresh weight increase linearly from 5 to 7 days fresh weight increase (5 to 7 days) Zea mays
trichoblasts combine diffusive expansion and polar growth
cylindrical state is initially generated by tip growth Ectocarpus
root growth consists of cell elongation
geometric structure and constraint have large influence on growth direction
actin filaments position endomembrane system
cells must receive accurate decisions for growth axis determination
cell turgor drives cell expansion and elongation
AO expression is high in expanding tissues
GLOBOSA2 (GLOT) stimulates cell elongation in the petal tube Primula
rapidly expanding cells have hydrostatic pressure reaching 5–10 MPa
cell wall loosening triggers vacuolar expansion
cell elongation occurs in direction perpendicular to alignment of cortical microtubules
Rubisco G404A mutant does not reduce growth rate under saturating irradiance and Ci Synechocystis PCC6803
(ABA2, ATABA2, ATSDR1, GIN1, ISI4, SDR1, SIS4, SRE1, AT1G52340) mutant improves root growth in shr and scr mutant backgrounds by enhancing cell elongation Arabidopsis thaliana
DYM internodes have similar maximum cell length Sorghum bicolor
XXXG integration into wall xyloglucan affects cell expansion
wall loosening accelerated by addition of XXXG promoted cell expansion Nicotiana tabacum
cells at the convex side are significantly longer than cells at the concave side Arabidopsis thaliana
Arabidopsis hybrids have increased cell size Arabidopsis thaliana
cells widening causes large, square faces bulge out Cardamine hirsuta
TsSPH1 promotes cell elongation Turnera subulata
vacuolar expansion represents additional strategy for plant cells to increase size without altering cytoplasmic or nuclear density
cell wall loosening enables water entry
hydrated gels ease sideway slippage of microfibrils during cell growth
yielding of cell walls ran ahead of water entry Zea mays
(ATXTH14, XTH14, XTR9, AT4G25820) (30 ng μl −1) treatment clearly impaired cell elongation Arabidopsis thaliana
mature root cortical cells show similar cell length at 4°C and 23°C treatment Arabidopsis thaliana
plant SNAREs function as molecular governors to coordinate cell expansion
rhizoid has limited growth Dictyota
vacuolar expansion drives rapid cell enlargement
vacuolar expansion allows rapid cell enlargement decoupled from transcriptional scaling
rigid walls constrain expansion
aluminium prevented increase in fresh weight in ALT301 cell line Nicotiana tabacum
deficiency of (ATTOP6B, BIN3, HLQ, HYP6, RHL3, TOP6B, AT3G20780) results in general growth defect Arabidopsis thaliana
atx1-1 mutant has abnormally large cells located near longitudinal boundaries of lateral root primordium (LRP) Arabidopsis thaliana
vacuolar expansion allows rapid cell enlargement decoupled from transcriptional scaling
volume changes of xylem and phloem tissue are dependent on irreversible turgor-driven growth Quercus robur L.; Fagus sylvatica L.
high concentrations of brefeldin A (BFA) lead to growth arrest of cells
coniferyl alcohol addition to growth medium decreased growth rates of YMM12 and wild-type and YMM12 expressing (ABCG29, AtABCG29, ATPDR1, PDR1, AT3G16340) Saccharomyces cerevisiae
organ swelling may result from interfering with diffuse growth Arabidopsis thaliana
dwarf phenotype is due to reduced cell elongation
auxin promotes elongation
TsSPH1 promotes endoreduplication Turnera subulata
polyploidization is associated with increased cell size
oxidative damage in zone I affects cell integrity and elongation
mechanism by which AO activity modulates cell growth may involve changes in apoplastic pool of oxidized ascorbate
non-adapted calli grew exponentially with specific growth rate (μ max) of 0.169 d −1
uptake of water increases cell volume
rapid cell enlargement without proportional increases in cytoplasmic or nuclear content reduces biosynthetic costs
50 μM CdSO4 treatment results in typical cell elongation Nicotiana tabacum
reduced height in SlTPR1 overexpression lines was related to smaller cell sizes Solanum lycopersicum
CsubMADS1 OX cells mimic cells of lag phase Coccomyxa subellipsoidea
actin filaments help to direct delivery of secreted wall material and membranes to sites of cell growth
RNAi plants of PpAGP1 resulted in cell length reduction Physcomitrella patens
pollen tube growth is strongly correlated with cell volume status
cell expansion increases cell size
recombinant and purified XTHs exhibit clear effect on cell elongation Arabidopsis thaliana
actin microfilaments undergo dynamic changes during cell elongation
plant cell wall is flexible to allow cell growth
microtubules contributes to growth heterogeneity Arabidopsis thaliana
present study aimed to determine how membrane dynamics are co-ordinated during growth
actin gene (Os01g64630) is down-regulated by arsenate treatment Oryza sativa
apoplastic ROS (aROS) activation of Ca2+-permeable non-selective cation channels (NSCCs) stimulates growth of Arabidopsis thaliana roots and pollen tubes Arabidopsis thaliana
pollen tube growth is strongly correlated with hydrodynamic flux
plant cell walls regulates cell growth
osmotic phase delays cell elongation
chloroplast number has been linked to cell volume
p-coumaryl alcohol exposure strongly retarded growth of YMM12 mutant Saccharomyces cerevisiae
turgor pressure equal within tissue could allow tissue tension combined with locally softer cell wall to explain swelling of young trichome cells
transmembrane conductivity partially limits growth Arabidopsis thaliana
Cell wall yielding results in growth Arabidopsis thaliana; Solanum lycopersicum
shade avoidance syndrome (SAS) and thermomorphogenesis promote cell elongation
retardation of root hair initiation and failed root hair growth leads to longer epidermal cells and roots
Ca2+ is implicated in regulating cell elongation
Ins(3,4,5,6)P4 affects pollen tube growth
hydrodynamic flow and apical volume increase–decrease could drive pollen tube growth
E. coli R832G mutant PEPC complements glutamate-requiring phenotype of E. coli F15 Escherichia coli
untreated control cells elongate during 36 h cultivation Nicotiana tabacum
different signals are thought to modulate organ growth through adjusting cell proliferation and cell expansion
Qa-SNARE syntaxin of plants 121 (AT-SYR1, ATSYP121, ATSYR1, PEN1, SYP121, SYR1, AT3G11820) plays critical roles in polarized cell growth
untreated cultures show continued increases in fresh weight Nicotiana tabacum
endoreplication increases ploidy level and cell size Arabidopsis thaliana
MsRBR and phospho-MsRBR proteins show reduced amounts in cells during the stationary phase of growth Medicago sativa
Aluminium treatment (50 μM) inhibits increase in fresh weight Nicotiana tabacum
expansin genes (Os01g14660, Os04g46650) are down-regulated by arsenate treatment Oryza sativa
tip growth is actin-dependent pollen tubes
cellulose microfibrils (CMFs) is likely to be main regulator of cell growth and orientation
Ljinv1-2 mutant leaves have enlarged cells Lotus japonicus
indole-3-acetic acid (IAA) plays essential role in cell elongation
(ARF5, IAA24, MP, AT1G19850) and (ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) function synergistically in cell expansion Arabidopsis thaliana
PME activity leads to reduced cell growth
cell wall loosening is required for cell elongation
length of bundle sheath (BS) cells increases approximately 2-fold width of BS cells Cleome angustifolia; Cleome gynandra
relative growth of strains AtTSPO-6×His and 6×His-AtTSPO was substantially reduced compared with EV control Saccharomyces cerevisiae
1-NOA results in increased cell elongation Nicotiana tabacum
pattern of cortical microtubules directs cell expansion
cell volume in the apical region oscillates with the same frequency as growth rate oscillations
higher doses of ancymidol completely inhibit cell elongation Nicotiana tabacum
indole-3-acetic acid (IAA) promotes cell elongation
pollen tubes have extremely rapid growth rates
epidermal cells of seed coat grow by vacuolar expansion Arabidopsis thaliana
reduced or aberrantly patterned cell growth in many tissues is feature of SCAR and (ARP2, ATARP2, WRM, AT3G27000) /3 complex mutant phenotypes Arabidopsis thaliana
studies on RALFs have been primarily conducted on tip-growing cells
cell expansion is associated with cortical array
gibberellin (GA) controls cell elongation Arabidopsis thaliana
PDGmax of midline epidermal cells showed stereotyped longitudinal orientation parallel to the long axis of the leaf Arabidopsis thaliana
higher turgor pressure in trichome causes cell to swell
stalling division failed to invert the growth trend in the model Arabidopsis thaliana
endoreplication is crucial process that maintains cellular and physiological functions
PMEI5oe plants have reduced cell elongation
pollen tubes are fastest growing eukaryotic cells
maize R894G mutant PEPC complemented slightly glutamate-requiring phenotype of E. coli F15 Zea mays; Escherichia coli
sweetening during active growth could influence rate of cell growth in perennial organ
dark-grown hypocotyls undergo growth predominantly by axial cell elongation Arabidopsis thaliana
ROS production is involved in regulating cell expansion
overexpression of ptATS2b in the ptATS2a mutants could partly restore algal cell growth Phaeodactylum tricornutum
Cell growth (GO:0016049) is conserved among upregulated genes at all four time points in meristem Hordeum vulgare
Differentially expressed genes in zmbell10-1 include genes corresponding to cell growth and differentiation Zea mays L.
bundle status of the actin array does not directly correlate with growth Arabidopsis thaliana
aluminium similarly inhibited fresh weight gain on all three carbon sources Nicotiana tabacum
bundle sheath (BS) as a whole enlarged because of additional cell division allows individual cells within it to remain the same size or be smaller
BR downregulation of CLASP does not affect cell elongation
as2-163 does not display higher growth anisotropy than Col-0 in basal blade/midrib region in individual time intervals Arabidopsis thaliana
average xylem cell area increased only very slowly over time time Arabidopsis thaliana
formin family proteins have been implicated in regulation of polarized cell growth
manipulation of pollen tube apical volume and membrane remodelling defined boundary of the growth zone
cell polarization and asymmetry occur in yeast, embryos, fungal hyphae, neurons, root hair cells, and pollen tubes
ZmMXAF is downregulated in zmbell10-1 Zea mays L.
SA reduces cell size Arabidopsis thaliana
growth is the dominant regulator of cell expansion
M1 strain shows moderately reduced growth Chlamydomonas reinhardtii
M1 strain exhibits slow growth in the dark phenotype Chlamydomonas reinhardtii
pollen tubes have cytoplasm organized into apical dome, subapical region, and tubular shank region
proximal meristem (PM) cells begin irreversible post-mitotic growth
bundle sheath (BS) cells of C3 Arabidopsis thaliana undergo significant endoreduplication but are small compared with bundle sheath (BS) cells of C4 Camelina gynandra Arabidopsis thaliana; Camelina gynandra
individual bundle sheath (BS) cell area was not larger than mesophyll (M) cell area Zea mays; Festuca trinervia; Setaria viridis
Cells in bb-1 petals begin to enlarge later than wild-type petal cells Arabidopsis thaliana
endoreplication is frequently correlated with increase in cell size Arabidopsis thaliana
cell-wall loosening is required for elongation growth
additional ethylene provision under salinity did not have effect on cell filling
oryzalin-treated SAMs have fewer-neighbored and small cells that grew slower Arabidopsis thaliana
smaller cells expand more than larger cells in untreated SAMs Arabidopsis thaliana
two regimes occur whatever the value of α a Arabidopsis thaliana
individual cell growth anisotropy monitored role of cell growth anisotropy Arabidopsis thaliana
post-proliferative phase is coupled with increase in cell size
parenchyma cells in mutants were larger than in wild-type (WT) Marchantia polymorpha
plant cells must undergo irreversible expansion of cell wall in response to turgor pressure
early root hair initiation and elongation leads to early completion of H cell growth in the anticlinal direction
osmotic drive θ is sufficiently large Arabidopsis thaliana
larger, elongated apertures primarily contribute to expansion latitudinally Arabidopsis thaliana
vip4-4 sepals adaxial cells exhibited 1.14-fold faster growth than vip4-4 sepals abaxial cells Arabidopsis thaliana
stress-related hormones reflect broader role involving inhibition of cell expansion Zea mays
auxin stimulates cell elongation
small stomatal lineage cells in lateral areas could more than double their size during 17 hr imaging period Arabidopsis thaliana
seed phenotype correlates with cell elongation alteration Arabidopsis thaliana
increase in nuclear DNA content is not always linked to larger cells Arabidopsis thaliana
inducible dominant negative mutant seedlings are defective in cell expansion Arabidopsis thaliana
reactive oxygen species (ROS) in radicle has been linked to cell elongation Helianthus annuus; Arabidopsis thaliana
estimates of ATP and NADPH costs of maintenance may be interpreted in terms of growth characteristics of cell line under three conditions Arabidopsis thaliana
cellulose synthase-microtubule coupling underlying directional growth Arabidopsis thaliana
smt15-1 pSMT15.1 line 64 shows rescue to near wild-type growth rate Chlamydomonas reinhardtii
actin cytoskeleton has central role in cell growth
previous studies have provided observations supporting acid growth model
(BADC1, BLP3, AT3G56130) (BADC3, BLP2, AT3G15690) cell suspension cultures exhibit normal growth compared with wild-type cultures Arabidopsis thaliana
width of epidermal cells in ABI1oe inflorescence stems was reduced by 27% relative to wild type Arabidopsis thaliana
predicted maximum growth rate without F-actin is significantly less than 5.5 ± 0.4 nm s −1 observed experimentally Physcomitrella patens
critical MC size of about 300 μm³ is obtained after 4 h in the light Chlamydomonas
domain length increase rate was lower than rate of increase in cell perimeter
reconstruction of the cell wall modulates cell expansion
pollen grain hydration is characterized by isotropic nature of expansion
polarized pectin deposition is important for regulating cell elongation
triple and quadruple mutants of Arabidopsis class XI myosins exhibited defects in diffuse growth Arabidopsis thaliana
type I ROPs function in polarized cell expansion
balance between AI cell growth and progression toward aposporous female gametophyte formation needs to be linked to cytoplasmic growth supported by macromolecular synthesis Hieracium spp.
ploidy level difference is correlated with increased size of EBC from lower peels relative to upper peels Mesembryanthemum crystallinum
increased genomic content and gene dosage effects can lead to larger cells
conditional suppression of two A622 copies via RNAi in Nicotiana tabacum hairy roots resulted in cell growth inhibition Nicotiana tabacum
extent of polar filament accumulation is positively correlated with rate of axial cell expansion Arabidopsis thaliana
LTR sequences of active LTR-REs were enriched with cis-elements associated with cell growth Phyllostachys edulis
endoreplication has been associated with rate of cellular growth
K+ transport assists cell growth
plastic deformation due to irreversible cell growth is formulated by irreversible increase of preferred area A0 Arabidopsis thaliana
(CDF5, AT1G69570) has role in promotion of cell elongation under inductive growth condition of (SDS, AT1G14750) Arabidopsis thaliana
variations of P Y are negligible when θ > θ T Arabidopsis thaliana
cells grow exponentially by plastic deformation Arabidopsis thaliana
correlation between ploidy, nuclear DNA content and cell size has been reported in Arabidopsis and many other plant species
correlation between ploidy, nuclear DNA content and cell size was also seen in tetraploid rice plant generated by CDKB2;1 inducible knockdown
cells in drop tests were first grown in SD-Ura medium to log phase Saccharomyces cerevisiae
lack of B results in inhibition of cell elongation
cell expansion is controlled by turgor pressure and wall relaxation
purely mechanical effect could involve expanding phloem cells might force growth upon neighboring cell files
threshold value θ T increases with increasing α a Arabidopsis thaliana
(PMEI5, AT2G31430) overexpression line (PMEI5oe) has reduced cell expansion Arabidopsis thaliana
cell growth anisotropy degree (GAD) is produced using principal directions of growth (PDGs) analysis in MGX Arabidopsis thaliana
(CDF5, AT1G69570) promotes cell elongation Arabidopsis thaliana
growth trend is sensitive to the balance between water flux and wall expansion Arabidopsis thaliana
additional ethylene provision under salinity could only have a subsequent negative effect on cell elongation
cell volumes in the floral meristem of wild-type and jag-1 mutant ranged from approximately 100 to 200 μm³ meristem cells
parallel arrays of cortical MTs affect signal-dependent cell elongation
Rho GTPase regulation of katanin-based MT-detachment regulates plant cell elongation
G is dominated by the variations of P Y Arabidopsis thaliana
as2-163;RCOg-V displays higher growth anisotropy than Col-0 in basal blade/midrib region in individual time intervals Arabidopsis thaliana
WT sepals adaxial cells and abaxial cells grew at similar rates adaxial and abaxial cell growth rates Arabidopsis thaliana
N_pos in wild-type decreased rapidly before trichome bulged out
negative-to-positive slope change of local growth heterogeneity captures a strong qualitative inversion of growth behavior Arabidopsis thaliana
some parameter sets predict negative correlation between growth rate and cell neighbor number Arabidopsis thaliana
RCO and KNOX1 act synergistically to elevate growth anisotropy Arabidopsis thaliana
proximal address may be held at fixed length
increasing osmotic pressure failed to invert the growth trend in the model Arabidopsis thaliana
quadrupling wall thickness can robustly trigger growth trend inversion Arabidopsis thaliana
cell expansion is often associated with endoreplication
protrusion-base cells in as2-163;RCOg-V show reduced growth along lateral direction relative to protrusion tip-base proximal-distal (PD) axis Arabidopsis thaliana
tubulin participates in polarity of growth
F302C, I447F and I287V variants showed similar growth rates to wild type Saccharomyces cerevisiae
light exposure increases cell volume Chlamydomonas reinhardtii
OspPLAII η overexpression suppresses cell elongation Oryza sativa
tubulin genes are associated with cell elongation
A0,max for PSE, PSE-LN and procambial cells was set to 100 μm^2 Arabidopsis thaliana
stress and strain are homogeneous when water movement is limiting for growth
irreversible expansion of cell wall in response to turgor pressure depends on cell-wall loosening
sinus cells in as2-163;RCOg-V grow with higher anisotropy compared to RCOg-V Arabidopsis thaliana
Catharantus roseus RLK1-like (Cr RLK1L) kinases are involved in polar growth
endoreplication has not been associated with growth anisotropy
proximal address does not have fixed size
korrigan1 mutant has increased cell expansion Arabidopsis thaliana
delay of (RSL4, AT1G27740) protein accumulation in H cells conferred by LRH is necessary for determination of the final length of the epidermal cells
endoreduplication is associated with increase in cell size
B2RNAiID-1 leaves show files of epidermal cells that are wider than those of wild-type
induced pET-28a-orf182-transformed cells showed significantly repressed growth Escherichia coli
expression of AtRbohH or -J under control of (ATRBOHC, RBOHC, RHD2, AT5G51060) cis-regulatory sequences did not fully complement root hair defects of (ATRBOHC, RBOHC, RHD2, AT5G51060) -5 mutant Arabidopsis thaliana
ubiquitination is involved in growth
oryzalin permits continuous, isotropic growth Arabidopsis thaliana
maximal growth directions of protrusion-base cells in as2-163;RCOg-V are unified toward leaflet tips Arabidopsis thaliana
Capsella hirsuta stm-1 mutants display more isotropic cell shape in sinuses and lobe bases Capsella hirsuta
guard cells in B2RNAiID-1 leaves were significantly larger
cytoskeleton governs cell growth
actin-filament bundles serve as tracks for polarized cell growth
DELLA-dependent modulation of ROS accumulation contributes to GA-mediated cell elongation Arabidopsis thaliana
cell length in pifqCDF5OX partially recovered in pifqCDF5OX compared to pifq Arabidopsis thaliana
cellular growth rate anticorrelates with cell size Arabidopsis thaliana
xyloglucan oligosaccharide (XXXG) accelerates cell division Nicotiana tabacum
(LRX2, AT1G62440) plays key role in cell elongation
auxin regulates cell expansion
trend in oryzalin-treated meristems corresponds to when θ is smaller than threshold θ T Arabidopsis thaliana
cell growth in rachises of wild-type Capsella hirsuta is highly anisotropic Capsella hirsuta
eob2-3 LofTAD petal limb epidermal cells were smaller wild-type petal limb epidermal cells Petunia axillaris
ptATS2a mutant shows similar growth and N consumption to wild-type (WT) in static cultures Phaeodactylum tricornutum
diffusion can easily support growth at upper bound estimate vesicle concentrations Physcomitrella patens
(ATRAPTOR1B, RAPTOR1, RAPTOR1B, AT3G08850) cells have defect in cell elongation Arabidopsis thaliana
cells lacking Sey1p grow normally normal growth Saccharomyces cerevisiae
HSF3- overexpression lines carrying additional mutations in (MED8, AT2G03070) had similar growth rates to (MED8, AT2G03070) single mutants Phaeodactylum tricornutum
strong and spatially graded expression differences not observed for expansins
fastest rates of cell elongation in plants occur after termination of cell division
(ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) might have no effect on growth of Phaeodactylum tricornutum Phaeodactylum tricornutum
CCMP1630 shows growth rate continued to increase up to 27°C without reaching a plateau Synechococcus spp.
(EMB2804, TFCB, AT3G10220) is required for cell growth
cell size homeostasis would be absent in oryzalin-treated SAMs Arabidopsis thaliana
α a is not too large Arabidopsis thaliana
fewer-neighbored and smaller cells grow faster Arabidopsis thaliana
epidermal cells in as2-163;RCOg-V petiolules form files and elongate toward tip Arabidopsis thaliana
bands of cellulose around the cell's short axis promote axial growth
cell size has a positive relationship with nuclear size and ploidy level
FERONIA (FER, AT3G51550) and rapid alkalinization factors (RALFs) functions as regulator of cell growth
pectin methylesterase (PME) affects cell elongation Zea mays L.
knockdown FERONIA mutants have limited capacity for cell expansion
plant pollen tubes are examples of polarized growth
cortical microtubules (MTs) exhibited highly aligned arrays transversely to direction of cell elongation Arabidopsis thaliana
ptATS2b mutant shows similar growth and N consumption to wild-type (WT) in static cultures Phaeodactylum tricornutum
cell wall matrix limits cell expansion
fer-4 mutant showed defect in epidermal cell growth Arabidopsis thaliana
moss protonemata are type of cell driven by tip growth
apical actin cluster is generated near cell apex
BUZZ represses elemental elongation Brachypodium distachyon
ZmBELL10 promotes cell elongation Zea mays L.
CP-depleted cells are significantly longer Arabidopsis thaliana
(ATBARD1, BARD1, ROW1, AT1G04020) accumulates at sites of active growth Ustilago maydis
CCMP841 has maximum growth rate temperature of ND (not determined) Synechococcus spp.
Epidermal cell size in zmbell10-1 is significantly decreased in zmbell10-1 compared to WT Zea mays L.
loss of (ADF4, ATADF4, AT5G59890) leads to enhanced hypocotyl cell elongation Arabidopsis thaliana
CCMP841 grew very slowly at 15°C Synechococcus spp.
SCARECROW-LIKE28 (At-SCL28, SCL28, AT5G18810) controls cell expansion Arabidopsis thaliana
cells in the elongation zone at 24–48 hr after induction of RAB-A5c[N125I] expression showed most pronounced abnormal expansion
MyoXI-4KO mutant suffers defects in cell elongation Arabidopsis thaliana
water-generated turgor pressure is driving force for expansion of plant cells
hydrogen peroxide (H2O2) is involved in cell elongation Arabidopsis thaliana
introduction of (REM11, VAL, AT5G60140) residue at position 119 in (ATTPS1, TPS1, AT1G78580) did not compromise yeast growth Saccharomyces cerevisiae
(TOR, AT1G50030) (target of rapamycin) pathway acts as key element in cell growth control
biogenesis can be evenly distributed within cells whose growth relies on global expansion
fungal hyphae are examples of polarized growth
overexpression of ptATS2a in the ptATS2b mutants could partly restore algal cell growth Phaeodactylum tricornutum
greater shoot sizes in HA–TWD1-Ct lines are caused by enhanced cell elongation
pyrophosphate degradation gives thermodynamic impulse to cell growth
ROP proteins play roles in tip growth Arabidopsis thaliana
cells growing at 34°C showed monophasic peak of increasing cell size between 0 and 10 h Chlamydomonas
apoplast acidification is vital for plant cell elongation
growth speed for vascular cells was set to 200 μm^2 per tissue growth period Arabidopsis thaliana
cell size homeostasis may contribute to smaller cells expanding more than larger cells Arabidopsis thaliana
model retrieves untreated SAM trends if transmembrane conductivity partially limits growth Arabidopsis thaliana
doubling and quadrupling wall thickness inverted the correlation of growth rate to neighbor number and cell size Arabidopsis thaliana
accumulated wall stress is relaxed by wall yielding (growth) with extensibility as the rate limit Arabidopsis thaliana
related LBDs may regulate cambial development by promoting cell growth Populus trichocarpa
Phosphatidylinositolphosphates (PIPs) have functions during polarized cell growth
median cell size in the meristem decreased in response to JAG activation
ratio of osmotic pressure to yield pressure; θ = Δ Π / P Y determines growth trend Arabidopsis thaliana
real-time dynamics of F-actin and MT in the apical cell would reveal driving forces of nuclear retention and radial cell expansion
M3 strain shows no detectable growth phenotype Chlamydomonas reinhardtii
transcriptional modules defined from genes showing opposite gene expression patterns during S3 and S5 stages included regulatory gene circuits (TFs–regulatory motifs–target genes) involved in cell size/growth Cicer arietinum
rapamycin-treated cells showed 11.2% decreased maximum mean cell volume (MCV) Chlamydomonas
endoreduplication is probably involved in cell expansion
genes encoding arabinogalactan proteins and peptides (AGPs) clearly stood out robust, comparatively high expression in bri T-RESCUE tissues compared with the bri TRIPLE mutant
strong correlation between brassinosteroid-dependent root cell morphology and the expression of AGPs matching biological role of AGPs in cellular growth
(TOR, AT1G50030) controls cellular growth Chlamydomonas
(ATRBOHC, RBOHC, RHD2, AT5G51060) -H and -J are required continuously at tip of growing root hair or pollen tube Arabidopsis thaliana
fresh weight of aluminium-treated cultures remained almost constant after 3 h of treatment Nicotiana tabacum
endoreduplication is coupled with cell elongation
superoxide radical (O2•–) accumulation is suggested to play a role in cell elongation
growth is defined as increase in predominantly cytoplasmic mass
plants expressing RAB-A5c[N125I] showed increased radial expansion
external cytokinin (CK) changes epidermal cell length Arabidopsis thaliana
S112R and L441P variants grew slower than wild type Saccharomyces cerevisiae
prolonged incubation of cells in presence of 4 mm hexan-1-ol resulted in complete inhibition of growth of Synechocystis Synechocystis
cell growth may recover from disruption from (ATRBR1, RB, RB1, RBR, RBR1, AT3G12280) suppression Arabidopsis
cell wall restricts cell expansion
bri T-RESCUE roots have essentially normal morphology of their mature cells
turgor pressure is uniform and isotropic Arabidopsis thaliana
(AGC1.5, AT3G12690) subfamily kinases are specifically expressed in tip-growing cells Arabidopsis thaliana
(TOR, AT1G50030) (target of rapamycin) controls cell growth by promoting anabolic processes, including translation, ribosome biogenesis, and transcription
α a compares balance of growth control by transmembrane water conductivity and by cell wall extensibility
higher turgor pressure associates with either faster or slower growth, depending on conditions Arabidopsis thaliana
G follows the prefactor Arabidopsis thaliana
cell length measurement is used to calculate cell elongation rate Arabidopsis thaliana
Met promotes cell growth in mammalian cells
15N-treated cells showed no effect on growth rate Arabidopsis thaliana
vacuolar function might be coordinated with overall macromolecular synthesis
growth rate (biomass accumulation) is cell culture growth parameter Arabidopsis thaliana
AHA, HPG and 15N were examined for effects on cell culture growth Arabidopsis thaliana
DDYM internodes have similar maximum cell length Sorghum bicolor
control cells grown under HC grew at doubling time of 10.1 ± 0.8 h Synechocystis
cell size is used in cell expansion
genes associated with cell tip growth are among over-represented groups among up-regulated genes Arabidopsis thaliana
Chlamydomonas strain CC-125 shows optimal growth pattern similar to Chlamydomonas strain CC-5152 Chlamydomonas reinhardtii
cell growth in roots of S. parvula is not strongly inhibited by salt treatment due, in part, to transcriptomic reprogramming Schrenkiella parvula
(ATHSF3, ATHSFA1B, HSF3, HSFA1B, AT5G16820) overexpression did not affect Phaeodactylum tricornutum growth Phaeodactylum tricornutum
CCMP1632 did not grow at 15°C and 27°C Synechococcus spp.
expansin (EXP) was found from noncanonical genes Arabidopsis thaliana
knock-out of aquaporin-like gene in Synechococcus sp. PCC7942 caused inhibition of cell growth Synechococcus sp. PCC7942
epidermal cell length in 4KOR-XI-Kpro plants is approximately 2.0-fold greater than epidermal cell length in 4KO Arabidopsis thaliana