全文获取类型
收费全文 | 109篇 |
免费 | 3篇 |
出版年
2021年 | 1篇 |
2019年 | 1篇 |
2016年 | 4篇 |
2015年 | 5篇 |
2014年 | 2篇 |
2013年 | 5篇 |
2012年 | 4篇 |
2011年 | 4篇 |
2010年 | 3篇 |
2009年 | 2篇 |
2008年 | 3篇 |
2007年 | 3篇 |
2006年 | 6篇 |
2005年 | 3篇 |
2004年 | 6篇 |
2003年 | 6篇 |
2002年 | 4篇 |
2001年 | 1篇 |
2000年 | 4篇 |
1999年 | 7篇 |
1998年 | 5篇 |
1997年 | 2篇 |
1995年 | 4篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1991年 | 1篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1988年 | 1篇 |
1986年 | 1篇 |
1985年 | 2篇 |
1984年 | 1篇 |
1983年 | 1篇 |
1982年 | 1篇 |
1981年 | 1篇 |
1977年 | 1篇 |
1940年 | 1篇 |
1909年 | 1篇 |
1897年 | 1篇 |
1889年 | 1篇 |
1888年 | 4篇 |
1875年 | 1篇 |
排序方式: 共有112条查询结果,搜索用时 15 毫秒
81.
82.
83.
Vasu Nair Sanjib Bera Travis Mickle Serge Van Calenbergh 《Nucleosides, nucleotides & nucleic acids》2013,32(4-5):577-579
Abstract Methodologies for the synthesis of novel isomeric dideoxynucleosides with unsaturation in the carbohydrate moiety have been developed. An example of the synthesis (Isod4A) is presented. Antiviral studies are in progress. 相似文献
84.
85.
Lysine is catabolized via the saccharopine pathway in plants and mammals. In this pathway, lysine is converted to α-aminoadipic-δ-semialdehyde (AASA) by lysine-ketoglutarate reductase/saccharopine dehydrogenase (LKR/SDH); thereafter, AASA is converted to aminoadipic acid (AAA) by α-aminoadipic-δ-semialdehyde dehydrogenase (AASADH). Here, we investigate the occurrence, genomic organization and functional role of lysine catabolic pathways among prokaryotes. Surprisingly, only 27 species of the 1478 analyzed contain the lkr and sdh genes, whereas 323 species contain aasadh orthologs. A sdh-related gene, identified in 159 organisms, was frequently found contiguously to an aasadh gene. This gene, annotated as lysine dehydrogenase (lysdh), encodes LYSDH an enzyme that directly converts lysine to AASA. Pipecolate oxidase (PIPOX) and lysine-6-aminotransferase (LAT), that converts lysine to AASA, were also found associated with aasadh. Interestingly, many lysdh–aasadh–containing organisms live under hyperosmotic stress. To test the role of the lysine-to-AASA pathways in the bacterial stress response, we subjected Silicibacter pomeroyi to salt stress. All but lkr, sdh, lysdh and aasadh were upregulated under salt stress conditions. In addition, lysine-supplemented culture medium increased the growth rate of S. pomeroyi under high-salt conditions and induced high-level expression of the lysdh–aasadh operon. Finally, transformation of Escherichia coli with the S. pomeroyi lysdh–aasadh operon resulted in increased salt tolerance. The transformed E. coli accumulated high levels of the compatible solute pipecolate, which may account for the salt resistance. These findings suggest that the lysine-to-AASA pathways identified in this work may have a broad evolutionary importance in osmotic stress resistance. 相似文献
86.
Phylogenetic analysis of slippage-like sequence variation in the V4 rRNA expansion segment in tiger beetles (Cicindelidae) 总被引:1,自引:1,他引:0
Sequence variation in the middle part of the small-subunit rRNA was studied
for representatives of the major groups in the family Cicindelidae
(Coleoptera). All taxa exhibited a much expanded segment in variable region
V4 compared to D. melanogaster. This expanded segment was not found in
other groups of beetles, including three taxa in the closely related
Carabidae. Secondary structure predictions indicate that the expanded
segment folds into a single stem-loop structure in all taxa. Despite its
structural conservation, the fragment differs strongly in primary sequence,
even between closely related sister taxa. Several features of these
sequences are consistent with slippage replication as the mechanism that
has generated this sequence variation: the level of internal sequence
repetition as measured by the relative simplicity factor (RSF), its
variation in length between close relatives, and the strong nucleotide bias
compared to the remainder of the gene. With few exceptions, there was also
a correlation between sequence length and the level of sequence repetition,
frequently interpreted as the result of slippage. Phylogenies inferred from
the expansion segment were not consistent with existing hypotheses from
other molecular data for the group. This indicates that DNA sequences in
this region are not homologous throughout the entire Cicindelidae, but it
leaves open the possibility that this expansion segment can be used for
phylogeny reconstruction within subgroups. The implications of a
phylogenetic approach to the understanding of slippage-like evolution are
discussed.
相似文献
87.
88.
89.
Nimmy Mohan Sudheesh AP Nimmy Francis Richard Anderson Rakesh S. Laishram 《Nucleic acids research》2015,43(14):7005-7020
Star-PAP is a nuclear non-canonical poly(A) polymerase (PAP) that shows specificity toward mRNA targets. Star-PAP activity is stimulated by lipid messenger phosphatidyl inositol 4,5 bisphoshate (PI4,5P2) and is regulated by the associated Type I phosphatidylinositol-4-phosphate 5-kinase that synthesizes PI4,5P2 as well as protein kinases. These associated kinases act as coactivators of Star-PAP that regulates its activity and specificity toward mRNAs, yet the mechanism of control of these interactions are not defined. We identified a phosphorylated residue (serine 6, S6) on Star-PAP in the zinc finger region, the domain required for PIPKIα interaction. We show that S6 is phosphorylated by CKIα within the nucleus which is required for Star-PAP nuclear retention and interaction with PIPKIα. Unlike the CKIα mediated phosphorylation at the catalytic domain, Star-PAP S6 phosphorylation is insensitive to oxidative stress suggesting a signal mediated regulation of CKIα activity. S6 phosphorylation together with coactivator PIPKIα controlled select subset of Star-PAP target messages by regulating Star-PAP-mRNA association. Our results establish a novel role for phosphorylation in determining Star-PAP target mRNA specificity and regulation of 3′-end processing. 相似文献
90.
Simultaneous saccharification and fermentation of straw to ethanol using the thermotolerant yeast strain Kluyveromyces marxianus imb3 总被引:1,自引:0,他引:1
The thermotolerant, ethanol-producing yeast strain Kluyveromyces marxianus IMB3 was grown at 45°C on media containing 2, 4 and 6 % (w/v) pulverized barley straw and supplemented with 2% (v/v) cellulase. Maximum ethanol concentrations produced were 2, 3 and 3.6g/l, respectively. When the pulverized straw was replaced by NaOH pretreated straw (at 2, 4 and 6% (w/v); based on original untreated straw), ethanol concentrations increased to maxima of 3.9, 8, and 12g/l, respectively. The ethanol yields amount to 20g ethanol from 100g of straw. 相似文献