Lorenzo Stella
Lorenzo Stella
Dept of Chemical Science and Technologies, University of Roma Tor Vergata
Verified email at - Homepage
Cited by
Cited by
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
Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia
E Flex, V Petrangeli, L Stella, S Chiaretti, T Hornakova, L Knoops, ...
The Journal of experimental medicine 205 (4), 751-758, 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Aggregation and water-membrane partition as major determinants of the activity of the antibiotic peptide trichogin GA IV
L Stella, C Mazzuca, M Venanzi, A Palleschi, M Didonč, F Formaggio, ...
Biophysical journal 86 (2), 936-945, 2004
Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes
S Martinelli, P Torreri, M Tinti, L Stella, G Bocchinfuso, E Flex, A Grottesi, ...
Human molecular genetics 17 (13), 2018-2029, 2008
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
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