DYNE, KATHARINE MARY
DYNE, KATHARINE MARY
DIPARTIMENTO DI BIOCHIMICA 'ALESSANDRO CASTELLANI' (attivo dal 01/01/1900 al 31/12/2011)
Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta.
1996-01-01 Dyne, KATHARINE MARY; Valli, Maurizia; Forlino, Antonella; Mottes, Monica; Kresse, Hans; Cetta, Giuseppe
Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta.
1993-01-01 Cetta, Giuseppe; Rossi, Antonio; Tenni, Ruggero; Valli, Maurizia; Forlino, Antonella; Zanaboni, Giuseppe; Dyne, KATHARINE MARY; R., Burgio
Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis.
1997-01-01 Zanaboni, Giuseppe; Viglio, Simona; Dyne, KATHARINE MARY; Grimm, Rodolf; Valli, Maurizia; Cetta, Giuseppe; Iadarola, Paolo
Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta.
1987-01-01 Dyne, KATHARINE MARY; Cetta, Giuseppe; Tenni, Ruggero; Rossi, Antonio; Finardi, E; Brunelli, Pc; Castellani, Alessandro
Mild, late-onset prolidase deficiency: another Italian case.
2001-01-01 Dyne, KATHARINE MARY; Zanaboni, Giuseppe; Cetta, Giuseppe; Viglio, Simona; Lupi, Anna; Iadarola, Paolo; Bertazzoni, M.
Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta.
1991-01-01 Tenni, Ruggero; Biglino, P; Dyne, KATHARINE MARY; Rossi, Antonio; Filocamo, M; Pendola, F; Brunelli, P; Buttitta, P; Borrone, C; Cetta, Giuseppe
Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects.
1987-01-01 Leoni, A; Cetta, Giuseppe; Tenni, Ruggero; Pasquali Ronchetti, I; Bertolini, F; Guerra, D; Dyne, KATHARINE MARY; Castellani, Alessandro
Proliferation characteristics and polyploidization of cultured myofibroblasts from a patient with fibroblastic rheumatism
2003-01-01 Lanni, Cristina; Bottone, MARIA GRAZIA; Bardoni, ANNA MARIA; Dyne, KATHARINE MARY; Soldani, C.; Pellicciari, Carlo; Caporali, Roberto; Montecucco, Carlomaurizio
Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity.
1988-01-01 Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Valli, Maurizia; Zanaboni, Giuseppe; Castellani, Alessandro
Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency.
2000-01-01 Marseglia, GIAN LUIGI; Maghnie, Mohamad; Dyne, KATHARINE MARY; Cetta, Giuseppe; Monafo, V.
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.
1988-01-01 Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Rossi, Antonio; Quacci, D; Lenzi, L; Castellani, Alessandro
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Deficient expression of the small proteoglycan decorin in a case of severe/lethal osteogenesis imperfecta. | 1-gen-1996 | Dyne, KATHARINE MARY; Valli, Maurizia; Forlino, Antonella; Mottes, Monica; Kresse, Hans; Cetta, Giuseppe | |
| Deposition of mutant type I collagen in the extracellular matrix of cultured dermal fibroblasts in osteogenesis imperfecta. | 1-gen-1993 | Cetta, Giuseppe; Rossi, Antonio; Tenni, Ruggero; Valli, Maurizia; Forlino, Antonella; Zanaboni, Giuseppe; Dyne, KATHARINE MARY; R., Burgio | |
| Direct monitoring of prolidase activity in cultured skin fibroblasts using capillary electrophoresis. | 1-gen-1997 | Zanaboni, Giuseppe; Viglio, Simona; Dyne, KATHARINE MARY; Grimm, Rodolf; Valli, Maurizia; Cetta, Giuseppe; Iadarola, Paolo | |
| Localization of a structural defect in type I procollagen in a patient affected with the severe non-lethal form of Osteogenesis imperfecta. | 1-gen-1987 | Dyne, KATHARINE MARY; Cetta, Giuseppe; Tenni, Ruggero; Rossi, Antonio; Finardi, E; Brunelli, Pc; Castellani, Alessandro | |
| Mild, late-onset prolidase deficiency: another Italian case. | 1-gen-2001 | Dyne, KATHARINE MARY; Zanaboni, Giuseppe; Cetta, Giuseppe; Viglio, Simona; Lupi, Anna; Iadarola, Paolo; Bertazzoni, M. | |
| Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta. | 1-gen-1991 | Tenni, Ruggero; Biglino, P; Dyne, KATHARINE MARY; Rossi, Antonio; Filocamo, M; Pendola, F; Brunelli, P; Buttitta, P; Borrone, C; Cetta, Giuseppe | |
| Prolidase deficiency in two siblings with chronic leg ulcerations. Clinical, biochemical, and morphologic aspects. | 1-gen-1987 | Leoni, A; Cetta, Giuseppe; Tenni, Ruggero; Pasquali Ronchetti, I; Bertolini, F; Guerra, D; Dyne, KATHARINE MARY; Castellani, Alessandro | |
| Proliferation characteristics and polyploidization of cultured myofibroblasts from a patient with fibroblastic rheumatism | 1-gen-2003 | Lanni, Cristina; Bottone, MARIA GRAZIA; Bardoni, ANNA MARIA; Dyne, KATHARINE MARY; Soldani, C.; Pellicciari, Carlo; Caporali, Roberto; Montecucco, Carlomaurizio | |
| Severe nonlethal osteogenesis imperfecta: biochemical heterogeneity. | 1-gen-1988 | Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Valli, Maurizia; Zanaboni, Giuseppe; Castellani, Alessandro | |
| Transient beneficial effect of GH replacement therapy and topical GH application on skin ulcers in a boy with prolidase deficiency. | 1-gen-2000 | Marseglia, GIAN LUIGI; Maghnie, Mohamad; Dyne, KATHARINE MARY; Cetta, Giuseppe; Monafo, V. | |
| 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. | 1-gen-1988 | Tenni, Ruggero; Cetta, Giuseppe; Dyne, KATHARINE MARY; Rossi, Antonio; Quacci, D; Lenzi, L; Castellani, Alessandro |