全文获取类型
收费全文 | 6979篇 |
免费 | 786篇 |
国内免费 | 1篇 |
出版年
2022年 | 54篇 |
2021年 | 75篇 |
2020年 | 64篇 |
2019年 | 67篇 |
2018年 | 100篇 |
2017年 | 78篇 |
2016年 | 122篇 |
2015年 | 200篇 |
2014年 | 214篇 |
2013年 | 323篇 |
2012年 | 380篇 |
2011年 | 344篇 |
2010年 | 239篇 |
2009年 | 224篇 |
2008年 | 316篇 |
2007年 | 329篇 |
2006年 | 274篇 |
2005年 | 260篇 |
2004年 | 282篇 |
2003年 | 244篇 |
2002年 | 259篇 |
2001年 | 158篇 |
2000年 | 191篇 |
1999年 | 155篇 |
1998年 | 107篇 |
1997年 | 75篇 |
1996年 | 72篇 |
1995年 | 63篇 |
1993年 | 61篇 |
1992年 | 136篇 |
1991年 | 119篇 |
1990年 | 163篇 |
1989年 | 101篇 |
1988年 | 109篇 |
1987年 | 106篇 |
1986年 | 93篇 |
1985年 | 94篇 |
1984年 | 84篇 |
1983年 | 61篇 |
1982年 | 93篇 |
1981年 | 77篇 |
1980年 | 72篇 |
1979年 | 89篇 |
1978年 | 77篇 |
1977年 | 72篇 |
1976年 | 54篇 |
1975年 | 68篇 |
1974年 | 55篇 |
1973年 | 55篇 |
1972年 | 53篇 |
排序方式: 共有7766条查询结果,搜索用时 15 毫秒
71.
North Carolina macular dystrophy (NCMD) is an autosomal dominant macular dystrophy causing impaired central vision at an early age, is completely penetrant, and is present in a single large family. With the development of the hypervariable microsatellite (CA repeats) markers in the human genome, it was possible to relatively rapidly screen most of the genome for linkage to the NCMD gene. After utilizing 124 genetic markers, which excluded over 95% of the human genome, three Marshfield microsatellites located at 6q13-q21 were linked to the NCMD locus. Marshfield marker (MFD) 131 gave a lod score of Z(theta) = 4.36 at theta = 0.137; MFD 171 gave a Z(theta) = 8.42 at theta = 0.004; and MFD 97 gave a Z(theta) = 13.10 at theta = 0.017. Other retinal diseases have been reported on 6q stressing the importance of this region and possibly suggesting that these diseases may be allelic or located in part of a large macular gene family. Locating and characterizing the NCMD gene may be an important step in understanding this group of maculopathies as well as age-related macular degeneration (AMD), a common cause of blindness in the elderly. 相似文献
72.
The effect of copper on the uptake of nitrogen and the tissue contents of inorganic nitrogen, amino acids and proteins were studied in cooper-sensitive Silene vulgaris (Moench) Garcke, grown at different nitrogen sources (NH4
+ or NO3
-). All the toxic copper levels tested, i.e. 4, 8, 16 M Cu2+, strongly inhibited the uptake of nitrogen, especially of NO3
-, and decreased the content of NO3
-, amino acids and proteins. Especially at 4 and 8 M Cu2+, NH4
+ accumulated in the plants, suggesting that the conversion of NH4
- into amino acids was inhibited. 相似文献
73.
The fat tumor suppressor gene in Drosophila encodes a novel member of the cadherin gene superfamily 总被引:24,自引:0,他引:24
Recessive lethal mutations in the fat locus of Drosophila cause hyperplastic, tumor-like overgrowth of larval imaginal discs, defects in differentiation and morphogenesis, and death during the pupal stage. Clones of mutant cells induced by mitotic recombination demonstrate that the overgrowth phenotype is cell autonomous. Here we show that the fat locus encodes a novel member of the cadherin gene superfamily: an enormous transmembrane protein of over 5000 amino acids with a putative signal sequence, 34 tandem cadherin domains, four EGF-like repeats, a transmembrane domain, and a novel cytoplasmic domain. Two recessive lethal alleles contain alterations in the fat coding sequence, and the dominant fat allele, Gull, contains an insertion of a transposable element in the 33rd cadherin domain. Thus, this novel member of the cadherin gene superfamily functions as a tumor suppressor gene and is required for correct morphogenesis. 相似文献
74.
A technique was developed in which the accessory sex glands of stallions were visualized with transrectal ultrasonography during ejaculation. The technique was judged to be effective, since 10 of 11 stallions were trained to tolerate transrectal ultrasonography during ejaculation; they ejaculated during 195 of 200 attempts, and acceptable visualization of their accessory sex glands and excurrent ducts occurred during 97 of 195 ejaculations. Sixty-five percent (89 136 ) of the recordings were successful for stallions that weighed more than 300 kg, whereas 14% (8 59 ) of the recordings were successful for stallions weighing less than 300 kg. The 98 unsuccessful attempts were caused by inaccurate transducer placement due to the small size of the pelvic canal(33 98 ), excessive transducer movement due to stallion movement (32 98 ), indistinct ultrasound images (28 98 ) and human error (5 98 ). The technique was judged to be safe, since no stallions or personnel sustained serious injuries during 200 data collection attempts. 相似文献
75.
76.
77.
Elisabetta Zappone Isabelle Dugast Panos Papadopoulos Kelly Theriault Veronique David Jean-Yves LeGall Kim Summers Lawrie Powell Jim Drysdale 《Human genetics》1991,86(6):557-561
Summary This paper addresses the question of whether abnormalities in ferritin expression in the iron storage disease hemochromatosis (HC) involve major deletions or alterations in regions containing the two ferritin H genes that lie near the disease locus on chromosome 6p. We present evidence from analyses of Southern blots that neither gene is deleted in hemochromatosis. We also describe a polymorphism in one of the genes that we have previously shown to be a processed pseudogene. This polymorphism does not correlate with the presence of HC. The PIC value for this polymorphism was calculated as 0.49. 相似文献
78.
Claudio Fortis Elisabetta Ferrero Mauro Biffi Silvia Heltai Carlo Besana Eraldo Bucci Moreno Tresoldi Claudio Rugarli 《Cancer immunology, immunotherapy : CII》1991,34(2):128-132
Summary Burkitt lymphoma (BL) lines can be grouped according to phenotypic characteristics. Group I cells exhibit the phenotype of resting B cells and grow as single cells. Such lines can be Epstein-Barr-virus(EBV)-negative or -positive. Group II and group III cells are always EBV-positive, they express B cell activation markers, grow in aggregates and resemble in varying degrees lymphoblastoid cell lines (LCL). We studied three groups of BL lines for their capacity to interact with allogeneic lymphocytes. The results showed that as long as the lines have the group I phenotype, they do not stimulate allogeneic T lymphocytes irrespective whether they carry the EBV genome. The group II and III cells are stimulatory. Generally there was no correlation between sensitivity to lymphocyte-mediated lysis and the phenotype of the lines. In one set of lines, the group I cells had higher sensitivity to both natural killer and lymphokine-activated killer effectors compared to the group II or III lines. However, such correlation could not be seen with the other two sets of lines. Among the phenotypic features investigated, expression of the adhesion molecules LFA-1 and LFA-3 correlated with the tendency for cell aggregation. 相似文献
79.
Diagnostic significance of coexpression of intermediate filaments in fine needle aspirates of human tumors 总被引:1,自引:0,他引:1
A study was undertaken of the diagnostic significance of the coexpression of intermediate filaments in fine needle aspirates of human tumors. Three types of coexpression were found: (1) true coexpression, in which tumor cells simultaneously express more than one intermediate filament protein; (2) pseudocoexpression, in which various tumor cell types from histogenetically different parts of a complex tumor show different results; and (3) false coexpression, in which tumor cells with one or two types of intermediate filaments are present together with benign cells expressing a different filament type. True coexpression of vimentin and keratin was documented in renal cell carcinomas, endometrial carcinomas, certain thyroid carcinomas and Hürthle cell adenomas. Coexpression of keratin and neurofilaments was seen in Merkel cell carcinomas, and coexpression of desmin and vimentin was found in leiomyosarcomas. Keratin, vimentin and neurofilament expression was seen in medullary thyroid carcinomas, and keratin, vimentin and glial fibrillary acidic protein expression was observed in pleomorphic adenomas of the salivary gland. Pseudocoexpression was noted in synovial sarcoma, epithelioid sarcoma, benign cystosarcoma phyllodes of the breast, teratocarcinoma, malignant granular cell tumor, progonoma, Wilms' tumor and triton tumor. Sources of false coexpression are also discussed. 相似文献
80.
Y Natsumeda Y Yamada Y Yamaji G Weber 《Biochemical and biophysical research communications》1988,153(1):321-327
Tiazofurin, an anti-cancer drug, which induces remissions in human leukemia, and ribavirin, an anti-viral agent, bind at separate sites (NADH and IMP-XMP sites, respectively) on the target enzyme, IMP dehydrogenase. Now we show that the binding to IMP dehydrogenase of these drugs at two separate sites is translated into synergistic inhibition of de novo guanylate biosynthesis and synergistic toxicity in rat hepatoma 3924A cells. These results may be utilized in the chemotherapy of neoplastic diseases and in the treatment of hepatitis virus infection and hepatocellular carcinoma. 相似文献