Glycoproteins and Disease

Glycoproteins and Disease, 1st Edition

Glycoproteins and Disease, 1st Edition,J. Montreuil,J.F.G. Vliegenthart,H. Schachter,ISBN9780444823960

New Comprehensive Biochemistry

Montreuil   &   Vliegenthart   &   Schachter   

Elsevier Science


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The elucidation during the latter half of the 20th century of the mechanisms by which information flows from nucleic acids to proteins has completely changed the face of biological research. Many diseases are caused by abnormalities in control mechanisms which are not immediately essential for life itself but which maintain the normal social behavior of differentiated cells in multicellular organisms. The complex sugar chains of glycoproteins and glycolipids are believed to play important roles in the control of cellular functions and in recognition between the cell and its cellular and fluid environment. Investigations into the abnormalities of complex sugar chain assembly are expected to yield an important new underatanding of the etiology and pathogenesis of human diseases. This volume discusses several representative diseases which emphasize the current status of glycopathology, and will stimulate further research in this exciting field.

J. Montreuil

Affiliations and Expertise

Universitá des Sciences et Technologies de Lille, Laboratoire de Chimie Biologique, (UMR no 111 du CNRS), 59655 Villeneuve d'Asq Cedex, France

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J.F.G. Vliegenthart

Affiliations and Expertise

Bijvoet Center for Biomolecular Research, Department of Bio-organic Chemistry, P.O. Box 80.075, 3508 Utrecht, The Netherlands

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H. Schachter

Affiliations and Expertise

Department of Biochemistry Research, Hospital for Sick Children, 555 University Avenue, Toronto, Ont. M5G 1X8, Canada

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Glycoproteins and Disease, 1st Edition

Preface. List of contributors. Previous volumes in the series. Preliminary contents of volume 29b.
Introduction to the volume (A. Kobata). 1a. Normal and Pathological catabolism of glycoproteins. The
enzymes (G.W. Jourdian). 1b. Normal and pathological catabolism of glycoproteins. Catabolic
pathways (J.-C. Michalski). 2a. Glycoproteins of parasites. Glycoproteins of Trypanosoma cruzi (B.K.
Hayes, G.W. Hart). 2b. Glycoproteins of parasites. Glycoconjugates of Leishmania (S.J.
Turco). 2c. Glycoproteins of parasites. Glycoproteins of malaria parasites (A. Dieckmann-Schuppert,
P. Gerold, R.T. Schwarz). 2d. Glycoproteins of parasites. Schistosoma glycoconjugates and
their role in host-parasite pathological interactions (G.J. van Dam, A.M. Deelder). 3. Cancer cells and
metastasis. Introduction (A. Kobata). 3a. Cancer cells and metastasis. Choriocarcinoma and hCG (R.
Nishimura, A. Kobata). 3b. Cancer cells and metastasis. Hepatocellular carcinoma (K. Yamashita, A.
Kobata). 3c. Cancer cells and metastasis. The Warren-Glick phenomenon - a molecular basis of
tumorigenesis and metastasis (A. Kobata). 3d. Cancer cells and metastasis. Carcinoembryonic antigen
and related normal antigens. (K. Yamashita, A. Kobata). 3. Cancer cells and metastasis. Concluding
remarks (A. Kobata). 4. Tumor-associated carbohydrate antigens and modified blood group antigens
(S. Hakomori). 5. Rheumatoid arthritis and serum IgG (T. Endo, K. Furukawa). 6. Glycoproteins in
inflammatory bowel disease (M. Tomana). 7. HEMPAS: A genetic disorder caused by a defect in N-
linked oligosaccharide synthesis (M.N. Fukuda). 8. Leukosialin and the Wiskott-Aldrich syndrome (M.
Fukuda). 9. Progeroid form of Ehlers-Danlos syndrome (H. Kresse). 10. Paroxysmal nocturnal
hemoglobinuria (M. Tomita). 11. Human mucosal mucins in diseases (P. Roussel, G. Lamblin). 12.
Glycoproteins and lectins in multiple sclerosis and immune demyelinating human diseases (J.-P.
Zanetta). 13. Leucocyte adhesion deficiency Type II (J.C. Paulson). 14. Polysialic acids of vertebrates:
biosynthesis, structural diversity, tissue expression and functions (J. Roth). 15. Glycosylation defects
in blood clotting (M. Matsuda). 16a. Carbohydrate-deficient glycoprotein syndrome. Type I (K.
Yamashita, K. Ohno). 16b. Carbohydrate-deficient glycoprotein syndrome. Type II: an autosomal
recessive disease due to mutations in the N-acetylglucosaminyltransferase II gene (J. Jaeken, G. Spik,
H. Schachter). Index.

Quotes and reviews

@qu:Clearly, this fascinating book should be of interest to glycobiologists, medical investigators and physiologists alike, whether they are involved in industrial or fundamental research.
@source:Carbohydrates in Europe
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