BP Alter, AD D'Andrea - Blood: Principles and Practice of Hematology, 1995 - books.google.com PARTS Stem Cell Disorders CHAPTER 8 Inherited Bone Marrow Failure Syndromes
Blanche P. Alter and Alan D. D'Andréa Constitutional aplastic anemia was
defined by O'Gorman Hughes (1) as" chronic bone marrow failure associated ... Cited by 430 - Related articles - BL Direct - All 4 versions
M Ho, R Jaffe, G Miller, MK Breinig, JS … - Transplantation, 1988 - journals.lww.com 720 TRANSPLANTATION Vol. 45, No. 4 cellular DNA, as estimated by optical
density, was digested with 40 units of Bam HI for 3 hr at 37°C and
electrophoresed in a 0.8% agarose gel. The DNA was transferred by Southern ... Cited by 332 - Related articles - All 4 versions
JI Cohen - New England Journal of Medicine, 2000 - content.nejm.org The EBV genome consists of a linear DNA molecule that encodes nearly 100 viral
proteins. 12 During viral replication, these proteins are important for
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- ►annals.org SE Straus, JI Cohen, G Tosato, J Meier - Annals of internal medicine, 1993 - Am Coll Physicians Epstein-Barr virus (EBV) encodes genes that ensure its persistence in human B
lymphocytes. Some of the genes encourage B-cell proliferation; others are poised
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KE Nichols, DP Harkin, S Levitz, M Krainer, … - Proceedings of the National Academy of Sciences of …, 1998 - National Acad Sciences X-linked lymphoproliferative syndrome (XLP) is an inherited immunodeficiency
characterized by increased susceptibility to Epstein–Barr virus (EBV). In
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AM Levine - Blood, 1992 - Am Soc Hematology . reserved Hematology; all rights Copyright 2007 by The American Society of
Suite 200, Washington DC 20036. semimonthly by the American Society of
Hematology, 1900 M St, NW, Blood (print ISSN 0006-4971, online ISSN ... Cited by 266 - Related articles - All 3 versions
TA Seemayer, H Grierson, SJ Pirruccello, TG … - Archives of Pediatrics & Adolescent Medicine, 1993 - archpedi.highwire.org In1975, Purtilo et al1 described a fatal X-linked condition that affected boys
in the Duncan kindred. The investi- gators surmised correctly that the disease
stemmed from a genetic inability to mount an effective immune response to ... Cited by 185 - Related articles - BL Direct - All 10 versions
- ►annals.org MC Sneller, W Strober, E Eisenstein, JS … - Annals of internal medicine, 1993 - ncbi.nlm.nih.gov Common variable immunodeficiency (CVI) is a heterogenous immunodeficiency
syndrome characterized by hypogammaglobulinemia, recurrent bacterial infections,
and various immunologic abnormalities. In addition to recurrent infections, ... Cited by 153 - Related articles - BL Direct - All 4 versions
ME Conley - Annual review of immunology, 1992 - Annual Reviews Although the X-linked immunodeficiencies-X-linked agammaglobulinemia (XLA),
X-linked severe combined immunodeficiency (XSCID), Wiskott Aldrich syndrome
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