Zobrazeno 1 - 10
of 17
pro vyhledávání: '"D. L. French"'
Publikováno v:
The Journal of Immunology. 146:2010-2016
Mutant mAb with increased Ag binding were generated from a hybridoma cell line, 36-65, that secretes an IgG1,kappa anti-p-azophenylarsonate-(Ars) specific antibody. The mutant antibodies were identified using an Ars-specific ELISA and sib selection s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac7d036f4ceeff432ddc455cc91cb4f6
https://doi.org/10.4049/jimmunol.146.6.2010
https://doi.org/10.4049/jimmunol.146.6.2010
Autor:
T. Oshima, E. Kakenaka, Y. Chen, A. Matsubara, H. Saji, K. Harada, M. Derogar, H. Abdelrazik, Makoto Kurachi, G. Awong, M. Koyama, T. Yabe, M. Satake, K. Nakajima, Y. Morishima, M. Onizuka, K. Tomizuka, K. Shibuya, K. Akashi, G. Spaggiari, A. Ogawa, K. Shibata, A. Shibuya, D. L. French, L. Moretta, Satoshi Ueha, O. Ringdén, G. Ma, G. Keller, Y. Wang, Z. Zhou, P. Pan, T. Nakamoto, H. Kai, P. Ljungman, S. Takashima, C. M. Divino, T. Nabekura, S. Ogawa, S. Eisenstein, Kouji Matsushima, Y. Yamashita, J. Abe, J. Zuniga-Pflucker, M. Takanashi, S. Chen, T. Sasazuki, S. Honda, K. Hirayasu, K. Kashiwase, S. Tahara-Hanaoka, Takanori Teshima, Y. Kodera, B. Omazic, Yusuke Shono, M. Kadowaki, K. Aoyama
Publikováno v:
International Immunology. 22:iv78-iv79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08abeb02c6cdc70b0bf5cf4db0cd6181
https://doi.org/10.1093/intimm/dxq328
https://doi.org/10.1093/intimm/dxq328
Autor:
D A, Wilcox, J C, Olsen, L, Ishizawa, P F, Bray, D L, French, D A, Steeber, W R, Bell, M, Griffith, G C, White
Publikováno v:
Blood. 95(12)
Glanzmann thrombasthenia is an inherited bleeding disorder characterized by qualitative or quantitative defects of the platelet-specific integrin, alphaIIbbeta(3). As a result, alphaIIbbeta(3) cannot be activated and cannot bind to fibrinogen, leadin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ad008542fa9591b86d82bc0c61513d3
https://pubmed.ncbi.nlm.nih.gov/10845892
https://pubmed.ncbi.nlm.nih.gov/10845892
Autor:
R B, Basani, D L, French, G, Vilaire, D L, Brown, F, Chen, B S, Coller, J M, Derrick, T K, Gartner, J S, Bennett, M, Poncz
Publikováno v:
Blood. 95(1)
Decreased expression of functional alphaIIbbeta3 complexes on the platelet surface produces Glanzmann thrombasthenia. We have identified mutations of alphaIIb(P145) in 3 ethnically distinct families affected by Glanzmann thrombasthenia. Affected Menn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1528c8aa2413452774196da926637004
https://pubmed.ncbi.nlm.nih.gov/10607701
https://pubmed.ncbi.nlm.nih.gov/10607701
This document presents detailed data, bar graphs, and pie charts on volume, radioactivity; isotopic identity, origin, and status of radioactive waste for calendar year 1998 at the Idaho National Engineering and Environmental Laboratory (INEEL). The d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c8938c822a1477e9c47558441bfdd60
https://doi.org/10.2172/771516
https://doi.org/10.2172/771516
Publikováno v:
British journal of haematology. 102(2)
Glanzmann thrombasthenia is an autosomal recessive bleeding disorder caused by mutations in the genes encoding platelet GPIIb or GPIIIa. Both genes map to chromosome 17q21 and polymorphisms within this chromosomal region have been identified. In the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b47305799ccf48bedbcb84e5810903de
https://pubmed.ncbi.nlm.nih.gov/9695977
https://pubmed.ncbi.nlm.nih.gov/9695977
Publikováno v:
Blood. 91(5)
Glanzmann thrombasthenia is an inherited bleeding disorder due to a functional reduction or absence of platelet GPIIb/IIIa (alphaIIbbeta3) integrin receptors. Based on a prolonged bleeding time and absence of platelet aggregation in response to physi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49c60404247dd387aa2a582a914d9801
https://pubmed.ncbi.nlm.nih.gov/9473221
https://pubmed.ncbi.nlm.nih.gov/9473221
Publikováno v:
Blood. 88(5)
A 20-year-old woman from a consanguineous family in the Hunan Province of the People's Republic of China was diagnosed as having Glanzmann's thrombasthenia based on (1) nearly a lifelong history of epistaxis, gum bleeding, petechiae, and purpura; (2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7034343d3d6104fd54a243fcc037fb86
https://pubmed.ncbi.nlm.nih.gov/8781422
https://pubmed.ncbi.nlm.nih.gov/8781422
Publikováno v:
Pharmaceutical research. 12(10)
The objective of this study is to correlate drug release mechanism with measured drug concentration profiles in gel layers of Carbopol matrices containing mesalamine or benzoic acid.Release rate experiments with Carbopol matrices were performed using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e93ba71898f6d168f4c95f92283b954
https://pubmed.ncbi.nlm.nih.gov/8584491
https://pubmed.ncbi.nlm.nih.gov/8584491
Publikováno v:
Cancer research. 55(2)
The purpose of this study was to correlate the presence of matrix metalloproteinase (MMP)-9 and MMP-2 and tissue inhibitors of metalloproteinase (TIMP)-1 and TIMP-2 mRNAs, detected in serial sections using the reverse transcriptase in situ PCR techni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a83dccd4fdcfaa9e8de643baea1517fd
https://pubmed.ncbi.nlm.nih.gov/7812956
https://pubmed.ncbi.nlm.nih.gov/7812956