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1 cord, and of structural coloration in fossil integument.
2 ity to accumulate dietary carotenoids in the integument.
3  often impeded polarized growth of the outer integument.
4 guments, or an apparently intermediate bifid integument.
5 espectively form dermis and epidermis of the integument.
6 ster of genes involved in development of the integument.
7 ion and asymmetric growth of the ovule outer integument.
8 ium in the cells that give rise to the outer integument.
9 ing epithelium that is part of a provisional integument.
10 hin the parenchyma cell layer underlying the integument.
11 mbs, which unfortunately lacks any preserved integument.
12 ally in lip and foot regions of the anterior integument.
13 onstrate that sea urchin larvae have a leaky integument.
14 ed only limited numbers of osteoderms in its integument.
15 her pigments such as melanins to color their integument.
16 hereas GPAT5 promoter is active in the outer integument.
17 are preferentially associated with the outer integument.
18  necessary to promote formation of the outer integument.
19 r confined to the abaxial layer of the inner integument.
20 rgan primordia, including those of the ovule integuments.
21      ant mutations affect initiation of both integuments.
22 ng the female gametophyte within sporophytic integuments.
23 ivocal evidence for feathers and/or downlike integuments.
24 ge and not readily released from the spore's integuments.
25 cessary to support laminar growth of the two integuments.
26                                    The short integuments 2 (sin2) mutation arrests cell division duri
27                        The Arabidopsis short integuments 2-1 (sin2-1) mutant produces ovules with sho
28            The inner cell layer of the outer integument also produces and degrades starch granules co
29  a suberized layer associated with the outer integument and a cutin-like polyester layer associated w
30  exclusively in the outer layer of the outer integument and in the female gametophyte of mature ovule
31 ccumulate complex, dynamic biofilms on their integument and in their gardens.
32 ized to have similar parallel roles in outer integument and leaf development.
33 r stages, and its expression was high in the integument and Malpighian tubules of last instar larvae
34 ing that elements controlling both the outer integument and tapetum expression are located within the
35 all reconstructions of the colors of reptile integument and the plumage of fossil birds and feathered
36 er gene resulted in congenital fusion of the integuments and altered seed morphology.
37 s we have isolated produces ovules that lack integuments and fail to complete megasporogenesis.
38 pment with reduced cell proliferation in the integuments and gametophyte abortion.
39  in the protoderm of the ovule primordia and integuments and gradually became restricted in its expre
40  a parasite requires an ability to cross the integuments and then to escape from the host immune defe
41  maintain the boundary between the two ovule integuments and to promote inner integument growth.
42  produce aberrant structures in place of the integuments and WUS is ectopically expressed in these st
43 heir own type of lateral determinate organs (integuments) and a model that considers carpels as analo
44 ssion is limited to embryo, endosperm, outer integument, and a small portion of the funiculus in deve
45 ss a fluorescence reporter gene primarily in integuments, anther tapetum, and seed coat with unique t
46                                    The inner integument appears to develop normally, resulting in ere
47  was expressed at the border between the two integuments at the time of their initiation, with expres
48  current knowledge of pigmentation in fossil integument beyond that of feathers, allowing for the rec
49          Metabolic scaling slopes of diverse integument-breathing species were significantly positive
50 weak ant mutant contain both inner and outer integuments but generally fail to produce a functional f
51 uggest that UCN suppresses ectopic growth in integuments by directly repressing the KANADI transcript
52 th regulator that maintains planar growth of integuments by repressing a developmental regulator invo
53 and tso1-4, but the shapes and alignments of integument cells became increasingly more disordered as
54 among Hispanics and African Americans, while integument damage was more frequent among African Americ
55 lity of Sin- plants is due to abnormal ovule integument development and aberrant differentiation of t
56 tant has reduced seed set due to outer ovule integument development arrest, leading to female sterili
57                            We found that the integument development gene INNER NO OUTER (INO) was und
58 egulators, act as positive factors for ovule integument development in a mechanism that involves tran
59 EGUMENTA (ANT) genes are essential for ovule integument development in Arabidopsis thaliana.
60 (sin2) mutation arrests cell division during integument development of the Arabidopsis ovule and also
61 ly gene, PFS2, reveals their contribution to integument development through interrelated mechanisms.
62 the mpk3(+/-) mpk6(-/-) ovules have abnormal integument development with arrested cell divisions at l
63 ith a primary role in these processes during integument development.
64 least partially independent processes during integument development.
65 -ZIPIII) genes leads to aberrations in ovule integument development.
66 wing fertilization, cells of the ovule outer integument differentiate into a unique cell type.
67                         When fertilized, the integuments differentiate into the seed coat and support
68                    In the pfs2-1 allele, the integuments display morphological abnormalities and 95%
69 uter (ino) mutant background, where an outer integument does not form, the ats mutation led to amorph
70 1 (sin2-1) mutant produces ovules with short integuments due to early cessation of cell division in t
71 A (PHV) are expressed adaxially in the inner integument during ovule development, independent of ABER
72 revealed that ANT regulates cell division in integuments during ovule development and is necessary fo
73 1 years; median, 2.75 years) with documented integument examination and 3.08 years +/- 1.36 (range, 0
74                   Dates of latest documented integument examination and latest interaction were recor
75              Clinical notes with and without integument examinations, pathologic records, and additio
76                                   The mutant integuments fail to accommodate the developing embryo sa
77 ss, a dependence on the presence of an inner integument for development of the embryo sac, and the ex
78 subunits remained with the spores' insoluble integument fraction, indicating that yields of purified
79 uld transmit to leaves, roots, and the ovule integument from which fibers originate.
80 uring this period the two-cell-layered outer integument goes through a dramatic differentiation proce
81 l regulator involved in the control of early integument growth and polarity.
82 In strong inner no outer (ino) mutants outer integument growth is eliminated, whereas in superman (su
83 liminated, whereas in superman (sup) mutants integument growth on the adaxial side is nearly equal to
84   Our analysis indicates that progression of integument growth requires ER-family signaling in a dosa
85 theses lead us to propose a model for normal integument growth that also explains the described mutan
86 AB3]) can substitute for INO in promotion of integument growth, but do not respond to SUP regulation.
87 larity genes result in amorphous or arrested integument growth, suggesting that polarity determinants
88 orm, the ats mutation led to amorphous inner integument growth.
89 egulates the expression of genes involved in integument growth.
90 e two ovule integuments and to promote inner integument growth.
91 of function of these genes leads to aberrant integument growth.
92 expression of INNER NO OUTER (INO) and outer integument growth.
93           In contrast, YAB5 fails to promote integument growth.
94  the primary influence on promotion of outer integument growth.
95 the outer integument without affecting inner integument growth.
96                           As a result, ovule integuments had arrested growth, and anthers grew abnorm
97 th and abaxial-adaxial polarity of the outer integument has been conserved between two divergent angi
98 gens, and Pseudonocardia bacteria on the ant integument has been popularized as an example of ant-Esc
99 nscription factor controlling ovule and seed integument identity, directly regulates PMEI6 and other
100  layer of the incipient and developing outer integument in Arabidopsis ovules.
101 ession of the gene in the megasporangium and integument in gymnosperms.
102 n the epidermal layer derived from the outer integument in the M. truncatula seed coat, starting from
103 lase and imply that ketolation occurs in the integument in zebra finches.
104 9 has a specific expression pattern in inner integuments in early steps of ovule development as well
105 t testa shape (ats) mutant produces a single integument instead of the two integuments seen in wild-t
106                           The underdeveloped integument is also a portal of entry for infection and t
107                                          The integument is well preserved and provides the first evid
108 and suberin polymerization in the seed outer integument layer.
109 es auxin transport from the endosperm to the integuments, leading to the removal of the PcG block on
110 ients with MFS have involvement of the skin, integument, lungs, and muscle tissue.
111 asis and sheet-like structure of Arabidopsis integuments make them an attractive model system to addr
112 A/PHB/PHV act in concert with ATS to control integument morphogenesis.
113 ribute transitions between each of the three integument morphologies to congenital fusion via a combi
114          Evidence of multiple transitions in integument morphology among Impatiens species suggests t
115                                Unusually for integument mutants, mnt does not impair female fertility
116                  In particular, reduction in integument number occurred early in the history of the a
117 hanisms of one such transition, reduction in integument number, which has occurred several times amon
118          Here we sample melanosomes from the integument of 181 extant amniote taxa and 13 lizard, tur
119                                    The outer integument of Arabidopsis ovules exhibits marked polarit
120 y to show that metals can be taken up by the integument of hagfish.
121 oparasite that lays large, yolky eggs on the integument of its host that develop much like the free-l
122 ne proteinase that is expressed in the outer integument of ovules during seed formation.
123                                    The outer integument of the Arabidopsis (Arabidopsis thaliana) ovu
124  a lipophilic polymer deposited in the outer integument of the Arabidopsis (Arabidopsis thaliana) see
125 cription of the differentiation of the outer integument of the Arabidopsis thaliana seed is presented
126                                          The integument of the Drosophila adult abdomen bears oriente
127                      Expression in the inner integument of the ovule appears to be an ancient express
128 igma, part of the transmitting tract and the integument of the ovules, while the L2 and L3 contribute
129 n electron microscopy reveals that the outer integument of the seed coat lost the electron-dense cuti
130  TH were significantly over-expressed in the integument of the SEM strain at late-prepupa and 0 h pup
131  which reveals the overall morphology of the integument of the wing and other connective structures a
132  in the cephalothorax of crustaceans and the integument of ticks are sources of secreted ecdysteroids
133 ent as well as in the funiculus, embryo, and integuments of developing seeds.
134 NAc) found in cell walls of fungi and in the integuments of insects and crustaceans.
135 s from another PAP, previously isolated from integuments of the same insect (PAP-1).
136 nt results from congenital fusion of the two integuments of the wild type.
137 noticeable effect on expression in the outer integument or tapetum.
138 ng ant mutants have ovules that fail to form integuments or a female gametophyte.
139 s, includes species with one integument, two integuments, or an apparently intermediate bifid integum
140 g the development of sepal margins and ovule integument outgrowth.
141  Hispanics from Texas and African Americans, integument (primarily scarring alopecia) in Hispanics fr
142           Ovules of ino mutants initiate two integument primordia, but the outer integument primordiu
143 ct in concert to define the boundary between integument primordia.
144 iate two integument primordia, but the outer integument primordium forms on the opposite side of the
145                                   A layer of integument protein that anchors the surface fibers is ac
146 urface fibers is similarly acquired when the integument protein-coated capsids pass through a second
147 to absent or symmetrical growth of the outer integument, respectively.
148 ification of polarity in the inner and outer integuments, respectively, that parallel the known roles
149 ker gene expression indicate that the single integument results from congenital fusion of the two int
150                              Analysis of ucn integuments reveals localized distortion of planar growt
151 duces a single integument instead of the two integuments seen in wild-type ovules.
152             Recessive mutations in the SHORT INTEGUMENT (SIN1) gene in Arabidopsis were previously sh
153                                    The short integument (sin1) mutation causes a female-specific infe
154 3 and MPK6 in promoting cell division in the integument specifically during ovule development.
155 o pollination, while expression in the outer integument started to develop from the micropylar end ou
156 factor in this is extra cell division in the integuments surrounding mnt mutant ovules, leading to th
157 h-instar larvae, including fat body, midgut, integument, testis, silk gland and haemocytes.
158 t is a biologically and clinically important integument that protects teeth against enamel deminerali
159 rm ovules include one, or more commonly two, integuments that cover the nucellus and female gametophy
160 e defects are the result of an alteration in integuments that fail to fully develop and are shorter t
161                     In ovules, expression in integument tissues was much higher in the micropylar reg
162 edge, Glycera jaws represent the first known integument to exploit melanin as a cohesive load- and sh
163 s of the Ericales, includes species with one integument, two integuments, or an apparently intermedia
164 nsible for morphological transitions between integument types in this group.
165       A fraction of cells in the chalaza and integuments underwent DNA fragmentation and programmed c
166                      Expression in the inner integument was apparent prior to pollination, while expr
167 tes were grafted to nude mice, the resulting integument was normal, and conversely, when transgenic b
168 nd their temporal expression patterns in the integument were compared during the larval-pupal metamor
169 s showed ATT1 promoter activity in the inner integument, whereas GPAT5 promoter is active in the oute
170 l toxins and enzymes that degrade the insect integument, which are normally repressed by QS at high i
171  are expressed in the epidermal layer of the integument, which could prevent or slow down the toxin f
172 transport of auxin from the endosperm to the integuments, which results in seed abortion.
173 r derived tyrannosauroids, indicates a scaly integument with high tactile sensitivity.
174 es the millipede by piercing the millipede's integument with its hollow sickle-shaped mandibles and a
175 481 bp that controls expression in the inner integument, with no noticeable effect on expression in t
176  eudicots, nearly all asterids have a single integument, with the only exceptions in the Ericales, a
177 bits a similar amorphous growth of the outer integument without affecting inner integument growth.

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