全文获取类型
收费全文 | 1310篇 |
免费 | 93篇 |
专业分类
1403篇 |
出版年
2023年 | 7篇 |
2022年 | 15篇 |
2021年 | 13篇 |
2020年 | 13篇 |
2019年 | 17篇 |
2018年 | 19篇 |
2017年 | 14篇 |
2016年 | 32篇 |
2015年 | 60篇 |
2014年 | 55篇 |
2013年 | 104篇 |
2012年 | 119篇 |
2011年 | 77篇 |
2010年 | 44篇 |
2009年 | 38篇 |
2008年 | 90篇 |
2007年 | 78篇 |
2006年 | 77篇 |
2005年 | 60篇 |
2004年 | 55篇 |
2003年 | 72篇 |
2002年 | 62篇 |
2001年 | 11篇 |
2000年 | 18篇 |
1999年 | 13篇 |
1998年 | 20篇 |
1997年 | 18篇 |
1996年 | 15篇 |
1995年 | 10篇 |
1994年 | 8篇 |
1993年 | 12篇 |
1992年 | 17篇 |
1991年 | 4篇 |
1989年 | 4篇 |
1987年 | 4篇 |
1986年 | 4篇 |
1982年 | 7篇 |
1981年 | 5篇 |
1979年 | 6篇 |
1977年 | 6篇 |
1975年 | 3篇 |
1974年 | 6篇 |
1973年 | 4篇 |
1971年 | 5篇 |
1970年 | 3篇 |
1966年 | 4篇 |
1965年 | 4篇 |
1964年 | 3篇 |
1948年 | 3篇 |
1947年 | 4篇 |
排序方式: 共有1403条查询结果,搜索用时 0 毫秒
11.
Muriel Bost Mary Berkaw O. Wesley McBride Guy Chazot Philippe Arnaud 《Human genetics》1995,96(2):239-240
Using a probe isolated from a human liver cDNA library, polymorphisms were observed in the human ceruloplasmin gene with the enzymes PstI and MspI. The PstI polymorphism was frequent (allele frequencies, 0.46 and 0.54) whereas the polymorphisms found with MspI were rare. 相似文献
12.
Suzanne Demczuk Annie Lévy Muriel Aubry Marie-Françoise Croquette Nicole Philip Marguerite Prieur Ursula Sauer Patrice Bouvagnet Guy A. Rouleau Gilles Thomas Alain Aurias 《Human genetics》1995,96(1):9-13
We have determined the parental origin of the deleted chromosome 22 in 29 cases of DiGeorge syndrome (DGS) using a CA-repeat mapping within the commonly deleted region, and in one other case by using a chromosome 22 short arm heteromorphism. The CA-repeat was informative in 21 out of 29 families studied and the deleted chromosome was of maternal origin in 16 cases (72%). When these data are pooled with recent results from the literature, 24 de novo DGS, velo-cardio-facial syndrome (VCFS) and isolated conotruncal cardiac disease deletions are found to be of maternal origin and 8 of paternal origin, yielding a 2 of 8 with a probability level lower than 0.01. These data, and review of the literature on familial DGS/VCFS and isolated conotruncal cardiopathies suggest that there is a strong tendency for the 22q11.2 deletions to be of maternal origin. 相似文献
13.
James E. Womack Muriel T. Davisson Eva M. Eicher Debra A. Kendall 《Biochemical genetics》1977,15(3-4):347-355
A method for detecting two alleles at Np-1 (nucleoside phosphorylase) and three alleles at Es-10 (esterase 10) from mouse blood by cellulose acetate electrophoresis is described. The allelic constitution at these loci for 44 inbred strains and stocks was determined. The location of Np-1 on chromosome 14 was established by backcross experiments in which alleles at Np-1 and Robertsonian translocations were segregating. Es-10 was shown to be linked to Np-1, and the following genetic map of Chr 14 was constructed: centromere-(8.9±4.0 cM)-[Np-1, Wc]-(10.2±1.9 cM)-Es-10-(15.5±3.7 cM)-s. The homologous human loci, NP and ES-D, are not linked.This work was supported by Contract E(11-1)-3267 with the Energy Research and Development Administration, by Contracts NO1-ES4-2156 and NO1-ES4-2159 with the National Institute of Environmental Health Sciences, and by Grants GM 19656 and GM 20919 from the National Institute of General Medical Sciences. D. A. K. was a participant in the 1975 Summer Program for College, Graduate, and Medical Students, which was supported, in part, by the Clark Foundation. The Jackson Laboratory is fully accredited by the American Association for Accreditation of Laboratory Animal Care. 相似文献
14.
Peleg Leah Nesbitt Muriel N. Ashkenazi Israel E. 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1982,147(1):137-142
Journal of Comparative Physiology A - A/J mice differ from C57BL/6J mice in the time of the daily peak of activity of glyceraldehyde-3-phosphate dehydrogenase (GAPD) in thymus and in thyroid.... 相似文献
15.
16.
Carlier L Couprie J le Maire A Guilhaudis L Milazzo-Segalas I Courçon M Moutiez M Gondry M Davoust D Gilquin B Zinn-Justin S 《Protein science : a publication of the Protein Society》2007,16(12):2750-2755
Human KIN17 is a 45-kDa eukaryotic DNA- and RNA-binding protein that plays an important role in nuclear metabolism and in particular in the general response to genotoxics. Its amino acids sequence contains a zinc finger motif (residues 28-50) within a 30-kDa N-terminal region conserved from yeast to human, and a 15-kDa C-terminal tandem of SH3-like subdomains (residues 268-393) only found in higher eukaryotes. Here we report the solution structure of the region 51-160 of human KIN17. We show that this fragment folds into a three-alpha-helix bundle packed against a three-stranded beta-sheet. It belongs to the winged helix (WH) family. Structural comparison with analogous WH domains reveals that KIN17 WH module presents an additional and highly conserved 3(10)-helix. Moreover, KIN17 WH helix H3 is not positively charged as in classical DNA-binding WH domains. Thus, human KIN17 region 51-160 might rather be involved in protein-protein interaction through its conserved surface centered on the 3(10)-helix. 相似文献
17.
Duncan J. Berger Elsa Lger Geetha Sankaranarayanan Mariama Sne Nicolas D. Diouf Muriel Rabone Aidan Emery Fiona Allan James A. Cotton Matthew Berriman Joanne P. Webster 《PLoS pathogens》2022,18(8)
Hybridization between different species of parasites is increasingly being recognised as a major public and veterinary health concern at the interface of infectious diseases biology, evolution, epidemiology and ultimately control. Recent research has revealed that viable hybrids and introgressed lineages between Schistosoma spp. are prevalent across Africa and beyond, including those with zoonotic potential. However, it remains unclear whether these hybrid lineages represent recent hybridization events, suggesting hybridization is ongoing, and/or whether they represent introgressed lineages derived from ancient hybridization events. In human schistosomiasis, investigation is hampered by the inaccessibility of adult-stage worms due to their intravascular location, an issue which can be circumvented by post-mortem of livestock at abattoirs for Schistosoma spp. of known zoonotic potential. To characterise the composition of naturally-occurring schistosome hybrids, we performed whole-genome sequencing of 21 natural livestock infective schistosome isolates. To facilitate this, we also assembled a de novo chromosomal-scale draft assembly of Schistosoma curassoni. Genomic analyses identified isolates of S. bovis, S. curassoni and hybrids between the two species, all of which were early generation hybrids with multiple generations found within the same host. These results show that hybridization is an ongoing process within natural populations with the potential to further challenge elimination efforts against schistosomiasis. 相似文献
18.
19.
20.
Common generalized vitiligo is an acquired depigmenting disorder characterized by a chronic and progressive loss of melanocytes from the epidermis and follicular reservoir. However, the mechanism of melanocyte disappearance has never been clearly understood, and the intervention of cellular and humoral autoimmune phenomena as primary events remains unproven. In this review, is discussed the data supporting the major theories of vitiligo, namely melanocyte destruction (autoimmune, neural and impaired redox status) and melanocyte inhibition or defective adhesion. Based on recent morphologic findings in vivo supporting a chronic detachment and transepidermal loss of melanocytes in common generalized vitiligo, a new theory is suggested proposing melanocytorrhagy as the primary defect underlying melanocyte loss, integrating most of the possible triggering/precipitating/enhancing effects of other known factors. 相似文献