Calcinosis cutis: part I. Diagnostic pathway
N Reiter, L El-Shabrawi, B Leinweber… - Journal of the American …, 2011 - Elsevier
Calcinosis cutis is characterized by the deposition of insoluble calcium salts in the skin and
subcutaneous tissue. The syndrome is separated into five subtypes: dystrophic calcification …
subcutaneous tissue. The syndrome is separated into five subtypes: dystrophic calcification …
[HTML][HTML] The role of senescence in cellular plasticity: Lessons from regeneration and development and implications for age-related diseases
Senescence is a cellular state which involves cell cycle arrest and a proinflammatory
phenotype, and it has traditionally been associated with cellular and organismal aging …
phenotype, and it has traditionally been associated with cellular and organismal aging …
Adipocyte dedifferentiation in health and diseases
Adipose tissues collectively as an endocrine organ and energy storage are crucial for
systemic metabolic homeostasis. The major cell type in the adipose tissue, the adipocytes or …
systemic metabolic homeostasis. The major cell type in the adipose tissue, the adipocytes or …
Calcinosis cutis: part II. Treatment options
N Reiter, L El-Shabrawi, B Leinweber… - Journal of the American …, 2011 - Elsevier
Because calcinosis cutis is a rare syndrome, there is a notable lack of controlled clinical
trials on its treatment. The efficacy of calcinosis treatment has only been reported in single …
trials on its treatment. The efficacy of calcinosis treatment has only been reported in single …
[HTML][HTML] Development of selective inhibitors and substrate of matrix metalloproteinase-12
L Devel, V Rogakos, A David, A Makaritis… - Journal of Biological …, 2006 - ASBMB
Four phosphinic peptide libraries with compounds having the general formula p-Br-Ph-(PO 2-
CH 2)-Xaa′-Yaa′-Zaa′-NH 2 have been prepared and screened against 10 matrix …
CH 2)-Xaa′-Yaa′-Zaa′-NH 2 have been prepared and screened against 10 matrix …
Association between tendon ruptures and use of fluoroquinolone, and other oral antibiotics: a 10-year retrospective study of 1 million US senior Medicare beneficiaries
S Baik, J Lau, V Huser, CJ McDonald - BMJ open, 2020 - bmjopen.bmj.com
Objectives To assess the association of fluoroquinolone use with tendon ruptures compared
with no fluoroquinolone and that of the four most commonly prescribed non-fluoroquinolone …
with no fluoroquinolone and that of the four most commonly prescribed non-fluoroquinolone …
Matrix metalloproteinase-11/stromelysin-3 exhibits collagenolytic function against collagen VI under normal and malignant conditions
ER Motrescu, S Blaise, N Etique, N Messaddeq… - Oncogene, 2008 - nature.com
The substrate of matrix metalloproteinase 11 (MMP11) remains unknown. We have recently
shown that MMP11 is a negative regulator of adipogenesis, able to reduce and even to …
shown that MMP11 is a negative regulator of adipogenesis, able to reduce and even to …
Cancer cells, adipocytes and matrix metalloproteinase 11: a vicious tumor progression cycle
ER Motrescu, MC Rio - 2008 - degruyter.com
This brief review focuses on the emerging role of matrix metalloproteinase 11 (MMP-11) in
cancer progression. It has recently been shown that MMP-11 is induced in adipose tissue by …
cancer progression. It has recently been shown that MMP-11 is induced in adipose tissue by …
Inhibition of angiogenesis and metastasis in two murine models by the matrix metalloproteinase inhibitor, BMS-275291
JG Naglich, M Jure-Kunkel, E Gupta, J Fargnoli… - Cancer research, 2001 - AACR
BMS-275291 is an po bioavailable, sulfhydryl-based matrix metalloproteinase (MMP)
inhibitor currently in clinical development for the treatment of cancer. This inhibitor was …
inhibitor currently in clinical development for the treatment of cancer. This inhibitor was …
Phosphinic pseudo-tripeptides as potent inhibitors of matrix metalloproteinases: a structure− activity study
S Vassiliou, A Mucha, P Cuniasse… - Journal of medicinal …, 1999 - ACS Publications
Several phosphinic pseudo-tripeptides of general formula R-XaaΨ (PO2-CH2) Xaa '-Yaa '-
NH2 were synthesized and evaluated for their in vitro activities to inhibit stromelysin-3 …
NH2 were synthesized and evaluated for their in vitro activities to inhibit stromelysin-3 …