Výsledky vyhledávání

Prospective analysis suggests susceptibility genes for deficiencies of IgA and several other immunoglobulins on the [HLA-B8, SC01, DR3] conserved extended haplotype

Autor: C A, Alper, D, Marcus-Bagley, Z, Awdeh, M S, Kruskall, G S, Eisenbarth, S J, Brink, A J, Katz, R, Stein, D H, Bing, E J, Yunis, P H, Schur

Publikováno v: Tissue antigens. 56(3)

The extended major histocompatibility complex (MHC) haplotype [HLA-B8, SC01, DR3] is increased in frequency among patients with immunoglobulin (Ig)A deficiency and common variable immunodeficiency. Because the genomic region from HLA-B to HLA-DR/DQ i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e4ea894feb91d8df607c499a7dd6a34e
https://pubmed.ncbi.nlm.nih.gov/11034556

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Summary of validation studies from twenty-six forensic laboratories in the United States and Canada on the use of the AmpliType PM PCR amplification and typing kit

Autor: C J, Word, T M, Sawosik, D H, Bing

Publikováno v: Journal of forensic sciences. 42(1)

A cooperative study was undertaken to collect and summarize the results of validation studies from forensic laboratories in the United States and Canada on the use of the AmpliType PM PCR amplification and typing kit for genetic typing of forensic bi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7ff0ef59804a941f6b3b5ed4302a183d
https://pubmed.ncbi.nlm.nih.gov/8988573

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Nonrandom inactivation of the X chromosome in early lineage hematopoietic cells in carriers of Wiskott-Aldrich syndrome

Autor: G, Wengler, J B, Gorlin, J M, Williamson, F S, Rosen, D H, Bing

Publikováno v: Blood. 85(9)

The Wiskott-Aldrich syndrome (WAS) is an X-linked (Xp11.22) recessive immunodeficiency syndrome characterized by susceptibility to opportunistic and pyogenic infections, thrombocytopenia, and eczema. Previous studies of obligate carriers of WAS docum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6853e9d77f24cf3344e99e13ef16f31e
https://pubmed.ncbi.nlm.nih.gov/7537115

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Genetic typing of the DQA1*4 alleles by restriction enzyme digestion of the PCR product obtained with the DQ Alpha Amplitype kit

Autor: M, Salazar, J, Williamson, D H, Bing

Publikováno v: Journal of forensic sciences. 39(2)

The three DQ Alpha 4 alleles, 4.1 (0501), 4.2 (0401), and 4.3 (0601) cannot be distinguished with the reverse dot blot DQ Alpha Amplitype Kit. A previous report (Yunis, I. et al., Tissue Antigens, Vol. 39, 1992, pp. 182-186) indicated that the typing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f2ed6807aa66302eb455b23d19bc5e14
https://pubmed.ncbi.nlm.nih.gov/8195762

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Akademický článek

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Transcriptional regulation of genes encoding the acute-phase proteins CRP, SAA, and C3

Autor: G Goldberger, D H Bing, J D Sipe, M Rits, H R Colten

Publikováno v: The Journal of Immunology. 138:3967-3971

Inflammation or acute tissue injury results in a programmed change in the concentration of several plasma proteins. Among these proteins, two--C-reactive protein (CRP) and serum amyloid A protein (SAA)--increase up to 1000-fold after an acute-phase s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b6554f91cc42f8f77bdde09b296de41
https://doi.org/10.4049/jimmunol.138.11.3967

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Computer-generated models of blood coagulation factor Xa, factor IXa, and thrombin based upon structural homology with other serine proteases

Autor: J P Burnier, Bruce Furie, D H Bing, R J Feldmann, D J Robison

Publikováno v: Journal of Biological Chemistry. 257:3875-3882

Computer-generated molecular models of the trypsin-like domains of blood coagulation factor IXa, Factor Xa, and thrombin have been prepared. These hypothetical models are based upon the sequence homology of the blood coagulation enzymes with the panc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b5aeb5310d18804c936d8b4ff0411ed9
https://doi.org/10.1016/s0021-9258(18)34864-6

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Further Studies on the Identification of the Subcomponents of the First Component of Complement After Affinity Chromatography of Human Serum on IgG-Sepharose

Autor: P. A. Taylor, S. Fink, D. H. Bing, R. H. Painter

Publikováno v: The Journal of Immunology. 118:1722-1727

Affinity chromatography of serum on IgG covalently linked to Sepharose results in the retention of the proteins of the first component of complement (C1). A fraction called pool II is eluted from this column with 0.025 M EDTA and has previously been

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::223530662048a1562c4f89c95f2cd842
https://doi.org/10.4049/jimmunol.118.5.1722

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Variability in purified dysfunctional C1(-)-inhibitor proteins from patients with hereditary angioneurotic edema. Functional and analytical gel studies

Autor: R A Harrison, F S Rosen, D H Bing, S Awad, C J Wagner, J Canar, Virginia H. Donaldson, G Kindness

Publikováno v: Journal of Clinical Investigation. 75:124-132

C1(-)-inhibitor (C1(-)-INH) proteins from normal persons and members of eight different kindred with dysfunctional C1(-)-INH proteins associated with hereditary angioneurotic edema (HANE) were compared with respect to their inhibitory activity agains

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422ca8f0153849e3c0ca466a8e514b85
https://doi.org/10.1172/jci111664

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