Detection of gelatinase B expression reveals osteoclastic bone resorption as a feature of early calvarial bone development (Q74045639)

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8 November 2019

title

Detection of gelatinase B expression reveals osteoclastic bone resorption as a feature of early calvarial bone development (English)

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8 November 2019

author name string

D P Rice

series ordinal

1

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8 November 2019

H J Kim

series ordinal

2

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8 November 2019

I Thesleff

series ordinal

3

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8 November 2019

publication date

1 December 1997

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8 November 2019

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8 November 2019

volume

21

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8 November 2019

issue

6

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8 November 2019

page(s)

479-486

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Isolation and characterization of skeletal acid ATPase--a new osteoclast marker?

8 November 2019

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Generation of osteoclastic function in mouse bone marrow cultures: multinuclearity and tartrate-resistant acid phosphatase are unreliable markers for osteoclastic differentiation.

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Cyclooxygenase inhibitors augment the production of pro-matrix metalloproteinase 9 (progelatinase B) in rabbit articular chondrocytes

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Histochemistry and biochemistry of tartrate-resistant acid phosphatase (TRAP) and tartrate-resistant acid adenosine triphosphatase (TrATPase) in bone, bone marrow and spleen: implications for osteoclast ontogeny

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Purification of a Type V Collagen Degrading Metalloproteinase from Rabbit Alveolar Macrophages

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The synthesis of collagenase, gelatinase-A (72 kDa) and -B (95 kDa), and TIMP-1 and -2 by human osteoblasts from normal and arthritic bone

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Bone acid phosphatase: tartrate-resistant acid phosphatase as a marker of osteoclast function

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A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

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Characterization of gelatinase from pig polymorphonuclear leucocytes. A metalloproteinase resembling tumour type IV collagenase

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7 January 2021

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

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7 January 2021

Ultrastructural localization of a tartrate-resistant acid ATPase in bone

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92-kDa type IV collagenase and TIMP-3, but not 72-kDa type IV collagenase or TIMP-1 or TIMP-2, are highly expressed during mouse embryo implantation

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9430236%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

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