Výsledky vyhledávání - "Wilma B. Bias"

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Normal Human Sera Cytotoxic to Cells of Human Acute Leukemia

Autor: Richard L. Humphrey, Wilma B. Bias, Bernice Z. Schacter

Publikováno v: Tissue Antigens. 8:289-298

Eight human sera from healthy individuals with no history of immunization with human transplantation antigens have demonstrated complement dependent cytotoxicity to cells of some patients with active acute leukemia. The antigen(s) detected by these s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4322d924b967712c7eaa6d54d75036f
https://doi.org/10.1111/j.1399-0039.1976.tb00581.x

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Identification of a C6/G21 translocation chromosome by the Q-M and Giemsa banding techniques in a patient with Down's syndrome, with possible assignment of Gm locus

Autor: Digamber S. Borgaonkar, Harvey M. Golomb, G.F. Bahr, G. Sadasivan, Gary A. Chase, Wilma B. Bias, H. M. Herr, Louis M. Kunkel

Publikováno v: Clinical Genetics. 4:53-57

A family with a C/G, probably 6/21, translocation chromosome was ascertained through a case of Down's syndrome. Genetic linkage analysis yields a possibility of localization of the Gm locus on autosome 6.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ea8ca0564ef7337ca94fc6741e04377
https://doi.org/10.1111/j.1399-0004.1973.tb01122.x

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Antigen, allele, and haplotype frequencies report of the ASHI minority antigens workshops: part 1, African-Americans

Autor: Wilma B. Bias, Andrea A. Zachary, Armead H. Johnson, Stephen M Rose, Mary S. Leffell

Publikováno v: Human Immunology. 62:1127-1136

HLA typing was performed on 977 African Americans residing throughout most of the United States. Class I and class II antigens and class II alleles were defined for all individuals and class I alleles were determined for a subset of individuals. The

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::42a530dcc04ab7d72bfccc0e81ba50b9
https://doi.org/10.1016/s0198-8859(01)00305-6

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A linkage study of the Marfan syndrome1

Autor: Wilma B. Bias, Gary A. Chase, Walker Ba, Victor A. McKusick, Freidhoff Lb, D A Schleutermann, J L Murdoch

Publikováno v: Clinical Genetics. 10:51-53

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f51bfe189e1c33cb3f07e006d00c8324
https://doi.org/10.1111/j.1399-0004.1976.tb00008.x

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Increased prevalence of systemic sclerosis in a native american tribe in oklahoma. Association with an amerindian HLA haplotype

Autor: H. Daniel Cameron, Trevor J. Hodge, Frank C. Arnett, Gabe Paxton, John D. Reveille, Egon Durban, Wilma B. Bias, Paul E. Weathers, Joann M. Moulds, Robert F. Howard, Filemon K. Tan

Publikováno v: Arthritis & Rheumatism. 39:1362-1370

Objective. To investigate a high prevalence of systemic sclerosis (SSc; scleroderma) in a well-defined population of 21,255 Choctaw Indians residing in 8 southeastern Oklahoma counties who were “users” of Indian Health Services. Methods. A case�

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef10c912f1deade3c9e616e15fbaa80f
https://doi.org/10.1002/art.1780390814

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THE FREQUENCIES OF HLA ALLELES AND HAPLOTYPES AND THEIR DISTRIBUTION AMONG DONORS AND RENAL PATIENTS IN THE UNOS REGISTRY1

Autor: Mary S. Leffell, Andrea A. Zachary, Arthur G. Steinberg, Wilma B. Bias

Publikováno v: Transplantation. 62:272-283

HLA allele and haplotype frequencies are used in transplantation, anthropology, forensic medicine, and studies of the associations between HLA factors and the immune response. The cost of determining these frequencies through family studies can be av

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f6042f87eaff48d6c2cc113edfa39855
https://doi.org/10.1097/00007890-199607270-00021

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The HLA-A3, Cw6, B47, DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region

Autor: Patricia A. Donohoue, Lisbeth A. Guethlein, Wilma B. Bias, Claude J. Migeon, C Van Dop, Malia M. Collins, B.J. Schmeckpeper

Publikováno v: Tissue Antigens. 46:163-172

The HLA-B47, DR7 haplotype in congenital adrenal hyperplasia (CAH) due to 21–hydroxylase deficiency contains a deletion of most of the active CYP21 gene and the entire adjacent C4B gene. The C4A gene produces a protein which is electrophoretically

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea36cee6dc42763aa6b9240dc44f7cec
https://doi.org/10.1111/j.1399-0039.1995.tb03115.x

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THE DISTRIBUTION OF HLA ANTIGENS AND PHENOTYPES AMONG DONORS AND PATIENTS IN THE UNOS REGISTRY

Autor: Arthur G. Steinberg, Wilma B. Bias, Mary S. Leffell, Andrea A. Zachary, Carol H. Machan

Publikováno v: Transplantation. 58:1119-1130

We have analyzed HLA data from the UNOS registry on 20,230 patients on the renal waiting list in 1991 and 18,708 donors from 1988-1992. Significant differences were found in the distribution of HLA antigens for comparisons of the total donor pool and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::31381a2a78d2b302173c5048ee030770
https://doi.org/10.1097/00007890-199411000-00011

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