1 pod-2 mutant embryos also exhibit a unique germline inhe
2 ists of a central hub and six spokes, with
a pod-like structure at the terminus of each spoke.
3 ALDO pod GC-A cKO mice demonstrated increased urinary albumin
4 Beverages prepared by espresso, capsule,
and pod machines had the lowest BAs contents, as a result of
5 flowering time control, seed development
and pod dehiscence.
6 have specific roles in seed development
and pod elongation, respectively.
7 l identity alterations as well as flower
and pod abnormalities (deformed flower and pod).
8 r and pod abnormalities (deformed flower
and pod).
9 In the VDBP-GFP
and pod::NTR-mCherry double-transgenic fish, induction of po
10 m the vegetative organs including leaves
and pod walls.
11 ive error, axial length, Gullstrand lens
and pod corneal power were all significant predictive factor
12 ted to the acquisition of DT, longevity,
and pod abscission.
13 nd tomato and leaf blade, petiole, stem,
and pod tissues from soybean plants.
14 Stems, leaves
and pods were also measured.
15 s through a spring-loaded mechanism known
as pod shatter, which is essential for dispersal of the see
16 that pod-2 functions in the same pathway
as pod-1.
17 phenology, and yield-related traits such
as pod number, localized to chromosome 4.
18 es commonly cultivated in Greece, as well
as pods from four commercial cultivars from North America w
19 Bean pod mottle virus (BPMV) is a bipartite, positive-sense (
20 Bean pod mottle virus (BPMV) is one of the most important pat
21 viruses, Cowpea mosaic virus (CPMV) and
Bean pod mottle virus (BPMV).
22 irus-induced gene silencing mediated by
Bean pod mottle virus.
23 Previously, two generations of
bean pod mottle virus (BPMV; genus Comovirus) vectors have be
24 monstrate the quantitative detection of
Bean pod mottle virus, a pathogen of great agricultural impor
25 the 5' untranslated region (UTR) of the
bean pod mottle comovirus (BPMV) RNA2, and found it to be ess
26 rticle bombardment in soybean and green
bean pods.
27 o be the causative agent of necrosis of
bean pods.
28 Tn5-containing derivatives of B728a on
bean pods, 26 strains that did not form disease lesions were
29 nt, in elucidating the epidemiology of
black pod disease of cocoa in Nigeria.
30 t be caused by variations in composition,
by pods of partial melt in a mostly solid matrix or by vari
31 ysis of 77 commercial coffee samples (
coffee pods, coffee capsules, and coffee beans).
32 lar bacteria matured into biofilms,
creating pod-like bulges on the bladder surface.
33 sa, we found that epithelial cells
developed pod-like clusters of intracellular bacteria with regiona
34 data covering multiple stages of
developing pod and seed are included in the LjGEA.
35 xpressed in the hair cells of the
developing pod, the likely location of vanillin biosynthesis.
36 issues including leaves, flowers,
developing pods, mature seed and roots.
37 Tunicate1 (Tu1) is a
dominant pod corn mutation in which kernels are completely enclos
38 Here, we characterize
Drosophila pod-1 (dpod1) and show that purified Dpod1 can crosslink
39 hed their sepals, petals, and anthers
during pod expansion and maturity, and these organs frequently
40 ly when heat waves were applied during
early pod developmental stages indicates the yield loss had mo
41 we describe spectacular extremely
expanded,
pod-like tibiae in males of a platycnemidid damselfly fr
42 n that is strictly associated with
explosive pod shatter across the Brassicaceae plant family.
43 lant tissues (i.e. leaf, root, stem,
flower,
pod and seed), with a developmental time series for pods
44 , nodules, stems, petioles, leaves,
flowers,
pods and seeds.
45 r, these results reveal novel activities
for pod-1 and show that proper levels of Dpod1, an actin/MT
46 velopment of separation layers essential
for pod shatter.
47 seed), with a developmental time series
for pods and seeds.
48 ensitive, allowing us to designate this
gene pod-2.
49 watcher boat traffic of three social
groups (
pods) of killer whales (Orcinus orca) living in the near
50 equired for a-p polarity, are delocalized
in pod-1 mutant embryos.
51 leaf tissue and only marginally expressed
in pod hair cells.
52 VLX cellular and subcellular localization
in pod walls suggest independent functions for these differ
53 SGlu7 mRNA also accumulated
in pods and flower buds.
54 served six-fold symmetric features
including pods, linkers and an ATPase complex, while fT3SSs probab
55 e generated podocyte-specific Shp2
knockout (
pod-Shp2 KO) mice.
56 e cell layer in the soybean (Glycine max
L.)
pod wall.
57 erformed on total RNA from root, stem,
leaf,
pod, flower bud, and hypocotyl using DNA probes for the
58 xpression in nodulated roots, source
leaves,
pods, and seed coats.
59 The discovery of intracellular biofilm-
like pods explains how bladder infections can persist in the
60 Following administration of
LPS,
pod-Shp2 KO mice exhibited lower proteinuria and blood u
61 ur" is produced by grinding the whole
mature pod, but in the traditional process most of the seeds ar
62 howed green anthers, central carpels,
mature pods, and seeds during senescence.
63 ice with podocyte specific podocin-cre
mice (
pod-Cre), which express cre at the time of glomerular ca
64 Nox5(
pod+) mice exhibited early onset albuminuria, podocyte f
65 man Nox5 in a podocyte-specific manner (
Nox5(
pod+)).
66 Subjecting
Nox5(
pod+) mice to streptozotocin-induced diabetes further ex
67 FRUITFULL may directly allow the control
of pod shatter in oilseed crops such as canola.
68 dehiscence may allow genetic manipulation
of pod shatter in crop plants.
69 cDNA library from specialized hair cells
of pods of the orchid Vanilla planifolia.
70 The regular production
of pods in this outcrossing species (tm = 0.979) indicates
71 al composition and nutritional value of
okra pods and the common practice of harvesting okra fruit wh
72 1 fmol (0.5 pg) causing neoplastic growth
on pods of all of the pea lines tested.
73 a weevil (Bruchus pisorum L.) oviposition
on pods of specific genetic lines of pea (Pisum sativum L.)
74 urs by a process called fruit dehiscence,
or pod shatter.
75 A
pea pod cDNA library was screened for sequences specific to
76 nes relies on a fine balance between the
pea pod, capsicum character of MPs and the passion fruit/gra
77 Four food-source ExPEC isolates (from
pea pods, turkey parts, ground pork, and vegetable dip) clos
78 rix was investigated, and an interesting
pea-
pod-like segregation of Au nanoparticles in PS domains w
79 s a waste material in the process to
produce pod flour.
80 For this
purpose,
pods from four okra cultivars and local landraces common
81 Terminal drought
reduces pod yield and affected the phenolic content of leaves, s
82 er membrane-attached export platform, C-
ring/
pods and ATPase complex.
83 ential gene expression in the explosive
seed pod of C. hirsuta.
84 vestigating the molecular mechanisms of
seed pod shattering has shown that the basic helix-loop-helix
85 Transformants derived from the same
seed pod contained independent T-DNA integration events.
86 We find that the
seed pod is optimally designed to minimize the cost of fractu
87 es and is present in stems, flowers and
seed pods but absent from the root where, according to immuno
88 was suppressed in leaves, flowers, and
seed pods.
89 many cells of the seeds and developing
seed pods.
90 cts from leaves, stems, roots, flowers,
seed pods, and cell suspension cultures were obtained.
91 in young leaves, flowers, and immature
seed pods, and increases in LOX7 and LOX8 transcripts were ob
92 patterned paper containers which, like
seed pods or insect prey, must be manipulated to extract food
93 size of plant organs, including seeds,
seed pods, and leaves, through a regulatory module that targe
94 It is highly expressed in sink organs (
seed,
pod, and seed coat) and undetectable in leaves.
95 nd alanine aminotransferase level on
seventh pod resulted significantly higher in group 2, conversely
96 VLXs also are prominent proteins in
soybean pod walls, representing approximately 12% of the total s
97 The MPL of
soybean pod walls may represent a novel multicellular compartmen
98 ch is highly expressed in developing
soybean pods.
99 n podocytes, we generated podocyte-
specific (
pod) GC-A conditional KO (cKO) mice.
100 edlings and reduced branching and
subsequent pod and seed production.
101 Gallotannins obtained from
tara pod extracts (EE) and from the products of acid hydrolys
102 Genetic analyses indicate
that pod-2 functions in the same pathway as pod-1.
103 Temperature-shift studies indicate
that pod-2 is required during oogenesis, indicating that aspe
104 Here, we show
that pod corn is caused by a cis-regulatory mutation and dupl
105 Our data suggest
that pod-2 may be required to properly position an a-p polari
106 The role of sepA and
the pod genes in controlling the spatial pattern of polarize
107 inergic itch-producing spicules covering
the pod of the legume Mucuna pruriens.
108 SF and SE were quantified in
the pod of Raphanus sativus L. var. caudatus Alef extracts (
109 ecific markers for a novel cell layer in
the pod wall.
110 our laboratory discovered a mutation in
the pod-1 gene (for polarity and osmotic defective) that uni
111 These neoplasms impede larval entry into
the pod.
112 trated that after mechanical wounding of
the pod wall, 40-kD fluorescein-dextran was able to move thr
113 re visualized during glomerulogenesis of
the pod-Cre;beta1(flox/flox) mice and proteinuria is present
114 erial often pools into a bulb located on
the pod.
115 ctions and work against each other until
the pod pops open from stress.
116 elaborate interdigitated network within
the pod wall.
117 We have generated a deletion within
the pod-1 gene.
118 s the spokes and the Spa33 protein forms
the pods.
119 y intradermal insertion of spicules from
the pods of a cowhage plant (Mucuna pruriens).
120 tions in the presence of boats for all
three pods, but only in recent recordings made following a per
121 ulation and of lipoxygenase activity
through pod wall development indicates that VLXD is the principa
122 Thus,
pod-2, along with pod-1, defines a new class of C. elega
123 ally expressed in germ-line-related
tissues (
pods and seeds), suggesting that they play a significant
124 Toxicant measures were linked
to pod, age, and birth order in genotyped individuals, prey
125 hsp70 heat shock protein hybridised only
to pod mRNA from pea lines where pod lignification occurred
126 In addition,
when pod walls are cut, an exudate flows from the MPL that is
127 idised only to pod mRNA from pea lines
where pod lignification occurred.
128 Thus, pod-2, along
with pod-1, defines a new class of C. elegans polarity genes.
129 Young pods and immature seeds had very low levels of the SMT t
130 are relatively abundant in flowers and
young pods undergoing rapid growth and most abundant in elonga
131 script levels in stems, roots, leaves,
young pods, and cotyledons of the yellow and black isolines bu
132 cible model of podocyte injury in
zebrafish (
pod::NTR-mCherry) by expressing a bacterial nitroreducta