全文获取类型
收费全文 | 99篇 |
免费 | 0篇 |
出版年
2021年 | 1篇 |
2018年 | 1篇 |
2017年 | 2篇 |
2016年 | 1篇 |
2015年 | 1篇 |
2014年 | 1篇 |
2013年 | 4篇 |
2012年 | 3篇 |
2011年 | 4篇 |
2010年 | 3篇 |
2009年 | 1篇 |
2008年 | 3篇 |
2007年 | 2篇 |
2006年 | 5篇 |
2005年 | 6篇 |
2004年 | 4篇 |
2003年 | 3篇 |
2002年 | 2篇 |
2001年 | 4篇 |
2000年 | 3篇 |
1999年 | 3篇 |
1998年 | 2篇 |
1996年 | 1篇 |
1995年 | 1篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1992年 | 1篇 |
1991年 | 1篇 |
1990年 | 1篇 |
1988年 | 1篇 |
1987年 | 4篇 |
1986年 | 1篇 |
1985年 | 3篇 |
1984年 | 3篇 |
1983年 | 2篇 |
1981年 | 4篇 |
1980年 | 1篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1977年 | 2篇 |
1972年 | 3篇 |
1970年 | 1篇 |
1969年 | 1篇 |
排序方式: 共有99条查询结果,搜索用时 15 毫秒
51.
On the domestication of the soybean 总被引:1,自引:0,他引:1
T. Hymowitz 《Economic botany》1970,24(4):408-421
52.
The Kunitz soybean proteinase inhibitors (SBTI-A2) of 13 soybean pure-lines were examined for variation in antitryptic activity. Extraction of the inhibitor from individual seeds, electrophoresis on polyacrylamide gels, and excision of the inhibitor region from the gels were used to prepare inhibitor samples for assay. Protein content of eluate from the gel portions was determined by absorbance at 280 nm after applying corrections for background absorbance due to gel chemicals. Enzyme inhibition and protein content of the gel eluate were used to calculate the specific activity of the inhibitor obtained from each seed. The coefficient of variation for specific activity measurement was about 12%, and analysis of variance on data from 13 pure-lines showed significant variation in inhibitor activity from genetic and environmental sources. There appeared to be three levels of inhibition averaging 21.9, 29.2, and 39.5 specific activity units.This investigation was supported in part by funds from the Illinois Agricultural Experiment Station, National Soybean Processor's Association, and a grant (FR 07030) from the U.S. Public Health Service. 相似文献
53.
Death-receptor O-glycosylation controls tumor-cell sensitivity to the proapoptotic ligand Apo2L/TRAIL 总被引:4,自引:0,他引:4
Wagner KW Punnoose EA Januario T Lawrence DA Pitti RM Lancaster K Lee D von Goetz M Yee SF Totpal K Huw L Katta V Cavet G Hymowitz SG Amler L Ashkenazi A 《Nature medicine》2007,13(9):1070-1077
Apo2L/TRAIL stimulates cancer cell death through the proapoptotic receptors DR4 and DR5, but the determinants of tumor susceptibility to this ligand are not fully defined. mRNA expression of the peptidyl O-glycosyltransferase GALNT14 correlated with Apo2L/TRAIL sensitivity in pancreatic carcinoma, non-small-cell lung carcinoma and melanoma cell lines, and up to 30% of samples from various human malignancies showed GALNT14 overexpression. RNA interference of GALNT14 reduced cellular Apo2L/TRAIL sensitivity, whereas overexpression increased responsiveness. Biochemical analysis of DR5 identified several ectodomain O-(N-acetyl galactosamine-galactose-sialic acid) structures. Sequence comparison predicted conserved extracellular DR4 and DR5 O-glycosylation sites; progressive mutation of the DR5 sites attenuated apoptotic signaling. O-glycosylation promoted ligand-stimulated clustering of DR4 and DR5, which mediated recruitment and activation of the apoptosis-initiating protease caspase-8. These results uncover a new link between death-receptor O-glycosylation and apoptotic signaling, providing potential predictive biomarkers for Apo2L/TRAIL-based cancer therapy. 相似文献
54.
AE Clarke S Bernatsky KH Costenbader MB Urowitz DD Gladman PR Fortin M Petri S Manzi DA Isenberg A Rahman D Wallace C Gordon C Peschken MA Dooley EM Ginzler C Aranow SM Edworthy O Nived S Jacobsen G Ruiz-Irastorza E Yelin SG Barr L Criswell G Sturfelt L Dreyer I Blanco L Gottesman CH Feldman R Ramsey-Goldman 《Arthritis research & therapy》2012,14(Z3):A16
55.
Hymowitz SG Compaan DM Yan M Wallweber HJ Dixit VM Starovasnik MA de Vos AM 《Structure (London, England : 1993)》2003,11(12):1513-1520
EDA is a tumor necrosis factor family member involved in ectodermal development. Splice variants EDA-A1 and EDA-A2 differ only by the presence of Glu 308 and Val 309 in the expected receptor binding region of EDA-A1 but not EDA-A2. This two amino acid difference functions as a switch controlling receptor specificity. EDA-A1 binds only to EDAR, while EDA-A2 is specific for XEDAR. In order to understand the structural basis of this switch, we determined the X-ray crystal structures of the TNF domain of both EDA-A1 and EDA-A2 at 2.3 A and 2.2 A, respectively. While the backbone conformation around the splice difference is similar in both isoforms, the conformation of the following loop, the surface charge, and the shape of the expected receptor binding site differ significantly. 相似文献
56.
BAFF/BLyS receptor 3 comprises a minimal TNF receptor-like module that encodes a highly focused ligand-binding site 总被引:4,自引:0,他引:4
Gordon NC Pan B Hymowitz SG Yin J Kelley RF Cochran AG Yan M Dixit VM Fairbrother WJ Starovasnik MA 《Biochemistry》2003,42(20):5977-5983
BAFF/BLyS, a member of the tumor necrosis family (TNF) superfamily of ligands, is a crucial survival factor for B cells. BAFF binds three receptors, TACI, BCMA, and BR3, with signaling through BR3 being essential for promoting B cell function. Typical TNF receptor (TNFR) family members bind their cognate ligands through interactions with two cysteine-rich domains (CRDs). However, the extracellular domain (ECD) of BR3 consists of only a partial CRD, with cysteine spacing distinct from other modules described previously. Herein, we report the solution structure of the BR3 ECD. A core region of only 19 residues adopts a stable structure in solution. The BR3 fold is analogous to the first half of a canonical TNFR CRD but is stabilized by an additional noncanonical disulfide bond. BAFF-binding determinants were identified by shotgun alanine-scanning mutagenesis of the BR3 ECD expressed on phage. Several of the key BAFF-binding residues are presented from a beta-turn that we have shown previously to be sufficient for ligand binding when transferred to a structured beta-hairpin scaffold [Kayagaki, N., Yan, M., Seshasayee, D., Wang, H., Lee, W., French, D. M., Grewal, I. S., Cochran, A. G., Gordon, N. C., Yin, J., Starovasnik, M. A, and Dixit, V. M. (2002) Immunity 10, 515-524]. Outside of the turn, mutagenesis identifies additional hydrophobic contacts that enhance the BAFF-BR3 interaction. The crystal structure of the minimal hairpin peptide, bhpBR3, in complex with BAFF reveals intimate packing of the six-residue BR3 turn into a cavity on the ligand surface. Thus, BR3 binds BAFF through a highly focused interaction site, unprecedented in the TNFR family. 相似文献
57.
Fully fertile plants with the expected chromosome number 2n=40 were regenerated from excised leaf sections of Glycine clandestina. Shoots formed directly on the explants through organogenesis. Utilizing the same media and procedures fully fertile plants were also regenerated from cotyledon and hypocotyl tissue of the same G. clandestina accession. We were not successful in regenerating plants from root tissue of G. clandestina.Abbreviations 6-BA
6-Benzyladenine
- FAA
Formalin
- NAA
Naphthalenacetic acid
- IAA
Indoleacetic acid
- Na2EDTA
Disodium salt Ethylenediamine tetraacetic acid
- Fe-NaEDTA
Ferric-Sodium salt Ethylenediamine tetraacetic acid 相似文献
58.
R. J. Singh T. Hymowitz 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1988,76(5):705-711
Summary This study was conducted with the objective of determining the genomic relationship between cultivated soybean (Glycine max) and wild soybean (G. soja) of the subgenus Soja, genus Glycine. Observations on cross-ability rate, hybrid viability, meiotic chromosome pairing, and pollen fertility in F
1 hybrids of G. max × G. soja and reciprocals elucidated that both species hybridized readily and set mature putative hybrid pods, generated vigorous F1 plants, had a majority of sporocytes that showed 18II + 1IV chromosome association at diakinesis and metaphase I, and had a pollen fertility that ranged from 49.2% to 53.3%. A quadrivalent was often associated with the nucleolus, suggesting that one of the chromosomes involved in the interchange is a satellited chromosome. Thus, G. max and G. soja genetic stocks used in this study have been differentiated by a reciprocal translocation. Pachytene analysis of F1 hybrids helped construct chromosome maps based on chromosome length and euchromatin and heterochromatin distribution. Chromosomes were numbered in descending order of 1–20. Pachytene chromosomes in soybean showed heterochromatin distribution on either side of the centromeres. Pachytene analysis revealed small structural differences for chromosomes 6 and 11 which were not detected at diakinesis and metaphase I. This study suggests that G. max and G. soja carry similar genomes and validates the previously assigned genome symbol GG.Research supported in part by the Illinois Agricultural Experiment Station and U.S. Department of Agriculture Competitive Research Grant (85-CRCR-1-1616) 相似文献
59.
Theodore Hymowitz 《Economic botany》1984,38(4):378-388
This paper is devoted to the analysis of the 4,451 soybean (Glycine max,) accessions collected by P. H. Dorsett and W. J. Morse during their plant exploration trip to east Asia 1929–1931. Until about 1950 the collection was used primarily for the development of vegetable type soybean cultivars. During this period many of the accessions were lost. Today only 945 of the original 4,451 accessions are available in the United States soybean germplasm collection. From the 1950s to the 1980s, as soybean production increased in the United States, so did plant pathogen problems. The Dorsett-Morse soybean accessions have been extremely valuable to plant pathologists and breeders as sources of resistance to certain pathogens. Individual genotypes in the collection have been used for genetic studies on morphological, physiological and biochemical traits. Due to the development and distribution of higher-yielding soybean cultivars, farmers in east Asia are no longer growing lower-yielding landraces. Although these landraces are now extinct in east Asia, many were collected by Dorsett and Morse and are preserved in the United States soybean collection. Over the years, the Dorsett-Morse collection has increased in value and will be as useful to soybean scientists in the future as it has been in its first 50 yr of existence. 相似文献
60.
Evolutionary rates for tuf genes in endosymbionts of aphids 总被引:5,自引:1,他引:4
The gene encoding elongation factor Tu (tuf) in aphid endosymbionts (genus
Buchnera) evolves at rates of 1.3 x 10(-10) to 2.5 x 10(-10) nonsynonymous
substitutions and 3.9 x 10(-9) to 8.0 x 10(-9) synonymous substitutions per
position per year. These rates, which are at present among the most
reliable substitution rates for protein-coding genes of bacteria, have been
obtained by calibrating the nodes in the phylogenetic tree produced from
the Buchnera EF-Tu sequences using divergence times for the corresponding
ancestral aphid hosts. We also present data suggesting that the rates of
nonsynonymous substitutions are significantly higher in the endosymbiont
lineages than in the closely related free-living bacteria Escherichia coli
and Salmonella typhimurium. Synonymous substitution rates for Buchnera
approximate estimated mutation rates for E. coli and S. typhimurium, as
expected if synonymous changes act as neutral mutations in Buchnera. We
relate the observed differences in substitution frequencies to the absence
of selective codon preferences in Buchnera and to the influence of Muller's
ratchet on small asexual populations.
相似文献