Loss of MMP-2 disrupts skeletal and craniofacial development and results in decreased bone mineralization, joint erosion and defects in osteoblast and osteoclast …

RA Mosig, O Dowling, A DiFeo… - Human molecular …, 2007 - academic.oup.com
The 'vanishing bone'or inherited osteolysis/arthritis syndromes represent a heterogeneous
group of skeletal disorders characterized by mineralization defects of affected bones and …

Differential effects between the loss of MMP2 and MMP9 on structural and tissuelevel properties of bone

JS Nyman, CC Lynch, DS Perrien… - Journal of Bone and …, 2011 - academic.oup.com
Matrix metalloproteinases (MMPs) are capable of processing certain components of bone
tissue, including type 1 collagen, a determinant of the biomechanical properties of bone …

MMP9 regulates the cellular response to inflammation after skeletal injury

X Wang, YY Yu, S Lieu, F Yang, J Lang, C Lu, Z Werb… - Bone, 2013 - Elsevier
Like other tissue injuries, bone fracture triggers an inflammatory response, which plays an
important role in skeletal repair. Inflammation is believed to have both positive and negative …

Impaired remodeling phase of fracture repair in the absence of matrix metalloproteinase-2

S Lieu, E Hansen, R Dedini… - Disease models & …, 2011 - journals.biologists.com
The matrix metalloproteinase (MMP) family of extracellular proteases performs crucial roles
in development and repair of the skeleton owing to their ability to remodel the extracellular …

A crucial role for matrix metalloproteinase 2 in osteocytic canalicular formation and bone metabolism

K Inoue, Y Mikuni-Takagaki, K Oikawa, T Itoh… - Journal of Biological …, 2006 - ASBMB
Extracellular matrix production and degradation by bone cells are critical steps in bone
metabolism. Mutations of the gene encoding MMP-2, an extracellular matrix-degrading …

Mutation of the matrix metalloproteinase 2 gene (MMP2) causes a multicentric osteolysis and arthritis syndrome

JA Martignetti, AA Aqeel, WA Sewairi, CE Boumah… - Nature …, 2001 - nature.com
The inherited osteolyses or'vanishing bone'syndromes are a group of rare disorders of
unknown etiology characterized by destruction and resorption of affected bones. The …

Altered fracture repair in the absence of MMP9

C Colnot, Z Thompson, T Miclau, Z Werb, JA Helms - 2003 - journals.biologists.com
The regeneration of adult skeletal tissues requires the timely recruitment of skeletal
progenitor cells to an injury site, the differentiation of these cells into bone or cartilage, and …

[HTML][HTML] Different roles of matrix metalloproteinase 2 in osteolysis of skeletal dysplasia and bone metastasis

X Li, L Jin, Y Tan - Molecular Medicine Reports, 2021 - spandidos-publications.com
Abstract Matrix metalloproteinase 2 (MMP2) is a well‑characterized protein that is
indispensable for extracellular matrix remodeling and other pathological processes, such as …

A novel matrix metalloproteinase 2 (MMP2) terminal hemopexin domain mutation in a family with multicentric osteolysis with nodulosis and arthritis with cardiac …

B Tuysuz, R Mosig, G Altun, S Sancak… - European journal of …, 2009 - nature.com
Multicentric osteolysis with nodulosis and arthropathy (MONA, NAO (OMIM no. 605156)) is
an autosomal recessive member of the 'vanishing bone'syndromes and is notable for the …

Matrix metalloproteinase Mmp-1a is dispensable for normal growth and fertility in mice and promotes lung cancer progression by modulating inflammatory responses

M Fanjul-Fernández, AR Folgueras, A Fueyo… - Journal of Biological …, 2013 - ASBMB
Human MMP-1 is a matrix metalloproteinase repeatedly associated with many pathological
conditions, including cancer. Thus, MMP1 overexpression is a poor prognosis marker in a …