Zobrazeno 1 - 10
of 18
pro vyhledávání: '"M B, Frank"'
Autor:
A. P. Reiner, S. M. Schwartz, M. B. Frank, W.T. Longstreth, L. A. Hindorff, G. Teramura, F. R. Rosendaal, L. K. Gaur, B. M. Psaty, D. S. Siscovick, J. R. Leclerc
Publikováno v:
Stroke. 32:2580-2587
Background and Purpose — Although family studies have suggested a genetic influence on hemorrhagic stroke, the underlying genetic risk factors remain poorly defined. Coagulation factor XIII, which is involved in hemostasis, fibrinolysis, vascular r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3f0aae8922ead90d380f227df33cf58
https://doi.org/10.1161/hs1101.098150
https://doi.org/10.1161/hs1101.098150
Publikováno v:
Scandinavian Journal of Immunology. 53:268-276
Anti-Ro (or SSA) is found in the sera of patients with autoimmune rheumatic illnesses. All patients with anti-Ro defined by precipitation bind a 60 000 Da antigen (60 kDa Ro), whereas some patients also bind a 52 000 Da molecule (52 kDa Ro). In gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::438cb369faddcd21cbb05c6b34b7fa65
https://doi.org/10.1046/j.1365-3083.2001.00870.x
https://doi.org/10.1046/j.1365-3083.2001.00870.x
Publikováno v:
The Journal of Immunology. 156:1668-1675
One cDNA clone (G7) was isolated from a lambda gt11 human liver cDNA library by the reaction with a serum containing anti-dsDNA Abs and was ligated into pGEX-1 lambda T vector. All the 10 SLE sera with anti-dsDNA, 2 samples of human monoclonal anti-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::166f41fc69fde0935a8778f2076a732f
https://doi.org/10.4049/jimmunol.156.4.1668
https://doi.org/10.4049/jimmunol.156.4.1668
Publikováno v:
Biochemical Journal. 305:359-362
The 52 kDa Ro/SSA protein is an intracellular autoantigen that is frequently recognized by antibodies in sera of patients with systemic lupus erythematosus or Sjogren's syndrome. While the function of this molecule is not known, zinc finger and leuci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0612e75a4d8492adfcf77b6c0a9fbbb
https://doi.org/10.1042/bj3050359
https://doi.org/10.1042/bj3050359
Publikováno v:
The Anatomical record. 96(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c6d263a01c509d010917b05daf69dbb6
https://pubmed.ncbi.nlm.nih.gov/20341470
https://pubmed.ncbi.nlm.nih.gov/20341470
Publikováno v:
Journal of Clinical Investigation. 90:559-570
Anti-PM-Scl antibodies are associated with polymyositis-scleroderma overlap or either disease alone. Among sera from 39 patients with anti-PM-Scl, 23 recognized the 100-kD band in immunoblot against HeLa cell extract, 16 of which also stained the 70-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ebbef9ca04dafe535cb6de0b4f6aeb
https://doi.org/10.1172/jci115895
https://doi.org/10.1172/jci115895
Publikováno v:
Lupus. 11(6)
Anti-dsDNA autoantibodiesare the hallmark of systemic lupus erythematosus(SLE) and frequently correlate with disease activity. In this study we report the isolation and characterization of human anti-Id monoclonal antibody fragments as single-chain F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71a4564c56030954c514f7718691c2c4
https://pubmed.ncbi.nlm.nih.gov/12139374
https://pubmed.ncbi.nlm.nih.gov/12139374
Autor:
A P, Reiner, S M, Schwartz, M B, Frank, W T, Longstreth, L A, Hindorff, G, Teramura, F R, Rosendaal, L K, Gaur, B M, Psaty, D S, Siscovick
Publikováno v:
Stroke. 32(11)
Although family studies have suggested a genetic influence on hemorrhagic stroke, the underlying genetic risk factors remain poorly defined. Coagulation factor XIII, which is involved in hemostasis, fibrinolysis, vascular remodeling, and tissue repai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f9764f57aa3851b766107898991d9e9e
https://pubmed.ncbi.nlm.nih.gov/11692020
https://pubmed.ncbi.nlm.nih.gov/11692020
Publikováno v:
American journal of hematology. 64(3)
Chronic neutrophilic leukemia (CNL) is a rare myeloproliferative disorder in which recurrent abnormalities of chromosome 20 have been reported. We report the case of a 76-year-old woman with CNL with partial deletion of the long arm of chromosome 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7439f0655b3324e417be5b3fcf83226e
https://pubmed.ncbi.nlm.nih.gov/10861824
https://pubmed.ncbi.nlm.nih.gov/10861824
Publikováno v:
Journal of Investigative Medicine. 52:S297-S298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1d9f77da33b1e930a82e94775d7c7df
https://doi.org/10.1097/00042871-200401001-00781
https://doi.org/10.1097/00042871-200401001-00781