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Recent findings confirm LIM domain kinases as emerging target candidates for cancer therapy

Current cancer drug targets, 2012-06, Vol.12 (5), p.543-560

Manetti, F

2012

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Targeting the Hedgehog Signaling Pathway with Small Molecules from Natural Sources

Current medicinal chemistry, 2015-01, Vol.22 (35), p.4058-4090

2015

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Targeting the human DEAD-box polypeptide 3 (DDX3) RNA helicase as a novel strategy to inhibit viral replication

Current medicinal chemistry, 2011-07, Vol.18 (20), p.3015-3027

2011

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SRC inhibitors and angiogenesis

Current pharmaceutical design, 2007-07, Vol.13 (21), p.2118-2128

2007

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New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold

Mini reviews in medicinal chemistry, 2007-01, Vol.7 (1), p.65-78

2007

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Pharmacophoric models and 3D QSAR studies of the adenosine receptor ligands

Current topics in medicinal chemistry, 2010-07, Vol.10 (10), p.1019-1035

2010

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Enlarging the NSAIDs family: ether, ester and acid derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents

Current medicinal chemistry, 2011-04, Vol.18 (10), p.1540-1554

2011

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Fibroblast growth factors and their inhibitors

Current pharmaceutical design, 2000-12, Vol.6 (18), p.1897-1924

2000

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Last findings on dual inhibitors of abl and SRC tyrosine-kinases

Mini reviews in medicinal chemistry, 2007-02, Vol.7 (2), p.191-201

2007

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New pyrazolo[3,4- d]pyrimidines endowed with A431 antiproliferative activity and inhibitory properties of Src phosphorylation

Bioorganic & medicinal chemistry letters, 2004-05, Vol.14 (10), p.2511-2517

2004

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Ductal carcinoma in situ of the breast, lessons learned after more than 10 years follow-up of a cohort of patients from a large western cancer centre

European journal of cancer (1990), 2024-03, Vol.200, p.113744, Article 113744

2024

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Prepectoral breast reconstruction with tissue expander covered by acellular dermal matrix: results and outcomes after the first 94 procedures

European journal of cancer (1990), 2024-03, Vol.200, p.113743, Article 113743

2024

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Synthesis, Biological Evaluation, and Pharmacophore Generation of Uracil, 4(3H)-Pyrimidinone, and Uridine Derivatives as Potent and Selective Inhibitors of Parainfluenza 1 (Sendai) Virus

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4554-4562

2001

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P146 New weapons are necessary to fight Mycobacterium abscessus

Journal of cystic fibrosis, 2020-06, Vol.19, p.S97-S97

2020

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Arylpiperazines with Affinity Toward a1-Adrenergic Receptors

Current medicinal chemistry, 2002-07, Vol.9 (13), p.1303-1321

2002

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Pyrazolo[3,4-d]pyrimidines as Potent Antiproliferative and Proapoptotic Agents toward A431 and 8701-BC Cells in Culture via Inhibition of c-Src Phosphorylation

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1549-1561

2006

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Medical Evaluation of Work-related Illness: Evaluations by a Treating Occupational Medicine Specialist and by Independent Medical Examiners Compared

International journal of occupational and environmental health, 2004-01, Vol.10 (1), p.1-12

2004

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Antimycobacterial compounds. New pyrrole derivatives of BM212

Bioorganic & medicinal chemistry, 2004-03, Vol.12 (6), p.1453-1458

2004

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HIV-Reverse Transcriptase Inhibition: Inclusion of Ligand-Induced Fit by Cross-Docking Studies

Journal of medicinal chemistry, 2005-01, Vol.48 (1), p.200-212

2005

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Computational comparison of microtubule-stabilising agents laulimalide and peloruside with taxol and colchicine

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (19), p.4825-4829

2004

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1,5-Diarylpyrrole-3-acetic Acids and Esters as Novel Classes of Potent and Highly Selective Cyclooxygenase-2 Inhibitors

Journal of medicinal chemistry, 2005-05, Vol.48 (9), p.3428-3432

2005

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Synthesis, biological evaluation, and pharmacophore generation of new pyridazinone derivatives with affinity toward alpha(1)- and alpha(2)-adrenoceptors

Journal of medicinal chemistry, 2001-06, Vol.44 (13), p.2118-2132

2001

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Antiproliferative activity of new 1-aryl-4-amino-1H-pyrazolo[3,4-d]pyrimidine derivatives toward the human epidermoid carcinoma A431 cell line

European journal of medicinal chemistry, 2004-11, Vol.39 (11), p.939-946

2004

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Antifungal Agents. 10. New Derivatives of 1-[(Aryl)[4-aryl-1H-pyrrol-3-yl]methyl]-1H-imidazole, Synthesis, Anti-Candida Activity, and Quantitative Structure−Analysis Relationship Studies

Journal of medicinal chemistry, 2002-06, Vol.45 (13), p.2720-2732

2002

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Synthesis, Biological Evaluation, and Pharmacophore Generation of New Pyridazinone Derivatives with Affinity toward α1- and α2-Adrenoceptors

Journal of medicinal chemistry, 2001-06, Vol.44 (13), p.2118-2132

2001

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Recent findings confirm LIM domain kinases as emerging target candidates for cancer therapy

Targeting the Hedgehog Signaling Pathway with Small Molecules from Natural Sources

Targeting the human DEAD-box polypeptide 3 (DDX3) RNA helicase as a novel strategy to inhibit viral replication

SRC inhibitors and angiogenesis

New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold

Pharmacophoric models and 3D QSAR studies of the adenosine receptor ligands

Enlarging the NSAIDs family: ether, ester and acid derivatives of the 1,5-diarylpyrrole scaffold as novel anti-inflammatory and analgesic agents

Fibroblast growth factors and their inhibitors

Last findings on dual inhibitors of abl and SRC tyrosine-kinases

New pyrazolo[3,4- d]pyrimidines endowed with A431 antiproliferative activity and inhibitory properties of Src phosphorylation

Ductal carcinoma in situ of the breast, lessons learned after more than 10 years follow-up of a cohort of patients from a large western cancer centre

Prepectoral breast reconstruction with tissue expander covered by acellular dermal matrix: results and outcomes after the first 94 procedures

Synthesis, Biological Evaluation, and Pharmacophore Generation of Uracil, 4(3H)-Pyrimidinone, and Uridine Derivatives as Potent and Selective Inhibitors of Parainfluenza 1 (Sendai) Virus

P146 New weapons are necessary to fight Mycobacterium abscessus

Arylpiperazines with Affinity Toward a1-Adrenergic Receptors

Pyrazolo[3,4-d]pyrimidines as Potent Antiproliferative and Proapoptotic Agents toward A431 and 8701-BC Cells in Culture via Inhibition of c-Src Phosphorylation

Medical Evaluation of Work-related Illness: Evaluations by a Treating Occupational Medicine Specialist and by Independent Medical Examiners Compared

Antimycobacterial compounds. New pyrrole derivatives of BM212

HIV-Reverse Transcriptase Inhibition: Inclusion of Ligand-Induced Fit by Cross-Docking Studies

Computational comparison of microtubule-stabilising agents laulimalide and peloruside with taxol and colchicine

1,5-Diarylpyrrole-3-acetic Acids and Esters as Novel Classes of Potent and Highly Selective Cyclooxygenase-2 Inhibitors

Synthesis, biological evaluation, and pharmacophore generation of new pyridazinone derivatives with affinity toward alpha(1)- and alpha(2)-adrenoceptors

Antiproliferative activity of new 1-aryl-4-amino-1H-pyrazolo[3,4-d]pyrimidine derivatives toward the human epidermoid carcinoma A431 cell line

Antifungal Agents. 10. New Derivatives of 1-[(Aryl)[4-aryl-1H-pyrrol-3-yl]methyl]-1H-imidazole, Synthesis, Anti-Candida Activity, and Quantitative Structure−Analysis Relationship Studies

Synthesis, Biological Evaluation, and Pharmacophore Generation of New Pyridazinone Derivatives with Affinity toward α1- and α2-Adrenoceptors

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