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Angiogenesis : in vivo systems. Part A / edited by David A. Cheresh
Angiogenesis : in vivo systems. Part A / edited by David A. Cheresh
Pubbl/distr/stampa Amsterdam [etc.], : Elsevier Academic Press, [2008]
Descrizione fisica v. ; 24 cm
Disciplina 572
Collana Methods in Enzymology
ISBN 9780123743138
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 444: Part A ; 445: Part B
Record Nr. UNINA-9910676795003321
Amsterdam [etc.], : Elsevier Academic Press, [2008]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Angiogenesis : in vitro systems / edited by David A. Cheresh
Angiogenesis : in vitro systems / edited by David A. Cheresh
Pubbl/distr/stampa Amsterdam [etc.], : Elsevier Academic Press, c2008
Descrizione fisica XLII, 356 p., [4] p. di tav. : ill. ; 24 cm.
Disciplina 572
Collana Methods in Enzymology
ISBN 9780123743152
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910676795103321
Amsterdam [etc.], : Elsevier Academic Press, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Anion-binding catalysis / / edited by Olga García Mancheño
Anion-binding catalysis / / edited by Olga García Mancheño
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2022]
Descrizione fisica 1 online resource (416 pages)
Disciplina 572
Soggetto topico Bioorganic chemistry
Soggetto genere / forma Electronic books.
ISBN 3-527-83065-0
3-527-83064-2
3-527-83066-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- List of Abbreviations -- Chapter 1 From Anion Recognition to Organocatalytic Chemical Reactions -- 1.1 Introduction and Background -- 1.1.1 Evolution of Thiourea‐Based Catalysts -- 1.1.2 Evolution of Triazole‐Based Catalysts -- 1.1.3 Progress on Halogen‐Binding‐Based Catalysts -- 1.1.4 Miscellaneous Anion‐Binding Catalysts -- 1.2 Concepts in Anion‐Binding Catalysis -- 1.2.1 Introduction -- 1.2.2 Anion‐Binding Catalysis in Addition Reactions -- 1.2.3 Anion‐Binding Catalysis in Substitution Reactions -- 1.2.4 Anion Binding in Cooperative Catalysis -- 1.2.5 Anion‐Binding in Lewis Acid Enhancement Catalysis -- 1.2.6 Anion‐Binding in Phase Transfer Catalysis -- 1.3 Summary and Outlook -- Acknowledgment -- References -- Chapter 2 Anion Recognition and Binding Constant Determination -- 2.1 Introduction to Supramolecular Chemistry and Binding Constant Determination -- 2.1.1 Chapter Overview -- 2.1.2 Supramolecular Chemistry and Its Connection to Anion‐Assisted Catalysis -- 2.1.3 Brief History of Advances in Supramolecular Anion Binding -- 2.1.4 Predicting the Model of Association and Simulating the Expected Species Distribution Profiles and Binding Curves -- 2.2 Equilibrium Constants, Binding Curves, Titration Conditions, and Errors -- 2.2.1 Physical Origins of Equilibrium Binding Constants -- 2.2.2 Explanation of the Basis for Titration Techniques and Binding Curves -- 2.2.3 Hirose's Rule and Picking the Right Concentration, Solvent, and Technique -- 2.2.4 Error Determination -- 2.3 Experimental Techniques: NMR Spectroscopy -- 2.3.1 When to Use -- 2.3.2 Slow Exchange vs. Fast Exchange -- 2.3.3 Determination of the Underlying Equilibria -- 2.3.4 Software for Non‐linear Regression Fitting -- 2.3.5 Common Issues -- 2.4 Experimental Techniques: UV-Vis Spectroscopy -- 2.4.1 When to Use.
2.4.2 Physical Origins of Optical Phenomena -- 2.4.3 Software for Non‐linear Regression Analysis of UV-Vis Titrations -- 2.4.4 Common Issues -- 2.5 Underappreciated Concerns in Binding Constant Determination: Multiple Binding Equilibria -- 2.5.1 When to Expect Additional Equilibria -- 2.5.2 How to Diagnose Additional Equilibria -- 2.5.3 How to Account for Additional Equilibria -- 2.6 Underappreciated Concerns in Binding Constant Determination: Ion Pairing -- 2.6.1 When to Expect Ion Pairing -- 2.6.2 Role of Solvent and Concentration in Ion Pairing -- 2.6.3 How to Diagnose Ion Pairing -- 2.7 Underappreciated Concerns in Binding Constant Determination: Kinetic Processes -- 2.8 Connecting Equilibrium Constants to Structures and Catalysis -- 2.9 Conclusion -- Acknowledgment -- References -- Chapter 3 (Thio)urea and Squaramide‐Catalyzed Anion‐Binding Catalysis with Halogen Anions -- 3.1 Introduction -- 3.2 History and Background -- 3.3 Asymmetric Catalysis by Catalyst Association with the Electrophile -- 3.3.1 Examples Utilizing the N‐Acyliminium Chloride Ion Pair -- 3.3.1.1 Pictet-Spengler Reaction and Variants -- 3.3.1.2 Intramolecular Cyclizations with Other (Hetero)aromatic Nucleophiles -- 3.3.1.3 Intramolecular and Intermolecular aza‐Sakurai Reaction -- 3.3.1.4 Mannich Reaction and Variants -- 3.3.1.5 Petasis‐Type Reactions -- 3.3.2 Examples Utilizing Electrophiles Other than N‐Acyliminium Ion Precursors -- 3.3.2.1 Utilization of Oxocarbenium and Pyrone Intermediates -- 3.3.2.2 Glycosylation Reactions Utilizing HBD-Halide Binding -- 3.3.2.3 Utilization of Non‐heteroatom‐Stabilized Carbocations as Electrophiles -- 3.4 Asymmetric Catalysis by Catalyst Association with the Nucleophile -- 3.4.1 Catalyst‐Nucleophile Association in Phase‐Transfer Catalysis -- 3.4.1.1 Investigation of Hydrogen‐Bonded Fluoride: Structure and Reactivity.
3.4.1.2 Development of Hydrogen‐Bonding Phase‐Transfer Catalysis (HBPTC) -- 3.4.1.3 Development of Acyl‐Transfer Catalysis with Hydrogen‐Bonded Fluoride -- 3.4.2 Catalyst-Nucleophile Association in Homogeneous Catalysis -- 3.5 Conclusions and Outlook -- Acknowledgments -- References -- Chapter 4 Chiral Ureas, Thioureas, and Squaramides in Anion‐Binding Catalysis with Co‐catalytic Brønsted/Lewis Acids -- 4.1 Introduction -- 4.2 Carboxylic Acid Co‐catalysts -- 4.3 Sulfonic Acid Co‐catalysts -- 4.4 Mineral Acid Co‐catalysts -- 4.5 Lewis Acid Co‐catalysts -- 4.6 Conclusions and Outlook -- References -- Chapter 5 Anion‐Binding Catalysis with Other Anions -- 5.1 Introduction -- 5.2 Cyanide Anion -- 5.2.1 Strecker Reaction -- 5.2.2 Acylcyanation of Imines -- 5.3 Oxygen‐Based Anions -- 5.3.1 Alkoxides and Enolates -- 5.3.2 Enolates of Lactones, Cyclic Anhydrides, and Imides -- 5.3.3 Carboxylates -- 5.4 Conclusions and Outlook -- References -- Chapter 6 Silanediols, Phosphoramides, and Other OH‐ and NH‐Based H‐Donor Catalysts -- 6.1 Introduction -- 6.2 Silanediols -- 6.2.1 Introduction -- 6.2.2 Overview of Silanols in Anion Binding and Catalysis -- 6.2.3 Silanediol Anion‐Binding Catalysis -- 6.2.4 Alkoxysilanediol Anion Binding Catalysis -- 6.3 Siloxanes -- 6.4 Thiophosphoramides -- 6.5 Cyclodiphosphazanes -- 6.6 Other Examples -- 6.6.1 Xanthene-Diamine Scaffold -- 6.6.2 Croconamides -- 6.6.3 Pyrrole‐Based Anion‐Binding Catalyst -- 6.6.4 Bisamidine Catalysts -- 6.7 Conclusions -- References -- Chapter 7 1,2,3‐Triazoles and 1,2,3‐Triazolium Ions as Catalysts -- 7.1 Introduction -- 7.2 Triazole‐Based Anion‐Binding Molecular Catalysts -- 7.3 Triazolium Ions as Organic Molecular Catalysts with Anion‐Binding Ability -- 7.4 Triazolium Ions in Dual Functional Catalysts -- 7.5 Conclusion -- References.
Chapter 8 Quaternary Ammonium, Phosphonium, and Tertiary Sulfonium Salts as Hydrogen‐Bonding Catalysts -- 8.1 Introduction -- 8.2 Hydrogen‐Bonding Ability of Quaternary Ammonium Salts -- 8.3 Hydrogen‐Bonding Catalysis of Quaternary Ammonium Salts -- 8.4 Hydrogen‐Bonding Catalysis of Quaternary Phosphonium Salts -- 8.5 Hydrogen‐Bonding Catalysis of Tertiary Sulfonium Salts -- 8.6 Conclusion -- References -- Chapter 9 Assisted and Dual Anion Binding in Amino and Nucleophilic Catalysis -- 9.1 Dual Amino/H‐Bond Donor Catalysis -- 9.1.1 Enamine Activation -- 9.1.2 Dienamine Activation -- 9.1.3 Iminium Ion Activation -- 9.1.4 Vinylogous Iminium Ion Activation -- 9.2 Thiourea - Pyridine‐Based Nucleophilic Dual Catalysis -- 9.2.1 Kinetic Resolution and Desymmetrization of Amines -- 9.2.2 Asymmetric Steglich Rearrangement -- 9.2.3 Other Acylation Reactions -- 9.2.4 Anion‐Binding‐Assisted Polymerization Reactions -- 9.3 Conclusions -- References -- Chapter 10 Anion‐Binding Catalysis by Halogen, Chalcogen, Pnictogen, and Tetrel Bonding -- 10.1 History of Halogen Bonding -- 10.2 History of Chalcogen Bonding -- 10.3 History of Pnictogen and Tetrel Bonding -- 10.4 Differences Between Hydrogen Bonding and Other Secondary Interactions -- 10.5 Secondary Bonding in Anion Recognition -- 10.6 Halogen Bonding in Anion‐Binding Catalysis -- 10.7 Chalcogen Bonding in Anion‐Binding Catalysis -- 10.8 Pnictogen and Tetrel Bonding in Anion‐Binding Catalysis -- 10.9 Conclusion -- References -- Chapter 11 New Trends and Supramolecular Approaches in Anion‐Binding Catalysis -- 11.1 General Introduction -- 11.2 Dual Photoredox and Anion‐Binding Catalysis -- 11.3 Combination of Metal and Anion‐Binding Catalysis -- 11.3.1 Anion‐Binding Assisted Hydrogenation Reactions -- 11.3.2 Hydroformylation Reactions -- 11.3.3 Anion‐Binding - Metal‐Catalyzed C-C Forming Reactions.
11.4 Supramolecular Approaches Involving Anion‐Binding Catalysis -- 11.4.1 Mechanically Interlocked Molecules in Anion‐Binding Catalysis -- 11.4.1.1 Molecular Knots as Anion‐Binding Catalysts -- 11.4.1.2 Rotaxanes as Anion‐Binding Catalysts -- 11.4.2 Molecular Motors in Anion‐Binding Catalysis -- 11.4.3 Macrocycles in Anion‐Binding Catalysis -- 11.5 Anion-π Catalysis -- 11.5.1 Anion-π‐Catalyzed Kemp Elimination Reaction -- 11.5.2 Anion-π Interactions in Enolate Chemistry -- 11.5.3 Epoxide‐Opening - Ether Cyclization Reactions -- 11.5.4 Enantioselective Anion-π Catalysis -- 11.5.5 Miscellaneous -- 11.6 Conclusion and Outlook -- References -- Index -- EULA.
Record Nr. UNINA-9910555108803321
Weinheim, Germany : , : Wiley-VCH, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Anion-binding catalysis / / edited by Olga García Mancheño
Anion-binding catalysis / / edited by Olga García Mancheño
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2022]
Descrizione fisica 1 online resource (416 pages)
Disciplina 572
Soggetto topico Catalysis
Anions
ISBN 3-527-83065-0
3-527-83064-2
3-527-83066-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- List of Abbreviations -- Chapter 1 From Anion Recognition to Organocatalytic Chemical Reactions -- 1.1 Introduction and Background -- 1.1.1 Evolution of Thiourea‐Based Catalysts -- 1.1.2 Evolution of Triazole‐Based Catalysts -- 1.1.3 Progress on Halogen‐Binding‐Based Catalysts -- 1.1.4 Miscellaneous Anion‐Binding Catalysts -- 1.2 Concepts in Anion‐Binding Catalysis -- 1.2.1 Introduction -- 1.2.2 Anion‐Binding Catalysis in Addition Reactions -- 1.2.3 Anion‐Binding Catalysis in Substitution Reactions -- 1.2.4 Anion Binding in Cooperative Catalysis -- 1.2.5 Anion‐Binding in Lewis Acid Enhancement Catalysis -- 1.2.6 Anion‐Binding in Phase Transfer Catalysis -- 1.3 Summary and Outlook -- Acknowledgment -- References -- Chapter 2 Anion Recognition and Binding Constant Determination -- 2.1 Introduction to Supramolecular Chemistry and Binding Constant Determination -- 2.1.1 Chapter Overview -- 2.1.2 Supramolecular Chemistry and Its Connection to Anion‐Assisted Catalysis -- 2.1.3 Brief History of Advances in Supramolecular Anion Binding -- 2.1.4 Predicting the Model of Association and Simulating the Expected Species Distribution Profiles and Binding Curves -- 2.2 Equilibrium Constants, Binding Curves, Titration Conditions, and Errors -- 2.2.1 Physical Origins of Equilibrium Binding Constants -- 2.2.2 Explanation of the Basis for Titration Techniques and Binding Curves -- 2.2.3 Hirose's Rule and Picking the Right Concentration, Solvent, and Technique -- 2.2.4 Error Determination -- 2.3 Experimental Techniques: NMR Spectroscopy -- 2.3.1 When to Use -- 2.3.2 Slow Exchange vs. Fast Exchange -- 2.3.3 Determination of the Underlying Equilibria -- 2.3.4 Software for Non‐linear Regression Fitting -- 2.3.5 Common Issues -- 2.4 Experimental Techniques: UV-Vis Spectroscopy -- 2.4.1 When to Use.
2.4.2 Physical Origins of Optical Phenomena -- 2.4.3 Software for Non‐linear Regression Analysis of UV-Vis Titrations -- 2.4.4 Common Issues -- 2.5 Underappreciated Concerns in Binding Constant Determination: Multiple Binding Equilibria -- 2.5.1 When to Expect Additional Equilibria -- 2.5.2 How to Diagnose Additional Equilibria -- 2.5.3 How to Account for Additional Equilibria -- 2.6 Underappreciated Concerns in Binding Constant Determination: Ion Pairing -- 2.6.1 When to Expect Ion Pairing -- 2.6.2 Role of Solvent and Concentration in Ion Pairing -- 2.6.3 How to Diagnose Ion Pairing -- 2.7 Underappreciated Concerns in Binding Constant Determination: Kinetic Processes -- 2.8 Connecting Equilibrium Constants to Structures and Catalysis -- 2.9 Conclusion -- Acknowledgment -- References -- Chapter 3 (Thio)urea and Squaramide‐Catalyzed Anion‐Binding Catalysis with Halogen Anions -- 3.1 Introduction -- 3.2 History and Background -- 3.3 Asymmetric Catalysis by Catalyst Association with the Electrophile -- 3.3.1 Examples Utilizing the N‐Acyliminium Chloride Ion Pair -- 3.3.1.1 Pictet-Spengler Reaction and Variants -- 3.3.1.2 Intramolecular Cyclizations with Other (Hetero)aromatic Nucleophiles -- 3.3.1.3 Intramolecular and Intermolecular aza‐Sakurai Reaction -- 3.3.1.4 Mannich Reaction and Variants -- 3.3.1.5 Petasis‐Type Reactions -- 3.3.2 Examples Utilizing Electrophiles Other than N‐Acyliminium Ion Precursors -- 3.3.2.1 Utilization of Oxocarbenium and Pyrone Intermediates -- 3.3.2.2 Glycosylation Reactions Utilizing HBD-Halide Binding -- 3.3.2.3 Utilization of Non‐heteroatom‐Stabilized Carbocations as Electrophiles -- 3.4 Asymmetric Catalysis by Catalyst Association with the Nucleophile -- 3.4.1 Catalyst‐Nucleophile Association in Phase‐Transfer Catalysis -- 3.4.1.1 Investigation of Hydrogen‐Bonded Fluoride: Structure and Reactivity.
3.4.1.2 Development of Hydrogen‐Bonding Phase‐Transfer Catalysis (HBPTC) -- 3.4.1.3 Development of Acyl‐Transfer Catalysis with Hydrogen‐Bonded Fluoride -- 3.4.2 Catalyst-Nucleophile Association in Homogeneous Catalysis -- 3.5 Conclusions and Outlook -- Acknowledgments -- References -- Chapter 4 Chiral Ureas, Thioureas, and Squaramides in Anion‐Binding Catalysis with Co‐catalytic Brønsted/Lewis Acids -- 4.1 Introduction -- 4.2 Carboxylic Acid Co‐catalysts -- 4.3 Sulfonic Acid Co‐catalysts -- 4.4 Mineral Acid Co‐catalysts -- 4.5 Lewis Acid Co‐catalysts -- 4.6 Conclusions and Outlook -- References -- Chapter 5 Anion‐Binding Catalysis with Other Anions -- 5.1 Introduction -- 5.2 Cyanide Anion -- 5.2.1 Strecker Reaction -- 5.2.2 Acylcyanation of Imines -- 5.3 Oxygen‐Based Anions -- 5.3.1 Alkoxides and Enolates -- 5.3.2 Enolates of Lactones, Cyclic Anhydrides, and Imides -- 5.3.3 Carboxylates -- 5.4 Conclusions and Outlook -- References -- Chapter 6 Silanediols, Phosphoramides, and Other OH‐ and NH‐Based H‐Donor Catalysts -- 6.1 Introduction -- 6.2 Silanediols -- 6.2.1 Introduction -- 6.2.2 Overview of Silanols in Anion Binding and Catalysis -- 6.2.3 Silanediol Anion‐Binding Catalysis -- 6.2.4 Alkoxysilanediol Anion Binding Catalysis -- 6.3 Siloxanes -- 6.4 Thiophosphoramides -- 6.5 Cyclodiphosphazanes -- 6.6 Other Examples -- 6.6.1 Xanthene-Diamine Scaffold -- 6.6.2 Croconamides -- 6.6.3 Pyrrole‐Based Anion‐Binding Catalyst -- 6.6.4 Bisamidine Catalysts -- 6.7 Conclusions -- References -- Chapter 7 1,2,3‐Triazoles and 1,2,3‐Triazolium Ions as Catalysts -- 7.1 Introduction -- 7.2 Triazole‐Based Anion‐Binding Molecular Catalysts -- 7.3 Triazolium Ions as Organic Molecular Catalysts with Anion‐Binding Ability -- 7.4 Triazolium Ions in Dual Functional Catalysts -- 7.5 Conclusion -- References.
Chapter 8 Quaternary Ammonium, Phosphonium, and Tertiary Sulfonium Salts as Hydrogen‐Bonding Catalysts -- 8.1 Introduction -- 8.2 Hydrogen‐Bonding Ability of Quaternary Ammonium Salts -- 8.3 Hydrogen‐Bonding Catalysis of Quaternary Ammonium Salts -- 8.4 Hydrogen‐Bonding Catalysis of Quaternary Phosphonium Salts -- 8.5 Hydrogen‐Bonding Catalysis of Tertiary Sulfonium Salts -- 8.6 Conclusion -- References -- Chapter 9 Assisted and Dual Anion Binding in Amino and Nucleophilic Catalysis -- 9.1 Dual Amino/H‐Bond Donor Catalysis -- 9.1.1 Enamine Activation -- 9.1.2 Dienamine Activation -- 9.1.3 Iminium Ion Activation -- 9.1.4 Vinylogous Iminium Ion Activation -- 9.2 Thiourea - Pyridine‐Based Nucleophilic Dual Catalysis -- 9.2.1 Kinetic Resolution and Desymmetrization of Amines -- 9.2.2 Asymmetric Steglich Rearrangement -- 9.2.3 Other Acylation Reactions -- 9.2.4 Anion‐Binding‐Assisted Polymerization Reactions -- 9.3 Conclusions -- References -- Chapter 10 Anion‐Binding Catalysis by Halogen, Chalcogen, Pnictogen, and Tetrel Bonding -- 10.1 History of Halogen Bonding -- 10.2 History of Chalcogen Bonding -- 10.3 History of Pnictogen and Tetrel Bonding -- 10.4 Differences Between Hydrogen Bonding and Other Secondary Interactions -- 10.5 Secondary Bonding in Anion Recognition -- 10.6 Halogen Bonding in Anion‐Binding Catalysis -- 10.7 Chalcogen Bonding in Anion‐Binding Catalysis -- 10.8 Pnictogen and Tetrel Bonding in Anion‐Binding Catalysis -- 10.9 Conclusion -- References -- Chapter 11 New Trends and Supramolecular Approaches in Anion‐Binding Catalysis -- 11.1 General Introduction -- 11.2 Dual Photoredox and Anion‐Binding Catalysis -- 11.3 Combination of Metal and Anion‐Binding Catalysis -- 11.3.1 Anion‐Binding Assisted Hydrogenation Reactions -- 11.3.2 Hydroformylation Reactions -- 11.3.3 Anion‐Binding - Metal‐Catalyzed C-C Forming Reactions.
11.4 Supramolecular Approaches Involving Anion‐Binding Catalysis -- 11.4.1 Mechanically Interlocked Molecules in Anion‐Binding Catalysis -- 11.4.1.1 Molecular Knots as Anion‐Binding Catalysts -- 11.4.1.2 Rotaxanes as Anion‐Binding Catalysts -- 11.4.2 Molecular Motors in Anion‐Binding Catalysis -- 11.4.3 Macrocycles in Anion‐Binding Catalysis -- 11.5 Anion-π Catalysis -- 11.5.1 Anion-π‐Catalyzed Kemp Elimination Reaction -- 11.5.2 Anion-π Interactions in Enolate Chemistry -- 11.5.3 Epoxide‐Opening - Ether Cyclization Reactions -- 11.5.4 Enantioselective Anion-π Catalysis -- 11.5.5 Miscellaneous -- 11.6 Conclusion and Outlook -- References -- Index -- EULA.
Record Nr. UNINA-9910830491403321
Weinheim, Germany : , : Wiley-VCH, , [2022]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Annual review of anthropology
Annual review of anthropology
Pubbl/distr/stampa Palo Alto : Annual reviews, 1972-
Disciplina 572
Soggetto topico Antropologia - Periodici
ISSN 0084-6570
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNISA-990001046480203316
Palo Alto : Annual reviews, 1972-
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Annual review of biochemistry
Annual review of biochemistry
Pubbl/distr/stampa Stanford, : Stanford university, 1932-
Descrizione fisica volumi : ill. ; 32 cm
Disciplina 572(Biochimica. Citochimica. Istochimica)
ISSN 0066-4154
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN0031647
Stanford, : Stanford university, 1932-
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Annual review of biochemistry
Annual review of biochemistry
Pubbl/distr/stampa Palo Alto (Calif.) : Annual Review Inc.
Disciplina 572
Soggetto topico Biochimica - Periodici
ISSN 0066-4154
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNISA-990000939970203316
Palo Alto (Calif.) : Annual Review Inc.
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Annual review of biochemistry
Annual review of biochemistry
Edizione [Stanford : Stanford university, 1932-]
Descrizione fisica Il luogo di pubblicazione e l'editore variano in: Palo Alto : Annual reviews.
Disciplina 572(Biochimica. Citochimica. Istochimica)
ISSN 0066-4154
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0031647
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Annual review of biochemistry
Annual review of biochemistry
Pubbl/distr/stampa Palo Alto, : Annual Reviews, Inc.
Disciplina 572
574.192
ISSN 0066-4154
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Note periodicità Annuale
Record Nr. UNINA-990008902190403321
Palo Alto, : Annual Reviews, Inc.
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Annual review of biochemistry
Annual review of biochemistry
Pubbl/distr/stampa Palo Alto, Calif., : Annual Review, Inc
Descrizione fisica 1 online resource
Disciplina 572
Soggetto topico Biochemistry
Biochimie
Biochemie
Soggetto genere / forma Periodicals.
ISSN 1545-4509
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910143938403321
Palo Alto, Calif., : Annual Review, Inc
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui

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