Joseph Fanous

发表

The role of molecular physicochemical properties and apolipoproteins in association of drugs with triglyceride‐rich lipoproteins: in‐silico prediction of uptake by chylomicrons

P. Gershkovich, A. Hoffman, S. Amselem, 2009, The Journal of pharmacy and pharmacology.

Overcoming the Lack of Oral Availability of Cyclic Hexapeptides: Design of a Selective and Orally Available Ligand for the Integrin αvβ3.

E. Novellino, H. Kessler, F. Rechenmacher, 2017, Angewandte Chemie.

Antibiotic chemotherapy against heterogeneous pathogen populations in complex host tissues

D. Bumann, F. Goormaghtigh, Joseph Fanous, 2019, F1000Research.

Tailoring of integrin ligands: probing the charge capability of the metal ion-dependent adhesion site.

E. Novellino, H. Kessler, Florian Manzenrieder, 2012, Journal of medicinal chemistry.

Superiority of the S,S conformation in diverse pharmacological processes: Intestinal transport and entry inhibition activity of novel anti-HIV drug lead.

M. Kotler, C. Gilon, A. Hoffman, 2015, International journal of pharmaceutics.

Outer membrane permeability: Antimicrobials and diverse nutrients bypass porins in Pseudomonas aeruginosa

D. Bumann, S. Hiller, Sandra Söderholm, 2021, Proceedings of the National Academy of Sciences.

Tissue compartmentalization enables Salmonella persistence during chemotherapy

D. Bumann, N. Chicherova, Beatrice Claudi, 2021, Proceedings of the National Academy of Sciences.

Quantitative contribution of efflux to multi-drug resistance of clinical Escherichia coli and Pseudomonas aeruginosa strains

D. Bumann, R. Neher, C. Kemmer, 2019, EBioMedicine.

Inhibition of inositol monophosphatase (IMPase) at the calbindin-D28k binding site: Molecular and behavioral aspects

M. Eisenstein, O. Almog, C. Gilon, 2013, European Neuropsychopharmacology.

The Calbindin-D28k binding site on inositol monophosphatase may allow inhibition independent of the lithium site of action

M. Eisenstein, O. Almog, C. Gilon, 2011 .

Enhancing Oral Bioavailability of Cyclic RGD Hexa-peptides by the Lipophilic Prodrug Charge Masking Approach: Redirection of Peptide Intestinal Permeability from a Paracellular to Transcellular Pathway.

H. Kessler, C. Gilon, A. Hoffman, 2018, Molecular pharmaceutics.

Development of a Novel Backbone Cyclic Peptide Inhibitor of the Innate Immune TLR/IL1R Signaling Protein MyD88

D. Karussis, C. Gilon, A. Hoffman, 2018, Scientific Reports.

Development of a Novel Backbone Cyclic Peptide Inhibitor of the Innate Immune TLR/IL1R Signaling Protein MyD88

D. Karussis, C. Gilon, A. Hoffman, 2018, Scientific Reports.

The role of molecular physicochemical properties and apolipoproteins in association of drugs with triglyceride-rich lipoproteins: in-silico prediction of uptake by chylomicrons.

Shimon Amselem, P. Gershkovich, A. Hoffman, 2009, The Journal of pharmacy and pharmacology.

Tailoring of integrin ligands: probing the charge capability of the metal ion-dependent adhesion site.

E. Novellino, H. Kessler, Florian Manzenrieder, 2012, Journal of medicinal chemistry.

Inhibition of inositol monophosphatase (IMPase) at the calbindin-D28k binding site: Molecular and behavioral aspects

M. Eisenstein, O. Almog, C. Gilon, 2013, European Neuropsychopharmacology.