| Fluorescence quenching and ligand binding: a critical discussion of a popular methodology M Van de Weert, L Stella Journal of Molecular Structure 998 (1-3), 144-150, 2011 | 665 | 2011 |
| Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia E Flex, V Petrangeli, L Stella, S Chiaretti, T Hornakova, L Knoops, ... Journal of Experimental Medicine 205 (4), 751-758, 2008 | 458 | 2008 |
| Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease M Tartaglia, S Martinelli, L Stella, G Bocchinfuso, E Flex, V Cordeddu, ... The American Journal of Human Genetics 78 (2), 279-290, 2006 | 447 | 2006 |
| Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype C Carta, F Pantaleoni, G Bocchinfuso, L Stella, I Vasta, A Sarkozy, ... The American Journal of Human Genetics 79 (1), 129-135, 2006 | 277 | 2006 |
| Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome F Kortüm, V Caputo, CK Bauer, L Stella, A Ciolfi, M Alawi, G Bocchinfuso, ... Nature genetics 47 (6), 661-667, 2015 | 228 | 2015 |
| Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis E Flex, M Jaiswal, F Pantaleoni, S Martinelli, M Strullu, EK Fansa, A Caye, ... Human molecular genetics 23 (16), 4315-4327, 2014 | 180 | 2014 |
| 7-Nitro-2, 1, 3-benzoxadiazole Derivatives, a New Class of Suicide Inhibitors for Glutathione S-Transferases MECHANISM OF ACTION OF POTENTIAL ANTICANCER DRUGS G Ricci, F De Maria, G Antonini, P Turella, A Bullo, L Stella, G Filomeni, ... Journal of Biological Chemistry 280 (28), 26397-26405, 2005 | 179 | 2005 |
| Mutations in PAX2 associate with Adult-Onset FSGS M Barua, E Stellacci, L Stella, A Weins, G Genovese, V Muto, V Caputo, ... J Am Soc Nephrol 25 (9), 1942-53, 2014 | 153 | 2014 |
| Amphipathic α-helical peptide, HP (2–20), and its analogues derived from Helicobacter pylori: pore formation mechanism in various lipid compositions SC Park, MH Kim, MA Hossain, SY Shin, Y Kim, L Stella, JD Wade, Y Park, ... Biochimica et Biophysica Acta (BBA)-Biomembranes 1778 (1), 229-241, 2008 | 150 | 2008 |
| SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype–phenotype correlations F Lepri, A De Luca, L Stella, C Rossi, G Baldassarre, F Pantaleoni, ... Human mutation 32 (7), 760-772, 2011 | 149 | 2011 |
| On the purported “backbone fluorescence” in protein three-dimensional fluorescence spectra A Bortolotti, YH Wong, SS Korsholm, NHB Bahring, S Bobone, S Tayyab, ... RSC Advances 6 (114), 112870-112876, 2016 | 146 | 2016 |
| Monomer− dimer equilibrium in glutathione transferases: a critical re-examination R Fabrini, A De Luca, L Stella, G Mei, B Orioni, S Ciccone, G Federici, ... Biochemistry 48 (43), 10473-10482, 2009 | 140 | 2009 |
| How Many Antimicrobial Peptide Molecules Kill a Bacterium? The Case of PMAP-23 D Roversi, V Luca, S Aureli, Y Park, ML Mangoni, L Stella ACS chemical biology 9 (9), 2003-2007, 2014 | 134 | 2014 |
| Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies M Niceta, E Stellacci, KW Gripp, G Zampino, M Kousi, M Anselmi, ... The American Journal of Human Genetics 96 (5), 816-825, 2015 | 133 | 2015 |
| Human Glutathione Transferase P1-1 and Nitric Oxide Carriers A NEW ROLE FOR AN OLD ENZYME ML Bello, M Nuccetelli, AM Caccuri, L Stella, MW Parker, J Rossjohn, ... Journal of Biological Chemistry 276 (45), 42138-42145, 2001 | 130 | 2001 |
| Different mechanisms of action of antimicrobial peptides: insights from fluorescence spectroscopy experiments and molecular dynamics simulations G Bocchinfuso, A Palleschi, B Orioni, G Grande, F Formaggio, C Toniolo, ... Journal of peptide science: an official publication of the European Peptide …, 2009 | 114 | 2009 |
| A reassessment of synchronous fluorescence in the separation of Trp and Tyr contributions in protein emission and in the determination of conformational changes S Bobone, M van de Weert, L Stella Journal of Molecular Structure 1077, 68-76, 2014 | 109 | 2014 |
| Mutations in ZBTB20 cause Primrose syndrome V Cordeddu, B Redeker, E Stellacci, A Jongejan, A Fragale, TEJ Bradley, ... Nature genetics 46 (8), 815-817, 2014 | 109 | 2014 |
| Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome CK Bauer, P Calligari, FC Radio, V Caputo, ML Dentici, N Falah, F High, ... The American Journal of Human Genetics 103 (4), 621-630, 2018 | 105 | 2018 |
| A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome V Caputo, L Cianetti, M Niceta, C Carta, A Ciolfi, G Bocchinfuso, E Carrani, ... The American Journal of Human Genetics 90 (1), 161-169, 2012 | 101 | 2012 |
Gianfranco BocchinfusoAssociate Professor - Chemistry Department - Rome Tor Vergata Universityยืนยันอีเมลแล้วที่ uniroma2.it