Search research articles
Contact Us
Filters
Showing results (41-50 of 54) with videos related to
Page
of 6
Sort By:
Biochimica Et Biophysica Acta
|
July 16, 1982
Desmosines in aneurysms of the ascending aorta (annulo-aortic ectasia)
T Halme, T Vihersaari, T Savunen, et al.
The Biochemical Journal
|
November 15, 1985
The borohydride-reducible compounds of human aortic elastin. Demonstration of a new cyclic amino acid in alkali hydrolysate, and changes with age and in patients with annulo-aortic ectasia including one with Marfan syndrome
T Halme, M Jutila, T Vihersaari, et al.
Archives of Dermatological Research
|
January 1, 1995
A fibroblast cell line cultured from a hypertrophic scar displays selective downregulation of collagen gene expression: barely detectable messenger RNA levels of the pro alpha 1(III) chain of type III collagen
L Q Zhang, M Laato, P Muona, et al.
Acta Neuropathologica
|
January 1, 1984
Neurofibromatosis tumor and skin cells in culture. II. Structural proteins with special reference to the cytoskeletal and cell surface components
J Peltonen, K Näntö-Salonen, H J Aho, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
October 1, 1984
Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder
K Näntö-Salonen, L J Pelliniemi, S Autio, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes
K Näntö-Salonen, T Halme, R Penttinen, et al.
Scandinavian Journal of Rheumatology
|
January 1, 1984
Xanthoma tendinosum in a normolipemic ectodermal dysplasia patient
S Jalava, M Hietarinta, S Einola, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline
K Näntö-Salonen, S Autio, E Härö, et al.
Connective Tissue Research
|
January 1, 1987
Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder
K Näntö-Salonen, H Larjava, A M Säämanen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1975
Patients with Ehlers-Danlos syndrome type IV lack type III collagen
F M Pope, G R Martin, J R Lichtenstein, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Biochimica Et Biophysica Acta
|
July 16, 1982
Desmosines in aneurysms of the ascending aorta (annulo-aortic ectasia)
T Halme, T Vihersaari, T Savunen, et al.
The Biochemical Journal
|
November 15, 1985
The borohydride-reducible compounds of human aortic elastin. Demonstration of a new cyclic amino acid in alkali hydrolysate, and changes with age and in patients with annulo-aortic ectasia including one with Marfan syndrome
T Halme, M Jutila, T Vihersaari, et al.
Archives of Dermatological Research
|
January 1, 1995
A fibroblast cell line cultured from a hypertrophic scar displays selective downregulation of collagen gene expression: barely detectable messenger RNA levels of the pro alpha 1(III) chain of type III collagen
L Q Zhang, M Laato, P Muona, et al.
Acta Neuropathologica
|
January 1, 1984
Neurofibromatosis tumor and skin cells in culture. II. Structural proteins with special reference to the cytoskeletal and cell surface components
J Peltonen, K Näntö-Salonen, H J Aho, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
October 1, 1984
Abnormal collagen fibrils in aspartylglycosaminuria. Altered dermal ultrastructure in a glycoprotein storage disorder
K Näntö-Salonen, L J Pelliniemi, S Autio, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes
K Näntö-Salonen, T Halme, R Penttinen, et al.
Scandinavian Journal of Rheumatology
|
January 1, 1984
Xanthoma tendinosum in a normolipemic ectodermal dysplasia patient
S Jalava, M Hietarinta, S Einola, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline
K Näntö-Salonen, S Autio, E Härö, et al.
Connective Tissue Research
|
January 1, 1987
Abnormal dermal proteoglycan in aspartylglycosaminuria: a possible mechanism for ultrastructural changes of collagen fibrils in a glycoprotein storage disorder
K Näntö-Salonen, H Larjava, A M Säämanen, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1975
Patients with Ehlers-Danlos syndrome type IV lack type III collagen
F M Pope, G R Martin, J R Lichtenstein, et al.
Page
of 6