By I. R. Peake (auth.), C. Th. Smit Sibinga, P. C. Das, E. Briët (eds.)
The invention of the constitution and serve as of DNA and the cracking of the genetic code have ended in speedy advances in gene remedy and screening and prognosis on a molecular foundation. whereas preliminary remedy has been for sufferers with unmarried gene defects, there's expanding curiosity in obtained affliction, utilizing the method of check or deal with melanoma. almost all tissues are being studied for genetic amendment, together with bone marrow and blood cells. The nineteenth overseas Symposium on Blood Transfusion concerned about hereditary illness and blood transfusion, demonstrating the relevance and value of transfusion medication. Gene remedy, even if for non permanent impact or long term aid, increases the security, dignity and caliber of lifestyles for a gaggle of sufferers with ailments, abnormalities and handicaps that experience hitherto merely been supported and palliated.
Audience: crucial studying for haematologists, Blood financial institution experts, pharmaceutical businesses and wellbeing and fitness care pros.
Read Online or Download Hereditary Diseases and Blood Transfusion: Proceedings of the Nineteenth International Symposium on Blood Transfusion, Groningen 1994, organized by the Red Cross Blood Bank Groningen-Drenthe PDF
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16. Ngo KV, Glotz VT, Koziol JA, et al. Homozygous and heterozygous deletions of the von Willebrand factor gene in patients and carriers of severe von Willebrand disease. 22 Proc Nat Acad Sci USA 1988;85:2753-57. 17. Peake IR, Liddell MB, Moodie P, et al. Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: Family studies that identify carriers of the condition and a compound heterozygous individual. Blood 1990;75:654-61. 18. Mancuso OJ, Tuley EA, Castillo R, de Bosch N, Mannucci PM, Sadler JE.
8. Patracchini P, Calzolari E, Aiello V, et al. 21) translocation. Hum Genet 1989;83:264-66. 9. Mancuso DJ, Tuley EA, Westfield LA, et al. Human von Willebrand factor gene and pseudogene. Structural analysis and differentiation by polymerase chain reaction. Biochemistry 1991 ;30:253-69. 10. Mancuso DJ, Tuley EA, Westfield LA, Worrall NK, Shelton-Inloes BB. Structure of the gene for human von Willebrand factor. J Bioi Chern 1989;264: 19514-27. 11. Sadler JE, Ginsburg D. A data base of polymorphisms in the von Willebrand factor gene and pseudogene.
13. Bertina RM, Koeleman BPC, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:64-67. 14. Reitsma PH, Poort SR, Bernardi F, et al. Protein C deficiency: A database of mutations. Thromb Haemost 1993;69:77-84. 15. Comp PC, Nixon RR, Cooper MR, Esmon CT. Familial protein S deficiency is associated with recurrent thrombosis. J Clin Invest 1984;74:2082-88. 16. Walker FJ. Regulation of activated protein C by protein S. The role of phospholipid in factor Va inactivation.