S. Selleri

发表

N-Nitrosulfonamides as Carbonic Anhydrase Inhibitors: A Promising Chemotype for Targeting Chagas Disease and Leishmaniasis.

C. Supuran, Alane Beatriz Vermelho, A. Nocentini, 2018, ACS medicinal chemistry letters.

DPA-714, a New Translocator Protein–Specific Ligand: Synthesis, Radiofluorination, and Pharmacologic Characterization

Denis Guilloteau, Roger R. Fulton, Sylvie Chalon, 2008, Journal of Nuclear Medicine.

Role of Natural Killer Cells in Intravenous Immunoglobulin-Induced Graft-versus-Host Disease Inhibition in NOD/LtSz-scidIL2rg(-/-) (NSG) Mice.

E. Haddad, S. Selleri, J. Gregoire-Gauthier, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

Novel 3-iodo-8-ethoxypyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide as promising lead for design of alpha5-inverse agonist useful tools for therapy of mnemonic damage.

C. Martini, C. Ghelardini, N. Galeotti, 2007, Bioorganic & medicinal chemistry.

Benzodiazepine receptor ligands. 8: synthesis and pharmacological evaluation of new pyrazolo[5,1-c] [1,2,4]benzotriazine 5-oxide 3- and 8-disubstituted: high affinity ligands endowed with inverse-agonist pharmacological efficacy.

C. Martini, B. Costa, F. Besnard, 2006, Bioorganic & medicinal chemistry.

Therapeutic efficacy of cord blood-derived mesenchymal stromal cells for the prevention of acute graft-versus-host disease in a xenogenic mouse model.

E. Haddad, C. Beauséjour, S. Selleri, 2012, Stem cells and development.

New 3-, 8-disubstituted pyrazolo[5,1-c][1,2,4]benzotriazines useful for studying the interaction with the HBp-3 area (hydrogen bond point area) in the benzodiazepine site on the γ-aminobutyric acid type A (GABAA) receptor.

C. Martini, S. Daniele, S. Selleri, 2011, Bioorganic & medicinal chemistry.

Novel 3-aroylpyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides 8-substituted, ligands at GABAA/benzodiazepine receptor complex: synthesis, pharmacological and molecular modeling studies.

C. Martini, C. Ghelardini, M. Montali, 2008, Bioorganic & medicinal chemistry.

In vivo T-cell dynamics during immune reconstitution after hematopoietic stem cell gene therapy in adenosine deaminase severe combined immune deficiency.

C. Cancrini, A. Aiuti, B. Cassani, 2011, The Journal of allergy and clinical immunology.

280 SGLT-1 as a novel immunological player in the intestinal mucosa

C. Rumio, A. Balsari, S. Selleri, 2008 .

Desmocollin 1 expression and desmosomal remodeling during terminal differentiation of human anagen hair follicle: an electron microscopic study

I. Barajon, E. Donetti, C. Rumio, 2004, Experimental dermatology.

Caveolin‐1 is expressed on multipotent cells of hair follicles and might be involved in their resistance to chemotherapy

C. Rumio, A. Balsari, S. Selleri, 2005, The British journal of dermatology.

Helper B Cells Promote Cytotoxic T Cell Survival and Proliferation Independently of Antigen Presentation through CD27/CD70 Interactions1

F. Marincola, E. Wang, D. Stroncek, 2008, The Journal of Immunology.

Development of ligands for the peripheral benzodiazepine receptor.

M. James, M. Kassiou, S. Selleri, 2006, Current medicinal chemistry.

Genomic scale analysis of racial impact on response to IFN-α

F. Marincola, M. Sabatino, A. Falus, 2009, Proceedings of the National Academy of Sciences.

GM-CSF/IL-3/IL-5 receptor common β chain (CD131) expression as a biomarker of antigen-stimulated CD8+ T cells

F. Marincola, E. Wang, D. Stroncek, 2008, Journal of Translational Medicine.

X-ray crystallography of Epacadostat in adduct with Carbonic Anhydrase IX.

C. Supuran, T. Peat, A. Angeli, 2020, Bioorganic chemistry.

Novel Pathogenic Mechanisms of Congenital Insensitivity to Pain with Anhidrosis Genetic Disorder Unveiled by Functional Analysis of Neurotrophic Tyrosine Receptor Kinase Type 1/Nerve Growth Factor Receptor Mutations*

M. Pierotti, M. Di Virgilio, G. Zanotti, 2002, The Journal of Biological Chemistry.

Sodium-dependent glucose transporter-1 as a novel immunological player in the intestinal mucosa.

C. Rumio, A. Balsari, S. Selleri, 2008, The Journal of Immunology.

Expression and Differential Effects of the Activation of Glucocorticoid Receptors in Mouse Gonadotropin-Releasing Hormone Neurons

F. Piva, A. Cariboni, M. Piccolella, 2006, Neuroendocrinology.

The Requirements for CTL-Mediated Rejectionof Cancer in Humans : NKG 2 D and Its Role in the Immune Responsiveness of Melanoma 55 Commentary on

E. Wang, S. Selleri, 2007 .

The Requirements for CTL-Mediated Rejection of Cancer in Humans: NKG2D and Its Role in the Immune Responsiveness of Melanoma

F. Marincola, E. Wang, S. Selleri, 2007, Clinical Cancer Research.

Rapamycin as an Adjunctive Therapy for NLRC4 Associated Macrophage Activation Syndrome

E. Haddad, S. Selleri, Isabel Fernández, 2018, Front. Immunol..

Polypharmacology of epacadostat: a potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII.

C. Supuran, M. Ferraroni, A. Angeli, 2019, Chemical communications.

Molecular purging of multiple myeloma cells by ex-vivo culture and retroviral transduction of mobilized-blood CD34+ cells

C. Voena, M. Roncarolo, S. Vai, 2007, Journal of Translational Medicine.

SecretionInduces Hormone, Chemokine, and Defensin Activation of Enteroendocrine Cells via TLRs

C. Rumio, A. Balsari, S. Selleri, 2007 .

The M581V mutation, associated with a mild form of congenital insensitivity to pain with anhidrosis, causes partial inactivation of the NTRK1 receptor.

M. Pierotti, A. Greco, S. Selleri, 2002, The Journal of investigative dermatology.

Cross-talk among Toll-like receptors and their ligands.

M. Bedoni, C. Rumio, A. Balsari, 2008, International immunology.

Therapeutic synergism of gemcitabine and CpG-oligodeoxynucleotides in an orthotopic human pancreatic carcinoma xenograft.

S. Ménard, G. Petrangolini, C. Rumio, 2005, Cancer research.

New fluoro derivatives of the pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide system: evaluation of fluorine binding properties in the benzodiazepine site on γ-aminobutyrric acid type A (GABA(A)) receptor. Design, synthesis, biological, and molecular modeling investigation.

C. Martini, C. Ghelardini, S. Daniele, 2010, Journal of medicinal chemistry.

Taurultams incorporating arylsulfonamide: First in vitro inhibition studies of α-, β- and γ-class Carbonic Anhydrases from Vibrio cholerae and Burkholderia pseudomallei.

C. Supuran, C. Capasso, A. Angeli, 2021, European journal of medicinal chemistry.

Small Molecule Alkoxy Oriented Selectiveness on Human Carbonic Anhydrase II and IX Inhibition

C. Supuran, A. Angeli, F. Carta, 2022, ChemMedChem.

A therapeutic dose of FK506 does not affect collagen turnover pathways in healthy human gingival fibroblasts.

G. Tartaglia, M. Gioia, C. Moscheni, 2008, Transplantation proceedings.

The effect of omega conotoxin GVIA, a peptide modulator of the N-type voltage sensitive calcium channels, on motor responses produced by activation of efferent and sensory nerves in mammalian smooth muscle

C. Maggi, P. Santicioli, A. Meli, 1988, Naunyn-Schmiedeberg's Archives of Pharmacology.

Improved synthesis of the peripheral benzodiazepine receptor ligand [11C]DPA-713 using [11C]methyl triflate.

M. Grégoire, B. Tavitian, M. James, 2006, Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine.

Remarkable Enhancement in Boron Uptake Within Glioblastoma Cells With Carboranyl-Indole Carboxamides.

C. Martini, M. Kassiou, R. Narlawar, 2018, Chemistry, an Asian journal.

A new class of pyrazolo[5,1-c][1,2,4]triazines as γ-aminobutyric type A (GABAA) receptor subtype ligand: synthesis and pharmacological evaluation.

C. Martini, S. Daniele, S. Selleri, 2018, Bioorganic & medicinal chemistry.

Synthesis and pharmacological evaluation of pyrazolo[1,5-a]pyrimidin-7(4H)-one derivatives as potential GABAA-R ligands.

C. Martini, C. Ghelardini, L. di Cesare Mannelli, 2017, Bioorganic & medicinal chemistry.

Development of ligands at γ-aminobutyrric acid type A (GABAA) receptor subtype as new agents for pain relief.

C. Martini, C. Ghelardini, L. di Cesare Mannelli, 2011, Bioorganic & medicinal chemistry.

Benzodiazepine receptor ligands. 4. Synthesis and pharmacological evaluation of 3-heteroaryl-8-chloropyrazolo[5,1-c][1,2,4] benzotriazine 5-oxides.

C. Martini, A. Lucacchini, B. Costa, 1999, Journal of medicinal chemistry.

Evidence for complex binding profiles and species differences at the translocator protein (TSPO) (18 kDa).

C. Martini, M. Kassiou, C. Luus, 2012, Current molecular medicine.

281 Low molecular weight hyaluronic acid increases the self defence of skin epithelium by induction of β-defensin 2 via TLR2 and 4

C. Rumio, A. Balsari, M. Sommariva, 2008 .

TLR 4-Defensin 2 via TLR 2 and β by Induction of Increases the Self-Defense of Skin Epithelium Low Molecular Weight Hyaluronic Acid

C. Rumio, A. Balsari, M. Sommariva, 2008 .

Toll‐like receptor agonists regulate β‐defensin 2 release in hair follicle

C. Rumio, A. Balsari, S. Selleri, 2007 .

Cord-blood-derived mesenchymal stromal cells downmodulate CD4+ T-cell activation by inducing IL-10-producing Th1 cells.

E. Haddad, C. Beauséjour, F. Le Deist, 2013, Stem cells and development.

Thiosemicarbazide-Substituted Coumarins as Selective Inhibitors of the Tumor Associated Human Carbonic Anhydrases IX and XII

C. Supuran, A. Angeli, F. Carta, 2022, Molecules.

Dual-Wavelength Passively Q-Switched Ytterbium-Doped Fiber Laser Based on Aluminum Oxide Nanoparticle Saturable Absorbers

A. Al-Janabi, S. Selleri, S. Al-Hayali, 2017 .

Tellurides bearing benzensulfonamide as carbonic anhydrase inhibitors with potent antitumor activity.

C. Supuran, C. Ghelardini, M. Pinteala, 2021, Bioorganic & medicinal chemistry letters.

Seleno Containing Compounds as Potent and Selective Antifungal Agents

C. Supuran, C. Capasso, A. Angeli, 2022, ACS infectious diseases.

Synthesis and benzodiazepine receptor affinity of pyrazolo[1,5-a]pyrimidine derivatives. 3. New 6-(3-thienyl) series as alpha 1 selective ligands.

C. Martini, B. Costa, F. Besnard, 2003, Journal of medicinal chemistry.

Synthesis and BZR affinity of pyrazolo[1,5-a]pyrimidine derivatives. Part 1: study of the structural features for BZR recognition.

C. Martini, B. Costa, S. Selleri, 1999, Bioorganic & medicinal chemistry.

Synthesis, benzodiazepine receptor affinity and in vivo testing of 3-aryl-4,7-dihydro-6-(N1′-alkylpyrazol-3′ - or 5′-yl)pyrazolo[1,5-a]pyrimidin-7-ones

C. Martini, A. Lucacchini, L. Giusti, 1998 .

New 2,3-substituted 4,7-dihydro-6-(1'H-pyrazol-3'-yl)pyrazolo[1,5-a] pyrimidin-7-ones and related compounds: synthesis and benzodiazepine receptor binding study.

C. Martini, A. Lucacchini, L. Giusti, 1995, Farmaco.

Reactivity of 7‐(2‐dimethylaminovinyl)pyrazolo[1,5‐a]pyrimidines: Synthesis of pyrazolo[1,5‐a]pyrido[3,4‐e]pyrimidine derivatives as potential benzodiazepine receptor ligands. 2

S. Selleri, G. Guerrini, F. Bruni, 1994 .

Synthesis of new pyrazolo[5,1-c][1,2,4] benzotriazines, pyrazolo[5,1-c]pyrido[4,3-e][1,2,4] triazines and their open analogues as cytotoxic agents in normoxic and hypoxic conditions.

E. Mini, S. Selleri, P. Failli, 2008, Bioorganic & medicinal chemistry.

Cytotoxic activity of 3-nitropyrazolo[5,1-c][1,2,4]benzotriazine derivatives: a new series of anti-proliferative agents

E. Mini, T. Mazzei, S. Selleri, 2005, Anti-cancer drugs.

Degranulation of paneth cells via toll-like receptor 9.

S. Ménard, C. Rumio, A. Balsari, 2004, The American journal of pathology.

2-Arylpyrazolo[1,5-a]pyrimidin-3-yl acetamides. New potent and selective peripheral benzodiazepine receptor ligands.

C. Martini, B. Costa, S. Selleri, 2001, Bioorganic & medicinal chemistry.

On the reactivity of 6-acetyl-7-(2-dimethylaminovinyl)pyrazolo[1,5-a]pyrimidines with 1,3- and 1,4-bisnucleophiles.

G. Viola, S. Selleri, S. Chimichi, 2008, Organic & biomolecular chemistry.

Insight into 2-phenylpyrazolo[1,5-a]pyrimidin-3-yl acetamides as peripheral benzodiazepine receptor ligands: synthesis, biological evaluation and 3D-QSAR investigation.

C. Martini, B. Costa, P. Gratteri, 2005, Bioorganic & medicinal chemistry.

Synthesis and preliminary evaluation of pyrazolo[1,5-a]pyrido[3,4-e]pyrimidin-6(7H)-ones and related compounds, as benzodiazepine receptor ligands and anticonvulsant agents

C. Martini, S. Selleri, G. Guerrini, 1992 .

A novel selective GABA(A) alpha1 receptor agonist displaying sedative and anxiolytic-like properties in rodents.

C. Martini, B. Costa, F. Besnard, 2005, Journal of medicinal chemistry.

Synthesis and study of the anti-inflammatory properties of some pyrazolo[1,5-a]pyrimidine derivatives.

S. Selleri, R. Fantozzi, G. Guerrini, 1993, Journal of pharmaceutical sciences.

Unambiguous structure determination of some pyrazolo [1,5‐a]pyrimidine derivatives by multinuclear NMR spectroscopy

B. Cosimelli, S. Selleri, S. Chimichi, 1992 .

Synthesis of 3-(1,3,4-thiadiazol-2-yl)pyrazolo[1,5-a] pyrimidine derivatives as potential antimicrobial agents.

S. Selleri, M. Clauser, G. Guerrini, 1990, Farmaco.

Pyrazolo(1,5-a)pyrido(3,4-e)pyrimidine: A New Heterocyclic Ring System.

B. Cosimelli, S. Selleri, S. Chimichi, 1990 .

Pyrazolo[1,5-a]pyrimidine acetamides: 4-Phenyl alkyl ether derivatives as potent ligands for the 18 kDa translocator protein (TSPO).

Annelaure Damont, Michael Kassiou, David Hibbs, 2010, Bioorganic & medicinal chemistry letters.

Benzodiazepine receptor ligands - Part II. Synthesis and biological evaluation of pyrazolo[5,1-c][1,2,4]benzotriazine 4-oxide

C. Martini, A. Lucacchini, B. Costa, 1998 .

gene therapy transcriptional activity of T cells from ADA-SCID patients treated with Integration of retroviral vectors induces minor changes in the

L. Naldini, F. Mavilio, A. Aiuti, 2014 .

Integration of retroviral vectors induces minor changes in the transcriptional activity of T cells from ADA-SCID patients treated with gene therapy.

C. Di Serio, L. Naldini, M. Roncarolo, 2009, Blood.

Low Molecular Weight Hyaluronic Acid Increases the Self-Defense of Skin Epithelium by Induction of β-Defensin 2 via TLR2 and TLR4

Marco Palazzo, C. Rumio, A. Balsari, 2008, The Journal of Immunology.

Human mesenchymal stromal cell-secreted lactate induces M2-macrophage differentiation by metabolic reprogramming

Ping Jin, Florina Moldovan, Francesco M. Marincola, 2016, Oncotarget.

Sodium-Dependent Glucose Transporter-1 as a Novel Immunological Player in the Intestinal Mucosa1

C. Rumio, A. Balsari, S. Selleri, 2008, The Journal of Immunology.

Discovery of new organoselenium compounds as antileishmanial agents.

Abdul-Malek S. Al-Tamimi, C. Supuran, A. Angeli, 2019, Bioorganic chemistry.

Azidothymidine “Clicked” into 1,2,3-Triazoles: First Report on Carbonic Anhydrase–Telomerase Dual-Hybrid Inhibitors

S. Carradori, C. Supuran, T. Peat, 2020, Journal of medicinal chemistry.

Discovery of β-Adrenergic Receptors Blocker-Carbonic Anhydrase Inhibitor Hybrids for Multitargeted Antiglaucoma Therapy.

R. Pecori, C. Supuran, E. Masini, 2018, Journal of medicinal chemistry.

Gene therapy of experimental brain tumors using neural progenitor cells

G. Finocchiaro, B. Pollo, R. Galli, 2000, Nature Medicine.

Efficient and Robust NK-Cell Transduction With Baboon Envelope Pseudotyped Lentivector

E. Haddad, J. Sanz, E. Verhoeyen, 2019, Front. Immunol..

The Tumor Microenvironment as a Model for Tissue-Specific Rejection

F. Marincola, C. Rumio, S. Selleri, 2008 .

Tumor microenvironment and the immune response.

F. Marincola, M. Sabatino, E. Wang, 2007, Surgical oncology clinics of North America.

Carbonic Anhydrase Inhibitors of Different Structures Dilate Pre-Contracted Porcine Retinal Arteries

C. Supuran, F. Carta, S. Selleri, 2019, International Journal of Molecular Sciences.

Heterologous expression and biochemical characterisation of the recombinant β-carbonic anhydrase (MpaCA) from the warm-blooded vertebrate pathogen malassezia pachydermatis

A. Scaloni, C. Supuran, V. De Luca, 2021, Journal of enzyme inhibition and medicinal chemistry.

Inhibitory Effects of Sulfonamide Derivatives on the β-Carbonic Anhydrase (MpaCA) from Malassezia pachydermatis, a Commensal, Pathogenic Fungus Present in Domestic Animals

A. Scaloni, C. Supuran, V. De Luca, 2021, International journal of molecular sciences.

N-aryl-N'-ureido-O-sulfamates: Potent and selective inhibitors of the human Carbonic Anhydrase VII isoform with neuropathic pain relieving properties.

C. Supuran, J. Winum, C. Ghelardini, 2019, Bioorganic chemistry.

Deciphering the Mechanism of Human Carbonic Anhydrases Inhibition with Sulfocoumarins: Computational and Experimental Studies.

C. Supuran, F. Carta, A. Nocentini, 2018, Chemistry.

Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides.

C. Supuran, M. Ferraroni, M. Pinteala, 2021, Journal of medicinal chemistry.

Conservation of genetic alterations in recurrent melanoma supports the melanoma stem cell hypothesis.

F. Marincola, M. Sabatino, E. Wang, 2008, Cancer research.

Bioisosteric Development of Multi-target Nonsteroidal Anti-inflammatory Drug - Carbonic Anhydrases Inhibitor Hybrids for the Management of Rheumatoid Arthritis.

C. Supuran, E. Masini, C. Ghelardini, 2020, Journal of Medicinal Chemistry.

Efficient and Robust NK-Cell Transduction With Baboon Envelope Pseudotyped Lentivector

E. Haddad, J. Sanz, E. Verhoeyen, 2019, bioRxiv.

Induction of pro-inflammatory programs in enteroendocrine cells by the Toll-like receptor agonists flagellin and bacterial LPS.

F. Marincola, E. Wang, C. Rumio, 2008, International immunology.

The motor response to ethylenediamine of the rat isolated duodenum: Involvement of GABAergic transmission?

C. Maggi, P. Santicioli, A. Meli, 1989, Naunyn-Schmiedeberg's Archives of Pharmacology.

Activation of smooth muscle and myenteric plexus cells of jejunum via toll‐like receptor 4

S. Akira, S. Ménard, S. Uematsu, 2006, Journal of cellular physiology.

Sequential gene profiling of basal cell carcinomas treated with imiquimod in a placebo-controlled study defines the requirements for tissue rejection

F. Marincola, E. Wang, Yingdong Zhao, 2007, Genome Biology.

Journal of Translational Medicine Molecular Signatures Induced by Interleukin-2 on Peripheral Blood Mononuclear Cells and T Cell Subsets

F. Marincola, E. Wang, D. Stroncek, 2022 .

Activation of Enteroendocrine Cells via TLRs Induces Hormone, Chemokine, and Defensin Secretion1

C. Rumio, A. Balsari, S. Selleri, 2007, The Journal of Immunology.

Leveraging interacting signaling pathways to robustly improve the quality and yield of human pluripotent stem cell-derived hepatoblasts and hepatocytes

B. Reversade, N. Baratang, G. Cagnone, 2022, Stem cell reports.

Spontaneous and treatment-induced cancer rejection in humans

F. Marincola, M. Sabatino, E. Wang, 2008 .

CMV pp65 and IE-1 T cell epitopes recognized by healthy subjects

F. Marincola, S. Adams, D. Stroncek, 2007, Journal of Translational Medicine.

Comprehensive epitope mapping of the Epstein–Barr virus latent membrane protein-2 in normal, non tumor-bearing individuals

F. Marincola, S. Adams, E. Wang, 2007, Cancer Immunology, Immunotherapy.

Benzodiazepine receptor ligands. III. Synthesis and biological evaluation of 2- and/or 3-substituted pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides.

C. Martini, A. Lucacchini, B. Costa, 1999, Farmaco.

Benzodiazepine receptor ligands. Synthesis and pharmacological evaluation of 3-, 7- and 8-substituted [5,1-c][1,2,4]benzotriazines and 5-oxide derivatives. Part I

C. Martini, A. Lucacchini, L. Giusti, 1996 .

Reactivity of 1-(2-nitrophenyl)-5-aminopyrazoles under basic conditions and synthesis of new 3-, 7-, and 8-substituted pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxides, as benzodiazepine receptor ligands

S. Selleri, G. Guerrini, F. Bruni, 1994 .

Synthesis of derivatives of pyrazolo[1,5-a]pyrrolo[1,2-c][1,3,6]-benzotriazocine, a new class of compounds with potential CNS activity

S. Selleri, G. Guerrini, F. Bruni, 1992 .

Epithelium–mesenchyme compartment interaction and oncosis on chemotherapy-induced hair damage

C. Rumio, A. Balsari, L. Vizzotto, 2004, Laboratory Investigation.

Synthesis of cns potentially active bicyclic and tricyclic derivatives of pyrazolo[1,5-a][1,3]diazepines

S. Selleri, F. Bruni, A. Costanzo, 1990 .

β3-Adrenoreceptor Activity Limits Apigenin Efficacy in Ewing Sarcoma Cells: A Dual Approach to Prevent Cell Survival

L. Filippi, Maura Calvani, A. Nocentini, 2019, International journal of molecular sciences.

Generation of Complex Syngeneic Liver Organoids from Induced Pluripotent Stem Cells to Model Human Liver Pathophysiology

S. Selleri, C. Raggi, Marie-Agnès M’Callum, 2022, Current protocols.

Associations between HLA Class I alleles and the prevalence of nasopharyngeal carcinoma (NPC) among Tunisians

F. Marincola, S. Adams, E. Wang, 2007, Journal of Translational Medicine.

Doxorubicin-induced alopecia is associated with sebaceous gland degeneration.

C. Zouboulis, C. Rumio, A. Balsari, 2006, The Journal of investigative dermatology.

Chemistry of substituted pyrazolo[1,5-a]pyrimidines. Part 4. A structural correction of a series of pyrazolo[5′,1′ : 2,3]pyrimido[5,4-d][1,2]diazepines on the basis of NMR spectroscopy and X-ray diffraction analysis

B. Cosimelli, G. Valle, S. Selleri, 1994 .

Chemistry of substituted pyrazolo[1,5-a]pyrimidines. Part 5. 7-Oxo-6-[pyrazol-3′(5′)-yl]-4,7-dihydropyrazolo[1,5-a]pyrimidines from 6-ethoxycarbonyl-7-(2-dimethylaminovinyl)pyrazolo[1,5-a]-pyrimidines: elucidation of the reaction mechanism through NMR spectroscopy and X-ray diffraction analysis

B. Cosimelli, G. Valle, S. Selleri, 1996 .

Chemistry of Substituted Pyrazolo(1,5-a)pyrimidines. Part 4. A Structural Correction of a Series of Pyrazolo(5′,1′:2,3)pyrimido(5,4-d) (1,2)diazepines on the Basis of NMR Spectroscopy and X-Ray Diffraction Analysis.

B. Cosimelli, G. Valle, S. Selleri, 1994 .

8H-Pyrazolo(5′,1′:2,3)pyrimido(5,4-d)(1,2)diazepine: A New Tricyclic System.

B. Cosimelli, S. Selleri, G. Guerrini, 1993 .

1H and 13C NMR study of the pyrazolo[1,5-a]pyrimidine system

B. Cosimelli, S. Selleri, S. Chimichi, 1992 .

Chemistry of Substituted Pyrazolo(1,5-a)pyrimidines. Part 5. 7-Oxo-6-( pyrazol-3′(5′)-yl)-4,7-dihydropyrazolo(1,5-a)pyrimidines from 6- Ethoxycarbonyl-7-(2-dimethylaminovinyl)pyrazolo(1,5-a)pyrimidines: Elucidation of the Reaction Mechanism Through NMR Spectroscopy and X- Ray Diffraction Analysis.

B. Cosimelli, G. Valle, S. Selleri, 1996 .

8H‐Pyrazolo(5′,1′:2,3)pyrimido(5,4‐d)(1,2)diazepine: A New Tricyclic System.

B. Cosimelli, S. Selleri, G. Guerrini, 1993 .

1H and 13C NMR Study of the Pyrazolo(1,5‐a)pyrimidine System.

B. Cosimelli, S. Selleri, S. Chimichi, 1992 .

Toll-like receptor agonists regulate beta-defensin 2 release in hair follicle.

C. Rumio, A. Balsari, S. Selleri, 2007, The British journal of dermatology.

Synthesis of new 1,3-dicyclohexyl barbituric acid derivatives with anti-inflammatory potential activity

P. Gratteri, S. Selleri, G. Orzalesi, 1990 .

Synthesis of New 1,3‐Dicyclohexyl Barbituric Acid Derivatives with Potential Anti‐Inflammatory Activity.

P. Gratteri, S. Selleri, G. Orzalesi, 1990 .

Polypharmacology of Epacadostat: a Potent and Selective Inhibitor of the Tumor Associated Carbonic Anhydrases IX and XII

C. Supuran, M. Ferraroni, A. Angeli, 2019 .

Glucose Biosensor With Extended Linearity

M. Mascini, S. Selleri, 1989 .

Ether analogues of DPA-714 with subnanomolar affinity for the translocator protein (TSPO).

Shane M. Wilkinson, C. Martini, M. Kassiou, 2015, European journal of medicinal chemistry.

Leveraging complex interactions between signaling pathways involved in liver development to robustly improve the maturity and yield of pluripotent stem cell-derived hepatocytes

B. Reversade, N. Baratang, G. Cagnone, 2020, bioRxiv.

Synthesis, in vivo evaluation, and molecular modeling studies of new pyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide derivatives. Identification of a bifunctional hydrogen bond area related to the inverse agonism.

C. Martini, C. Ghelardini, M. Montali, 2009, Journal of medicinal chemistry.

Benzodiazepine receptor ligands. 7. Synthesis and pharmacological evaluation of new 3-esters of the 8-chloropyrazolo[5,1-c][1,2,4]benzotriazine 5-oxide. 3-(2-Thienylmethoxycarbonyl) derivative: an anxioselective agent in rodents.

C. Martini, B. Costa, F. Besnard, 2002, Journal of medicinal chemistry.

Spontaneous and treatment-induced cancer rejection in humans.

F. Marincola, M. Sabatino, E. Wang, 2008, Expert opinion on biological therapy.

Deletion of exons 11–17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease

G. Finocchiaro, G. Uziel, D. Pareyson, 2000, Journal of Neurology.

Handling drug-target selectivity: A study on ureido containing Carbonic Anhydrase inhibitors.

C. Supuran, A. Angeli, F. Carta, 2020, European journal of medicinal chemistry.

Synthesis of 6-[¹⁸F]fluoro-PBR28, a novel radiotracer for imaging the TSPO 18 kDa with PET.

Annelaure Damont, Raphaël Boisgard, Bertrand Tavitian, 2011, Bioorganic & medicinal chemistry letters.

DNA recognition by peptide nucleic acid-modified PCFs: from models to real samples

Stefano Selleri, Enrico Coscelli, Annamaria Cucinotta, 2010, Photonics Europe.

Comprehensive Epitope Mapping of the Epstein-Barr Virus Latent Membrane Protein-2 in Ethnically Diverse Populations

F. Marincola, S. Adams, E. Wang, 2005 .

Conservation of genetic alterations in recurrent melanoma supports the melanoma stem cell hypothesis.

F. Marincola, M. Sabatino, E. Wang, 2008, Cancer research.

Role of Natural Killer Cells in Intravenous Immunoglobulin-Induced Graft-versus-Host Disease Inhibition in NOD/LtSz-scidIL2rg(-/-) (NSG) Mice.

E. Haddad, S. Selleri, L. Benchimol, 2015, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

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This information is current as Interactions Antigen Presentation through CD 27 / CD 70 Survival and Proliferation Independently of Helper B Cells Promote Cytotoxic T Cell

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2-Substituted-4,7-dihydro-4-ethylpyrazolo[1,5-a]pyrimidin-7-ones alleviate LPS-induced inflammation by modulating cell metabolism via CD73 upon macrophage polarization.

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