M. Agostini

Details der Publikationsliste

Zeitraum

1983 - 2009

Anzahl

18

Co-Autoren

On the statistics of edge fluctuations: comparative study between various fusion devices (2009)

Sattin, F., Agostini, M., Scarin, P., Vianello, N., Cavazzana, R., Marrelli, L., ...

In this paper we present a statistical study of edge fluctuations taken with the Gas Puffing Imaging (GPI) diagnostics. We carry out a comparison of GPI signal from an extensive database including...

About the parabolic relation existing between the skewness and the kurtosis in time series of experimental data (2009)

Sattin, F., Agostini, M., Cavazzana, R., Serianni, G., Scarin, P., Vianello, N.

In this work we investigate the origin of the parabolic relation between skewness and kurtosis often encountered in the analysis of experimental time-series. We argue that the numerical values of the...

Statistical features of edge turbulence in RFX-mod from Gas Puffing Imaging (2006)

Sattin, F., Scarin, P., Agostini, M., Cavazzana, R., Serianni, G., Spolaore, M., ...

Plasma density fluctuations in the edge plasma of the RFX-mod device are measured through the Gas Puffing Imaging Diagnostics. Statistical features of the signal are quantified in terms of the...

A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis (2006)

Baris, I, Arisoy, AE, Smith, A, Agostini, M, Mitchell, CS, Park, SM, ...

Background: Thyroid dysgenesis is the most frequent cause of congenital hypothyroidism (CH), and its genetic basis is largely unknown. Hitherto, two mutations in the human thyroid transcription...

Non-DNA binding, dominant-negative, human PPAR gamma mutations cause lipodystrophic insulin resistance (2006)

Agostini, M, Schoenmakers, E, Mitchell, C, Szatmari, I, Savage, D, Smith, A, ...

PPAR gamma is essential for adipogenesis and metabolic homeostasis. We describe mutations in the DNA and ligand binding domains of human PPAR gamma in lipodystrophic, severe insulin resistance. These...

A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis (2006)

Baris, I, Arisoy, AE, Smith, A, Agostini, M, Mitchell, CS, Park, SM, ...

Background: Thyroid dysgenesis is the most frequent cause of congenital hypothyroidism (CH), and its genetic basis is largely unknown. Hitherto, two mutations in the human thyroid transcription...

Non-DNA binding, dominant-negative, human PPAR gamma mutations cause lipodystrophic insulin resistance (2006)

Agostini, M, Schoenmakers, E, Mitchell, C, Szatmari, I, Savage, D, Smith, A, ...

PPAR gamma is essential for adipogenesis and metabolic homeostasis. We describe mutations in the DNA and ligand binding domains of human PPAR gamma in lipodystrophic, severe insulin resistance. These...

Tyrosine Agonists reverse the molecular defects associated with dominant-negative mutations in human peroxisome proliferator-activated receptor gamma (2004)

Agostini, M, Gurnell, M, Savage, DB, Wood, EM, Smith, AG, Rajanayagam, O, ...

Loss-of-function mutations in the ligand-binding domain of human peroxisome proliferator-activated receptor gamma (PPARgamma) are associated with a novel syndrome characterized by partial...

Tyrosine Agonists reverse the molecular defects associated with dominant-negative mutations in human peroxisome proliferator-activated receptor gamma (2004)

Agostini, M, Gurnell, M, Savage, DB, Wood, EM, Smith, AG, Rajanayagam, O, ...

Loss-of-function mutations in the ligand-binding domain of human peroxisome proliferator-activated receptor gamma (PPARgamma) are associated with a novel syndrome characterized by partial...

Alternative antibiotics for the treatment of pseudomonas infections in cystic fibrosis (1983)

Mastella, G., Agostini, M., Barlocco, G., Bonomi, U., Borgo, G., Bozzino, L., ...

We have investigated the effectiveness of seven new β-lactam antibiotics, azlocillin, piperacillin, ceftazidime, cefsulodin, cefoperazone, latamoxef (moxalactam), and cefotaxime, against acute...

The "fully no-touch" technique for the internal thoracic-coronary artery anastomosis.

Dottori, V, Spagnolo, S, Agostini, M, Parodi, E, Giambuzzi, M, DeGaetano, G, ...

Extreme technical accuracy is crucial in coronary artery surgery. Although late graft patency depends mostly upon the patient's own biochemical status in chronic ischemic patients who have undergone...

A role for helix 3 of the TRbeta ligand-binding domain in coactivator recruitment identified by characterization of a third cluster of mutations in resistance to thyroid hormone.

Collingwood, T N, Wagner, R, Matthews, C H, Clifton-Bligh, R J, Gurnell, M, Rajanayagam, O, ...

Resistance to thyroid hormone (RTH) has hitherto been associated with thyroid hormone beta receptor (TRbeta) mutations which cluster in two regions (alphaalpha 310-353 and alphaalpha 429-461) of the...

The "fully no-touch" technique for the internal thoracic-coronary artery anastomosis.

Dottori, V, Spagnolo, S, Agostini, M, Parodi, E, Giambuzzi, M, DeGaetano, G, ...

Extreme technical accuracy is crucial in coronary artery surgery. Although late graft patency depends mostly upon the patient's own biochemical status in chronic ischemic patients who have undergone...

A role for helix 3 of the TRbeta ligand-binding domain in coactivator recruitment identified by characterization of a third cluster of mutations in resistance to thyroid hormone.

Collingwood, T N, Wagner, R, Matthews, C H, Clifton-Bligh, R J, Gurnell, M, Rajanayagam, O, ...

Resistance to thyroid hormone (RTH) has hitherto been associated with thyroid hormone beta receptor (TRbeta) mutations which cluster in two regions (alphaalpha 310-353 and alphaalpha 429-461) of the...