scholarly article | Q13442814 |
P2093 | author name string | J Groffen | |
N Heisterkamp | |||
V Kaartinen | |||
Y A DeClerck | |||
A Lazaryev | |||
L Blavier | |||
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Onset of the acquired potentiality for fusion in the palatal shelves of rats | Q72922671 | ||
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover | Q73082300 | ||
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Cloning, expression, and type II collagenolytic activity of matrix metalloproteinase-13 from human osteoarthritic cartilage | Q24562729 | ||
Molecular cloning and expression of collagenase-3, a novel human matrix metalloproteinase produced by breast carcinomas | Q28116247 | ||
Pathogenesis of cleft palate in TGF-beta3 knockout mice | Q28141234 | ||
Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction | Q28284617 | ||
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The TIMP2 membrane type 1 metalloproteinase "receptor" regulates the concentration and efficient activation of progelatinase A. A kinetic study | Q28619177 | ||
Matrix metalloproteinases: a review | Q29620220 | ||
The fate of medial edge epithelial cells during palatal fusion in vitro: an analysis by DiI labelling and confocal microscopy | Q30784811 | ||
Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor loci | Q35196271 | ||
Matrix metalloproteinase stromelysin-1 triggers a cascade of molecular alterations that leads to stable epithelial-to-mesenchymal conversion and a premalignant phenotype in mammary epithelial cells | Q36255048 | ||
Induction of cell scattering by expression of beta1 integrins in beta1-deficient epithelial cells requires activation of members of the rho family of GTPases and downregulation of cadherin and catenin function | Q36313391 | ||
Transforming growth factor-beta 3 is required for secondary palate fusion | Q37373842 | ||
Tissue inhibitor of metalloproteinases-2 is expressed in the interstitial matrix in adult mouse organs and during embryonic development | Q37386958 | ||
Matrix-dependent Tiam1/Rac signaling in epithelial cells promotes either cell-cell adhesion or cell migration and is regulated by phosphatidylinositol 3-kinase | Q38330900 | ||
Palate development | Q39577154 | ||
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Role of tissue inhibitor of metalloproteinases-2 (TIMP-2) in regulation of pro-gelatinase A activation catalyzed by membrane-type matrix metalloproteinase-1 (MT1-MMP) in human cancer cells | Q41020537 | ||
Focalized proteolysis: spatial and temporal regulation of extracellular matrix degradation at the cell surface | Q41239020 | ||
ECM and cell surface proteolysis: regulating cellular ecology | Q41656253 | ||
Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure | Q41663663 | ||
Differential expression of TGF beta isoforms in murine palatogenesis. | Q41903122 | ||
Molecular and morphologic changes during the epithelial-mesenchymal transformation of palatal shelf medial edge epithelium in vitro | Q42148147 | ||
Migration of neutrophils across human pulmonary endothelial cells is not blocked by matrix metalloproteinase or serine protease inhibitors. | Q42472543 | ||
Medial edge epithelium transforms to mesenchyme after embryonic palatal shelves fuse | Q42489698 | ||
Medial edge epithelium fate traced by cell lineage analysis during epithelial-mesenchymal transformation in vivo | Q43704984 | ||
Transforming growth factor-beta3 regulates transdifferentiation of medial edge epithelium during palatal fusion and associated degradation of the basement membrane | Q44769796 | ||
Immunodetection of the transforming growth factors beta 1 and beta 2 in the developing murine palate | Q44902866 | ||
Epithelial immaturity and multiorgan failure in mice lacking epidermal growth factor receptor | Q46766121 | ||
Diminished matrix metalloproteinase 2 (MMP-2) in ectomesenchyme-derived tissues of the Patch mutant mouse: regulation of MMP-2 by PDGF and effects on mesenchymal cell migration. | Q52175351 | ||
TGFbeta3 promotes transformation of chicken palate medial edge epithelium to mesenchyme in vitro. | Q52191961 | ||
Expression of interstitial collagenase is restricted to skeletal tissue during mouse embryogenesis. | Q52210294 | ||
Expression of interstitial collagenase during skeletal development of the mouse is restricted to osteoblast-like cells and hypertrophic chondrocytes | Q58326928 | ||
MMP2 activation by collagen I and concanavalin A in cultured human hepatic stellate cells | Q59571869 | ||
Transforming growth factor-beta induces collagenase-3 expression by human gingival fibroblasts via p38 mitogen-activated protein kinase | Q64381116 | ||
Differential expression of genes encoding TGFs β1, β2, and β3 during murine palate formation | Q67672314 | ||
P433 | issue | 5 | |
P304 | page(s) | 1457-1466 | |
P577 | publication date | 2001-05-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | TGF-beta3-induced palatogenesis requires matrix metalloproteinases | |
P478 | volume | 12 |
Q47881863 | A TGF-beta-induced gene, betaig-h3, is crucial for the apoptotic disappearance of the medial edge epithelium in palate fusion |
Q39483974 | Ablation of the Sox11 Gene Results in Clefting of the Secondary Palate Resembling the Pierre Robin Sequence |
Q41781930 | Alteration of medial-edge epithelium cell adhesion in two Tgf-beta3 null mouse strains. |
Q36838700 | Analysis of Zfhx1a mutant mice reveals palatal shelf contact-independent medial edge epithelial differentiation during palate fusion. |
Q92570962 | Anterior cleft palate due to Cbfb deficiency and its rescue by folic acid |
Q36087151 | Association of MMP3 and TIMP2 promoter polymorphisms with nonsyndromic oral clefts. |
Q28507415 | Atrioventricular cushion transformation is mediated by ALK2 in the developing mouse heart |
Q46627704 | Cell autonomous requirement for Tgfbr2 in the disappearance of medial edge epithelium during palatal fusion |
Q36329382 | Cellular and Molecular Mechanisms of Palatogenesis |
Q84548187 | Cleft lip and palate |
Q33671456 | Cleft lip and palate genetics and application in early embryological development |
Q42439306 | Cleft palate cells can regenerate a palatal mucosa in vitro |
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Q36857821 | Complexity in interpretation of embryonic epithelial-mesenchymal transition in response to transforming growth factor-beta signaling |
Q48100669 | Computational Model of Secondary Palate Fusion and Disruption. |
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Q44678396 | Cross-talk between interleukin-6 and transforming growth factor-beta3 regulates extracellular matrix production by human fibroblasts from subjects with non-syndromic cleft lip and palate. |
Q38967887 | Deciphering TGF-β3 function in medial edge epithelium specification and fusion during mouse secondary palate development |
Q57727521 | Detection of gelatinolytic activity in developing basement membranes of the mouse embryo head by combining sensitive in situ zymography with immunolabeling |
Q51914657 | Development of secondary palate requires strict regulation of ECM remodeling: sequential distribution of RECK, MMP-2, MMP-3, and MMP-9. |
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Q34890656 | Epigenetic analysis of laser capture microdissected fetal epithelia |
Q36205671 | Epithelial-mesenchymal transformation during craniofacial development. |
Q92542941 | Extracellular Matrix Composition and Remodeling: Current Perspectives on Secondary Palate Formation, Cleft Lip/Palate, and Palatal Reconstruction |
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Q33936577 | Functional Significance of MMP3 and TIMP2 Polymorphisms in Cleft Lip/Palate. |
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Q28584886 | Functional role of transforming growth factor-beta type III receptor during palatal fusion |
Q51800972 | Gene-expression analysis of matrix metalloproteinases 1 and 2 and their tissue inhibitors in chronic periapical inflammatory lesions. |
Q26799998 | Genomic expression in non syndromic cleft lip and palate patients: A review |
Q36640967 | Heparanase localization during palatogenesis in mice. |
Q44533433 | Homocysteine oxidation and apoptosis: a potential cause of cleft palate |
Q43216183 | Human cleft lip and palate fibroblasts and normal nicotine-treated fibroblasts show altered in vitro expressions of genes related to molecular signaling pathways and extracellular matrix metabolism. |
Q89849515 | Identification of Smad-dependent and -independent signaling with transforming growth factor-β type 1/2 receptor inhibition in palatogenesis |
Q36164819 | Induction of palate epithelial mesenchymal transition by transforming growth factor β3 signaling |
Q37239895 | Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence. |
Q36321204 | Intracellular collagen degradation mediated by uPARAP/Endo180 is a major pathway of extracellular matrix turnover during malignancy |
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Q28512267 | Jag2-Notch1 signaling regulates oral epithelial differentiation and palate development |
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Q36498019 | Loss of singleminded-2s in the mouse mammary gland induces an epithelial-mesenchymal transition associated with up-regulation of slug and matrix metalloprotease 2. |
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Q36324816 | MT1-MMP-dependent, apoptotic remodeling of unmineralized cartilage: a critical process in skeletal growth |
Q28592084 | Matrix metalloproteinase-25 has a functional role in mouse secondary palate development and is a downstream target of TGF-β3 |
Q37407289 | Matrix metalloproteinases 2 and 9 are dispensable for pancreatic islet formation and function in vivo |
Q52548422 | Matrix metalloproteinases have a role in palatogenesis. |
Q35893613 | Mechanisms of tissue fusion during development. |
Q35107597 | Membrane type-matrix metalloproteinases (MT-MMP) |
Q53625816 | Membrane-type 1 matrix metalloproteinase is required for normal alveolar development. |
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