全文获取类型
收费全文 | 599篇 |
免费 | 166篇 |
国内免费 | 1篇 |
专业分类
766篇 |
出版年
2021年 | 4篇 |
2019年 | 4篇 |
2018年 | 5篇 |
2016年 | 9篇 |
2015年 | 21篇 |
2014年 | 16篇 |
2013年 | 21篇 |
2012年 | 32篇 |
2011年 | 16篇 |
2010年 | 8篇 |
2009年 | 11篇 |
2008年 | 16篇 |
2007年 | 23篇 |
2006年 | 21篇 |
2005年 | 11篇 |
2004年 | 36篇 |
2003年 | 83篇 |
2002年 | 94篇 |
2001年 | 61篇 |
2000年 | 37篇 |
1999年 | 25篇 |
1998年 | 4篇 |
1997年 | 9篇 |
1996年 | 4篇 |
1994年 | 5篇 |
1993年 | 7篇 |
1992年 | 9篇 |
1991年 | 6篇 |
1990年 | 5篇 |
1989年 | 6篇 |
1988年 | 4篇 |
1987年 | 5篇 |
1986年 | 6篇 |
1985年 | 7篇 |
1984年 | 11篇 |
1982年 | 5篇 |
1981年 | 7篇 |
1980年 | 6篇 |
1979年 | 4篇 |
1977年 | 11篇 |
1976年 | 4篇 |
1973年 | 4篇 |
1972年 | 5篇 |
1971年 | 3篇 |
1970年 | 5篇 |
1969年 | 4篇 |
1967年 | 4篇 |
1955年 | 3篇 |
1942年 | 3篇 |
1913年 | 3篇 |
排序方式: 共有766条查询结果,搜索用时 12 毫秒
1.
The spontaneous allele quakingviable (qk
v
) exerts effects on myelination and spermiogenesis. The defects generated by qk
v
were not separated in a multilocus mapping cross that provided a mapping resolution of 0.1 centiMorgans (cM). Furthermore, no distortions suggestive of a large chromosomal anomaly associated with qk
v
were apparent. One plausible interpretation is that the quaking locus contains more than one functional domain, either organized into overlapping genes or expressed by alternative splicing mechanisms. The cloning needed to analyze this locus will be enhanced by the very high resolution of the meiotic mapping cross reported here. The recombinational distances on this qk
v
map were compressed compared with those previously reported in a high-resolution map for qk
1–1, an embryonic lethal allele of quaking induced by ethylnitrosourea. Additional crosses confirmed prior reports that the sex and the genetic background of the heterozygous parent can affect recombinational distances. These joint effects on recombination are strong enough to account for the discrepancy between the two maps. This variability of two-factor map values leads to the preferred multilocus map-building protocol discussed in the accompanying paper. 相似文献
2.
3.
4.
The activities of -2-l-fucosyltransferase and -3-l-fucosyltransferase were measured in human platelets and leucocytes from normal donors, -2-l-Fucosyltransferase was found in platelets but not in leucocytes. In contrast -3-l-fucosyltransferase was not detected in platelets but was present in leucocytes where it was demonstrated in the neutrophil, monocyte and lymphocyte fractions. 相似文献
5.
A soluble Lewis blood-group gene associated -3/4-L-fucosyltransferase has been purified from human milk by a series of steps involving hydrophobic chromatography on Phenyl Sepharose 4B, ion exchange chromatography on CM-Sephadex C-50, affinity chromatography on GDP-hexanolamine Sepharose 4B and gel filtration on Sephacryl S-200. The first step separated -3-L-fucosyltransferase activity directed towardsN-acetylglucosamine in Type 2 (Gal1-4GlcNAc-R) acceptors from an -3/4-fucosyltransferase fraction acting on both Type 1 (Gal1-3GlcNAc-R) and Type 2 acceptors. Further purification of this latter fraction on CM-Sephadex and GDP-hexanolamine Sepharose gave a single peak of fucosyltransferase activity that catalysed the addition of fucose toN-acetylglucosamine in both Type 1 and Type 2 acceptors and to theO-3 position of glucose in lactose-based oligosaccharides. The enzyme preparation at this stage resembled previously described -3/4-fucosyltransferase preparations purified from human milk. However, gel filtration of this preparation on Sephacryl S-200 or Sephadex G-150 separated further amounts of -3-fucosyltransferase activity acting solely on Type 2 acceptors and left a residual -3/4-fucosyltransferase that retained strong -4 activity with the Type 1 acceptor, lacto-N-biose 1, and -3 activity with 2-fucosyllactose, but had relatively little -3 activity withN-acetyllactosamine and virtually no capacity to transfer fucose to glycoproteins withN-linked oligosaccharide chains having unsubstituted terminal Type 2 structures. 相似文献
6.
Evidence is presented of the ability of H-2 class I antigens to function as teratocarcinoma transplantation (Gt) antigens. Coisogenic immunization against H-2 class I antigens expressed on transfected L cells is shown to induce resistance to embryonic carcinoma (EC) cell allografts. The Kb, Db, Dd, and, in appropriate recipients, Ld antigens can function as Gt antigens. The protocol presented may be useful for the molecular identification of other genes encoding histocompatibility antigens. 相似文献
7.
A clone coding for Schizophyllum commune beta-glucosidase: homology with a yeast beta-glucosidase 总被引:3,自引:0,他引:3
F Moranelli J R Barbier M J Dove R M MacKay V L Seligy M Yaguchi G E Willick 《Biochemistry international》1986,12(6):905-912
Three identical clones coding for a partial sequence of the Schizophyllum commune beta-glucosidase were isolated from a cDNA library in lambda gt11, using polyclonal antibody to the enzyme. The identity was confirmed by comparison of the amino-terminus of a peptide from a protease lys-C digest with the sequence inferred from the cDNA sequence. A comparison of the sequence with that reported for a beta-glucosidase from Candida pelliculosa revealed a region in the latter with 43% identity in amino acid sequence. There was also a similarity in the S. commune beta-glucosidase to an active site sequence proposed for a S. commune endoglucanase, suggesting the possibility of a common catalytic mechanism for these two glucolytic enzymes. 相似文献
8.
9.
10.
Mutation analysis of the cystic fibrosis transmembrane regulator gene in native American populations of the southwest
下载免费PDF全文
![点击此处可从《American journal of human genetics》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Theresa A. Grebe Winifred W. Doane Sarah F. Richter Carol Clericuzio R. A. Norman William K. Seltzer Susan N. Rhodes Bruce E. Goldberg Lucy S. Hernried Melody McClure Gail Kaplan 《American journal of human genetics》1992,51(4):736-740
We report DNA and clinical analyses of cystic fibrosis (CF) in two previously unstudied, genetically isolated populations: Pueblo and Navajo Native Americans. Direct mutation analysis of six mutations of the CFTR gene--namely, delta F508, G542X, G551D, R553X, N1303K, and W1282X--was performed on PCR-amplified genomic DNA extracted from blood samples. Haplotype analyses with marker/enzyme pairs XV2c/TaqI and KM19/PstI were performed as well. Of the 12 affected individuals studied, no delta F508 mutation was detected; only one G542X mutation was found. None of the other mutations was detected. All affected individuals have either an AA, AC, or CC haplotype, except for the one carrying the G542X mutation, who has the haplotype AB. Clinically, six of the affected individuals examined exhibit growth deficiency, and five (all from the Zuni Pueblo) have a severe CF phenotype. Four of the six Zunis with CF are also microcephalic, a finding not previously noted in CF patients. Our DNA data have serious implications for risk assessment of CF carrier status for these people. 相似文献