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31.
Previous publications have shown how a combination of X-ray computed tomography and spherical harmonic series could be used to characterize the 3-D shape of rocks used for aggregates in concrete. The X-ray computed tomography was used to obtain the raw 3-D numerical data for the coordinates of the aggregate surface. In this paper, we demonstrate how laser detection and ranging (LADAR) numerical data can replace X-ray computed tomography data and be used in conjunction with spherical harmonic series analysis to analyze the 3-D shape of aggregates. 相似文献
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H. E. N. Stone 《Journal of Materials Science》1992,27(6):1701-1703
Ten samarium-structure alloys have been oxidation tested in air to estimate the thermal oxidation parameter, T
p, and hence the ratio T
p/TSm, where T
Sm is the temperature of decomposition of the appropriate structure and the ratio is a measure of the strength and type of bonding. The ratio decreases with (a) increasing distance apart in the 4f series of the components, and (b) increasing average Group number. 相似文献
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Localization of putative tumor suppressor loci by genome-wide allelotyping in human pancreatic endocrine tumors 总被引:1,自引:0,他引:1
DC Chung SB Brown F Graeme-Cook LG Tillotson AL Warshaw RT Jensen A Arnold 《Canadian Metallurgical Quarterly》1998,58(16):3706-3711
Only two tumor suppressor gene loci, one on 3p25 and the MEN1 gene on 11q13, have thus far been implicated in the pathogenesis of sporadic human pancreatic endocrine tumors (PETs). A genome-wide allelotyping study of 28 human PETs was undertaken to identify other potential tumor suppressor gene loci. In addition to those on chromosomes 3p and 11q, frequent allelic deletions were identified on 3q (32%), 11p (36%), 16p (36%), and 22q (29%). Finer deletion mapping studies localized the smallest regions of common deletion to 3q27, 11p13, and 16p12.3-13.11. Potential candidate genes at these loci include WT1 (11p13), TSC2 (16p13), and NF2 (22q12), but no known tumor suppressor gene localizes to 3q27. The mean fractional allelic loss among these human PETs is 0.126, and no correlation was observed between allelic loss and clinical parameters, including age, sex, hormonal subtype, and disease stage. These findings highlight novel locations of tumor suppressor gene loci that contribute to the pathogenesis of human PETs, and several of these on 3p, 3q, and 22q are syntenic with loci on mouse chromosomes 9 and 16 that are implicated in a murine transgenic model of PETs. 相似文献
38.
RT Loder RN Hensinger PD Alburger DD Aronsson JH Beaty DR Roy RP Stanton R Turker 《Canadian Metallurgical Quarterly》1998,18(5):630-636
We reviewed 32 children with 41 radiation-therapy associated slipped capital femoral epiphyses (RTASCFE). Ten were from the authors' institutions and 22 from the literature. Gender distribution was equal. The age at diagnosis of the malignancy was 4.3 +/- 3.1 years; the amount of radiation was 4,240 +/- 1,445 rads. Children with RTASCFE presented younger (10.4 +/- 3.2 years) than a routine SCFE. The average symptom duration was 5 +/- 6 months. Children with RTASCFE are usually thin (median weight, 10th percentile) in contrast to children with typical SCFE, who are usually obese (<95th percentile). The majority (82%) of the slips were mild, compared to routine SCFEs (approximately 50%); 28% were bilateral. There was a positive linear relationship between the age at presentation of the SCFE and the age at diagnosis of the malignancy; there was a negative linear relationship between the age at presentation of the SCFE and the amount of radiation therapy. 相似文献
39.
CD28 is a major T cell costimulatory molecule, delivering signals distinct from those of the CD3/TCR complex, which regulate cytokine and cytokine receptor expression, cell proliferation, and cell viability. CD28 needs to be cross-linked to initiate signals, yet both of its ligands, CD80 and CD86, are expressed as monomers. Previously, we determined the cytoplasmic tail of CD80 is required for CD28-mediated costimulation and subcellular relocalization of CD80 in lymphocytes. In this study, we report that Reh B cell transfectants expressing CD80 with mutations in the cytoplasmic tail region either at 275-278 (RRNE-->AAAA, CD80/4A) or serine 284 (S-->A, CD80/SA) can bind ligand similar to transfectants expressing wild-type CD80, yet are unable to costimulate T cell proliferation. These mutant CD80 molecules are expressed on the surface of the Reh cells in small clusters or foci indistinguishable from those of wild-type CD80 molecules. However, mutant CD80 molecules unlike wild-type CD80 cannot be readily induced by ligand into caps. Thus, small clusters of CD80 found on APC are insufficient to initiate CD28-mediated signals, and the formation of CD80 caps appears to be a critical factor regulating the initiation of T cell costimulation. A 30-kDa phosphoprotein that associates with the cytoplasmic tail of CD80 in activated cells may play a role in CD80 redistribution and thus CD28-mediated costimulation. These results indicate two distinct regions of the CD80 cytoplasmic tail regulate its costimulatory function, and both regions are required for CD80 function. 相似文献
40.
A Stone 《Canadian Metallurgical Quarterly》1998,101(6):1738-1739