R Sztrolovics
Overview
Explore the profile of R Sztrolovics including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
155
Followers
0
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Recent Articles
1.
Sztrolovics R, Alini M, Mort J, Roughley P
Spine (Phila Pa 1976)
. 1999 Sep;
24(17):1765-71.
PMID: 10488504
Study Design: An analysis of proteoglycans of the intervertebral disc using immunoblotting of tissue extracts. Objectives: To investigate the changes in structure and abundance of fibromodulin and lumican in human...
2.
Sztrolovics R, White R, Poole A, Mort J, Roughley P
Biochem J
. 1999 Apr;
339 ( Pt 3):571-7.
PMID: 10215595
A bovine nasal-cartilage culture system has been utilized to analyse the catabolic events occurring in response to interleukin-1beta over a 14-day period. An early event following the start of interleukin-1...
3.
Sztrolovics R, Alini M, Roughley P, Mort J
Biochem J
. 1997 Aug;
326 ( Pt 1):235-41.
PMID: 9337874
Aggrecan degradation in human intervertebral disc and articular cartilage has been studied by using anti-neoepitope antibodies specific for the N-terminal degradation products generated by cleavage within the interglobular domain at...
4.
Sztrolovics R, Wang S, Lapierre P, Chen H, Robert M, Mitchell G
Mamm Genome
. 1997 Feb;
8(2):86-9.
PMID: 9060404
Hormone-sensitive lipase (Lipe) catalyzes both the release lease of fatty acids from storage triglycerides in adipocytes and the liberation of cholesterol from cholesterol esters in steroidogenic tissues. Lipe activity is...
5.
Sztrolovics R, Chen X, Grover J, Roughley P, Korenberg J
Genomics
. 1994 Oct;
23(3):715-7.
PMID: 7851907
No abstract available.
6.
Sztrolovics R, Rimoin D, Rodriguez E, Roughley R
Matrix Biol
. 1994 Aug;
14(4):307-12.
PMID: 7827753
The coding regions of the human decorin, biglycan and fibromodulin cDNAs have been examined utilizing the method of single-strand conformation polymorphism analysis. Analysis of total RNA from a group of...
7.
Sztrolovics R, Glorieux F, Travers R, van Der Rest M, Roughley P
Bone
. 1994 May;
15(3):321-8.
PMID: 7520724
Osteogenesis imperfecta (OI) is a group of inherited disorders characterized by a predisposition to bone fracturing, and usually resulting from mutations in the genes encoding type I collagen. This report...
8.
Sztrolovics R, van Der Rest M, Roughley P
Matrix Biol
. 1994 Jan;
14(1):9-19.
PMID: 8061924
This study has examined the frequency and distribution of polymorphisms in the type I collagen coding sequences. RNA from a group of human skin fibroblast cell lines was analyzed by...
9.
Sztrolovics R, Glorieux F, van Der Rest M, Roughley P
Hum Mol Genet
. 1993 Aug;
2(8):1319-21.
PMID: 8401517
No abstract available.