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Membrane-type MMPs enable extracellular matrix permissiveness and mesenchymal cell proliferation during embryogenesis
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scholarly article
1 reference
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PubMed
PubMed ID
18022611
retrieved
24 January 2017
title
Membrane-type MMPs enable extracellular matrix permissiveness and mesenchymal cell proliferation during embryogenesis
(English)
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
main subject
Matrix metallopeptidase 16
1 reference
stated in
GOA release 2020-03-11
Matrix metallopeptidase 14 (membrane-inserted)
1 reference
stated in
GOA release 2020-03-11
embryogenesis
1 reference
based on heuristic
inferred from title
author name string
Joanne Shi
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Mi-Young Son
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Susan Yamada
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Ludmila Szabova
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Stacie Kahan
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Kaliopi Chrysovergis
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Lauren Wolf
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Andrew Surmak
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
Kenn Holmbeck
series ordinal
9
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 January 2008
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
published in
Developmental Biology
1 reference
stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
volume
313
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PubMed
PubMed ID
18022611
retrieved
24 January 2017
issue
1
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stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
page(s)
196–209
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stated in
PubMed
PubMed ID
18022611
retrieved
24 January 2017
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Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels
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Identification of the second membrane-type matrix metalloproteinase (MT-MMP-2) gene from a human placenta cDNA library. MT-MMPs form a unique membrane-type subclass in the MMP family
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Matrix metalloproteinase dependent and independent collagen degradation
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MT1-MMP-dependent neovessel formation within the confines of the three-dimensional extracellular matrix.
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Altered endochondral bone development in matrix metalloproteinase 13-deficient mice
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Osteoclast differentiation at growth plate cartilage-trabecular bone junction in newborn rat femur
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MT1-MMP-dependent, apoptotic remodeling of unmineralized cartilage: a critical process in skeletal growth
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Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I
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29 September 2017
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29 September 2017
Specific degradation of the collagen molecule by tadpole collagenolytic enzyme
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29 September 2017
An extracellular matrix infrastructure provides support for murine secondary palatal shelf remodelling
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PubMed Central
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29 September 2017
Organization and cellular biology of the perichondrial ossification groove of ranvier: a morphological study in rabbits
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29 September 2017
Functional characterization of MT3-MMP in transfected MDCK cells: progelatinase A activation and tubulogenesis in 3-D collagen lattice.
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2 June 2018
Mode of growth, fate and functions of cartilage canals
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2 June 2018
Palatal closure in the mouse as demonstrated in frozen sections.
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2 June 2018
Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast growth
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PubMed Central
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27 November 2018
Expression pattern of four membrane-type matrix metalloproteinases in the normal and diseased mouse mammary gland.
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27 November 2018
Chondrocytes are released as viable cells during cartilage resorption associated with the formation of intrachondral canals in the rat tibial epiphysis.
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27 November 2018
The role of cartilage canals in endochondral and perichondral bone formation: are there similarities between these two processes?
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27 November 2018
Membrane type I matrix metalloproteinase usurps tumor growth control imposed by the three-dimensional extracellular matrix.
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27 November 2018
Characterization of a truncated recombinant form of human membrane type 3 matrix metalloproteinase.
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27 November 2018
Unaltered secretion of beta-amyloid precursor protein in gelatinase A (matrix metalloproteinase 2)-deficient mice.
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PubMed Central
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27 November 2018
Dissolution of type I collagen fibrils by gingival fibroblasts isolated from patients of various periodontitis categories
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retrieved
7 January 2021
MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.YDBIO.2007.10.017
retrieved
7 January 2021
Membrane type 1-matrix metalloproteinase is involved in the formation of hepatocyte growth factor/scatter factor-induced branching tubules in madin-darby canine kidney epithelial cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.YDBIO.2007.10.017
retrieved
7 January 2021
Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.YDBIO.2007.10.017
retrieved
7 January 2021
Involvement of Membrane-Type Matrix Metalloproteinases (MT-MMPs) in Capillary Tube Formation by Human Endometrial Microvascular Endothelial Cells: Role of MT3-MMP
2 references
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FJ.YDBIO.2007.10.017
retrieved
7 January 2021
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18022611
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.YDBIO.2007.10.017
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3594783
OpenCitations bibliographic resource ID
3594783
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3594783
PMCID
2262846
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3594783
PubMed ID
18022611
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3594783
ResearchGate publication ID
5823795
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