Zobrazeno 1 - 10
of 16
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
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
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
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
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
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)
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
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
Autor:
C L, Librach, S L, Feigenbaum, K E, Bass, T Y, Cui, N, Verastas, Y, Sadovsky, J P, Quigley, D L, French, S J, Fisher
Publikováno v:
The Journal of biological chemistry. 269(25)
During early human pregnancy, fetal cytotrophoblasts rapidly invade the uterus. This process has many similarities to tumor invasion, except that the extent and the timing of cytotrophoblast invasion are carefully regulated. Therefore, this system is