المؤلفون: Sandler Topelius, N., Shokraneh, F., Bahman, M., Lahtinen, J., Hassinen, N., Airaksinen, S., Verma, S., Hrizanovska, L., Lass, J., Paaver, U., Tähnas, J., Kern, C., Lagarce, F., Fenske, D., Malik, J., Scherliess, H., Cruz, S.P., Paulsson, M., Dekker, J., Kammonen, K., Rautamo, M., Lück, H., Pierrot, A., Stareprawo, S., Tubic-Grozdanis, M., Zibolka, S., Lösch, U., Jeske, M., Griesser, U., Hummer, K., Thalmeier, A., Harjans, A., Kruse, A., Heimke-Brinck, R., Khoukh, K., Bruno, F.

المصدر: Pharmaceutics, vol. 16, no. 5

مصطلحات موضوعية: automated compounding, hospital and community pharmacies, integrated quality control, pharma inks

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38794340; info:eu-repo/semantics/altIdentifier/pissn/1999-4923; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_211F3EB3399E7; https://serval.unil.ch/notice/serval:BIB_211F3EB3399E; https://serval.unil.ch/resource/serval:BIB_211F3EB3399E.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_211F3EB3399E
https://doi.org/10.3390/pharmaceutics16050678
https://serval.unil.ch/resource/serval:BIB_211F3EB3399E.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_211F3EB3399E7

المؤلفون: Bahman, M., Jalili, H., Etesam, M., Amrane, A.

المساهمون: University of Tehran, Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 2214-7144 ; Journal of Water Process Engineering ; https://hal.science/hal-03691395 ; Journal of Water Process Engineering, 2022, 47, pp.102820. ⟨10.1016/j.jwpe.2022.102820⟩.

مصطلحات موضوعية: Codeine phosphate, Metronidazole, Pharmaceutical compounds removal, Rosuvastatin, Wastewater treatment, [CHIM]Chemical Sciences

Relation: hal-03691395; https://hal.science/hal-03691395

الاتاحة: https://hal.science/hal-03691395
https://doi.org/10.1016/j.jwpe.2022.102820

المؤلفون: Roberto Pellicciari, Antimo Gioiello, Gabriele Costantino, Bahman M. Sadeghpour, Giovanni Rizzo, Udo Meyer, Derek J. Parks, Antonio Entrena-guadix, Stefano Fiorucci

المساهمون: The Pennsylvania State University CiteSeerX Archives

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.378.2447

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.378.2447

المؤلفون: Bahman, M. R., Feldman, N. B., Orekhov, S. N., Sedyakina, N. E., Gromovykh, T. I., Lutsenko, S. V.

المصدر: Nanobiotechnology Reports; March 2021, Vol. 16 Issue: 2 p239-245, 7p

المؤلفون: Johan Auwerx, Roberto Pellicciari, Gianluca Giorgi, Kristina Schoonjans, Hiroyuki Sato, Bahman M. Sadeghpour, Gabriele Costantino, Antimo Gioiello, Antonio Macchiarulo

المساهمون: Institut de génétique et biologie moléculaire et cellulaire (IGBMC), Université Louis Pasteur - Strasbourg I-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Clinique de la Souris (ICS), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Louis Pasteur - Strasbourg I

المصدر: Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2007, 50 (18), pp.4265-8. ⟨10.1021/jm070633p⟩

مصطلحات موضوعية: Models, Molecular, medicine.medical_treatment, Receptors, Cytoplasmic and Nuclear, MESH: Cricetinae, MESH: Receptors, G-Protein-Coupled, Crystallography, X-Ray, Ligands, Receptors, G-Protein-Coupled, chemistry.chemical_compound, MESH: Structure-Activity Relationship, 0302 clinical medicine, MESH: Cricetulus, Cricetinae, Chenodeoxycholic acid, Drug Discovery, MESH: Ligands, MESH: Animals, Receptor, 0303 health sciences, Molecular Structure, Bile acid, Chemistry, Ursodeoxycholic Acid, TGR5, Stereoisomerism, MESH: Transcription Factors, G protein-coupled bile acid receptor, DNA-Binding Proteins, FXR, Biochemistry, 030220 oncology & carcinogenesis, Molecular Medicine, MESH: Models, Molecular, Agonist, medicine.drug_class, Stereochemistry, MESH: Molecular Structure, CHO Cells, MESH: Bile Acids and Salts, MESH: Receptors, Cytoplasmic and Nuclear, Methylation, Steroid, Bile Acids and Salts, MESH: Methylation, Structure-Activity Relationship, 03 medical and health sciences, Cricetulus, MESH: CHO Cells, medicine, Animals, Humans, bile acid, Structure–activity relationship, 030304 developmental biology, G protein-coupled receptor, MESH: Humans, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, MESH: Crystallography, X-Ray, MESH: Stereoisomerism, MESH: Ursodeoxycholic Acid, MESH: DNA-Binding Proteins, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3cfa699a9b29607cfb7429c74274dd
https://doi.org/10.1021/jm070633p

المؤلفون: ROBERTO PELLICCIARI, HIROYUKI SATO, ANTIMO GIOIELLO, GABRIELE COSTANTINO, ANTONIO MACCHIARULO, BAHMAN M. SADEGHPOUR, KRISTINA SCHOONJANS, JOHAN AUWERX, GIORGI, GIANLUCA

المساهمون: Roberto, Pellicciari, Hiroyuki, Sato, Antimo, Gioiello, Gabriele, Costantino, Antonio, Macchiarulo, BAHMAN M., Sadeghpour, Giorgi, Gianluca, Kristina, Schoonjan, Johan, Auwerx

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000249150700002; volume:50; firstpage:4265; lastpage:4268; journal:JOURNAL OF MEDICINAL CHEMISTRY; http://hdl.handle.net/11365/10060; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-34548508190

الاتاحة: http://hdl.handle.net/11365/10060

المؤلفون: Gioiello, Antimo, Sardella, Roccaldo, Rosatelli, Emiliano, Sadeghpour, Bahman M., Natalini, Benedetto, Pellicciari, Roberto

المصدر: Steroids ; volume 77, issue 3, page 250-254 ; ISSN 0039-128X

الاتاحة: http://dx.doi.org/10.1016/j.steroids.2011.11.012
https://api.elsevier.com/content/article/PII:S0039128X11003424?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0039128X11003424?httpAccept=text/plain

المؤلفون: Bruno Tamburini, Bahman M. Sadeghpour, Roberto Pellicciari, Tino Rossi, Carla Marchioro, Giorgio Tarzia

المصدر: Tetrahedron. 51:10723-10730

مصطلحات موضوعية: Reaction sequence, Chemistry, Yield (chemistry), Radical, Organic Chemistry, Drug Discovery, Organic chemistry, Nanotechnology, Stereoselectivity, Biochemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3cc8548614d44db23c64fab9b5ab7639
https://doi.org/10.1016/0040-4020(95)00637-n

المؤلفون: Roccaldo Sardella, Bahman M. Sadeghpour, Emiliano Rosatelli, Benedetto Natalini, Antimo Gioiello, Roberto Pellicciari

مصطلحات موضوعية: Magnetic Resonance Spectroscopy, Clinical Biochemistry, Silica Gel, Biochemistry, High-performance liquid chromatography, chemistry.chemical_compound, Endocrinology, Column chromatography, Pregnenediones, Organic chemistry, Cellulose, Molecular Biology, Commiphora, Chromatography, High Pressure Liquid, Pharmacology, Chloroform, Chromatography, Molecular Structure, Chemistry, Organic Chemistry, Stereoselective synthesis, Regioselectivity, Reproducibility of Results, Stereoisomerism, FXR, Guggulsterone, HPLC, Wittig reaction, Stereoselectivity, Androstenes, Carbamates, Oxidation-Reduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a51b1e587fe050540f0508d8b33cc6f3
http://hdl.handle.net/11391/546497

المؤلفون: Taj, Sh., Shirvani, H., Bahman, M., Ziya, A.A.

مصطلحات موضوعية: bank efficiency, ефективність банку, глобальный кризис, bank, эффективность банка, global crisis, глобальна криза, банк

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2001::c53cdd6bca74d70ace1e9a8ea23aa271
http://essuir.sumdu.edu.ua/handle/123456789/63328

المؤلفون: Bahman M. Sadeghpour, Roberto Luneia, Benedetto Natalini, Roberto Pellicciari, Joseph B. Monahan, J. P. Snyder, Maura Marinozzi, Marinella Roberti, Giovanni C. Rosato, F. Moroni

المصدر: ChemInform. 24

مصطلحات موضوعية: Agonist, chemistry.chemical_compound, chemistry, medicine.drug_class, Stereochemistry, medicine, Enantioselective synthesis, NMDA receptor, General Medicine, Sulfate, Pipecolic acid

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::590c90733c0ff2a7a42f1053cad8fce7
https://doi.org/10.1002/chin.199328257

المؤلفون: Benedetto Natalini, Giovanni C. Rosato, A. Ursini, Roberto Pellicciari, Bahman M. Sadeghpour

المصدر: ChemInform. 25

مصطلحات موضوعية: inorganic chemicals, chemistry.chemical_compound, chemistry, Organic chemistry, Diazo, General Medicine, Boron trifluoride

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::c244a756562e696a0a655861d1d512d8
https://doi.org/10.1002/chin.199419092

المؤلفون: Roberto Pellicciari, Carla Marchioro, Tino Rossi, Bahman M. Sadeghpour, Bruno Tamburini, Giorgio Tarzia

المصدر: ChemInform. 27

مصطلحات موضوعية: Reaction sequence, Chemistry, Radical, Yield (chemistry), Stereoselectivity, General Medicine, Medicinal chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e67d59307a474b463bb576d9f4a745bf
https://doi.org/10.1002/chin.199603261

المؤلفون: T. Rossi, Giorgio Tarzia, Roberto Pellicciari, Carla Marchioro, Bahman M. Sadeghpour, Antonella Ursini, Bruno Tamburini

المصدر: ChemInform. 27

مصطلحات موضوعية: medicine.drug_class, Chemistry, Antibiotics, medicine, Nanotechnology, General Medicine, Combinatorial chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::e1c4da567571c49ee4c4a525cac610d2
https://doi.org/10.1002/chin.199603260

المؤلفون: Giovanni Rizzo, Daniela Passeri, Loredana Donadio, Moshe Levi, G. Rizzo, Xiaoxin X. Wang, Luciano Adorini, Bahman M. Sadeghpour, Stefano Orlandi, Mark Pruzanski, Gianmario Ciaccioli, Tao Jiang, Francesca De Franco

المصدر: Molecular pharmacology. 78(4)

مصطلحات موضوعية: Agonist, Male, medicine.medical_specialty, medicine.drug_class, Mice, Obese, Receptors, Cytoplasmic and Nuclear, CHO Cells, Biology, Receptors, G-Protein-Coupled, Bile Acids and Salts, Mice, Cricetulus, Internal medicine, Cricetinae, medicine, Animals, Humans, Liver X receptor, Receptor, Pharmacology, Bile acid, Cytochrome P450, Hep G2 Cells, Articles, G protein-coupled bile acid receptor, Mice, Inbred C57BL, Endocrinology, Nuclear receptor, Mice, Inbred DBA, biology.protein, NIH 3T3 Cells, Molecular Medicine, Farnesoid X receptor

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a94ea0a7d9f2c73faabac3d94bc323e6
https://pubmed.ncbi.nlm.nih.gov/20631053

المؤلفون: Pellicciari, Roberto, Gioiello, Antimo, Costantino, Gabriele, Sadeghpour, Bahman M., Rizzo, Giovanni, Meyer, Udo, Parks, Derek J., Entrena-Guadix, Antonio, Fiorucci, Stefano

المصدر: Journal of Medicinal Chemistry ; volume 49, issue 14, page 4208-4215 ; ISSN 0022-2623 1520-4804

الاتاحة: http://dx.doi.org/10.1021/jm060294k
https://pubs.acs.org/doi/pdf/10.1021/jm060294k

المؤلفون: Roberto, Pellicciari, Hiroyuki, Sato, Antimo, Gioiello, Gabriele, Costantino, Antonio, Macchiarulo, Sadeghpour, BAHMAN M., Giorgi, Gianluca, Kristina, Schoonjans, Johan, Auwerx

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1820::1703f497543d6473a0d426bc38458625
http://hdl.handle.net/11365/10060

المؤلفون: Pellicciari, Roberto, Costantino, Gabriele, Camaioni, Emidio, Sadeghpour, Bahman M., Entrena, Antonio, Willson, Timothy M., Fiorucci, Stefano, Clerici, Carlo, Gioiello, Antimo

المصدر: Journal of Medicinal Chemistry ; volume 47, issue 18, page 4559-4569 ; ISSN 0022-2623 1520-4804

الاتاحة: http://dx.doi.org/10.1021/jm049904b
https://pubs.acs.org/doi/pdf/10.1021/jm049904b

المؤلفون: Antimo Gioiello, Stefano Fiorucci, Derek J. Parks, Gabriele Costantino, Roberto Pellicciari, Udo Meyer, Giovanni Rizzo, ⊥ and Antonio Entrena-Guadix, Bahman M. Sadeghpour

مصطلحات موضوعية: Models, Molecular, Receptors, Steroid, Stereochemistry, Fluorescence spectrometry, Receptors, Cytoplasmic and Nuclear, Chenodeoxycholic Acid, Ligands, Response Elements, Transfection, chemistry.chemical_compound, Transactivation, Structure-Activity Relationship, Nuclear Receptor Coactivator 1, Genes, Reporter, Chenodeoxycholic acid, Cell Line, Tumor, Drug Discovery, FXR, Bile Acid, Carbammate, SBARM, Structure-Activity Relationship, antagonism, Fluorescence Resonance Energy Transfer, Humans, Luciferases, Histone Acetyltransferases, Chemistry, Carbammate, antagonism, Nuclear receptor coactivator 1, DNA-Binding Proteins, Förster resonance energy transfer, Nuclear receptor, FXR, Docking (molecular), Drug Design, Molecular Medicine, Farnesoid X receptor, SBARM, Bile Acid, Transcription Factors

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a94eedafd7ff148496d38a4d81d1b8f
http://hdl.handle.net/11391/270690

المؤلفون: Mattia Clementi, Giuseppe Sabatino, Kenneth D.R. Setchell, Roberto Pellicciari, Bahman M. Sadeghpour, Danilo Castellani, Olivia Morelli, Stefania Asciutti, Emidio Camaioni, Monia Baldoni, Antonio Morelli, Barbara Renga, Stefano Fiorucci, Carlo Alfredo Clerici, Nancy C. O'Connell, Alessandro Mazzocchi, Elisabetta Nardi, Vittorio Giuliano, Stefano Orlandi

المصدر: Toxicology and applied pharmacology. 214(2)

مصطلحات موضوعية: Male, medicine.medical_specialty, medicine.drug_class, Bicarbonate, Toxicology, Cholesterol 7 alpha-hydroxylase, Hyodeoxycholic acid, Ethinyl Estradiol, Gas Chromatography-Mass Spectrometry, Rats, Sprague-Dawley, chemistry.chemical_compound, Cholestasis, Internal medicine, medicine, Animals, Bile, Steroid 12-alpha-Hydroxylase, RNA, Messenger, Cholesterol 7-alpha-Hydroxylase, Chromatography, High Pressure Liquid, Micelles, Phospholipids, Pharmacology, Bile acid, Dose-Response Relationship, Drug, Molecular Structure, Chemistry, Biliary fistula, Ursodeoxycholic Acid, Cholic acid, medicine.disease, Ursodeoxycholic acid, Rats, Endocrinology, Cholanes, Bile Ducts, medicine.drug, Deoxycholic Acid, Steroids, Fluorinated

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19b50a6fc0b496116b1fc5dad3e640d1
https://pubmed.ncbi.nlm.nih.gov/16487557