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1 sting that BMPER may play a role in coronary vascular development.
2 not been specifically implicated in coronary vascular development.
3 al role for seryl-tRNA synthetase (SerRS) in vascular development.
4  of synaptic connectivity and is involved in vascular development.
5    Neurons have an important role in retinal vascular development.
6 bryonic lethality at E11 because of impaired vascular development.
7 o1 protein senses mechanical force to enable vascular development.
8 rane receptors involved in axon guidance and vascular development.
9 il1-Dll4/Notch1 axis that controls embryonic vascular development.
10 ty between E11.5 and E12.5 due to defects in vascular development.
11 (FGFR) signalling as a critical regulator of vascular development.
12 + cells in the kidney and its role in kidney vascular development.
13 en have been established to be regulators of vascular development.
14 aintaining normal mitochondrial function and vascular development.
15 th Norrin/Frizzled4 signaling to control CNS vascular development.
16 t important and complex signaling systems in vascular development.
17      Capillaries expressed gene programs for vascular development.
18 mine if the oxidase activity was crucial for vascular development.
19 of the most critical events during embryonic vascular development.
20 /RhoA-mediated pathway to promote vertebrate vascular development.
21 , functionally equivalent ligands of ALK1 in vascular development.
22 omolog (dcbld2) in zebrafish impaired normal vascular development.
23 mediate touch perception, proprioception and vascular development.
24 ions and directed cell rearrangements during vascular development.
25  that Nrf2 is increased and activated during vascular development.
26 tion, and their specification is crucial for vascular development.
27  essential function of glutaredoxin 2 during vascular development.
28 acts in part via Wnt5a to regulate pulmonary vascular development.
29 nal repression by microRNAs, to allow normal vascular development.
30 c cell signaling that is required for normal vascular development.
31 es, with absence of any detectable defect in vascular development.
32 (SRF) is known to be important for embryonic vascular development.
33 icroRNAs contribute to its repression during vascular development.
34 d in the vascular tissues and regulate shoot vascular development.
35 s through vascular S1P receptors to regulate vascular development.
36 4 is dispensable for embryonic viability and vascular development.
37 y for monolignol polymerization during plant vascular development.
38 scent vessels and arterial maturation during vascular development.
39 trin-4-induced biological effects related to vascular development.
40 the canonical Wnt pathway to control retinal vascular development.
41  cause appreciable defects in normal retinal vascular development.
42 transcription factor FoxC1 regulates corneal vascular development.
43 death receptors DR6 and TROY in CNS-specific vascular development.
44 s high plasticity and cell type diversity in vascular development.
45  these cadherins play a nonredundant role in vascular development.
46 ta introduce LRP1 as a critical regulator of vascular development.
47 ause its role has been implicated in retinal vascular development.
48 reveal a crucial role for GATA2 in lymphatic vascular development.
49 ment, as an important regulator of lymphatic vascular development.
50 n of proper lung epithelial, mesenchymal and vascular development.
51 hway and mediates stem cell self-renewal and vascular development.
52 d for the involvement of the Wnt pathways in vascular development.
53 pported by observations of Wnt signalling in vascular development.
54 ges expression of multiple genes involved in vascular development.
55 modulation of Wnt signaling during embryonic vascular development.
56 pected role for this transcription factor in vascular development.
57 en shown to control shoot meristem, root and vascular development.
58 dination of lung epithelial, mesenchymal and vascular development.
59 ivate SLP-76 signaling to regulate embryonic vascular development.
60  signaling is required to regulate lymphatic vascular development.
61 ene Prox1 is crucial for mammalian lymphatic vascular development.
62 mary and lung morphogenesis as well as blood vascular development.
63 obiotic metabolizing enzymes, and in hepatic vascular development.
64 ve and migratory properties essential during vascular development.
65 , leading to both increased and well-ordered vascular development.
66 might contribute to fibronectin assembly and vascular development.
67 mechanism for physiologic processes, such as vascular development.
68 le precursor vessel, a process essential for vascular development.
69 1b, are primarily expressed during embryonic vascular development.
70 sted KANK genes were co-opted for vertebrate vascular development.
71 ed GPCR crosstalk, which plays a key role in vascular development.
72 erscore the importance of the S1P pathway in vascular development.
73 T signaling and Sox17 to ensure normal brain vascular development.
74  receptor APLNR, is known to be important in vascular development.
75 n in pregnancy characteristics and childhood vascular development.
76 cating that MCs mostly cover arteries during vascular development.
77 ut mice have previously implicated MAP3K3 in vascular development.
78  while secondary vascular stem cells sustain vascular development.
79  levels, demonstrated a similar reduction in vascular development.
80 ein alpha-parvin (alpha-pv) is essential for vascular development.
81 f mice to study its role in angiogenesis and vascular development.
82 of endoreduplication, KAK may play a role in vascular development.
83 yonic lethality because of severe defects in vascular development.
84 t Mekk3 plays an intrinsic role in embryonic vascular development.
85 ming and extent of GPCR-mediated cardiac and vascular development.
86 ates angiogenic SLIT3-ROBO4 signaling during vascular development.
87 g the requirement of WNK1-OSR1 signaling for vascular development.
88 mice displayed significantly delayed retinal vascular development, absence of deep layer retinal vess
89 lishing the venous identity during embryonic vascular development, also regulates the pathophysiologi
90 vity, protein metabolism, cell adhesion, and vascular development, among others.
91 ia probably plays an important role in plant vascular development and adaptation to land environments
92 ults in the profound impairment of postnatal vascular development and adult angiogenesis, lymphangiog
93          Here we show that it also regulates vascular development and adult angiogenesis.
94                                              Vascular development and angiogenesis initially depend o
95 ignaling family, plays a fundamental role in vascular development and angiogenesis.
96 ental processes and has an essential role in vascular development and angiogenesis.
97 nd Notch ligand, plays a fundamental role in vascular development and angiogenesis.
98 in-dependent transcription recapitulated the vascular development and barrier defects associated with
99 5) and LRP6 had redundant functions in brain vascular development and barrier maintenance; however, l
100 hat loss of NDST1 causes defective diaphragm vascular development and CDH and that heparan sulfate fa
101 n plays a crucial role in both physiological vascular development and common blinding diseases.
102 4 as a critical regulator of early lymphatic vascular development and demonstrate that mutations in t
103 ist regarding our understanding of pulmonary vascular development and disease in preterm infants at r
104 different pathways in growth factor actions, vascular development and disease, and are worthy of furt
105 phatase-5 (DUSP5), and its role in embryonic vascular development and disease, we hypothesized that m
106 o summarize the emerging roles of lncRNAs in vascular development and disease.
107  now emerging as key regulators of mammalian vascular development and disease.
108  in endothelial cells is required for normal vascular development and embryonic viability.
109 nstream signals that play essential roles in vascular development and endothelial integrity, control
110 s with FZD4, a receptor important in retinal vascular development and frequently mutated in Norrie di
111 he molecular mechanisms underlying lymphatic vascular development and function are not well understoo
112 tch signaling pathway is required for normal vascular development and function, and genetic associati
113 shear forces have established roles in blood vascular development and function, but whether such forc
114  critical requirement for the Abl kinases in vascular development and function, which may have import
115 GF-A) is a master regulator of angiogenesis, vascular development and function.
116 terial-venous differentiation is crucial for vascular development and function.
117 ntrol GATA4 exercises over specialized liver vascular development and function.
118        However, VEGFA also regulates retinal vascular development and functions as a retinal neural s
119  have uncovered a critical role for Egfl7 in vascular development and have shown that some of these f
120                       They are important for vascular development and hematopoiesis, immune and infla
121  an essential role in gene regulation during vascular development and hematopoietic differentiation.
122 orm to uncover the molecular determinants of vascular development and heterogeneity and potentially r
123 d support a critical role for VEGF-D in lung vascular development and homeostasis.
124  ATOH7, especially its importance in retinal vascular development and hyaloid regression.
125  analyses suggest that PVE1 functions during vascular development and in mediolateral and dorsiventra
126 xact contribution of these components in CNS vascular development and in specification of the blood-b
127 a mutant rootstock results in restoration of vascular development and lateral root initiation.
128 r processes, particularly those that lead to vascular development and maintenance.
129 n of endothelial cell adhesion is central to vascular development and maintenance.
130 growth factor (VEGF)-dependent regulation of vascular development and metabolism, little is understoo
131 he KIF11 gene likely plays a role in retinal vascular development and mutations in this gene can lead
132           Notch signaling mediates embryonic vascular development and normal vascular remodeling; Not
133 f cytotrophoblasts to facilitate appropriate vascular development and oxygenation during pregnancy.
134 al growth factor trap (VEGF Trap) on retinal vascular development and pathologic neovascularization (
135 -beta co-receptor, play an essential role in vascular development and pathological angiogenesis.
136 nses to fluid shear stress are essential for vascular development and physiology, and determine the f
137 1-phosphate (S1P) signaling is essential for vascular development and postnatal vascular homeostasis.
138 lnutrition specifically impacts fetal kidney vascular development and prevents full functionality of
139 recent contributions to the understanding of vascular development and remodelling.
140                               Thus, abnormal vascular development and resulting hypoxia may contribut
141 well as their basis in general mechanisms of vascular development and stability.
142 that are believed to play important roles in vascular development and stability.
143 ical role in a number of processes including vascular development and stabilization, lymphocyte migra
144 ith the usual role of flow directionality in vascular development and suggests that the full spatial
145 helial Notch signaling is critical for early vascular development and survival.
146 gest a pathway that integrates initiation of vascular development and testis cord morphogenesis, and
147 tor-beta (TGFbeta) play pivotal roles during vascular development and the pathogenesis of vascular di
148 ngineered vessels and play a crucial role in vascular development and the pathogenic events of vascul
149 s a matricellular protein involved in normal vascular development and tissue repair.
150 though Twist1 also plays a role in embryonic vascular development and tumor angiogenesis, the molecul
151 by regulating endothelial genes critical for vascular development and vascular endothelial growth fac
152 as lymphocyte trafficking, cardiac function, vascular development, and inflammation.
153  trafficking, organization of immune organs, vascular development, and neuroinflammation.
154 ial ligand for endothelial Alk1 in embryonic vascular development, and provide evidence that circulat
155 thesis, secondary cell wall biosynthesis and vascular development, and regulation of growth were alte
156  cell (SMC) differentiation is essential for vascular development, and TGF-beta signaling plays a cri
157 l processes such as branching morphogenesis, vascular development, and the differentiation of multipo
158   The VEGF-A isoforms play a crucial role in vascular development, and the VEGF signaling pathway is
159  the major approaches used in studying plant vascular development, and we cover the mechanisms and ge
160  vitro models for the investigation of renal vascular development are limited.
161 ower root diameter, indehiscent anthers, and vascular development arrest with lack of lignification.
162 Focal adhesion kinase (FAK) is essential for vascular development as endothelial cell (EC)-specific k
163 e demonstrate that YAP/TAZ are essential for vascular development as endothelium-specific deletion of
164 iogenesis, is a central process in embryonic vascular development as well as in adult tissues.
165 suggest that anthracycline treatment impairs vascular development as well as progenitor cell function
166 egulating endothelial cadherin levels during vascular development, as well as microvascular patternin
167 characterized by an arrest in normal retinal vascular development associated with microvascular degen
168  overexpression in the early embryo inhibits vascular development at midgestation, but Edn2 overexpre
169 ion in newborn mice not only blocked retinal vascular development but also suppressed astrocytic diff
170        Integrin alpha5beta1 is essential for vascular development but it remains unclear precisely wh
171 ephrinB2 are known key regulators of retinal vascular development, but due to their capacity for bidi
172         A lack of opticin does not influence vascular development, but opticin is antiangiogenic and
173 dependent and -dependent functions of FAK in vascular development by creating and analyzing an EC-spe
174 emonstrate that platelets regulate lymphatic vascular development by directly interacting with lympha
175  is to examine the role of p120 in mammalian vascular development by generating a conditionally mutan
176 gnaling specifies arterial fate during early vascular development by inducing the transcription of De
177 thelin-2 (Edn2) in the mouse retina perturbs vascular development by inhibiting endothelial cell migr
178 eal that EC Map4k4 is critical for lymphatic vascular development by regulating EC quiescence and lym
179 tch1-Delta-like 4 (Dll4) signalling controls vascular development by regulating endothelial cell (EC)
180 upport a critical role for GIT1 in pulmonary vascular development by regulating VEGF-induced PLCgamma
181 n regulating secondary wall formation during vascular development by tissue- or cell-specific modulat
182 s Review, we will discuss how the process of vascular development can be used to guide approaches to
183 zed that somatic mosaic mutations disrupting vascular development cause both the Sturge-Weber syndrom
184 tion, bone/joint formation, axonal guidance, vascular development, cell proliferation and cell moveme
185  not single knockout mice displayed dramatic vascular development defects.
186     Thus, the essential function of SerRS in vascular development depends on UNE-S.
187 -2 function is required for proper lymphatic vascular development during embryogenesis.
188 ght an essential role of mammalian Piezo1 in vascular development during embryonic development.
189 in vivo monitoring of hemodynamic status and vascular development, especially in the brain.
190 provides new insights into the mechanisms of vascular development, function, and dysfunction.
191 logical responses, the involvement of EVs in vascular development, growth, and maturation has been wi
192          Our understanding of the process of vascular development has gained significant refinement i
193 rphogenesis, but how NRP1 functions to guide vascular development has not been completely elucidated.
194 erization of an endogenous role for VEGFD in vascular development has remained elusive.
195 -1 (Ang-1) and angiopoietin-2 (Ang-2) during vascular development have been extensively investigated,
196 iogenesis and vessel wall integrity), FOXC2 (vascular development), hemochromatosis (involved in veno
197 minant-negative PKA in mice led to perturbed vascular development, hemorrhage and embryonic lethality
198 at microRNAs (miRNAs) play a pivotal role in vascular development, homeostasis and a variety of disea
199                 Forces play diverse roles in vascular development, homeostasis and disease.
200 ch signaling pathway (Notch) is essential to vascular development, homeostasis, and sprouting angioge
201   We give particular attention to aspects of vascular development, homoeostasis, and response to envi
202                    TGF-beta is essential for vascular development; however, excess TGF-beta signaling
203 rtant yet little understood aspects of brain vascular development, implicating for the first time a f
204  cytokine biosynthesis, and angiogenesis and vascular development in (adjusted P<0.1).
205 ient SEMA3-NRP1 signaling on fetal pulmonary vascular development in a mouse model.
206 ermline Vegfr-1(-/-) embryos die of abnormal vascular development in association with excessive endot
207 lant secondary cell walls forms the basis of vascular development in land plants, with xylem tissues
208  reported lack of yolk-sac hematopoiesis and vascular development in Ldb1(-/-) mouse result from a de
209 d in vivo application of GW9662 also reduced vascular development in Matrigel plugs.
210 132, anti-miR-132, reduced postnatal retinal vascular development in mice.
211                   Many genes associated with vascular development in other species show enriched expr
212 g adequate comparison of normal and abnormal vascular development in pregnancy disease.
213 ortant role of Wnt signaling in pathological vascular development in retinopathy and show a novel fun
214  RPE and iris development, ocular growth and vascular development in the anterior chamber, whereas Vh
215 Itgb8) have been shown to result in abnormal vascular development in the CNS, including prenatal and
216 l NOTCH ligand, due to its essential role in vascular development in the context of cardiovascular fe
217  receptor of SLIT3, aggravated the defect in vascular development in the diaphragm and CDH.
218 urine endothelium (Ndst1ECKO mice) disrupted vascular development in the diaphragm, which led to hypo
219 uxin accumulation in auxin-mediated root and vascular development in the embryo.
220 r of angiogenic sprouting and is involved in vascular development in the embryo.
221 e in utero during early gestation for normal vascular development in the eye.
222 nd pro-angiogenic miR-130a affect airway and vascular development in the fetal lungs.
223 gated the hypothesis that opticin influences vascular development in the posterior segment of the eye
224 leiotropic abnormalities, including impaired vascular development in the yolk sac (YS).
225 n of angiogenesis, a direct role for TARS in vascular development in the zebrafish could be demonstra
226                                              Vascular development in UBR4-deficient YS normally advan
227 of FRG1 protein is critical for muscular and vascular development in vertebrates; however, its precis
228          However, their role on vSMCs during vascular development in vivo remains unclear.
229  angiogenesis in vitro and postnatal retinal vascular development in vivo.
230 of Elmo1 and Dock180 in human ECs and during vascular development in zebrafish embryos.
231 es endothelial migration, tube formation and vascular development in zebrafish that is, CLEC14A regul
232 and s1pr2 function cooperatively to regulate vascular development in zebrafish.
233 azoans and is required for many processes in vascular development, including arterial-venous differen
234 ent that influences several aspects of plant vascular development, including cell division in the vas
235 expression of endothelial genes critical for vascular development, including vascular endothelial gro
236                                              Vascular development is a complex process regulated by d
237 tic proteins (BMPs) and their antagonists in vascular development is increasingly being recognized.
238 idence that demonstrates a role for ENOX1 in vascular development is lacking.
239 ted IOP, demonstrating that anterior chamber vascular development is sensitive to Tek gene dosage and
240       A key cell type that regulates retinal vascular development is the astrocyte.
241                          The role of p120 in vascular development is unknown.
242 gh the function of VEGF-NRP1 interactions in vascular development is well described, the importance o
243 sence of NG2(+) glia drastically affects the vascular development leading to severe reduction of rami
244 ve been recently described to play a role in vascular development, lineage commitment, and in mesoder
245 st that Etv2 is dynamically regulated during vascular development, little is known about the mechanis
246 melanoma cells together with VEGF to promote vascular development mediated by (V600E)B-Raf signaling.
247 are affected, S1P signaling is essential for vascular development, neurogenesis, and lymphocyte traff
248 ad range of investigations of mural cells in vascular development, neurovascular coupling and neuropa
249                                              Vascular development of the central nervous system and b
250 r1 and s1pr2 is suppressed, severely reduced vascular development of the intersegmental vessels was o
251  differentiation of retinal pericytes during vascular development of the retina.
252 IVNV without affecting physiological retinal vascular development or overall pup growth.
253 ut adversely affecting physiological retinal vascular development or pup weight gain.
254 ulating effects of Vegf during early retinal vascular development, our data suggest a modest involvem
255 Etv2 gene ceases at midgestation; therefore, vascular development past this stage must continue indep
256                                       During vascular development, physical forces originating from a
257  HTS data with the cell-agent based model of vascular development predicted adverse effects of a refe
258  cuticle formation and epidermal patterning, vascular development, programmed cell death, organ absci
259  increased apical meristem life, and altered vascular development relative to the null controls.
260 ectors that modulate Notch signalling during vascular development remain largely undefined.
261 1/Dock180 regulates endothelial function and vascular development remained elusive.
262            Blood flow plays crucial roles in vascular development, remodeling and homeostasis, but th
263 e kinase 1 (ALK1) plays an important role in vascular development, remodeling, and pathologic angioge
264  that juvenile doxorubicin exposure impaired vascular development, resulting in abnormal vascular arc
265           Our analysis of pre- and perinatal vascular development revealed that vasculogenesis and an
266 at endothelial PKA activity is essential for vascular development, specifically regulating the transi
267 und to mechanistically retard melanoma tumor vascular development, subsequently affecting tumor cell
268 n between astrocyte distribution and retinal vascular development, the factors that guide astrocytes
269                                       During vascular development, the meristematic cambial cells div
270         Despite its functional importance in vascular development, the physiological ligand or ligand
271 eta) is known to regulate various aspects of vascular development, the signaling mechanism of TGF-bet
272  functions of FAK can support EC survival in vascular development through E13.5 but are insufficient
273 indicate that the DGCR8 gene is required for vascular development through the regulation of VSMC prol
274 angiogenesis and promote physiologic retinal vascular development, toxicity from broad and targeted i
275 in decidualization that resulted in abnormal vascular development, trophoblast defects, and a deficie
276  of the most recent experimental advances in vascular development using the mouse as a model organism
277 ve analysis in embryonic and adult models of vascular development, using intravascular injection of a
278 or any other source of S1P was essential for vascular development, vascular integrity, or hemostasis/
279 eptors is dynamically regulated and controls vascular development, vessel stability and immune cell t
280 ulation is a critical regulator of lymphatic vascular development via activation of Wnt/beta-catenin
281 ophospholipid S1P, which regulates embryonic vascular development via its receptors.
282 acid (RA) as an important regulator of brain vascular development via non-cell-autonomous and cell-au
283 n opticin knockout mouse was established and vascular development was compared between knockout and w
284                           Moreover, when gut vascular development was impaired, either genetically in
285                                  Its role in vascular development was validated in zebrafish embryos
286 ck (HS)-induced RCD, but not reproductive or vascular development, was found to involve a ferroptosis
287 d that neuropilin 2 (NRP2), a key factor for vascular development, was significantly downregulated du
288 hip of migrating ENCC, ENS formation and gut vascular development we combined fate-mapping of ENCC wi
289 genic mouse models for the study of coronary vascular development, we show that extracardiac septum t
290 giopoietin signaling pathways, which mediate vascular development, were downregulated from early stag
291 lish a new role for Notch signaling in brain vascular development whereby Notch3 signaling promotes e
292 e macrophages in the very early phase of CNS vascular development, which in turn are recruited from s
293 y (FEVR) is characterized by delayed retinal vascular development, which promotes hypoxia-induced pat
294 er, VEGF is also required for normal retinal vascular development, which raises concerns about inhibi
295 e found that Col4a1 mutations cause abnormal vascular development, which triggers small-vessel diseas
296                Gall formation also perturbed vascular development with a significant reduction in xyl
297 pression are highly dynamic during zebrafish vascular development, with both apparent during early so
298 gh the importance of neuronal progenitors in vascular development within the CNS is well recognized,
299 he zebrafish embryo to characterize cerebral vascular development within the embryonic hindbrain.
300 enriched in transcripts for innate immunity, vascular development, WNT signaling pathway, and cell mi

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