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 HDA-1 zygotic expression results in specific
postembryonic defects in gonadogenesis and vulval develo
31 nt production of Ca(2+) spikes may influence
postembryonic dendritic remodeling.
32 These transcription factors are
postembryonic determinants of the ground tissue stem cel
33 ession of CLPS3-TAP fusion caused a range of
postembryonic development abnormalities, including early
34 R pathway antagonize one another to regulate
postembryonic development and adult longevity.
35 THs are key during embryonic and
postembryonic development and critical for cell metaboli
36 ctive system as the major SUMO target during
postembryonic development and highlight LIN-11 as a phys
37 er our understanding of gene function during
postembryonic development and in disease.
38 During
postembryonic development and throughout life, neurons a
39 l the growth rate of internal tissues during
postembryonic development are poorly understood.
40 ibian metamorphosis is strikingly similar to
postembryonic development around birth in mammals, with
41 specification in embryogenesis and vascular
postembryonic development but also for leaf flatness.
42 regulates gene expression during vertebrate
postembryonic development by using T(3)-dependent amphib
43 However, the regulation of
postembryonic development has received less attention as
44 als that modulate neuroblast activity during
postembryonic development have been identified.
45 Here we use
postembryonic development in Arabidopsis plants to inves
46 ted by the decapping complex is required for
postembryonic development in Arabidopsis.
47 Taken together, our findings show that
postembryonic development in the SEG is mediated by a su
48 neural lineages, or any other aspect of the
postembryonic development in the SEG.
49 Furthermore, the severe block to
postembryonic development in vcs and tdt and the accompa
50 of adult intestinal adult stem cells during
postembryonic development in vertebrates.
51 ment cell development and patterning, and in
postembryonic development more generally.
52 ) and root apical meristem are necessary for
postembryonic development of aboveground tissues and roo
53 During
postembryonic development of C. elegans, non-gonadal mes
54 During
postembryonic development of Caenorhabditis elegans, the
55 l of ecdysis behaviors may change during the
postembryonic development of Drosophila.
56 Seed germination and
postembryonic development of fry1 are more sensitive to
57 In the
postembryonic development of insects, ecdysone is synthe
58 The
postembryonic development of lateral roots and nodules i
59 /alphaVolado), are all known to regulate the
postembryonic development of synaptic terminal arborizat
60 at governs neuronal temporal identity during
postembryonic development of the Drosophila brain.
61 We find that the mutations can disrupt the
postembryonic development of the male-specific blast cel
62 and protein undergoes dynamic changes during
postembryonic development of the mosquito.
63 may serve as a mechanism by which extensive
postembryonic development of the mushroom bodies can occ
64 onsiderable information has been obtained on
postembryonic development of the neuroblasts and their l
65 ent center in the stem cell niche during the
postembryonic development of the root system.
66 a dormant phase that separates embryonic and
postembryonic development of the sporophyte.
67 opus metamorphosis as a model for vertebrate
postembryonic development to identify direct T3 response
68 During
postembryonic development, a larval skeletal muscle moto
69 gans in vertebrates often takes place during
postembryonic development, a period around birth in mamm
70 d diploid Xenopus tropicalis, as a model for
postembryonic development, a period around birth in mamm
71 organ-specific stem cells during vertebrate
postembryonic development, a period characterized by hig
72 ressed in the AWC sensory neurons throughout
postembryonic development, and regulates terminal differ
73 including energy homeostasis, embryonic and
postembryonic development, and the stress response.
74 processes is crucial for both embryonic and
postembryonic development, as well as for the maintenanc
75 This pathway is nonessential during
postembryonic development, but it is required to termina
76 ose in Arabidopsis thaliana is essential for
postembryonic development, but the underlying mechanism
77 , their potential function during vertebrate
postembryonic development, especially in organ-specific
78 ve timing and sequence of many events during
postembryonic development, including the terminal differ
79 ession in song control nuclei changes during
postembryonic development, peaking during an early phase
80 During late
postembryonic development, the Caenorhabditis elegans ma
81 During
postembryonic development, the nervous system must adapt
82 To understand the genetic control of
postembryonic development, we performed a dominant scree
83 ne that uniquely expresses P granules during
postembryonic development.
84 display severe defects in embryogenesis and
postembryonic development.
85 required for organismal thermotolerance and
postembryonic development.
86 tinct roles at later stages of embryonic and
postembryonic development.
87 ing muscles and neurons during embryonic and
postembryonic development.
88 elegans establish axonal connections during
postembryonic development.
89 l status to control arrest and initiation of
postembryonic development.
90 ll vertebrates, thyroid hormones (TH) affect
postembryonic development.
91 ating development in different organs during
postembryonic development.
92 evels oscillate relative to the molts during
postembryonic development.
93 ealing functions in various processes during
postembryonic development.
94 ed on paired antennules--undergoes continual
postembryonic development.
95 imuli that modulate fiber-type plasticity in
postembryonic development.
96 ession becomes restricted and dynamic during
postembryonic development.
97 yogenesis and in vulval morphogenesis during
postembryonic development.
98 esult in any obvious defects in embryonic or
postembryonic development.
99 generated, maintained, and recruited during
postembryonic development.
100 enetic screen to isolate mutations affecting
postembryonic development.
101 of neural crest stem cells during zebrafish
postembryonic development.
102 gnaling in the Arabidopsis embryo and during
postembryonic development.
103 their essential functions are restricted to
postembryonic development.
104 o the approximately 6-hour molting cycles of
postembryonic development.
105 for all nongonadal mesoderm formation during
postembryonic development.
106 in an environmentally adaptive manner during
postembryonic development.
107 sential epidermal factor required for proper
postembryonic development.
108 ination--both in the early embryo and during
postembryonic development.
109 ear architectural schemes during Arabidopsis
postembryonic development.
110 m cell-like neuroblasts during embryonic and
postembryonic development.
111 age-specific manner in these lineages during
postembryonic development.
112 ran metamorphosis serves as a model to study
postembryonic development.
113 le of activating mab-5 in the V cells during
postembryonic development; however, during normal develo
114 terochronic gene pathway, which ensures that
postembryonic developmental events are appropriately tim
115 ne lin-14 specifies the temporal sequence of
postembryonic developmental events.
116 egulation and thereby controls the timing of
postembryonic developmental events.
117 amined potential functional roles of fish in
postembryonic developmental processes, including those i
118 The timing of
postembryonic developmental programs in Caenorhabditis e
119 ent kinase inhibitors, and functions to link
postembryonic developmental programs to cell cycle progr
120 In the
postembryonic developmental stages, defects in NMT1 lead
121 assess the effect of FPS down-regulation at
postembryonic developmental stages, we generated Arabido
122 yecdysone (ecdysone) is the key regulator of
postembryonic developmental transitions in insects and c
123 g insect development, coordinating the major
postembryonic developmental transitions, including molti
124 These data indicate that targeted
postembryonic disruption of the acinar cell fate can res
125 isting cell-division mutations: some disrupt
postembryonic divisions and affect formation of the gona
126 is elegans hermaphrodite is generated by the
postembryonic divisions of two somatic precursors, Z1 an
127 s, none of the gonad progenitors undergo any
postembryonic divisions.
128 The hbl-1/lin-57 3'UTR is required for
postembryonic downregulation in the hypodermis and nervo
129 Postembryonic dPDZ-GEF mutant cells generated in mosaic
130 regulation of these transitions, we used the
postembryonic epithelial stem (seam) cell lineages of Ca
131 egans, lin-4 and let-7 control the timing of
postembryonic events by translational repression of targ
132 n of wings will be knowledge of the earliest
postembryonic events promoting wing outgrowth.
133 unction and malfunction of key embryonic and
postembryonic events.
134 We studied their embryonic and
postembryonic expression domains and grouped them into t
135 Ectopic,
postembryonic expression of LEC2 in transgenic plants in
136 Ectopic
postembryonic expression of the LEC1 gene in vegetative
137 elegans Hox gene in depth, we determined the
postembryonic expression pattern of egl-5, the C. elegan
138 ILM and VB in chick and human embryonic and
postembryonic eye development.
139 ed to the yet little studied stem cell based
postembryonic eye primordium of primitive insects.
140 ether Patched 2 function is essential in the
postembryonic eye.
141 the embryonic formation of the larva and the
postembryonic formation of the adult body plan are tempo
142 is work is the first to establish a specific
postembryonic function for dosage compensation in any or
143 g morphogenesis, thereby revealing the first
postembryonic function for Pkn.
144 into N-myristoylation in plants by ascribing
postembryonic functions of Arabidopsis NMT1 that involve
145 t staining of adherens junctions confirmed a
postembryonic fusion of hyp6 with hyp7, the major syncyt
146 To sustain plants'
postembryonic growth and development in a structure of c
147 Caenorhabditis elegans halts
postembryonic growth and development shortly after hatch
148 C. elegans hatch in a food-free environment,
postembryonic growth and development stall, but sensory
149 strally have been involved in the control of
postembryonic growth and reproduction.
150 ion to differentiation, thereby impinging on
postembryonic growth capacity of the root meristem.
151 neration is a unique and complex instance of
postembryonic growth observed in certain metazoans that
152 encompass stem/progenitor cells that sustain
postembryonic growth of all plant organs.
153 stem, these results suggest a model in which
postembryonic growth of hypodermal cells is regulated by
154 Continuous formation of plant tissues during
postembryonic growth requires asymmetric divisions and t
155 he position and connections of nerves during
postembryonic growth.
156 s in radial patterning of both embryonic and
postembryonic growth.
157 ut smaller animals because of a reduction in
postembryonic growth.
158 mporal patterns of gene expression and early
postembryonic growth.
159 perception to mediate temperature-dependent
postembryonic growth.
160 ls in the utricle, which undergoes continual
postembryonic hair cell production, but it is absent fro
161 v6 as a selective and essential regulator of
postembryonic HSCs.
162 In zebrafish, a high level of
postembryonic hypothalamic neurogenesis has been observe
163 petence for change, became restricted to one
postembryonic instar.
164 3)-dependent Xenopus metamorphosis resembles
postembryonic intestinal maturation in mammals.
165 expression can be dramatically visualized in
postembryonic larval tissues.
166 splays stunted root growth and fails to form
postembryonic leaves.
167 These
postembryonic leg motoneurons are produced by five neuro
168 Moreover, oli is expressed in
postembryonic leg-innervating motoneuron lineages and re
169 ical regulators of embryonic development and
postembryonic life, but little is know about the upstrea
170 at the larval neuromuscular junction during
postembryonic life.
171 gressive loss of dopaminergic neurons during
postembryonic life.
172 , unambiguous identification of 23 of the 25
postembryonic lineages based on the expression of 15 tra
173 s that occupied positions similar to the six
postembryonic lineages in Manduca.
174 n drosha and pasha/dgcr8 null alleles in two
postembryonic lineages in the Drosophila brain: eliminat
175 sexta and is restricted to six identifiable
postembryonic lineages in the moth's thoracic hemigangli
176 Cells that form the
postembryonic lineages in wild-type animals do not enter
177 sly shown to cause ectopic neurogenesis from
postembryonic lineages.
178 ectivity and recruiting newborn neurons from
postembryonic lineages.
179 ow here that besides being components of the
postembryonic locomotory circuit, these embryonic motone
180 Furthermore,
postembryonic loss of opa expression alone causes head d
181 ht correspondence between both embryonic and
postembryonic loss-of-function punt and dpp phenotypes i
182 neddylation activity are required to sustain
postembryonic meristem function in Arabidopsis.
183 n of the striated BWM fate in the C. elegans
postembryonic mesoderm, implicating a remarkable level o
184 In the C. elegans
postembryonic mesoderm, this subdivision is a result of
185 e (BWM) fate specification in the C. elegans
postembryonic mesoderm.
186 lin-39 and mab-5, in diversification of the
postembryonic mesoderm.
187 the exd ortholog ceh-20 in patterning of the
postembryonic mesoderm.
188 SEM-2, in the M lineage, which produces the
postembryonic mesoderm.
189 A role for CeTwist in
postembryonic mesodermal cell fate specification was ind
190 The C. elegans
postembryonic mesodermal lineage arises from a single ce
191 The
postembryonic mesodermal lineage in C. elegans provides
192 The C. elegans
postembryonic mesodermal lineage, the M lineage, allows
193 the same expression pattern as CeMyoD in the
postembryonic mesodermal lineage, the M lineage, and tha
194 mesoderm development in C. elegans using the
postembryonic mesodermal M lineage as a model system.
195 is elegans member of this family (CeMyoD) in
postembryonic mesodermal patterning.
196 ect of adding TH to the rearing water of the
postembryonic Mexican axolotl was reinvestigated under c
197 Here we examine their roles in the
postembryonic migration of the P cell neuroblasts and th
198 of actin filaments appear during each of the
postembryonic molts when new cuticles are synthesized.
199 entify genes and cell behaviors required for
postembryonic morphogenesis and differentiation.
200 osophila RhoA (Rho1) GTPase is essential for
postembryonic morphogenesis of leg and wing imaginal dis
201 a number of fundamental processes within the
postembryonic muscle lineage, such as cell division pola
202 t did not indicate the production of glia by
postembryonic mushroom body neuronal precursors.
203 te hypothalamus as a model for Wnt-regulated
postembryonic neural progenitor differentiation and defi
204 We show that expression of pal-1 in the
postembryonic neuroblast cell V6 can be initiated by two
205 adherin DE-cadherin is expressed globally by
postembryonic neuroblasts and their lineages ("secondary
206 Two of these
postembryonic neuroblasts generate solely motoneurons th
207 iously attributed to cytokinesis failures in
postembryonic neuroblasts.
208 ession of a C. elegans Hox gene, egl-5, in a
postembryonic neuroectodermal cell lineage.
209 Postembryonic neurogenesis has been observed in several
210 tion will be important for future studies on
postembryonic neurogenesis in Drosophila.
211 that additional behaviors may be affected by
postembryonic neurogenesis in this brain structure.
212 ation of distinct neuronal cell types during
postembryonic neurogenesis.
213 al changes affect lineage progression during
postembryonic neurogenesis.
214 affect the number of ABLKs generated during
postembryonic neurogenesis.
215 , which contain 25 individually identifiable
postembryonic neuronal lineages.
216 ons as a permissive signal for embryonic and
postembryonic neuronal migration in the nematode C. eleg
217 s are important for the accurate guidance of
postembryonic neuronal migrations in the nematode Caenor
218 acking exon 19 or exon 23 effectively blocks
postembryonic neuronal morphogenesis.
219 The GABA phenotype is lineally determined in
postembryonic neurons in the tobacco hawkmoth, Manduca s
220 the reaper and grim genes act in concert in
postembryonic neurons to induce apoptosis.
221 t and differentiation of discrete subsets of
postembryonic neurons.
222 ate the specification and differentiation of
postembryonic neurons: for example, Nkx6 is necessary an
223 We conclude that betaPS integrin at the
postembryonic NMJ is a critical determinant of morpholog
224 PS integrins appear at
postembryonic NMJs coincident with the onset of rapid mo
225 o investigate in vivo the role of ST3 during
postembryonic organ development in vertebrates.
226 s have been reported on the roles of MMPs in
postembryonic organ development.
227 he function of MMPs during embryogenesis and
postembryonic organ development.
228 oration of developmental pre-patterns during
postembryonic organ development.
229 e for Arabidopsis thaliana embryogenesis and
postembryonic organ formation.
230 lateral roots represents one example of such
postembryonic organogenesis.
231 a gene regulatory network (GRN) that directs
postembryonic organogenesis.
232 l for elucidating the mechanisms controlling
postembryonic organogenesis.
233 m cell populations is critical for extensive
postembryonic organogenesis.
234 sible for the initiation of all above-ground
postembryonic organs, in most plants the vast majority o
235 Legume roots form two types of
postembryonic organs, lateral roots and symbiotic nodule
236 yogenesis and the formation of embryonic and
postembryonic organs.
237 These data suggest that
postembryonic partial loss of AgRP/NPY neurons leads to
238 ive auxin gradients as well as embryonic and
postembryonic patterning are severely compromised.
239 e lipids and are essential for embryonic and
postembryonic patterning.
240 Both cdr-4 and cdr-6 are transcribed in
postembryonic pharyngeal and intestinal cells in C. eleg
241 plant stem cells remain quiescent until the
postembryonic phase of development.
242 The
postembryonic phase produces the adult specific compound
243 quiescence separating distinct embryonic and
postembryonic phases of proliferation.
244 studying the genetic and cellular bases for
postembryonic phenotypes.
245 y, also for other polarization events during
postembryonic plant life.
246 e to form new organs is a key feature of the
postembryonic plasticity of plant development, and the e
247 alphaPS2 is essential for both embryonic and
postembryonic processes, while this portion of alphaPS1
248 Postembryonic production of hair cells, the highly speci
249 Postembryonic production of inner ear hair cells occurs
250 e potential and lineage segregation of these
postembryonic progenitors is poorly understood, and it i
251 Postembryonic RCN1 function is required to maintain norm
252 idence also implicates these pathways in the
postembryonic regulation of stem-cell number in epitheli
253 study addresses this goal by describing the
postembryonic remodeling of the excitability and dendrit
254 basement membrane to insulate axons from the
postembryonic remodeling of their targets.
255 Similar defects are observed upon
postembryonic removal of two C2H2 zinc finger transcript
256 g the correct cell types and patterns during
postembryonic replacement of sensory epithelial cells in
257 xpression, ptc-3(RNAi) reveals an additional
postembryonic requirement for ptc-3 activity.
258 In addition, we document
postembryonic requirements for punt activity.
259 enerate the rod photoreceptor lineage in the
postembryonic retina.
260 Postembryonic RNA interference of PAR-1 causes a protrud
261 Here, we define a new
postembryonic role for gooseberry.
262 ressed embryonically, and plays an essential
postembryonic role in tissue integrity, it is not requir
263 e activity plays a unique role in regulating
postembryonic root development and stress response.
264 ristem maintenance and cell expansion during
postembryonic root development in Arabidopsis.
265 -borne beneficial bacteria to interfere with
postembryonic root developmental programs.
266 date, we initially describe the diversity of
postembryonic root forms.
267 s callus formation precedes specification of
postembryonic root founder cells, from which roots are i
268 undamental structure that is responsible for
postembryonic root growth.
269 any meristem 3 (BAM3) perfectly suppress the
postembryonic root meristem growth defect and the associ
270 However, many other programs of
postembryonic root organogenesis exist in angiosperms.
271 embryos, leading to a loss of embryonic and
postembryonic root stem cells and vascular specification
272 The discovery of emp2 mutant phenotypes in
postembryonic shoots reveals that the duplicate genes em
273 oughout the embryo and to a few well-defined
postembryonic sites.
274 Postembryonic SKN-1 functions have not been elucidated.
275 Their expression is initiated at a precise
postembryonic stage, long after PVT has been generated i
276 e posterior telencephalic roof, activated at
postembryonic stages and persisting lifelong.
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 tanding paradox of ESC dispensability during
postembryonic times.
292 n formation during embryonic development and
postembryonic tissue homeostasis.
293 s in transcriptional activation by TR during
postembryonic tissue remodeling by using amphibian metam
294 cells in long-distance communication during
postembryonic tissue remodeling.
295 hog (Hh) signaling during development and in
postembryonic tissues requires activation of the 7TM onc
296 uring embryos and seeds; it also occurred in
postembryonic tissues, especially in association with va
297 ads to severe phenotypes in embryos and many
postembryonic tissues.
298 s to the maintenance of dFMRFa expression by
postembryonic Tv neurons, although the strength of its r
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