Molecular bases of human diseases : proceedings of the international meeting, held in Milan, Italy, September 27-Octover 1, 1992 /

Molecular bases of human diseases : proceedings of the international meeting, held in Milan, Italy, September 27-Octover 1, 1992 /

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Bibliographic Details
Imprint:Amsterdam ; New York : Excerpta Medica, 1993.
Description:ix, 305 p. : ill. ; 25 cm.
Language:English
Subject:
Pathology, Molecular -- Congresses.
Medical genetics -- Congresses.
Medical genetics.
Pathology, Molecular.
Conference papers and proceedings.
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/1497987
Hidden Bibliographic Details
Other authors / contributors:Polli, E. E. (Elio E.)
ISBN:0444815635 (acid-free paper)
Notes:Includes bibliographical references and index.

MARC

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245 0 0 |a Molecular bases of human diseases :  |b proceedings of the international meeting, held in Milan, Italy, September 27-Octover 1, 1992 /  |c editor, E.E. Polli. 
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300 |a ix, 305 p. :  |b ill. ;  |c 25 cm. 
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504 |a Includes bibliographical references and index. 
505 0 0 |t From basic science to clinical practice /  |r E. E. Polli --  |t Structural and functional diversity of HLA class II molecules /  |r D. Charron --  |t Peptide binding to HLA: An overview /  |r G. Frumento and G. B. Ferrara --  |t Universal heteroduplex generators: Reagents for genotyping of HLA and of human diseases /  |r J. L. Bidwell, N. A. P. Wood, L. A. Tyfield, T. M. Clay, D. Culpan, J. M. Evans, M. C. Pursall and B. A. Bradley --  |t HLA oligonucleotide genotyping: From theory to clinic /  |r J.-M. Tiercy, M. Jeannet and B. Mach --  |t HLA-DR compatibility in cadaver kidney transplantation: From serology to DNA typing /  |r F. Poli, M. Scalamogna, L. Mascaretti, A. Nocco, M. Pappalettera, G. Piccolo, L. Crespiatico, L. Lecchi, D. Trezzi, A. Archenti and G. Sirchia --  |t HLA expression and autoimmunity /  |r I. Todd and G. F. Bottazzo --  |t The cellular and molecular basis of fibrosis in scleroderma /  |r E. S. Smith and E. C. LeRoy --  |t Characterization of anti-endothelial cell antibodies in antiphospholipid syndrome /  |r N. del Papa, G. Conforti, D. Gambini, W. Barcellini, M. O. Borghi, C. Fain, A. Tincani, G. Balestrieri, F. Tedesco and P. L. Meroni --  |t T cell receptor repertoire in human autoimmune diseases /  |r A. Albertini, A. Sottini, C. Mazza, A. Bettinardi, R. Gorla, E. Prati, D. Primi and L. Imberti --  |t The molecular genetics of acute promyelocytic leukemia /  |r F. Grignani, M. Fagioli, M. Alcalay, P. F. Ferrucci, L. Tomassoni, D. Rogaia, F. Grignani and P. G. Pelicci --  |t PCR approach for the evaluation of minimal residual disease in acute leukemia /  |r A. Biondi, A. Rambaldi, V. Rossi, A. Luciano, M. Cavana, F. lo Coco, D. Diverio, P. P. Pandolfi, M. Alcalay, C. R. Bartram and P. G. Pelicci --  |t Molecular defects in haemophilia A /  |r M. R. A. Lalloz, E. G. D. Tuddenham, R. Schwaab and D. David --  |t Molecular basis of haemophilia B /  |r F. Giannelli, S. Saad, G. Rowley and P. M. Green --  |t The molecular bases of Von Willebrand disease /  |r A. M. Randi, P. M. Mannucci and J. E. Sadler --  |t Molecular defects in rare coagulopathies /  |r F. Bernardi, P. Patracchini, F. Conconi and G. Marchetti --  |t The molecular genetics of protein C deficiency /  |r D. N. Cooper and P. H. Reitsma --  |t Relationship of the structure, function, and regulation of the thyrotropin receptor to its role in autoimmune thyroid disease /  |r L. D. Kohn, T. Ban, F. Okajima, H. Shimura, Y. Shimura, A. Hidaka, C. Giuliani, G. Napolitano, S. Kosugi, S. Ikuyama and M. Saji --  |t Molecular bases of thyroid hormone resistance syndromes /  |r P. Beck-Peccoz, L. Persani, D. Cortelazzi, F. Forloni, C. Asteria, D. Preziati and S. Borgato --  |t Alpha-subunit mutations of Gs protein and endocrine disorders /  |r A. Spada, L. Vallar, M. Arosio and G. Faglia --  |t Use of transgenic models in the study of hypothalamic-pituitary function /  |r F. F. P. Giraldi, Z. D. Horowitz, M. Mizobuchi, T. R. Downs, A. Kier, J. J. Kopchick and L. A. Frohman --  |t A molecular approach to the understanding of primary defects in glucose homeostasis /  |r J. Philippe and M. Cordier-Bussat --  |t Polyhormones: The examples of PTH and PTH-related peptide /  |r L. E. Mallette --  |t The human genome project, unstable DNA and peculiar genetics: Lessons from fragile X syndrome /  |r D. L. Nelson --  |t Sequence analysis of the Dystrophin gene deletion 'hot-spot' /  |r A. Pizzuti and C. T. Caskey --  |t Molecular biology of neurotrophic factors in the central nervous system /  |r V. Silani and G. Scarlato --  |t Mitochondrial encephalomyopathy: From the gene to the phenotypes /  |r N. Bresolin, G. P. Comi, F. Mazzucchelli, A. Bardoni and G. Scarlato --  |t Spectrum of primary cutaneous CD30 (Ki-1) positive lymphoproliferative disorders /  |r R. Willemze and R. C. Beljaards --  |t Inflammatory diseases that stimulate lymphomas: The cutaneous pseudolymphomas /  |r L. Cerroni and H. Kerl --  |t The bcl-2 protein and its gene in haematological and epithelial tumours /  |r F. Pezzella --  |t Oncogenes analysis in cutaneous lymphomas /  |r S. A. Garatti, E. Roscetti, D. Trecca, E. Berti and A. Neri --  |t Genotypic and phenotypic analysis in cutaneous T-cell lymphomas /  |r L. Crosti, A. Biondi, E. Berti and R. Caputo --  |t Genetic hemochromatosis: Molecular study in the HLA-A class I region /  |r A. Piperno, M. Sampietro, C. Arosio, C. Camaschella, P. Gasparini and G. Fiorelli --  |t Genetic hemochromatosis: Molecular regulation of iron proteins /  |r M. W. Hentze --  |t Molecular regulation of iron metabolism in genetic hemochromatosis /  |r A. Pietrangelo, G. Cairo, D. Quaglino, G. Casalgrandi, R. Gualdi, D. Conte, L. Cesarini and E. Ventura --  |t Porphyria cutanea tarda and hepatoerythropoietic porphyria: Recent advances in molecular pathology /  |r H. de Verneuil, F. Moreau-Gaudry, M. Bensidhoum, I. Hombrados and C. Ged --  |t Detection of the p53 codon 249 mutation by ARMS-PCR in Italian patients with hepatocellular carcinoma /  |r M. Sampietro, L. Ambrosio, L. Fossati, A. L. Fracanzani, A. Piperno, G. Ronchi, Y.-M. D. Lo and G. Fiorelli. 
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