Zobrazeno 1 - 10
of 25
pro vyhledávání: '"L J, Sandell"'
Publikováno v:
Rheumatology. 46:938-943
Objectives. The 5-yr longitudinal study tested the hypothesis that serum and urinary markers of type II collagen metabolism would be associated with radiological progression of disease in patients with mild-to-moderate knee osteoarthritis (OA). Metho
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :1066-1069
We have measured the concentration of cartilage-derived retinoic-acid-sensitive protein (CD-RAP) in synovial fluid (SF) from the knees of 49 patients with osteoarthritis (OA) and 79 with rheumatoid arthritis (RA) in order to investigate the correlati
Autor:
L J, Sandell
Publikováno v:
Journal of musculoskeletalneuronal interactions. 8(4)
Publikováno v:
The Journal of bone and joint surgery. British volume. 84(7)
We have measured the concentration of cartilage-derived retinoic-acid-sensitive protein (CD-RAP) in synovial fluid (SF) from the knees of 49 patients with osteoarthritis (OA) and 79 with rheumatoid arthritis (RA) in order to investigate the correlati
Publikováno v:
Orthopedics. 24(8)
Osteochondromas are chondro-osseous protuberances that occur in metaphyses of long bones. The cartilaginous cap is assumed to be responsible for the growth of the lesions during childhood and adolescence, but mitotic figures are rarely seen in the ca
Publikováno v:
American journal of veterinary research. 60(10)
To isolate, clone, and determine primary nucleotide sequence of equine insulin-like growth factor I (IGF-I) and to examine IGF-I gene expression in tissues and cartilage from horses.Horses of various ages.Total RNA was isolated from tissues and purif
Publikováno v:
Arthritis and rheumatism. 42(7)
To test for the reexpression of the chondroprogenitor splice variant of the gene COL2A1, type IIA procollagen (containing a cysteine-rich NH2 propeptide), in adult articular chondrocytes in osteoarthritic (OA) joint disease.In situ hybridization and
Autor:
W H, Raskind, E U, Conrad, M, Matsushita, E M, Wijsman, D E, Wells, N, Chapman, L J, Sandell, M, Wagner, J, Houck
Publikováno v:
Human mutation. 11(3)
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by growth of benign bone tumors. Three chromosomal loci have been implicated in this genetically heterogeneous disease: EXT1 at 8q24, EXT2 at 11p13, and EXT3 on 19p.
Publikováno v:
The Journal of rheumatology. 24(6)
To examine the phenotypic expression and geographic distribution of collagens in early stages of osteoarthrosis and their relationship to ultrastructural events in cartilage.In situ hybridization was used to localize articular expression of total typ
Autor:
A K, Bosserhoff, S, Kondo, M, Moser, U H, Dietz, N G, Copeland, D J, Gilbert, N A, Jenkins, R, Buettner, L J, Sandell
Publikováno v:
Developmental dynamics : an official publication of the American Association of Anatomists. 208(4)
A cDNA encoding a novel protein has been previously isolated from two independent sources: melanoma cell cultures and chondrocytes. The protein from human melanoma cell lines and tumors is called melanoma inhibitory activity (MIA) (Blesch et al. [199