Zobrazeno 1 - 10
of 21
pro vyhledávání: '"B G, Hepkema"'
Autor:
A. E. Greijer, S. J. Stevens, S. A. Verkuijlen, H. Juwana, S. C. Fleig, E. A. Verschuuren, B. G. Hepkema, J. J. Cornelissen, R. A. Brooimans, L. F. Verdonck, J. M. Middeldorp
Publikováno v:
Clinical and Developmental Immunology, Vol 2012 (2012)
Epstein-Barr virus (EBV) driven post-transplant lymphoproliferative disease (PTLD) is a heterogeneous and potentially life-threatening condition. Early identification of aberrant EBV activity may prevent progression to B-cell lymphoma. We measured EB
Externí odkaz:
https://doaj.org/article/12c2b2ea59524b99b7fc650f42e40e2d
Publikováno v:
Journal of Medical Virology, 80(3), 467-477. Wiley
Rapid diagnosis of human herpesvirus primary infections or reactivations is facilitated by quantitative PCRs. Quantitative PCR assays with a standard thermal cycling profile permitting simultaneous detection of herpes simplex virus (HSV), varicella z
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::232f3b01a9a501321743d6f7532d9e21
https://research.rug.nl/en/publications/84a88401-4814-424e-b1da-dbdc50eef244
https://research.rug.nl/en/publications/84a88401-4814-424e-b1da-dbdc50eef244
Publikováno v:
Tissue antigens. 86(6)
Human leukocyte antigens (HLA)-DQA1*01:07 was identified as an HLA-DQ blank specificity that segregated with the serological HLA-A2, -B7, -DR14, -DR52 haplotype, which carried DQB1*05:03. The blank specificity of DQA1*01:07-DQB1*05:03 may be because
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3879199813365b390380a5fef2512b85
https://pubmed.ncbi.nlm.nih.gov/26555242
https://pubmed.ncbi.nlm.nih.gov/26555242
Autor:
D A J, Dijck-Brouwer, B G, Hepkema, F P L, van der Dijs, H N, Steward, J M C, de Windt-Hol, F A J, Muskiet
Publikováno v:
The West Indian medical journal. 53(3)
Epidemiological studies indicate a positive relation between iron status and coronary artery disease (CAD) risk The HFE C282Y allele is associated with increased iron status and higher CAD risk. We investigated whether HFE C282Ymight be a CAD risk fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6420ca14b37745b0baec84a410d8b573
https://pubmed.ncbi.nlm.nih.gov/15352740
https://pubmed.ncbi.nlm.nih.gov/15352740
Identification of three new DRB1 alleles, DRB1*0107, *0425 and *13012 and confirmation of DRB4*01033
Publikováno v:
Tissue antigens. 61(5)
The characterization of three novel DRB1 alleles is described, DRB1*0107, DRB1*0425 and DRB1*13012 as well as confirmation of DRB4*01033. Two alleles, DRB1*0107 and *0425, showed amino acid differences with previously identified HLA molecules. In DRB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b1ddcd814256b6f1229c895e89328019
https://pubmed.ncbi.nlm.nih.gov/12753659
https://pubmed.ncbi.nlm.nih.gov/12753659
Publikováno v:
Tissue antigens. 61(1)
In this report, the novel allele B*40351 is presented. The allele was identified in a Caucasian individual by sequence-based typing. B*4035 is identical to B*4002 in exon 2, but differs in exon 3 at position 463, where it has an A in stead of a C. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf5fc66a758753f906884e3b8f3fba95
https://pubmed.ncbi.nlm.nih.gov/12622780
https://pubmed.ncbi.nlm.nih.gov/12622780
Publikováno v:
Tissue antigens. 60(4)
In this report we describe a novel HLA-A*34 allele, A*3404, which was initially detected by an unusual serological pattern in two unrelated individuals. Sequencing revealed that the new allele was identical to A*3402 in exons 2 and 3, except for a si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e12b9de26cd9ba828eb21e00f77209f8
https://pubmed.ncbi.nlm.nih.gov/12472662
https://pubmed.ncbi.nlm.nih.gov/12472662
Publikováno v:
Tissue antigens. 58(1)
In our recent study using high-resolution HLA-B locus typing by sequence-based typing (SBT) we identified 9 new alleles in a total of 355 unrelated individuals (4). Three of them concerned an allele belonging to the B22 group. One of them, B*5607, sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe971fed3ac18420f67392996c9d129c
https://pubmed.ncbi.nlm.nih.gov/11580856
https://pubmed.ncbi.nlm.nih.gov/11580856
Autor:
A, de Haan, A P, van den Berg, W, van der Bij, B G, Hepkema, E, Bruin-van Dijk, I, van der Gun, S P, Lems, M J, Slooff, E B, Haagsma, L F, de Leij, J, Prop
Publikováno v:
Transplantation. 71(6)
A decrease in donor-specific T cell precursor frequencies as seen late, one or more years, after transplantation is assumed to reflect transplantation tolerance, a condition important for long term acceptance of the allograft. However, such late decr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2a76326095d00c4961c1b2a9133eb11
https://pubmed.ncbi.nlm.nih.gov/11330529
https://pubmed.ncbi.nlm.nih.gov/11330529
Publikováno v:
Transplantation. 69(8)
After solid organ transplantation most alloantigens are presented to the recipient's immune system by normal tissue cells, which can be considered to act as nonprofessional antigen-presenting cells (APC). It is well accepted that such nonprofessional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::02680b8433ed4d93a0a7ebc618c360d8
https://pubmed.ncbi.nlm.nih.gov/10836375
https://pubmed.ncbi.nlm.nih.gov/10836375