全文获取类型
收费全文 | 9603篇 |
免费 | 887篇 |
国内免费 | 1篇 |
专业分类
10491篇 |
出版年
2023年 | 75篇 |
2022年 | 126篇 |
2021年 | 306篇 |
2020年 | 149篇 |
2019年 | 191篇 |
2018年 | 254篇 |
2017年 | 220篇 |
2016年 | 348篇 |
2015年 | 568篇 |
2014年 | 609篇 |
2013年 | 743篇 |
2012年 | 804篇 |
2011年 | 874篇 |
2010年 | 517篇 |
2009年 | 399篇 |
2008年 | 609篇 |
2007年 | 596篇 |
2006年 | 470篇 |
2005年 | 442篇 |
2004年 | 412篇 |
2003年 | 321篇 |
2002年 | 305篇 |
2001年 | 84篇 |
2000年 | 76篇 |
1999年 | 74篇 |
1998年 | 64篇 |
1997年 | 52篇 |
1996年 | 46篇 |
1995年 | 60篇 |
1994年 | 40篇 |
1993年 | 33篇 |
1992年 | 32篇 |
1991年 | 38篇 |
1990年 | 36篇 |
1989年 | 29篇 |
1988年 | 29篇 |
1987年 | 28篇 |
1986年 | 27篇 |
1985年 | 22篇 |
1984年 | 41篇 |
1983年 | 21篇 |
1982年 | 15篇 |
1981年 | 23篇 |
1980年 | 15篇 |
1978年 | 15篇 |
1977年 | 20篇 |
1976年 | 18篇 |
1975年 | 19篇 |
1974年 | 15篇 |
1973年 | 15篇 |
排序方式: 共有10000条查询结果,搜索用时 0 毫秒
21.
Joseph C. Polacco Adam K. Judd Jody K. Dybing Silvia R. Cianzio 《Molecular & general genetics : MGG》1989,217(2-3):257-262
Summary We reported earlier the recovery of two classes of soybean urease mutants in soybean (Glycine max L. Merr. cv. Williams). Class I mutants lack the embryo-specific urease while class II mutants lack the activities of both
urease isozymes, the embryo-specific and the ubiquitous urease, the latter found in all tissues examined. We report here the
recovery of a true-breeding mutant, aj3, which represents the third phenotypic class: normal levels of embryo-specific urease
and little or no ubiquitous urease. Unlike class II mutant plants which lack urease in all tissue, aj3 lacks urease activity
only in leaves (ca. 2% normal activity); its roots have near normal urease activity. Callus derived from leaves of aj3 has
14% to 40% the urease activity of Williams 82 callus. This partial reduction in urease activity in aj3 callus is sufficient
to reduce growth with urea as sole nitrogen source and to confer resistance to 50 mM urea added to callus maintenance medium.
Leaves of aj3 produce more than 40 times the urease antigen expected from their urease activity. The aj3 trait is due to a
single recessive lesion which is not allelic with lesions at theEu2, Eu3 (class II) orEu1 (class I) loci. We designate the aj3 genotype aseu4/eu4. 相似文献
22.
Comparison of 16S rRNA sequences from the family Pasteurellaceae: phylogenetic relatedness by cluster analysis 总被引:2,自引:0,他引:2
The taxonomy of the family Pasteurellaceae has remained controversial despite investigations of biochemistry, serology, and nucleic acid relatedness. In an attempt to resolve some of this confusion, we have partially sequenced the 16S rRNAs of seven members of the family, representing all three genera. The sequences were aligned, similarity scores calculated, and single, average and complete linkage cluster analysis of the resulting distance matrix performed. In this way, an evolutionary branching pattern of these closely related species was reconstructed, and the approximate phylogenetic position of the family determined. Actinobacillus (Haemophilus) actinomycetemcomitans clustered with Haemophilus instead of Actinobacillus, supporting transfer of this species to the genus Haemophilus. Thus cluster analysis of phylogenetic relatedness was found to be particularly useful for studying closely related organisms, and could be performed using a microcomputer. 相似文献
23.
24.
R D Adam 《Nucleic acids research》1992,20(12):3057-3061
Giardia lamblia trophozoites contain at least five sets of chromosomes that have been categorized by chromosome-specific probes. Pulsed field separations of G. lamblia chromosomes also demonstrated minor bands in some isolates which stained less intensely with ethidium than the major chromosomal bands. Two of the minor bands of the E11 clone of the ISR isolate, MBa and MBb, were similar to each other and to chromosomal band I by hybridization to total chromosomal DNA and by hybridization of specific probes. In order to determine the extent of this similarity, I have developed a panel of probes for many of the Pacl restriction fragments and have shown that most of the Pacl and Notl fragments found in MBa are also present in MBb. The differences are found in both telomeric regions. At one end, MBb contains a 300 kb region not found in MBa. At the other end of MBb is a 160 kb region containing the rDNA repeats which is bounded on one end by the telomeric repeat and on the other by sites for multiple enzymes that do not digest the rDNA repeats. The corresponding region of MBa is 23 kb in size. The size difference is consistent with the eightfold greater number of rDNA repeats in MBb than MBa and suggests that 30% of the size difference is accounted for by different numbers of copies of the rDNA repeat. MBa of another ISR clone (ISR G5) is 150 kb larger in size than MBa of ISR E11. The data suggest that MBa and MBb are homologous chromosomes of different sizes and that a portion of the size difference is accounted for by different copy numbers of the rDNA repeat. 相似文献
25.
26.
Mitochondrial boundary membrane contact sites in brain: points of hexokinase and creatine kinase location, and control of Ca2+ transport 总被引:1,自引:0,他引:1
M Kottke V Adam I Riesinger G Bremm W Bosch D Brdiczka G Sandri E Panfili 《Biochimica et biophysica acta》1988,935(1):87-102
The location of hexokinase at the surface of brain mitochondria was investigated by electron microscopy using immuno-gold labelling techniques. The enzyme was located where the two mitochondrial limiting membranes were opposed and contact sites were possible. Disruption of the outer membrane by digitonin did not remove bound hexokinase and creatine kinase from brain mitochondria, although the activity of outer membrane markers and adenylate kinase decreased, suggesting a preferential location of both enzymes in the contact sites. In agreement with that, a membrane fraction was isolated from osmotically lysed rat brain mitochondria in which hexokinase and creatine kinase were concentrated. The density of this kinase-rich fraction was specifically increased by immuno-gold labelling of hexokinase, allowing a further purification by density gradient centrifugation. The fraction was composed of inner and outer limiting membrane components as shown by the specific marker enzymes, succinate dehydrogenase and NADH-cytochrome-c-oxidase (rotenone insensitive). As reported earlier for the enriched contact site fraction of liver mitochondria the fraction from brain mitochondria contained a high activity of glutathione transferase and a low cholesterol concentration. Moreover, the contacts showed a higher Ca2+ binding capacity in comparison to outer and inner membrane fractions. This finding may have regulatory implications because glucose phosphorylation via hexokinase activated the active Ca2+ uptake system and inhibited the passive efflux, resulting in an increase of intramitochondrial Ca2+. 相似文献
27.
mRNA polyadenylate-binding protein: gene isolation and sequencing and identification of a ribonucleoprotein consensus sequence. 总被引:111,自引:30,他引:81 下载免费PDF全文
S A Adam T Nakagawa M S Swanson T K Woodruff G Dreyfuss 《Molecular and cellular biology》1986,6(8):2932-2943
We identified and produced antibodies to the major proteins that interact with poly(A)+ RNAs in the yeast Saccharomyces cerevisiae. The major proteins which were cross-linked by UV light to poly(A)+ RNA in intact yeast cells had apparent molecular weights of 72,000, 60,000, and 50,000. The poly(A) segment of the RNA was selectively cross-linked to the 72,000-molecular-weight protein (72K protein). Mice immunized with purified UV-cross-linked RNA-protein (RNP) complexes produced antibodies to the three major RNP proteins. A yeast genomic DNA library constructed in the lambda gt11 expression vector was screened with the anti-RNP serum, and recombinant bacteriophage clones were isolated. One recombinant phage, lambda YPA72.1, bearing a 2.5-kilobase insert, produced a large beta-galactosidase-RNP fusion protein. Affinity-selected antibodies from the anti-RNP serum on this fusion protein recognized a single 72K protein which was cross-linked to the poly(A) segment of RNA in the intact cell. Furthermore, the fusion protein of lambda YPA72.1 had specific poly(A)-binding activity. Therefore, lambda YPA72.1 encodes the 72K poly(A)-binding protein. Immunofluorescence microscopy showed that this protein was localized in the cytoplasm. Hybrid-selected mRNA translated in vitro produced the 72K poly(A)-binding protein, and mRNA blot analysis detected a single 2.1-kilobase mRNA. DNA blot analysis suggested a single gene for the poly(A)-binding protein. DNA sequence analysis of genomic clones spanning the entire gene revealed a long open reading frame encoding a 64,272-molecular-weight protein with several distinct domains and repeating structural elements. A sequence of 11 to 13 amino acids is repeated three times in this protein. Strikingly, this repeated sequence (RNP consensus sequence) is highly homologous to a sequence that is repeated twice in a major mammalian heterogeneous nuclear RNP protein, A1. The conservation of the repetitive RNP consensus sequence suggests an important function and a common evolutionary origin for messenger RNP and heterogeneous nuclear RNP proteins. 相似文献
28.
NMR, CD and IR spectroscopies of a tridecanucleotide containing a no-base residue: coexistence of B and Z conformations. 总被引:3,自引:3,他引:0 下载免费PDF全文
S Pochet T Huynh-Dinh J M Neumann S Tran-Dinh S Adam J Taboury E Taillandier J Igolen 《Nucleic acids research》1986,14(2):1107-1126
The synthesis of the tridecadeoxynucleotide d(CGm5CGCGxACATGT), where x is the 1-cyano-2-deoxy-beta-D-erythropentofuranose, is described. The NMR, IR, CD studies at various salt concentrations and temperatures of this oligomer show that the B and Z conformations are simultaneously present in the same short DNA fragment. A single apurinic residue is sufficient for the coexistence of the B and Z helices on this oligomer. 相似文献
29.
Donald Spencer Peter M. Chandler Thomas J. V. Higgins Adam S. Inglis Michael Rubira 《Plant molecular biology》1983,2(5):259-267
Serological studies and comparison of N-terminal amino acid sequences with the amino acid sequence deduced from a cDNA clone have been used to establish the sequence relationships between the subunits of the pea seed storage protein, vicilin. Subunits smaller than Mr~50 000 (i.e., Mr 34 000, 30 000, 25 000, 18 000, 14 000, 13 000 and 12 000) show extensive homology with molecules within Mr~50 000 group. Both the sequencing and serological data confirm earlier evidence from studies on vicilin synthesisin vivo andin vitro which indicated that the vicilin subunits smaller than Mr~50 000 arose by endoproteolytic cleavage of parent molecules within the Mr~50 000 group. Cleavage in different Mr 50 000 parent molecules containing either one or both of two susceptible processing sites accounts for the formation of all the vicilin subunits smaller than Mr~50 000, with the possible exception of the Mr34 000 polypeptide. The position of these sites in the putative parents were defined by reference to a complete amino acid sequence deduced from the sequence of DNA complementary to mRNA for one member of the Mr~50 000 group. 相似文献
30.