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1 ined analyses examining its emergence during organogenesis.
2 rphogenesis and other symmetry breaks during organogenesis.
3 how that this region is essential for nodule organogenesis.
4 , heterogeneity, and functions during kidney organogenesis.
5 hrogenesis as niches remodel and grow during organogenesis.
6 ole in controlling retinoid gradients during organogenesis.
7 odel for the study of complex human endoderm organogenesis.
8 mutants revealed that NiCK4 promotes nodule organogenesis.
9 essing sites that are implicated in prostate organogenesis.
10 ated cytokinin signaling in symbiotic nodule organogenesis.
11 . elegans vulval development, a paradigm for organogenesis.
12 ing programs and are essential for mammalian organogenesis.
13 on of appropriate lineage differentiation in organogenesis.
14 a paradigm for understanding many aspects of organogenesis.
15 ent despite loss of LTbetaR-mediated medulla organogenesis.
16 pecies are needed to infer the principles of organogenesis.
17 ad implications for understanding epithelial organogenesis.
18 cell expansion during murine salivary gland organogenesis.
19 d its known roles in plant growth and floral organogenesis.
20 ear how lineages are regulated during kidney organogenesis.
21 rucial for postnatal tissue homoeostasis and organogenesis.
22 he establishment of vascular networks during organogenesis.
23 sible for KIT(+) progenitor expansion during organogenesis.
24 ts are critical for proper embryogenesis and organogenesis.
25 proach to study the mechanism of human liver organogenesis.
26 ty in nephron progenitor cells during kidney organogenesis.
27 required for multiple aspects of pancreatic organogenesis.
28 -1958 bp) affects minor or major aspects of organogenesis.
29 offers an attractive model for investigating organogenesis.
30 hy of periodic patterning modes operating in organogenesis.
31 and fate determination critically influences organogenesis.
32 ghly migratory and significant to vertebrate organogenesis.
33 emains one of the least understood phases of organogenesis.
34 subset transcripts associated with prostate organogenesis.
35 of estrogen's direct effect on mammary gland organogenesis.
36 apitulate cell interactions occurring during organogenesis.
37 ester, the etiologically relevant period for organogenesis.
38 l, differentiation, and proliferation during organogenesis.
39 mice by study of embryos undergoing advanced organogenesis.
40 e, specification of pancreatic cell fate and organogenesis.
41 nds on its adequate supply to achieve proper organogenesis.
42 e lineage-restricted progenitor cells during organogenesis.
43 specify this cellular spatial domain during organogenesis.
44 oth cell types during fate specification and organogenesis.
45 ate the role of Pol II pausing in vertebrate organogenesis.
46 soderm interactions that orchestrate foregut organogenesis.
47 o the liver vasculature and defects in liver organogenesis.
48 nately induce rhizobial infection and nodule organogenesis.
49 liferation to differentiation is crucial for organogenesis.
50 an integrated transcriptomic atlas of human organogenesis.
51 the meristematic competence of cells during organogenesis.
52 acid (RA) metabolism is critical for spleen organogenesis.
53 gnaling pathway, which is essential for skin organogenesis.
54 for infection thread progression and nodule organogenesis.
55 e specification and organ development during organogenesis.
56 es during mammalian cell differentiation and organogenesis.
57 ECM markers, contribute to morphogenesis and organogenesis.
58 controls both rhizobial infection and nodule organogenesis.
59 at ligand back-signaling contributed to skin organogenesis.
60 ial for specific aspects of auditory-related organogenesis.
61 I) endocrine-committed cells during pancreas organogenesis.
62 ing the fate of epithelial stem cells during organogenesis.
63 ndoderm patterning, organ specification, and organogenesis.
64 he nucleus and cytoplasm during lateral root organogenesis.
65 late later developmental events during petal organogenesis.
66 o define how this hypertrophy contributes to organogenesis.
67 ed by massive cell death and defect in liver organogenesis.
68 rebrain and establish novel roles of Pax6 in organogenesis.
69 es such as proliferation, transcription, and organogenesis.
70 l the transcriptional programs that underpin organogenesis.
71 ly tractable model of complex self-organized organogenesis.
72 cations across thirteen tissues during human organogenesis.
73 ue specificity during gastrulation and early organogenesis.
74 rphogenesis during embryonic development and organogenesis.
75 opmental program is used in Lotus for nodule organogenesis.
76 for stem cell niche re-establishment during organogenesis.
77 is known to control plant growth and floral organogenesis.
78 uxin-dependent transcription associated with organogenesis.
79 ss to the regulatory blueprint for mammalian organogenesis.
80 cluding immune responses, hematopoiesis, and organogenesis.
81 he complex morphogenetic processes of native organogenesis.
82 n and differentiation are coordinated during organogenesis.
83 gene expression dynamics during human heart organogenesis.
84 ighlight a vital role for MYOCD in mammalian organogenesis.
85 d," are mainly cis elements that act late in organogenesis.
86 ls, which is a prerequisite for lateral root organogenesis.
87 dal signaling cascade to initiate asymmetric organogenesis.
88 ophila larval wing disc, a genetic model for organogenesis.
89 indings define a novel mechanism of impaired organogenesis, accelerated ubiquitin-directed proteasoma
92 amental communication between tissues during organogenesis and are primarily regulated by growth fact
95 that regulate fundamental processes, such as organogenesis and cell growth, and elevated TEAD activit
100 ithelial-mesenchymal signaling in human lung organogenesis and help to explain the histopathological
103 ole for polyamine biosynthesis in pancreatic organogenesis and identified that it may be possible to
105 cent work in understanding the regulation of organogenesis and in particular leaf formation, highligh
106 ntral role in cross signaling between nodule organogenesis and infection processes; and Symbiosis Rec
108 for thymic tolerance segregates from medulla organogenesis and instead involves LTbetaR-mediated regu
109 ysis of Mnx1 function during murine pancreas organogenesis and into the adult uncovered novel stage-s
110 into the requirement of 12-LOX in pancreatic organogenesis and islet formation, and additionally prov
112 peripheral tissues, where they contribute to organogenesis and later constitute the first line of pro
113 aning), with only a small effect on pancreas organogenesis and no deficiencies in their female counte
114 extend our understanding of gastrointestinal organogenesis and of how Wnt and BMP might coordinate ge
115 transcription factor involved in endodermal organogenesis and pancreatic precursor cell differentiat
117 erved hedgehog (Hh) pathway is essential for organogenesis and plays critical roles in postnatal tiss
119 al primary afferent neurons of the TG during organogenesis and provide a rationale to explore whether
120 r ANKS6 in regulating Hippo signaling during organogenesis and provides mechanistic insights into the
121 rcing the view that the capacity for de novo organogenesis and regeneration from mature plant tissues
126 capitulated several aspects of hepatobiliary organogenesis and resulted in concomitant formation of p
128 ed and new roles of senescence in vertebrate organogenesis and support the view that cellular senesce
130 r early nodulation to coordinate root nodule organogenesis and the progression of bacterial infection
131 ith an essential yet uncharacterized role in organogenesis and tissue homeostasis, was identified as
134 lay crucial roles in vertebrate development, organogenesis and when dysfunctional result in pleiotrop
136 for malformations and spontaneous abortion (organogenesis), and the second/third trimesters are the
138 the discrete action of extrinsic factors in organogenesis, and allow for the discovery of relationsh
140 for deciphering the molecular mechanisms of organogenesis, and has thus been of longstanding interes
141 during early development through to terminal organogenesis, and it regulates many aspects of cell pos
142 ultiple stages to regulate infection, nodule organogenesis, and nitrogen fixation in L. japonicus.
143 essential for cell-type differentiation and organogenesis, and plant cells produce amounts of GlcCer
144 critical and non-redundant roles for Ano1 in organogenesis, and show that chloride channels are essen
145 gnals act on tissue-level mechanics to drive organogenesis, and suggest a possible mechanism by which
146 reciated role of metabolic regulation during organogenesis, and suggests that it might contribute to
147 erning organelle biogenesis are simpler than organogenesis, and therefore organelle size scaling in t
148 embryos revealed major tissue types in early organogenesis as well as fine features like microvascula
149 phage differentiation is an integral part of organogenesis, as colonization of organ anlagen by pMacs
155 yed as a recurrent module to stimulate plant organogenesis, at least in part by enabling rapid cellul
156 signalling cascade is essential for lymphoid organogenesis, B cell maturation, osteoclast differentia
159 t Pals1 is not only essential for cerebellum organogenesis, but also for preventing premature differe
160 tein 1 (FSTL1) plays a critical role in lung organogenesis, but is downregulated during lung cancer d
161 g plays important roles in the regulation of organogenesis, but its impact on cardiovascular differen
162 hoid tissue inducer (LTi) cells and lymphoid organogenesis, but its role in postnatal ILC3s is unknow
163 gous pluripotent cells can result in de-novo organogenesis, but the technique is complex, not widely
164 transcription factors are known to regulate organogenesis, but their molecular targets and function
166 cale-bridging, in vivo studies of vertebrate organogenesis by cell-accurate structure-function mappin
167 t potassium deficiency inhibits lateral root organogenesis by delaying early stages in the formation
168 chimeric hosts and allows for initiation of organogenesis by donor mouse pluripotent stem cells (PSC
169 Blood vessels serve as key regulators of organogenesis by providing oxygen, nutrients and molecul
170 together, our data show that normal blastema organogenesis cannot occur without timely infiltration o
173 have emerged as a valuable tool for studying organogenesis, cell-to-cell stromal communication and di
178 ging from pharyngeal pouch endoderm in early organogenesis, differential Foxa1/Foxa2 expression disti
179 naling pathway and involved in regulation of organogenesis, differentiation, cell migration and proli
182 ta1 and PI4KIIIbeta2 is essential for the LR organogenesis driven by endocytic trafficking to the vac
186 ine by embryonic day (E) 13.5 and, before PP organogenesis (E14.5-15), are broadly dispersed in the p
188 e-resident myeloid cells that develop during organogenesis from yolk-sac erythro-myeloid progenitors
189 gnals required for successful ectopic kidney organogenesis, given the established role of NIK in neov
191 temporal gene expression trajectories during organogenesis have been challenging because diverse cell
192 XCL12 mediate directed cell migration during organogenesis, immune responses, and metastatic disease.
196 e mechanisms behind nephrogenesis and kidney organogenesis in an ex vivo organ culture/organoid setti
202 osure during pregnancy on prenatal/postnatal organogenesis in offspring and in predisposing metabolic
207 se factors have been shown to play a role in organogenesis in various diverse model species, revealin
209 pathway directs cell differentiation during organogenesis, in part by restricting proliferation.
210 dvances in stem cell-derived models of human organogenesis, in the form of three-dimensional organoid
211 ANT and AIL6/PLT3 regulate aspects of floral organogenesis, including floral organ initiation, growth
212 -coding RNAs, that potentially contribute to organogenesis, including tissue-specific regulation betw
214 cking to the vacuole positively regulates LR organogenesis independently of the auxin complex recepto
215 ological processes, including hematopoiesis, organogenesis, inflammation, tissue repair, and thermoge
223 hemical and transcriptional factors to shape organogenesis is an important question in developmental
235 ed Hair follicle Neogenesis (WIHN), an adult organogenesis model where stem cells regenerate de novo
238 asing recognition as important regulators of organogenesis motivate the development of methods to eff
239 tresia-like phenotypes and hepatitis in late organogenesis mouse embryos, but the molecular and cellu
240 functions for some members of this family in organogenesis, neurodevelopment, myelination, angiogenes
245 ROPICA (DGT), have been shown to abolish the organogenesis of lateral roots; however, a mechanistic e
247 verse regulatory and patterning roles during organogenesis of the intestine and in the regulation of
249 BX4 is an essential transcription factor for organogenesis of the lungs, pelvis, and hindlimbs in hum
254 y overlap with genes associated with SIX1 in organogenesis or human tumors, and show coincident regul
255 processes including tissue remodeling during organogenesis, organ homeostasis, repair following injur
260 ing the genetic switches controlling the NLS organogenesis program in crops, especially cereals, can
262 ctions, ILC3s crucially orchestrate lymphoid organogenesis, promote tissue protection or regeneration
264 noids, three-dimensional cultures that model organogenesis, provide a new platform to investigate hum
269 the model plant Arabidopsis thaliana, floral organogenesis requires AINTEGUMENTA (ANT) and AINTEGUMEN
272 otes lateral root growth but prevents nodule organogenesis, rhizobial infection, and the induction of
273 ring the hyperglycemia-susceptible period of organogenesis significantly reduced NTDs and cell apopto
274 transcription factor Pdx1 controls pancreas organogenesis, specification of endocrine pancreas proge
275 ns, they have been shown to be important for organogenesis, spermatogenesis, and male hormone product
276 Dnaaf2 mouse embryos fail to progress beyond organogenesis stages with many abnormalities including l
277 of arachidonic acid increase sharply during organogenesis stages, and that this increase is blocked
278 ination between the genes suppressing female organogenesis (SUPPRESSOR OF FEMALE FUNCTION) and promot
281 es have advanced our understanding of nodule organogenesis, the functioning of symbiotic cells, and t
284 potential of mESCs to execute key aspects of organogenesis through the coordinated development of mul
286 as a major driver of embryonic development, organogenesis, tissue homeostasis, and tumor disseminati
287 of a cell's genome) frequently arises during organogenesis, tissue repair, and age-associated disease
288 across developmental time points from early organogenesis to adulthood for human, rhesus macaque, mo
291 izobial invasion of the epidermis and nodule organogenesis was unaffected but rhizobia remain restric
292 prehensive chromatin landscapes during early organogenesis, we mapped chromatin accessibility in 19,4
293 d an indispensable role for Pdx1 in pancreas organogenesis, we used Elastase-Cre-mediated recombinati
296 tly undergo fundamental steps of early heart organogenesis with an in-vivo-like spatiotemporal fideli
297 anscription factors, important regulators of organogenesis, with the Hippo tumor suppressor pathway t
298 , genes of signaling components important in organogenesis (Wnt, TGFbeta/ BMP, FGF, Notch, SHH, Erbb)
299 in efforts to disentangle the complexity of organogenesis, yet adoption of the potent new toolbox pr
300 l and systemic roles in murine mammary gland organogenesis, yet specific functions remain undefined.