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1 opically reminiscent of the adjacent natural cranial suture.
2  of FGFR2c to multiple FGFs expressed in the cranial suture.
3 osis of the coronal suture, as well as other cranial sutures.
4 the fibrous joints between the bones, termed cranial sutures.
5 l features caused by the premature fusion of cranial sutures.
6 th defect resulting from premature fusion of cranial sutures.
7 ed endochondral-like ossification within the cranial sutures.
8 nd results from the premature fusion of >/=1 cranial sutures.
9 al stem/progenitor cells are resident in the cranial sutures.
10 tween subjects guided by the location of the cranial sutures.
11                           These mice exhibit cranial suture and sternal fusions that are exacerbated
12 rtilage heterotopic ossification (HO) within cranial sutures and fontanels of the mouse model, leadin
13 ts in a more severe delay in ossification of cranial sutures and fontanels than occurs with Runx2 hap
14     We also observed premature fusion of the cranial sutures and low bone density in newborn FGFR3(G3
15 nalling dynamics, whereby development of the cranial sutures and sternum follows a morphogen mode, wh
16 NCCs impairs the formation of normal midline cranial sutures and, consequently, the overlying skin, r
17 zed by craniosynostosis (premature fusion of cranial sutures) and severe syndactyly of the hands and
18 h as the mandibular condyle, calvarial bone, cranial suture, and subcutaneous adipose tissue--have be
19 splasia characterized by short stature, wide cranial sutures, and increased bone density and fragilit
20 suture mesenchyme of patent, but not fusing, cranial sutures, and that noggin expression is suppresse
21 craniofacial geometry, irregular patterns of cranial suturing, and ectopic bone formation.
22                                              Cranial sutures are major growth centers for the calvari
23                                          The cranial sutures are proposed to be a stem cell niche, ha
24 by the premature fusion of one or more major cranial sutures at birth or soon after.
25 at differences in the morphology of selected cranial sutures between species that span the fish-tetra
26  new insights, both into normal and abnormal cranial suture biogenesis and into problems of broad int
27 arpenter syndrome implicates HH signaling in cranial-suture biogenesis--an unexpected finding, given
28 synostosis based on current understanding of cranial suture biology and molecular and developmental p
29  animal models and improved uncerstanding of cranial suture biology and pathology may lead to complem
30      This work addressed a hypothesis that a cranial suture can be tissue-engineered from autologous
31                          Premature fusion of cranial sutures, caused by deficiency in intramembranous
32 l neural crest cells, giving rise to midline cranial suture cells that express keratinocyte-promoting
33 quencing (scRNA-seq) of normal neonatal mice cranial suture chondrocytes showed a Hedgehog (Hh) inact
34  to growth plate abnormalities and premature cranial suture closure because of precocious maturation
35 ithelium during palatal fusion and postnatal cranial suture closure during skull development.
36 ovel molecule overexpressed during premature cranial suture closure in patients with craniosynostosis
37 h a series of tissue interactions within the cranial suture complex.
38 hat the Mgp promoter is highly active at the cranial sutures, cranial base synchondroses, and nasal s
39 idermal hyperplasia and premature closure of cranial sutures (craniosynostosis) due to abnormal cell
40       Premature fusion of one or more of the cranial sutures (craniosynostosis) in humans causes over
41                      Premature fusion of the cranial sutures (craniosynostosis), affecting 1 in 2000
42 trate the roles of osteoprogenitor cells and cranial suture-derived stem cells for proper calvarial g
43                                              Cranial suture development involves a complex interactio
44 reviously unsuspected role for Zic1 in early cranial suture development, potentially by regulating en
45 tional modules active at different stages of cranial suture development.
46 ipally the mouse, because of similarities in cranial suture development.
47 osis (CS) is caused by a premature fusion of cranial sutures during development.
48                                              Cranial sutures either originate from the neural crest o
49 ach may be refined for tissue engineering of cranial sutures for craniosynostosis patients.
50 congenital malformation in which one or more cranial sutures fuse prematurely.
51 enetically determined disorders of premature cranial suture fusion (craniosynostosis) provide one rou
52 a skull deformity characterized by premature cranial suture fusion due to the loss of the GNAS gene a
53          Since noggin misexpression prevents cranial suture fusion in vitro and in vivo, we suggest t
54 nai1 and Snai2 mutations to enhance aberrant cranial suture fusion, demonstrating that genetic intera
55               Craniosynostosis, or premature cranial suture fusion, results in an abnormal skull shap
56 ribe the pathways and processes that lead to cranial suture fusion.
57 numerous syndromes associated with premature cranial suture fusion.
58 tudy the biomolecular mechanisms that govern cranial suture fusion.
59 kull and cognitive defects, due to premature cranial suture fusion.
60                               This pediatric cranial suture growth model constitutes a necessary tool
61 mes of craniosynostosis (premature fusion of cranial sutures) have homologues in the CeTwist pathway.
62 replication with growth, chondrogenesis, and cranial suture homeostasis.
63   Over-expression of Nell1 in the developing cranial sutures in both human and mouse induces craniosy
64                         Premature closure of cranial sutures in intramembranous ossification is a fea
65 ative spatial transcriptomic analysis of the cranial sutures in vivo confirmed a positive association
66 ex craniosynostosis (premature fusion of the cranial sutures) in humans and mice.
67 fined by premature fusion of one or multiple cranial sutures, is a common congenital defect affecting
68 niosynostosis, the premature ossification of cranial sutures, is a developmental disorder of the skul
69 raniosynostosis, the premature fusion of the cranial sutures, is a heterogeneous disorder with a prev
70 st cells (NCCs), which normally form midline cranial suture mesenchymal cells that express keratinocy
71 e was de novo formation of tissue-engineered cranial suture, microscopically reminiscent of the adjac
72 enital disorder of premature ossification of cranial sutures, occurring in one of approximately every
73          In the mutants, premature fusion of cranial sutures occurs at early postnatal stages.
74               We therefore, investigated why cranial sutures of same tissue origin adopt a different
75                           Interestingly, the cranial sutures of the mutant mice showed normal anatomi
76 ostosis, the premature fusion of one or more cranial sutures of the skull, provides a paradigm for in
77                                  Analyses of cranial suture patency and palatal fusion during develop
78 ortant role for BCL11B in the maintenance of cranial suture patency.
79 with the pathways that are known to regulate cranial suture patency.
80 T/E dimers plays a central role in governing cranial suture patency.
81 tudy abnormal development in the presence of cranial suture pathology.
82                                    MSC-based cranial suture regeneration offers a paradigm shift in t
83 ostosis results from premature fusion of the cranial suture(s), which contain mesenchymal stem cells
84                                              Cranial sutures separate neighboring skull bones and are
85                        The tissue-engineered cranial suture showed radiolucency on radiographic image
86 Cs, we successfully regenerated a functional cranial suture that corrects skull deformity, normalizes
87 ricular surfaces, pubic symphyseal face, and cranial sutures, to produce a multifactorial narrower ag
88                         Premature closure of cranial sutures, which serve as growth centers for the s