1 the expression pattern and possible roles of
postembryonic accumulation of AGL15.
2 The
postembryonic acquisition of behavior requires alteratio
3 attern formation and viability, and that its
postembryonic activity is required for several processes
4 backbone, we propose a scenario in which the
postembryonic addition of segments that occurs in most s
5 The requirements for
postembryonic adult body plan formation in the larval ru
6 a persistent action of retinoic acid in the
postembryonic and adult songbird brain and provide furth
7 l in plants because development is primarily
postembryonic and continuous over a plant's life span.
8 Plant development is predominantly
postembryonic and tuned in to respond to environmental c
9 We found that
postembryonic antagonism of Ptf1a, a master regulator of
10 We show that
postembryonic arborization and neurosecretory terminal t
11 uced Dscam expression but minimally affected
postembryonic axonal morphogenesis.
12 found that this is the case for of a pair of
postembryonic blast cells in the tail.
13 efects that result from the inability of the
postembryonic blast cells to escape G(1) cell cycle arre
14 In lin-23 null mutants, all
postembryonic blast cells undergo extra divisions, creat
15 tant exhibits extensive DNA rereplication in
postembryonic BLAST cells, similar to what is observed i
16 tively, are necessary for proper division of
postembryonic blast cells.
17 cye-1 lead to the underproliferation of many
postembryonic blast lineages as well as defects in ferti
18 eas, and nearly all TH-ir cell groups of the
postembryonic brain were already established.
19 These results link embryonic and
postembryonic cell behaviour, and help to explain the co
20 The initiation of
postembryonic cell divisions by the gonadal precursors o
21 c viable allele (ku233), all of which affect
postembryonic cell divisions including those of the vulv
22 chromatin organization and severe defects in
postembryonic cell divisions, including the mesodermal l
23 was previously shown to negatively regulate
postembryonic cell divisions.
24 tions show that ESCL associates with E(Z) in
postembryonic cells and chromatin immunoprecipitations s
25 determine the polarity of both embryonic and
postembryonic cells.
26 unlabeled hosts, allowing us to discern the
postembryonic central and peripheral projections of each
27 present evidence that supports the idea that
postembryonic changes in individual sensilla may be resp
28 how that gsb becomes widely expressed in the
postembryonic CNS, including within mature motoneurons.
29 e measured current and voltage noise in 18 d
postembryonic cultured neurons from the rat hippocampus,
30 single cells from embryonic day 11.5 (E11.5)
postembryonic day 5 (P5) gonads and performed lineage tr
31 HDA-1 zygotic expression results in specific
postembryonic defects in gonadogenesis and vulval develo
32 nt production of Ca(2+) spikes may influence
postembryonic dendritic remodeling.
33 These transcription factors are
postembryonic determinants of the ground tissue stem cel
34 ession of CLPS3-TAP fusion caused a range of
postembryonic development abnormalities, including early
35 R pathway antagonize one another to regulate
postembryonic development and adult longevity.
36 THs are key during embryonic and
postembryonic development and critical for cell metaboli
37 ctive system as the major SUMO target during
postembryonic development and highlight LIN-11 as a phys
38 er our understanding of gene function during
postembryonic development and in disease.
39 During
postembryonic development and throughout life, neurons a
40 l the growth rate of internal tissues during
postembryonic development are poorly understood.
41 ibian metamorphosis is strikingly similar to
postembryonic development around birth in mammals, with
42 specification in embryogenesis and vascular
postembryonic development but also for leaf flatness.
43 regulates gene expression during vertebrate
postembryonic development by using T(3)-dependent amphib
44 However, the regulation of
postembryonic development has received less attention as
45 als that modulate neuroblast activity during
postembryonic development have been identified.
46 Here we use
postembryonic development in Arabidopsis plants to inves
47 ted by the decapping complex is required for
postembryonic development in Arabidopsis.
48 Taken together, our findings show that
postembryonic development in the SEG is mediated by a su
49 neural lineages, or any other aspect of the
postembryonic development in the SEG.
50 Furthermore, the severe block to
postembryonic development in vcs and tdt and the accompa
51 of adult intestinal adult stem cells during
postembryonic development in vertebrates.
52 ment cell development and patterning, and in
postembryonic development more generally.
53 ) and root apical meristem are necessary for
postembryonic development of aboveground tissues and roo
54 During
postembryonic development of C. elegans, non-gonadal mes
55 During
postembryonic development of Caenorhabditis elegans, the
56 l of ecdysis behaviors may change during the
postembryonic development of Drosophila.
57 Seed germination and
postembryonic development of fry1 are more sensitive to
58 In the
postembryonic development of insects, ecdysone is synthe
59 The
postembryonic development of lateral roots and nodules i
60 /alphaVolado), are all known to regulate the
postembryonic development of synaptic terminal arborizat
61 at governs neuronal temporal identity during
postembryonic development of the Drosophila brain.
62 We find that the mutations can disrupt the
postembryonic development of the male-specific blast cel
63 and protein undergoes dynamic changes during
postembryonic development of the mosquito.
64 may serve as a mechanism by which extensive
postembryonic development of the mushroom bodies can occ
65 onsiderable information has been obtained on
postembryonic development of the neuroblasts and their l
66 ent center in the stem cell niche during the
postembryonic development of the root system.
67 a dormant phase that separates embryonic and
postembryonic development of the sporophyte.
68 opus metamorphosis as a model for vertebrate
postembryonic development to identify direct T3 response
69 During
postembryonic development, a larval skeletal muscle moto
70 gans in vertebrates often takes place during
postembryonic development, a period around birth in mamm
71 d diploid Xenopus tropicalis, as a model for
postembryonic development, a period around birth in mamm
72 organ-specific stem cells during vertebrate
postembryonic development, a period characterized by hig
73 ressed in the AWC sensory neurons throughout
postembryonic development, and regulates terminal differ
74 including energy homeostasis, embryonic and
postembryonic development, and the stress response.
75 processes is crucial for both embryonic and
postembryonic development, as well as for the maintenanc
76 This pathway is nonessential during
postembryonic development, but it is required to termina
77 ose in Arabidopsis thaliana is essential for
postembryonic development, but the underlying mechanism
78 , their potential function during vertebrate
postembryonic development, especially in organ-specific
79 ve timing and sequence of many events during
postembryonic development, including the terminal differ
80 ession in song control nuclei changes during
postembryonic development, peaking during an early phase
81 The initial step modified
postembryonic development, resulting in the nymph-adult
82 During late
postembryonic development, the Caenorhabditis elegans ma
83 During
postembryonic development, the nervous system must adapt
84 To understand the genetic control of
postembryonic development, we performed a dominant scree
85 ne that uniquely expresses P granules during
postembryonic development.
86 display severe defects in embryogenesis and
postembryonic development.
87 required for organismal thermotolerance and
postembryonic development.
88 tinct roles at later stages of embryonic and
postembryonic development.
89 ing muscles and neurons during embryonic and
postembryonic development.
90 elegans establish axonal connections during
postembryonic development.
91 l status to control arrest and initiation of
postembryonic development.
92 ll vertebrates, thyroid hormones (TH) affect
postembryonic development.
93 ating development in different organs during
postembryonic development.
94 evels oscillate relative to the molts during
postembryonic development.
95 ealing functions in various processes during
postembryonic development.
96 ed on paired antennules--undergoes continual
postembryonic development.
97 imuli that modulate fiber-type plasticity in
postembryonic development.
98 ession becomes restricted and dynamic during
postembryonic development.
99 yogenesis and in vulval morphogenesis during
postembryonic development.
100 esult in any obvious defects in embryonic or
postembryonic development.
101 generated, maintained, and recruited during
postembryonic development.
102 enetic screen to isolate mutations affecting
postembryonic development.
103 of neural crest stem cells during zebrafish
postembryonic development.
104 gnaling in the Arabidopsis embryo and during
postembryonic development.
105 their essential functions are restricted to
postembryonic development.
106 o the approximately 6-hour molting cycles of
postembryonic development.
107 and PKC-3, but not PAR-3, are essential for
postembryonic development.
108 in an environmentally adaptive manner during
postembryonic development.
109 a series of morphological events resembling
postembryonic development.
110 ear architectural schemes during Arabidopsis
postembryonic development.
111 m cell-like neuroblasts during embryonic and
postembryonic development.
112 age-specific manner in these lineages during
postembryonic development.
113 ran metamorphosis serves as a model to study
postembryonic development.
114 le of activating mab-5 in the V cells during
postembryonic development; however, during normal develo
115 terochronic gene pathway, which ensures that
postembryonic developmental events are appropriately tim
116 ne lin-14 specifies the temporal sequence of
postembryonic developmental events.
117 egulation and thereby controls the timing of
postembryonic developmental events.
118 amined potential functional roles of fish in
postembryonic developmental processes, including those i
119 The timing of
postembryonic developmental programs in Caenorhabditis e
120 ent kinase inhibitors, and functions to link
postembryonic developmental programs to cell cycle progr
121 In the
postembryonic developmental stages, defects in NMT1 lead
122 assess the effect of FPS down-regulation at
postembryonic developmental stages, we generated Arabido
123 yecdysone (ecdysone) is the key regulator of
postembryonic developmental transitions in insects and c
124 g insect development, coordinating the major
postembryonic developmental transitions, including molti
125 These data indicate that targeted
postembryonic disruption of the acinar cell fate can res
126 isting cell-division mutations: some disrupt
postembryonic divisions and affect formation of the gona
127 s, none of the gonad progenitors undergo any
postembryonic divisions.
128 s (JH), which function in both embryonic and
postembryonic domains and control the stage-specifying g
129 The hbl-1/lin-57 3'UTR is required for
postembryonic downregulation in the hypodermis and nervo
130 Postembryonic dPDZ-GEF mutant cells generated in mosaic
131 regulation of these transitions, we used the
postembryonic epithelial stem (seam) cell lineages of Ca
132 egans, lin-4 and let-7 control the timing of
postembryonic events by translational repression of targ
133 n of wings will be knowledge of the earliest
postembryonic events promoting wing outgrowth.
134 unction and malfunction of key embryonic and
postembryonic events.
135 We studied their embryonic and
postembryonic expression domains and grouped them into t
136 Ectopic,
postembryonic expression of LEC2 in transgenic plants in
137 Ectopic
postembryonic expression of the LEC1 gene in vegetative
138 elegans Hox gene in depth, we determined the
postembryonic expression pattern of egl-5, the C. elegan
139 ILM and VB in chick and human embryonic and
postembryonic eye development.
140 ed to the yet little studied stem cell based
postembryonic eye primordium of primitive insects.
141 ether Patched 2 function is essential in the
postembryonic eye.
142 In plants,
postembryonic formation of new organs helps shape the ad
143 the embryonic formation of the larva and the
postembryonic formation of the adult body plan are tempo
144 is work is the first to establish a specific
postembryonic function for dosage compensation in any or
145 g morphogenesis, thereby revealing the first
postembryonic function for Pkn.
146 into N-myristoylation in plants by ascribing
postembryonic functions of Arabidopsis NMT1 that involve
147 t staining of adherens junctions confirmed a
postembryonic fusion of hyp6 with hyp7, the major syncyt
148 llagen recruitment to Caenorhabditis elegans
postembryonic gonadal and pharyngeal BMs.
149 To sustain plants'
postembryonic growth and development in a structure of c
150 Caenorhabditis elegans halts
postembryonic growth and development shortly after hatch
151 C. elegans hatch in a food-free environment,
postembryonic growth and development stall, but sensory
152 nd is essential for embryogenesis and normal
postembryonic growth and development.
153 JH also acquired a potent role in regulating
postembryonic growth and development.
154 strally have been involved in the control of
postembryonic growth and reproduction.
155 However,
postembryonic growth and the sucrose-Tre6P relationship
156 ion to differentiation, thereby impinging on
postembryonic growth capacity of the root meristem.
157 neration is a unique and complex instance of
postembryonic growth observed in certain metazoans that
158 encompass stem/progenitor cells that sustain
postembryonic growth of all plant organs.
159 stem, these results suggest a model in which
postembryonic growth of hypodermal cells is regulated by
160 Continuous formation of plant tissues during
postembryonic growth requires asymmetric divisions and t
161 perception to mediate temperature-dependent
postembryonic growth.
162 he position and connections of nerves during
postembryonic growth.
163 s in radial patterning of both embryonic and
postembryonic growth.
164 ut smaller animals because of a reduction in
postembryonic growth.
165 mporal patterns of gene expression and early
postembryonic growth.
166 ls in the utricle, which undergoes continual
postembryonic hair cell production, but it is absent fro
167 v6 as a selective and essential regulator of
postembryonic HSCs.
168 In zebrafish, a high level of
postembryonic hypothalamic neurogenesis has been observe
169 petence for change, became restricted to one
postembryonic instar.
170 3)-dependent Xenopus metamorphosis resembles
postembryonic intestinal maturation in mammals.
171 splays stunted root growth and fails to form
postembryonic leaves.
172 These
postembryonic leg motoneurons are produced by five neuro
173 Moreover, oli is expressed in
postembryonic leg-innervating motoneuron lineages and re
174 jor portion of embryogenesis was deferred to
postembryonic life with the evolution of holometaboly, J
175 ical regulators of embryonic development and
postembryonic life, but little is know about the upstrea
176 at the larval neuromuscular junction during
postembryonic life.
177 gressive loss of dopaminergic neurons during
postembryonic life.
178 , unambiguous identification of 23 of the 25
postembryonic lineages based on the expression of 15 tra
179 n drosha and pasha/dgcr8 null alleles in two
postembryonic lineages in the Drosophila brain: eliminat
180 Cells that form the
postembryonic lineages in wild-type animals do not enter
181 sly shown to cause ectopic neurogenesis from
postembryonic lineages.
182 ectivity and recruiting newborn neurons from
postembryonic lineages.
183 ow here that besides being components of the
postembryonic locomotory circuit, these embryonic motone
184 Furthermore,
postembryonic loss of opa expression alone causes head d
185 neddylation activity are required to sustain
postembryonic meristem function in Arabidopsis.
186 n of the striated BWM fate in the C. elegans
postembryonic mesoderm, implicating a remarkable level o
187 In the C. elegans
postembryonic mesoderm, this subdivision is a result of
188 SEM-2, in the M lineage, which produces the
postembryonic mesoderm.
189 e (BWM) fate specification in the C. elegans
postembryonic mesoderm.
190 lin-39 and mab-5, in diversification of the
postembryonic mesoderm.
191 the exd ortholog ceh-20 in patterning of the
postembryonic mesoderm.
192 The C. elegans
postembryonic mesodermal lineage arises from a single ce
193 The
postembryonic mesodermal lineage in C. elegans provides
194 The C. elegans
postembryonic mesodermal lineage, the M lineage, allows
195 the same expression pattern as CeMyoD in the
postembryonic mesodermal lineage, the M lineage, and tha
196 mesoderm development in C. elegans using the
postembryonic mesodermal M lineage as a model system.
197 Here we examine their roles in the
postembryonic migration of the P cell neuroblasts and th
198 entify genes and cell behaviors required for
postembryonic morphogenesis and differentiation.
199 osophila RhoA (Rho1) GTPase is essential for
postembryonic morphogenesis of leg and wing imaginal dis
200 a number of fundamental processes within the
postembryonic muscle lineage, such as cell division pola
201 t did not indicate the production of glia by
postembryonic mushroom body neuronal precursors.
202 te hypothalamus as a model for Wnt-regulated
postembryonic neural progenitor differentiation and defi
203 We show that expression of pal-1 in the
postembryonic neuroblast cell V6 can be initiated by two
204 adherin DE-cadherin is expressed globally by
postembryonic neuroblasts and their lineages ("secondary
205 Two of these
postembryonic neuroblasts generate solely motoneurons th
206 iously attributed to cytokinesis failures in
postembryonic neuroblasts.
207 ession of a C. elegans Hox gene, egl-5, in a
postembryonic neuroectodermal cell lineage.
208 Postembryonic neurogenesis has been observed in several
209 tion will be important for future studies on
postembryonic neurogenesis in Drosophila.
210 that additional behaviors may be affected by
postembryonic neurogenesis in this brain structure.
211 ation of distinct neuronal cell types during
postembryonic neurogenesis.
212 al changes affect lineage progression during
postembryonic neurogenesis.
213 affect the number of ABLKs generated during
postembryonic neurogenesis.
214 , which contain 25 individually identifiable
postembryonic neuronal lineages.
215 ons as a permissive signal for embryonic and
postembryonic neuronal migration in the nematode C. eleg
216 s are important for the accurate guidance of
postembryonic neuronal migrations in the nematode Caenor
217 acking exon 19 or exon 23 effectively blocks
postembryonic neuronal morphogenesis.
218 t and differentiation of discrete subsets of
postembryonic neurons.
219 ate the specification and differentiation of
postembryonic neurons: for example, Nkx6 is necessary an
220 We conclude that betaPS integrin at the
postembryonic NMJ is a critical determinant of morpholog
221 PS integrins appear at
postembryonic NMJs coincident with the onset of rapid mo
222 o investigate in vivo the role of ST3 during
postembryonic organ development in vertebrates.
223 s have been reported on the roles of MMPs in
postembryonic organ development.
224 he function of MMPs during embryogenesis and
postembryonic organ development.
225 oration of developmental pre-patterns during
postembryonic organ development.
226 e for Arabidopsis thaliana embryogenesis and
postembryonic organ formation.
227 l for elucidating the mechanisms controlling
postembryonic organogenesis.
228 m cell populations is critical for extensive
postembryonic organogenesis.
229 lateral roots represents one example of such
postembryonic organogenesis.
230 a gene regulatory network (GRN) that directs
postembryonic organogenesis.
231 sible for the initiation of all above-ground
postembryonic organs, in most plants the vast majority o
232 Legume roots form two types of
postembryonic organs, lateral roots and symbiotic nodule
233 yogenesis and the formation of embryonic and
postembryonic organs.
234 These data suggest that
postembryonic partial loss of AgRP/NPY neurons leads to
235 ive auxin gradients as well as embryonic and
postembryonic patterning are severely compromised.
236 e lipids and are essential for embryonic and
postembryonic patterning.
237 Both cdr-4 and cdr-6 are transcribed in
postembryonic pharyngeal and intestinal cells in C. eleg
238 plant stem cells remain quiescent until the
postembryonic phase of development.
239 The
postembryonic phase produces the adult specific compound
240 quiescence separating distinct embryonic and
postembryonic phases of proliferation.
241 studying the genetic and cellular bases for
postembryonic phenotypes.
242 It is essential for embryonic and
postembryonic plant development and it affects growth ra
243 y, also for other polarization events during
postembryonic plant life.
244 irst larval stage and fail in two assays for
postembryonic plasticity of neuronal structure.
245 e to form new organs is a key feature of the
postembryonic plasticity of plant development, and the e
246 Postembryonic production of hair cells, the highly speci
247 Postembryonic production of inner ear hair cells occurs
248 e potential and lineage segregation of these
postembryonic progenitors is poorly understood, and it i
249 Postembryonic RCN1 function is required to maintain norm
250 idence also implicates these pathways in the
postembryonic regulation of stem-cell number in epitheli
251 study addresses this goal by describing the
postembryonic remodeling of the excitability and dendrit
252 basement membrane to insulate axons from the
postembryonic remodeling of their targets.
253 Similar defects are observed upon
postembryonic removal of two C2H2 zinc finger transcript
254 g the correct cell types and patterns during
postembryonic replacement of sensory epithelial cells in
255 xpression, ptc-3(RNAi) reveals an additional
postembryonic requirement for ptc-3 activity.
256 In addition, we document
postembryonic requirements for punt activity.
257 enerate the rod photoreceptor lineage in the
postembryonic retina.
258 Postembryonic RNA interference of PAR-1 causes a protrud
259 Here, we define a new
postembryonic role for gooseberry.
260 ressed embryonically, and plays an essential
postembryonic role in tissue integrity, it is not requir
261 e activity plays a unique role in regulating
postembryonic root development and stress response.
262 ristem maintenance and cell expansion during
postembryonic root development in Arabidopsis.
263 -borne beneficial bacteria to interfere with
postembryonic root developmental programs.
264 date, we initially describe the diversity of
postembryonic root forms.
265 s callus formation precedes specification of
postembryonic root founder cells, from which roots are i
266 undamental structure that is responsible for
postembryonic root growth.
267 any meristem 3 (BAM3) perfectly suppress the
postembryonic root meristem growth defect and the associ
268 However, many other programs of
postembryonic root organogenesis exist in angiosperms.
269 embryos, leading to a loss of embryonic and
postembryonic root stem cells and vascular specification
270 iferation and organ initiation essential for
postembryonic shoot growth.
271 The discovery of emp2 mutant phenotypes in
postembryonic shoots reveals that the duplicate genes em
272 oughout the embryo and to a few well-defined
postembryonic sites.
273 Postembryonic SKN-1 functions have not been elucidated.
274 Their expression is initiated at a precise
postembryonic stage, long after PVT has been generated i
275 e posterior telencephalic roof, activated at
postembryonic stages and persisting lifelong.
276 at is specific to the embryo and absent from
postembryonic stages in water striders (Gerromorpha).
277 gene engrailed, which at embryonic and early
postembryonic stages is expressed in extant panarthropod
278 ansmitter-expressing neurons in the brain at
postembryonic stages of development.
279 on of TH-ir cells and fibers in the brain of
postembryonic stages of the shark Scyliorhinus canicula.
280 ession of engrailed during late embryonic to
postembryonic stages, and the development of the dorsal
281 in the embryonic VB, their sharp decline at
postembryonic stages, and their very low abundance in th
282 To analyze EMP2 function during
postembryonic stages, plants mosaic for sectors of emp2
283 During
postembryonic stages, SKN-1 regulates a key Phase II det
284 ontrast, most Dscams lack exons 19 and 23 at
postembryonic stages.
285 ESC, is expressed with peak abundance during
postembryonic stages.
286 s of neurogenesis that are characteristic of
postembryonic stages.
287 e mature egg, lethality is delayed until the
postembryonic stages.
288 whereas asm-2 is predominantly expressed in
postembryonic stages.
289 significantly influence seizure behavior at
postembryonic stages.
290 ce for a functional role of integrins at the
postembryonic synapse.
291 We present data for 58 of 66
postembryonic thoracic lineages, excluding the motor neu
292 tanding paradox of ESC dispensability during
postembryonic times.
293 n formation during embryonic development and
postembryonic tissue homeostasis.
294 s in transcriptional activation by TR during
postembryonic tissue remodeling by using amphibian metam
295 cells in long-distance communication during
postembryonic tissue remodeling.
296 hog (Hh) signaling during development and in
postembryonic tissues requires activation of the 7TM onc
297 uring embryos and seeds; it also occurred in
postembryonic tissues, especially in association with va
298 ads to severe phenotypes in embryos and many
postembryonic tissues.
299 adult intestinal stem cell formation during
postembryonic vertebrate development.
300 in vivo identification and classification of
postembryonic wound closure genes has yet to be develope