Zobrazeno 1 - 10
of 13
pro vyhledávání: '"D L, Haviland"'
Autor:
X Wang, D T Fleischer, W T Whitehead, D L Haviland, S I Rosenfeld, J P Leddy, R Snyderman, R A Wetsel
Publikováno v:
The Journal of Immunology. 154:5464-5471
Hereditary C5 deficiency has been reported in several families of different ethnic backgrounds and from different geographic regions, but the molecular genetic defect causing C5 deficiency has not been delineated in any of them. To examine the molecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::053922c2454abcd47457bf1fbebcd53b
https://doi.org/10.4049/jimmunol.154.10.5464
https://doi.org/10.4049/jimmunol.154.10.5464
Autor:
D L Haviland, R L McCoy, W T Whitehead, H Akama, E P Molmenti, A Brown, J C Haviland, W C Parks, D H Perlmutter, R A Wetsel
Publikováno v:
The Journal of Immunology. 154:1861-1869
The small-complement C5 activation fragment, C5a, is a potent phlogistic molecule that, on binding to the C5a Receptor (C5aR), mediates contraction of smooth muscle, enhances vascular permeability, and promotes leukocyte functions such as directed ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40171eb27ca9de8d5bbf30a605bda43f
https://doi.org/10.4049/jimmunol.154.4.1861
https://doi.org/10.4049/jimmunol.154.4.1861
Publikováno v:
Journal of immunological methods. 390(1-2)
Monocytes have been used to assess immune dysfunction and disease. While mouse models are a useful longitudinal analog, few researchers have assessed changes in mouse monocytes. The purpose of this study was to provide recommendations for the sample
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c1f4743ae19fac44c0ead78ac7a17d1
https://pubmed.ncbi.nlm.nih.gov/21466808
https://pubmed.ncbi.nlm.nih.gov/21466808
Publikováno v:
The Journal of Immunology. 146:362-368
Two truncated human C5 clones, pHC5A and pHC5B, were isolated from an adult human liver cDNA library, and contained inserts of 2930 and 2181 bp, respectively. Both clones were polyadenylated and encoded the 5'-end of the C5 pro-molecule, thereby comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2f4cee2a24c77bc76430ef8292b4e1a
https://doi.org/10.4049/jimmunol.146.1.362
https://doi.org/10.4049/jimmunol.146.1.362
Autor:
X, Wang, D T, Fleischer, W T, Whitehead, D L, Haviland, S I, Rosenfeld, J P, Leddy, R, Snyderman, R A, Wetsel
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 154(10)
Hereditary C5 deficiency has been reported in several families of different ethnic backgrounds and from different geographic regions, but the molecular genetic defect causing C5 deficiency has not been delineated in any of them. To examine the molecu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a16e57652b556fde8f98fb6ebaace77
https://pubmed.ncbi.nlm.nih.gov/7730648
https://pubmed.ncbi.nlm.nih.gov/7730648
Publikováno v:
The Journal of biological chemistry. 266(28)
Human C5 cDNA fragments were used to identify five overlapping cosmid clones that spanned the entire C5 gene. Partial sequencing and Southern analysis of the clones were performed to identify intron/exon boundaries and to map intron size. The human C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6d1def6c005c218ad26823501427415e
https://pubmed.ncbi.nlm.nih.gov/1917999
https://pubmed.ncbi.nlm.nih.gov/1917999
Publikováno v:
The Journal of biological chemistry. 266(18)
To understand fifth complement component (C5) gene regulation, splicing, and C5 protein deficiency at the molecular level, the organization of the murine C5 gene was determined. The C5 structural gene is present as a single copy in the mouse genome a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6a4d2c3fbd751fa9d3aa0ac758c9c6a
https://pubmed.ncbi.nlm.nih.gov/1711041
https://pubmed.ncbi.nlm.nih.gov/1711041
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 146(1)
Two truncated human C5 clones, pHC5A and pHC5B, were isolated from an adult human liver cDNA library, and contained inserts of 2930 and 2181 bp, respectively. Both clones were polyadenylated and encoded the 5'-end of the C5 pro-molecule, thereby comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e608e4c07afc61cb686a3f07bde62184
https://pubmed.ncbi.nlm.nih.gov/1984448
https://pubmed.ncbi.nlm.nih.gov/1984448
Publikováno v:
The Journal of biological chemistry. 265(5)
To ascertain the molecular mechanism that causes murine C5 deficiency, genomic and cDNA libraries were constructed from mouse liver DNA and mRNA employing the congenic strains B10.D2/nSnJ and B10.D2/oSnJ that are sufficient and deficient for C5, resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb9e6b4a4c19df7f5623dc3dc4d9d488
https://pubmed.ncbi.nlm.nih.gov/2303408
https://pubmed.ncbi.nlm.nih.gov/2303408
Publikováno v:
The Journal of Immunology. 135:4034-4043
Several cloned lines of IL 2-dependent human T cells derived from alloantigen, mitogen, or IL 2-stimulated peripheral blood lymphocytes were examined for their surface marker expression, cytolytic activity in a 51Cr-release assay, and capacity to rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f906999e910ed09778d2f98d7e1ed4a
https://doi.org/10.4049/jimmunol.135.6.4034
https://doi.org/10.4049/jimmunol.135.6.4034