Dyne K - Search Results

1

Type I procollagen in the severe non-lethal form of osteogenesis imperfecta. Defective pro-alpha 1(I) chains in a patient with abnormal proteoglycan metabolism and mineral deposits in the dermis.

Tenni R, Cetta G, Dyne K, Rossi A, Quacci D, Lenzi L, Castellani AA. Tenni R, et al. Among authors: dyne k. Hum Genet. 1988 Jul;79(3):245-50. doi: 10.1007/BF00366245. Hum Genet. 1988. PMID: 3402997

2

Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta.

Tenni R, Biglino P, Dyne K, Rossi A, Filocamo M, Pendola F, Brunelli P, Buttitta P, Borrone C, Cetta G. Tenni R, et al. Among authors: dyne k. J Inherit Metab Dis. 1991;14(2):189-201. doi: 10.1007/BF01800591. J Inherit Metab Dis. 1991. PMID: 1886404

3

Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity.

Tenni R, Cetta G, Dyne K, Valli M, Zanaboni G, Castellani AA. Tenni R, et al. Among authors: dyne k. Ann N Y Acad Sci. 1988;543:73-82. doi: 10.1111/j.1749-6632.1988.tb55317.x. Ann N Y Acad Sci. 1988. PMID: 3214054 No abstract available.

4

Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta.

Dyne K, Cetta G, Tenni R, Rossi A, Finardi E, Brunelli PC, Castellani AA. Dyne K, et al. Ital J Biochem. 1987 Jul-Aug;36(4):256-66. Ital J Biochem. 1987. PMID: 3429209

5

Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.

Cetta G, Rossi A, Tenni R, Valli M, Forlino A, Zanaboni G, Dyne K, Burgio GR. Cetta G, et al. Among authors: dyne k. Connect Tissue Res. 1993;29(1):41-9. doi: 10.3109/03008209309061965. Connect Tissue Res. 1993. PMID: 8339545

6

Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta.

Dyne KM, Valli M, Forlino A, Mottes M, Kresse H, Cetta G. Dyne KM, et al. Am J Med Genet. 1996 May 3;63(1):161-6. doi: 10.1002/(SICI)1096-8628(19960503)63:1<161::AID-AJMG28>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8723103 Review.

7

Biochemical, morphological and stereological study of the dermis in three members of a large family with type IV Ehlers-Danlos syndrome.

Vitellaro-Zuccarello L, Dyne K, Cetta G. Vitellaro-Zuccarello L, et al. Among authors: dyne k. Connect Tissue Res. 1989;23(1):1-17. doi: 10.3109/03008208909103900. Connect Tissue Res. 1989. PMID: 2632142

8

Low levels of serum type III procollagen aminoterminal propeptide confirmed type III collagen deficiency in patients without typical clinical symptoms of Ehlers-Danlos type IV.

Dyne KM, Zanaboni G, Annoni G, De Agostini MP, Cetta G. Dyne KM, et al. Eur J Clin Invest. 1989 Aug;19(4):362-6. doi: 10.1111/j.1365-2362.1989.tb00242.x. Eur J Clin Invest. 1989. PMID: 2506053

9

Ehlers-Danlos syndrome type VIII: biochemical, stereological and immunocytochemical studies on dermis from a child with clinical signs of Ehlers-Danlos syndrome and a family history of premature loss of permanent teeth.

Dyne KM, Vitellaro-Zuccarello L, Bacchella L, Lanzi G, Cetta G. Dyne KM, et al. Br J Dermatol. 1993 Apr;128(4):458-63. doi: 10.1111/j.1365-2133.1993.tb00211.x. Br J Dermatol. 1993. PMID: 8494762

10

Type I collagen CNBr peptides: species and behavior in solution.

Rossi A, Zuccarello LV, Zanaboni G, Monzani E, Dyne KM, Cetta G, Tenni R. Rossi A, et al. Among authors: dyne km. Biochemistry. 1996 May 14;35(19):6048-57. doi: 10.1021/bi9518151. Biochemistry. 1996. PMID: 8634246

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