Sfoglia per Autore  

Opzioni
Mostrati risultati da 1 a 20 di 90
Titolo Data di pubblicazione Autore(i) File
The antiangiogenic tissue kallikrein pattern of endothelial cells in systemic sclerosis. 2005 B.GIUSTI; S.SERRATI'; F.MARGHERI; L.PAPUCCI; L.ROSSI; F.POGGI; A.MAGI; A.DEL ROSSO; M.CINELLI; S.GUIDUCCI; B.KAHALEH; M.MATUCCI CERINIC; R.ABBATE; G. FIBBI; M.DEL ROSSO
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients. 2006 Giusti B;Fibbi G;Margheri F;Serratì S;Rossi L;Poggi F;Lapini I;Magi A;Del Rosso A;Cinelli M;Guiducci S;Kahaleh B;Bazzichi L;Bombardieri S;Matucci Cerinic M;Gensini GF;Del Rosso M;Abbate R
Using a calibration experiment to assess gene-specific information: full Bayesian and empirical Bayesian models for two-channel microarray data. 2006 M.Blangiardo; S.Toti; B.Giusti; R.Abbate; A.Magi; F.Poggi; L.Rossi; F.Torricelli; A.Biggeri.
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm. 2008 B.Giusti; C.Saracini; P.Bolli; A.Magi; I.Sestini; E.Sticchi; G.Pratesi; R.Pulli; C.Pratesi; R.Abbate
High-throughput multiplex single-nucleotide polymorphism (SNP) analysis in genes involved in methionine metabolism 2008 B.Giusti; I.Sestini; C.Saracini; E.Sticchi; P.Bolli; A.Magi; AM.Gori; R.Marcucci; GF.Gensini; R.Abbate
Gene expression profile of rat left ventricles reveals persisting changes following chronic mild exercise protocol: implications for cardioprotection 2009 Giusti B; Marini M; Rossi L; Lapini I; Magi A; Capalbo A; Lapalombella R; di Tullio S; Samaja M; Esposito F; Margonato V; Boddi M; Abbate R; Velcsteinas A
Gene expression profiling of peripheral blood in patients with abdominal aortic aneurysm 2009 Giusti B; Rossi L; Lapini I; Magi A; Pratesi G; Lavitrano M; Blasi GM; Pulli R; Pratesi C; Abbate R
Early-onset ischaemic stroke: analysis of 58 polymorphisms in 17 genes involved in methionine metabolism 2010 B.Giusti; C.Saracini; P.Bolli; A.Magi; I.Martinelli; F.Peyvandi; M.Rasura; M.Volpe; LA.Lotta; S.Rubattu; P.M.Mannucci; R.Abbate
A very fast and accurate method for calling aberrations in array-CGH data. 2010 M. Benelli;G. Marseglia;G. Nannetti;R. Paravidino;F. Zara;F. D. Bricarelli;F. Torricelli;A. Magi
Assessment of fibrinolytic activity by measuring the lysis time of a tissue-factor-induced clot: a feasibility evaluation. 2010 A.P. Cellai; D. Lami; A. Magi; A.A. Liotta; A. Rogolino; E. Antonucci ; B. Bandinelli; R. Abbate; D. Prisco
A shifting level model algorithm that identifies aberrations in array-CGH data 2010 A. Magi;M. Benelli;G. Marseglia;G. Nannetti;M. R. Scordo;F. Torricelli
Bioinformatics for Next Generation Sequencing Data 2010 Magi A.; Benelli M.; Gozzini A.; Girolami F.; Torricelli F.; Brandi M.L.
Carotid artery disease: Novel pathophysiological mechanisms identified by gene-expression profiling of peripheral blood 2010 Rossi L, Lapini I, Magi A, Pratesi G, Lavitrano M, Biasi GM, Pulli R, Pratesi C, Abbate R, Giusti B
Sphingosine 1-phosphate induces differentiation of mesoangioblasts towards smooth muscle. A role for GATA6. 2011 C. Donati; G. Marseglia; A. Magi; S. Serratì; F. Cencetti; C. Bernacchioni; G. Nannetti; M. Benelli; S. Brunelli; F. Torricelli; G. Cossu; P. Bruni
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm. 2011 A. Magi;M. Benelli;S. Yoon;F. Roviello;F. Torricelli
EX-HOM (EXome HOMozygosity): A Proof of Principle. 2011 T. Pippucci;M. Benelli;A. Magi;P. L. Martelli;P. Magini;F. Torricelli;R. Casadio;M. Seri;G. Romeo
WNP: A Novel Algorithm for Gene Products Annotation from Weighted Functional Networks. 2012 Magi A, Tattini L, Benelli M, Giusti B, Abbate R, Ruffo S
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuria. 2012 Mannelli F;Bencini S;Peruzzi B;Cutini I;Sanna A;Benelli M;Magi A;Gianfaldoni G;Rotunno G;Carrai V;Gelli AM;Valle V;Santini V;Notaro R;Luzzatto L;Bosi A
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants. 2012 B. Giusti;A. Vestrini; C. Poggi; A. Magi; E. Pasquini; R. Abbate; C. Dani
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization. 2012 Striano P; Coppola A; Paravidino R; Malacarne M; Gimelli S; Robbiano A; Traverso M; Pezzella M; Belcastro V; Bianchi A; Elia M; Falace A; Gazzerro E; Ferlazzo E; Freri E; Galasso R; Gobbi G; Molinatto C; Cavani S; Zuffardi O; Striano S; Ferrero GB; Silengo M; Cavaliere ML; Benelli M; Magi A; Piccione M; Dagna Bricarelli F; Coviello DA; Fichera M; Minetti C; Zara F.
Mostrati risultati da 1 a 20 di 90
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile