全文获取类型
收费全文 | 18943篇 |
免费 | 1398篇 |
国内免费 | 541篇 |
出版年
2024年 | 16篇 |
2023年 | 133篇 |
2022年 | 308篇 |
2021年 | 578篇 |
2020年 | 405篇 |
2019年 | 513篇 |
2018年 | 583篇 |
2017年 | 487篇 |
2016年 | 712篇 |
2015年 | 1086篇 |
2014年 | 1187篇 |
2013年 | 1386篇 |
2012年 | 1775篇 |
2011年 | 1616篇 |
2010年 | 983篇 |
2009年 | 905篇 |
2008年 | 1154篇 |
2007年 | 986篇 |
2006年 | 892篇 |
2005年 | 747篇 |
2004年 | 743篇 |
2003年 | 657篇 |
2002年 | 593篇 |
2001年 | 248篇 |
2000年 | 227篇 |
1999年 | 224篇 |
1998年 | 159篇 |
1997年 | 152篇 |
1996年 | 148篇 |
1995年 | 115篇 |
1994年 | 106篇 |
1993年 | 118篇 |
1992年 | 115篇 |
1991年 | 108篇 |
1990年 | 80篇 |
1989年 | 77篇 |
1988年 | 61篇 |
1987年 | 65篇 |
1986年 | 53篇 |
1985年 | 52篇 |
1984年 | 39篇 |
1983年 | 48篇 |
1982年 | 27篇 |
1981年 | 28篇 |
1980年 | 18篇 |
1979年 | 15篇 |
1978年 | 22篇 |
1976年 | 14篇 |
1974年 | 14篇 |
1972年 | 16篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
91.
Luciana A. Haddad Regina C. Mingroni-Netto Angela M. Vianna-Morgante Sérgio D. J. Pena 《Human genetics》1996,97(6):808-812
Ever since the identification of the genetic cause of fragile X syndrome as the expansion of an unstable trinucleotide sequence,
several diagnostic strategies have evolved from molecular studies. However, we still lack a simple test suitable for population
screening. We have therefore developed a nonisotopic polymerase chain reaction (PCR)-based technique for the identification
of fragile X full mutations among men, with easy visualization of the PCR products on silver-stained polyacrylamide gels.
The technique consists of PCR amplification with primers that flank the trinucleotide repeats, with a product of 557 bp for
the (CGG)29 allele. Conditions were established such that full mutations failed to amplify and were thus identified with 98% sensitivity
compared with Southern blot analysis. To produce an indispensable internal control we added to the reaction a third primer,
internal to this fragment, allowing the multiplex amplification of a monomorphic band corresponding to a CG-rich stretch 147
bp upstream of the polymorphic region. In trials involving 41 patients and 74 controls, the PCR-based test here described
showed specificity of more than 98.6%, accuracy of 99% and a sensitivity of 98%. Thus, although not suitable for medical diagnosis,
it constitutes a useful tool for screening for the fragile X syndrome in populations of mentally retarded males.
Received: 31 May 1995 / Revised: 4 October 1995 相似文献
92.
Maria de Fatima Bonaldo Pierre Jelenc Long Su Lee Lawton M. -T. Wu Dorothy Warburton Marcelo Bento Soares 《Human genetics》1996,97(4):441-452
A study was conducted on the feasibility of isolating genes and pseudogenes that map to chromosome 13 by a hybridization-based approach using a 13-specific library and pools of repeat-free cDNA clones. Five pairs of cDNA and chromosome 13 genomic clones were identified and characterized. Partial or full-length sequence was derived from all cDNAs, and database searches were performed for putative gene identification. Partial sequence was also obtained from the chromosome 13 genomic clones for comparison with those of the hybridizing cDNAs. As a result of these analyses we identified three genes, a putative homologue of a porcine mRNA encoding an unidentified hepatic protein, a putative homologue of a yeast integral membrane protein, and a gene for a translationally controlled tumor protein, and two processed pseudogenes, ribosomal proteins L23a and S3a. The latter was formerly identified as the v-fos transformation effector gene, Fte-1, and recently cited as a possible candidate for the BRCA2 gene on chromosome 13. All genes and pseudogenes were localized to cytogenetic bands by in situ hybridization of metaphase chromosomes with probes derived from the chromosome 13 genomic clones. 相似文献
93.
Márcia Camargo-De-Morais Marta De Freitas Angela G. De Mattos Nádia Schröder Ana C. Zilles Carla S. F. Lisboa Nice Arteni Armando Barlem Rejane Schierholt Guilherme Zwetsch Carlos A. B. Souza Regina Pessoa-Pureur Carlos A. Netto 《Neurochemical research》1996,21(5):595-602
Neurofilaments subunits (NF-H, NF-M, NF-L) and glial fibrillary acidic protein (GFAP) were investigated in the hippocampus
of rats after distinct periods of reperfusion (1 to 15 days) following 20 min of transient global forebrain ischemia in the
rat. In vitro [14Ca]leucine incorporation was not altered until 48 h after the ischemic insult, however concentration of intermediate filament
subunits significantly decreased in this period. Three days after the insult, leucine incorporation significantly increased
while the concentration NF-H, NF-M, and NF-L were still diminished after 15 days of reperfusion. In vitro incorporation of32P into NF-M and NF-L suffered immediately after ischemia, but returned to control values after two days of reperfusion. GFAP
levels decreased immediately after ischemia but quickly recovered and significantly peaked from 7 to 10 days after the insult.
These results suggest that transient ischemia followed by reperfusion causes proteolysis of intermediate filaments in the
hippocampus, and that proteolysis could be facilitated by diminished phosphorylation levels of NF-M and NF-L. 相似文献
94.
Ma Rosario de la Torre Angela Casado Ma Encarnación López-Fernández Diana Carrascosa Ma Concepción Casado Domenico Venarucci Vincenzo Venarucci 《Neurochemical research》1996,21(8):885-888
In order to investigate the role of two free radical detoxificant enzymes in patients with aging brain disorders, superoxide
dismutase (SOD) and catalase (CAT) activities have been measured in blood from male and female human patients of different
ages with several types of aging brain disorders. When compared with activities in the normal population, we have detected:
1) SOD and CAT activities are decreased in patients with Parkinson disease. 2) SOD activity seems to be normal and CAT activity
is decreased in patients with dementia. 3) In the patients with stroke, SOD activity is normal, while CAT activity is decreased.
SOD activity was measured in red blood cells using the Minami and Yoshikawa method. CAT activity was measured in hemolysates
by the method of Aebi. We can conclude that SOD and CAT activities in patients with Parkinson disease are decreased. 相似文献
95.
菜用大豆产量相关性状的遗传分析 总被引:7,自引:0,他引:7
对 19个菜用大豆品种与产量有关的10个农艺性状进行遗传分析的结果表明,生育期和主茎节数遗传力偏高;单株荚数、分枝数遗传力偏低;单株产量、单株荚数的遗传变异系数很大,其遗传进度的值也较大;生育期的遗传变异系数小, 遗传进度也小,遗传相关分析结果表明,产量与生育期、单株结荚数相关关系密切。菜用大豆遗传参数分析结果与前人对食用大豆的研究结果趋势一致。 相似文献
96.
懒猴属的核糖体DNA变异及其种间分化关系 总被引:5,自引:2,他引:3
用15种限制性内切酶和人28S、18SrDNA探针构建了懒猴属各物种核糖体DNA重复单位的限制性内切酶图谱。在进化速率较高的非转录间隔区,在大、中、小懒猴中分别定位了23、24、24个酶切位点。大懒猴与中懒猴有12个位点不同,与小懒猴有14个位点不同,而中、小懒猴间则只有一个位点的差异。经过计算,大懒猴与中懒猴的遗传距离值为12.65%,与小懒猴的差异为14.24%,中、小懒猴间的差异则仅为0.7 相似文献
97.
云南姬鼠的蛋白多态性及其遗传分化关系 总被引:3,自引:0,他引:3
本文采用蛋白电泳技术对来源于云南省若干地区的姬鼠属(Apodemus)的3种姬鼠──高山姬鼠(A.chevrieri)8只,中华姬鼠(A.draco)3只和大耳姬鼠(A.latronum)1只,以及作为外群的同科的绒鼠属的大绒鼠(Hapalomysdelalori)3只进行了分析。共检测遗传座位27个,发现21个座位存在多态性。根据蛋白多态的数据对研究对象进行遗传分化关系的探讨,用系统分析软件PHYLIP计算它们之间的分化关系,得到了一棵无根系统树。结果表明,作为外群的大绒鼠明显不同于其它3种姬鼠而聚在最外面。8只高山姬鼠个体汇聚成独立的一支,中华姬鼠的3个个体也聚成一支,但大耳姬鼠却聚在中华姬鼠一支中,因此我们认为大耳姬鼠同中华姬鼠的分化时间可能比较晚近。 相似文献
98.
99.