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Titolo Data di pubblicazione Autore(i) File
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients 1-gen-1995 Gennarelli, M.; Lucarelli, Marco; Capon, F.; Pizzuti, Antonio; Merlini, L.; Angelini, C.; Novelli, G.; Dallapiccola, B.
Different expression of the myotonin protein kinase gene in discrete areas of human brain 1-gen-1995 Gennarelli, M.; Lucarelli, Marco; Zelano, G.; Pizzuti, Antonio; Novelli, G.; Dallapiccola, B.
Screening of thyrotropin receptor mutations by fine-needle aspiration biopsy in autonomous functioning thyroid nodules in multinodular goiters. 1-gen-1999 V., Tassi; A., DI CERBO; A., Porcellini; E., Papini; C., Cisternino; A., Crescenzi; A., Scillitani; Pizzuti, Antonio; A., Ratti; Trischitta, Vincenzo; V. E., Avvedimento; G. FENZI V., DE FILIPPIS
A polymorphism (K121Q) of the human glycoprotein PC-1 coding region is strongly associated with insulin resistance 1-gen-1999 Pizzuti, Antonio; Frittitta, L; Argiolas, A; Baratta, R; GOLDFINE I., D; Bozzali, M; Ercolino, T; Scarlato, G; Iacoviello, L; Vigneri, R; Tassi, V; Trischitta, Vincenzo
Erratum: A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance (Diabetes (1999) 48 (1881-1884)) 1-gen-1999 Pizzuti, A.; Frittitta, L.; Argiolas, A.; Baratta, R.; Goldfine, I. D.; Bozzali, M.; Ercolino, T.; Scarlato, G.; Iacoviello, L.; Vigneri, R.; Tassi, V.; Trischitta, V.
Association between the human glycoprotein PC-1 gene and elevated glucose and insulin levels in a paired-sibling analysis 1-gen-2000 H. F., Gu; P., Almgren; E., Lindholm; L., Frittitta; Pizzuti, Antonio; Trischitta, Vincenzo; L. C., Groop
The K121Q variant of human PC-1 gene is not associated with insulin resistance or type 2 diabetes mellitus among Danish Caucasians 1-gen-2000 S. K., Rasmussen; S. A., Urhammer; Pizzuti, Antonio; S. M., Echwald; C. T., Ekstrom; L., Hansen; T., Hansen; K., BORCH JOHNSEN; L., Frittitta; Trischitta, Vincenzo; O., Pedersen
A PC-1 aminoacid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria. 1-gen-2000 S., DE COSMO; A., Argiolas; G., Miscio; S., Thomas; Gp, Piras; R., Trevisan; P., CAVALLO PERIN; S., Bacci; L., Zucaro; M., Margaglione; L., Frittitta; Pizzuti, Antonio; V., Tassi; Gc, Viberti; Trischitta, Vincenzo
The Q121 PC-1 variant and obesity have additive and independent effects in causing insulin resistance. 1-gen-2001 L., Frittitta; R., Baratta; D., Spampinato; R., DI PAOLA; Pizzuti, Antonio; R., Vigneri; Trischitta, Vincenzo
A cluster of 3 single nucleotide polymorphisms in the 3\'-untranslated region of human glycoprotein PC-1 gene stabilizes mRNA and associates with increased protein content and insulin resistance related abnormalities 1-gen-2001 Lucia, Frittitta; Tonino, Ercolino; Maura, Bozzali; Alessandra, Argiolas; Salvo, Graci; MARIA G., Santagati; Daniela, Spampinato; ROSA DI, Paola; Vittorio, Tassi; Riccardo, Vigneri; Pizzuti, Antonio; Trischitta, Vincenzo
The Q allele variant (GLN121) of membrane glycoprotein PC-1 interacts with the insulin receptor and inhibits insulin signaling more effectively than the common K allele variant (LYS121) 1-gen-2001 B. V., Costanzo; Trischitta, Vincenzo; R., Di Paola; D., Spampinato; Pizzuti, Antonio; R., Vigneri; L., Frittitta
An ATG repeat in the 3’UTR of the hResistin gene is associated with a decreased risk of insulin resistance 1-gen-2002 Pizzuti, Antonio; Argiolas, A; DI PAOLA, R; Baratta, R; Rauseo, A; Bozzali, M; Vigneri, R; Dallapiccola, B; Trischitta, Vincenzo; Frittitta, L.
Leiomyosarcoma of the larynx: Case report with pathologic and surgical considerations 1-gen-2002 Fusconi, Massimo; Magliulo, Giuseppe; Pizzuti, Antonio; Caterina, Ceccarini; Soldo, Pietro; DE VINCENTIIS, Marco
Novel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia 1-gen-2002 Francesco, Brancati; Giovanni, Defazio; Caputo, Viviana; Enza Maria, Valente; Pizzuti, Antonio; Paolo, Livrea; Berardelli, Alfredo; Bruno, Dallapiccola
The role of PC-1 and ACE genes in diabetic nephropathy in type 1 diabetic patients: Evidence for a polygenic control of kidney disease progression 1-gen-2002 De Cosmo, S.; Miscio, G.; Zucaro, L.; Margaglione, M.; Argiolas, A.; Thomas, S.; Piras, G.; Trevisan, R.; Perin, P. C.; Bacci, S.; Frittitta, L.; Pizzuti, A.; Tassi, V.; Di Minno, G.; Viberti, G.; Trischitta, V.
Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene 1-gen-2002 Maria Cristina, Digilio; Emanuela, Conti; Anna, Sarkozy; Rita, Mingarelli; Tania, Dottorini; MARINO TAUSSIG DE BODONIA, Bruno; Pizzuti, Antonio; DALLA PICCOLA, Bruno
DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 Gene 1-gen-2003 Conti, E; Grifone, N; Sarkozy, A; Tandoi, C; Marino Taussig De Bodonia, Bruno; Digilio, Mc; Mingarelli, R; Pizzuti, Antonio; Dalla Piccola, Bruno
Hereditary Gingival Fibromatosis (Hgf) with hypertrichosis is unlinked to the Hgf1 and Hgf2 Loci 1-gen-2003 Mangino, M; Bonfante, A; Cucchiara, E; Pizzuti, Antonio; Dallapiccola, B.
. Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A. 1-gen-2003 Brancati, F; Valente, Em; Davies, Np; Sarkozy, A; Sweeney, Mg; Lomonaco, M; Pizzuti, Antonio; Hanna, Mg; Dallapiccola, B.
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes 1-gen-2003 A., Sarkozy; E., Conti; D., Seripa; M. C., Digilio; N., Grifone; C., Tandoi; V. M., Fazio; V., Di Ciommo; MARINO TAUSSIG DE BODONIA, Bruno; Pizzuti, Antonio; DALLA PICCOLA, Bruno
Mostrati risultati da 1 a 20 di 151
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