Zobrazeno 1 - 10
of 29
pro vyhledávání: '"K. Witzel-Schlömp"'
Publikováno v:
European Journal of Immunogenetics. 28:515-522
Summary C9 is the last of the human complement components creating the membrane attack complex. The single chain serum protein is encoded by a gene located on chromosome 5p13 that is composed of 11 exons. With the aid of inverse PCR, the hitherto unk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e25fa51a4fc9bab5b919376837342d62
https://doi.org/10.1046/j.0960-7420.2001.00248.x
https://doi.org/10.1046/j.0960-7420.2001.00248.x
Publikováno v:
Immunogenetics. 53:1-9
Intron 9 contains the complete endogenous retrovirus HERV-K(C4) as a 6.4-kb insertion in 60% of human C4 genes. The retroviral insertion is in reverse orientation to the C4 coding sequence. Therefore, expression of C4 could lead to the transcription
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf6ce7618e16f312e8451a8e5e2633ad
https://doi.org/10.1007/s002510000288
https://doi.org/10.1007/s002510000288
Autor:
Beate Stradmann-Bellinghausen, Constanze Steinhauer, K. Witzel-Schlömp, Peter M. Schneider, Christian Rittner
Publikováno v:
Experimental and Clinical Immunogenetics. 18:130-134
The fourth component of complement (C4) is coded for by two tandem-duplicated genes located in the class III region of the MHC of humans as well as a number of primates. A C4 gene size polymorphism giving rise to two gene variants of 16 and 22.3 kb l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0531e2b61be34682b9cba1d1b8b39308
https://doi.org/10.1159/000049192
https://doi.org/10.1159/000049192
Autor:
Thomas Kaufmann, Christian Rittner, Reinhard Würzner, A. Orren, K. Witzel-Schlömp, M. J. Hobart, B A Fernie, Peter M. Schneider
Publikováno v:
Immunogenetics. 48:144-147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bff5ecb6a063643f718ad3ce2344b10
https://doi.org/10.1007/s002510050415
https://doi.org/10.1007/s002510050415
Publikováno v:
The Journal of Immunology. 158:5043-5049
The ninth component of human complement (C9) is the last of the terminal complement components creating the membrane attack complex. C9 is a single-chain serum protein that is encoded by a gene located on chromosome 5p. Deficiency of terminal complem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb03bad9e856069565883bbdbbbd4d06
https://doi.org/10.4049/jimmunol.158.10.5043
https://doi.org/10.4049/jimmunol.158.10.5043
Publikováno v:
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics. 28(5)
C9 is the last of the human complement components creating the membrane attack complex. The single chain serum protein is encoded by a gene located on chromosome 5p13 that is composed of 11 exons. With the aid of inverse PCR, the hitherto unknown reg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a87a63aee608b41ba3d32b9f3f0b4da
https://pubmed.ncbi.nlm.nih.gov/11881818
https://pubmed.ncbi.nlm.nih.gov/11881818
Publikováno v:
Experimental and clinical immunogenetics. 15(4)
The results of the present (VIIth Complement Genetics Workshop and Conference, Mainz, May 1998) and past reference typing workshops for the terminal complement components C6, C7 and C9 are compiled and discussed both on the protein level and on the D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc8b260a2304fbb890f8e0bd0173eff5
https://pubmed.ncbi.nlm.nih.gov/10072638
https://pubmed.ncbi.nlm.nih.gov/10072638
Autor:
Zuheir L. Awdeh, Lennart Truedsson, K. Witzel-Schlömp, Chester A. Alper, Birgitta Gullstrand, Gunilla Nordin Fredrikson, Peter M. Schneider, Anders G. Sjöholm
Publikováno v:
Human immunology. 59(11)
The genetic basis of complete C4 deficiency in a patient with SLE was investigated. Previous studies have demonstrated that this patient has two different major histocompatibility complex (MHC) haplotypes that each contain a major deletion and a non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c00d0c47ba58b3150942a958a5e6e60
https://pubmed.ncbi.nlm.nih.gov/9796739
https://pubmed.ncbi.nlm.nih.gov/9796739
Autor:
Diego Bellavia, K. Tokunaga, C. Yung Yu, B. Bellinghausen, M. J. Hobart, Marina Botto, V. Bala Subramanian, Gottfried Mauff, A. Cortelazzo, Jonathan Cohen, Reinhard Würzner, Chester A. Alper, P.M. Schneider, Joann M. Moulds, P. Otremba, Takahiko Horiuchi, M. Cuccia, R. L. Dawkins, H. Schröder, Birgit Luther, B A Fernie, A. Correns, J.M. Moulds, K. Witzel-Schlömp, B. Stradmann, R. Würzner, B. Stradmann-Bellinghausen, F. Zhang, L. Truedsson, Gunther Geserick, A. Frank, J. Schifferli, G. Mauff, Yasuo Fukumori, Ch. Rittner, Beate Stradmann-Bellinghausen, M. Brai, G.W. Wu, Marie Lin, A. Orren, S. Sadallah, John P. Atkinson, Peter M. Schneider, Christian Rittner
Publikováno v:
Experimental and Clinical Immunogenetics. 15:I-II
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6360c13e426a815c1716c818f3039ac2
https://doi.org/10.1159/000019072
https://doi.org/10.1159/000019072
Autor:
M. Brai, J.P. Atkinson, Reinhard Würzner, G.W. Wu, Diego Bellavia, K. Tokunaga, M. J. Hobart, P. Otremba, Gunther Geserick, Marie Lin, V. Bala Subramanian, P. Schneider, M. Cuccia, B. Bellinghausen, S. Sadallah, H. Schröder, B A Fernie, R. L. Dawkins, Yasuo Fukumori, Gottfried Mauff, R. Würzner, B. Stradmann-Bellinghausen, Beate Stradmann-Bellinghausen, Takahiko Horiuchi, B. Stradmann, Ch. Rittner, C. Yung Yu, Peter M. Schneider, L. Truedsson, Jonathan Cohen, F. Zhang, Marina Botto, Christian Rittner, Joann M. Moulds, A. Correns, A. Frank, G. Mauff, J.M. Moulds, Chester A. Alper, Birgit Luther, K. Witzel-Schlömp, A. Cortelazzo, A. Orren, J. Schifferli
Publikováno v:
Experimental and Clinical Immunogenetics. 15:299-300
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6124d8cdff3d3aeacb6938959740282
https://doi.org/10.1159/000019088
https://doi.org/10.1159/000019088