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Primary immunodeficiency diseases: an experimental model for molecular medicine
Author(s): Fischer A
Source: LANCET    Volume: 357    Issue: 9271    Pages: 1863-1869    Published: JUN 9 2001  
Times Cited: 56     References: 61     
Abstract: Primary immunodeficiency diseases represent a vast array of inherited disorders of the immune system. Major advances in the understanding of genetic basis and molecular mechanisms have occurred within the past 10 years, as a result of the tools of modern genetics. About three quarters of 100 primary immunodeficiency diseases can now be reliably diagnosed with molecular probes. In many cases, gene identification has enabled significant insight into the physiopathology of the related conditions. Therapeutic progress based on protein engineering and possibly gene therapy will also ensue.
Document Type: Article
Language: English
Reprint Address: Fischer, A (reprint author), Hop Necker Enfants Malad, INSERM, U429, 149 Rue Sevres, F-75015 Paris, France
Addresses:
1. Hop Necker Enfants Malad, INSERM, U429, F-75015 Paris, France
Publisher: LANCET LTD, 84 THEOBALDS RD, LONDON WC1X 8RR, ENGLAND
Subject Category: Medicine, General & Internal
IDS Number: 440DN
ISSN: 0140-6736
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