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Ganglioside Biochemistry / / by Cheorl-Ho Kim
Ganglioside Biochemistry / / by Cheorl-Ho Kim
Autore Kim Cheorl-Ho
Edizione [1st ed. 2020.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Descrizione fisica 1 online resource (XVI, 214 p. 57 illus., 48 illus. in color.)
Disciplina 596.0188
Soggetto topico Molecular genetics
Cancer
Genetics
Biochemistry
Biological transport
Cell membranes
Molecular Genetics
Cancer Biology
Genetics and Genomics
Membrane Trafficking
ISBN 981-15-5815-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preface: Carbohydrates- the third life chain -- 1. Glycosylation -- 2. N-Glycan and O-glycan glycosylation in eukaryotes -- 3. Sialyltransferase, sialylation and sulfoylation -- 4. Congenital disorders of glycosylation (CDG) of N-glycoprotein -- 5. Neuraminic acids/sialic acids (N-acetyl- and N-glycolylneuraminic acid) -- 6. Biosynthesis of sialic acid -- 7. Neu5Gc (N-glycolylneuraminic acid) -- 8. Gangliosides -- 9. Gangliosides and tumor-associated ganglioside (TAG) modulate receptor-tyrosine kinases (RTKs) -- 10. Sialic acids and TAGs of tumor cells to escape immunesurveillance and immuneediting -- 11. Tumor characteristics in tumor related carbohydrates.
Record Nr. UNINA-9910416110403321
Kim Cheorl-Ho  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Glycobiology of Innate Immunology / / by Cheorl-Ho Kim
Glycobiology of Innate Immunology / / by Cheorl-Ho Kim
Autore Kim Cheorl-Ho
Edizione [1st ed. 2022.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2022
Descrizione fisica 1 online resource (673 pages)
Disciplina 301
Collana Biomedical and Life Sciences Series
Soggetto topico Genetics
Medical genetics
Biology
Membranes (Biology)
Biological transport
Cell membranes
Genetics and Genomics
Medical Genetics
Biological Sciences
Biological Membranes
Membrane Trafficking
ISBN 981-16-9080-4
981-16-9081-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Part 1. Glycans in innate immunity of dendritic cells -- Chapter 1) Historical expansion of defense system -- Chapter 2) Columbus era to modern revolution in immunological defense system -- Chapter 3) Historical profile of defense constituents and progress in innte immune repertoire -- Chapter 4) The outline of innate immunity -- Chapter 5) Autophagy from microbial invaders and self-associated molecular patterns (SAMPs) of innate immune cells -- Part 2. Dendritic cells (DCs) -- Chapter 6) General biology of DCs -- Chapter 7) Classification and different function of DCs -- Chapter 8) Glycan biosynthesis in eukaryotes -- Chapter 9) Glycans in cell recognition and evolutionary adaptation in organisms -- Chapter 10) Changes in glycan structure involve in co-regulated expression of glycan-binding lectin counterparts -- Chapter 11) Evolution of lectin: alternative splicing contributes to variation for glycan binding receptors -- Chapter 12) Glycan regulation of NK cell receptors -- Chapter 13) Carbohydrate recognition of target antigens by DCs during infection and inflammation -- Chapter 14) Glycan-specific trafficking receptors in DCs maturation -- Chapter 15) Glycan ligands in trafficking of DC migration -- Chapter 16) Chemokine receptors in DCs trafficking -- Chapter 17) Glycan structure-recognizing selectins in DC-endothelium interaction during infection and inflammation -- Chapter 18) Glycans activate the innate immune system -- Chapter 19) Innate immune lectin receptors of Siglec, DC-SIGN, Galectin and TLR in DCs -- Chapter 20) Galectins -- Chapter 21) DC-specific ICAM-3-grabbing non-integrin, DC-SIGNB (CD209) -- Chapter 22) Other DCs-derivd receptors -- Chapter 23) Toll-like receptors (TLRs) -- Chapter 24) CD33 and CD33-related Siglecs in pathogen recognition and endocytosis of DC in the innate immune system -- Chapter 25) Pathogenic suppression of the pathogen-specific host immune response -- Chapter 26) DCs tumor immunotherapy through sialyl binding of DCs to T cells.
Record Nr. UNINA-9910743362403321
Kim Cheorl-Ho  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Glycoimmunology in Xenotransplantation / / by Cheorl-Ho Kim
Glycoimmunology in Xenotransplantation / / by Cheorl-Ho Kim
Autore Kim Cheorl-Ho
Edizione [1st ed. 2024.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024
Descrizione fisica 1 online resource (378 pages)
Disciplina 617.954
Soggetto topico Biology
Biological Sciences
ISBN 9789819976911
981997691X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preface -- Table of Contents -- Keywords -- Chapter 1 Origin of Life and Diversity of Glycan -- Chapter 2 Current State of Xenotransplantation -- Chapter 3 Pig as Best Source for Clinical Xenotransplantation -- Chapter 4 Glycan Antigens of Pig Interfering with Xenotransplantation: Three Immune Responses from the Glycans -- Chapter 5 Glycosylation in Eukaryotes -- Chapter 6 Human Red Blood Cell (RBC) Blood Groups System -- Chapter 7 Non-ABO Blood Group Systems -- Chapter 8 Conceptual Aspect of Xenotransplantation from ABO Blood Type-incompatible Organ Allotransplantation -- Chapter 9 Classification of Rejection in Host Recipients in Xenotransplantation -- Chapter 10 Hyper Acute Rejection (HAR) -- Chapter 11 Non-α1,3Gal Carbohydrate Antigenic Epitopes -- Chapter 12. Other non-a1,3Gal Antigens -- Chapter 13 Blood Mediated Inflammatory Reaction (IBMIR) and Prevention of IBMIR -- Chapter 14 Protection of Cellular Antigens from Xenoreactive Responses as Overcoming Strategies -- Chapter 15 Delayed Rejection of Xenograft (DRX) -- Chapter 16 Blood Coagulation as Coagulation Dysregulation -- Chapter 17 Xenogeneic and Allogenic Cellular Rejection (CR) -- Chapter 18 Induction of Xenograft Tolerance and Chimerism as an Alternative Prevention of Xenograft Rejection -- Chapter 19 Genome Editing and Transgenes in Pigs -- Chapter 20 Solid Xenoorgan Xenotransplantation -- Chapter 21 Infectious Risk and Protection -- Chapter 22 Concept of Chimeric Organisms such as Human-non-human chimera (HNH-chimera) -- Chapter 23 Intra-bone Bone Marrow Transplantation -- Chapter 24 The Future of Pig Organ and Cell Xenotransplantation -- Chapter 25 Conclusions.
Record Nr. UNINA-9910838279503321
Kim Cheorl-Ho  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2024
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Glycosphingolipids Signaling / / by Cheorl-Ho Kim
Glycosphingolipids Signaling / / by Cheorl-Ho Kim
Autore Kim Cheorl-Ho
Edizione [1st ed. 2020.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Descrizione fisica 1 online resource (XVII, 181 p. 30 illus., 25 illus. in color.)
Disciplina 571.74
Soggetto topico Molecular genetics
Cancer
Genetics
Biochemistry
Biological transport
Cell membranes
Molecular Genetics
Cancer Biology
Genetics and Genomics
Membrane Trafficking
ISBN 981-15-5807-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. Glycosphingolipids (GSLs) -- 2. Mammal GSL synthesis via ER and Golgi network -- 3. The GSL dependent signaling -- 4. Viral protein interaction with host cells GSLs -- 5. Bacterial toxin protein interaction with host cells GSL -- 6. GSL signaling regulation.
Record Nr. UNINA-9910437632003321
Kim Cheorl-Ho  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
GM3 Signaling / / by Cheorl-Ho Kim
GM3 Signaling / / by Cheorl-Ho Kim
Autore Kim Cheorl-Ho
Edizione [1st ed. 2020.]
Pubbl/distr/stampa Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Descrizione fisica 1 online resource (VII, 138 p. 32 illus., 26 illus. in color.)
Disciplina 378.1662
Soggetto topico Molecular genetics
Cancer
Genetics
Biochemistry
Biological transport
Cell membranes
Molecular Genetics
Cancer Biology
Genetics and Genomics
Membrane Trafficking
ISBN 981-15-5652-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto 1. History of sialic acids, gangliosides and GM3 -- 2. Synthesis of GM3 -- 3. Molecular localization of GM3 in cells -- 4. Basic function of GM3 as an interacting molecule -- 5. GD3 mimetics with a neurite forming capacity -- 6. GM3 as a pathogenic infection receptor -- 7. GM3 and related gangliosides prevent inflammation and atherosclerosis -- 8. GM3 has an anti-tumor capacity -- 9. GM3 suppresses tumor angiogenesis -- 10. Interaction between EGFR and GM3 -- 11. Membrane ganglioside-specific neuraminidase 3 (NEU3) regulates GM3 signaling -- 12. Regulation of GM3-mediated EGFR signaling by NEU3 sialidase -- 13. VEGFR-GM3 interaction in angiogenesis -- 14. GM3, competing with GM1, interaction with urokinase plasminogen activator receptor (uPAR) in endothelial caveolar-lipid rafts inhibits angiogenesis -- 15. GM3 interacts with TGFβ Rs in the epithelial-mesenchymal transition (EMT) during posterior capsular opacification (PCO) formation -- 16. Galectin-1 promotes tumor growth and escapes immune surveillance -- 17. GM3-HGFR, FGFR and PDGFR cancer cell behavior, and IGF-1R in diabetic wound healing -- 18. GM3, caveolin-1 and insulin receptor in insulin resistance -- 19. GM3 suppresses arthritis -- 20. GM3 protects cochlear hair cells and hearing from corti degeneration -- 21. GM3 increases osteoclast differentiation via direct GM3 cooperation with RANKL and IGF-1 -- 22. GM3 in leukemic cells into terminal differentiation -- 23. α2,3-Sialyllactose (3SL) or α2,6-sialyllactose (6SL) of GM3 glycan in innate immunity. .
Record Nr. UNINA-9910416108503321
Kim Cheorl-Ho  
Singapore : , : Springer Nature Singapore : , : Imprint : Springer, , 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui