全文获取类型
收费全文 | 2314篇 |
免费 | 137篇 |
出版年
2022年 | 7篇 |
2021年 | 18篇 |
2019年 | 13篇 |
2018年 | 26篇 |
2017年 | 27篇 |
2016年 | 38篇 |
2015年 | 63篇 |
2014年 | 66篇 |
2013年 | 179篇 |
2012年 | 134篇 |
2011年 | 146篇 |
2010年 | 78篇 |
2009年 | 76篇 |
2008年 | 114篇 |
2007年 | 153篇 |
2006年 | 124篇 |
2005年 | 113篇 |
2004年 | 125篇 |
2003年 | 134篇 |
2002年 | 141篇 |
2001年 | 43篇 |
2000年 | 39篇 |
1999年 | 41篇 |
1998年 | 33篇 |
1997年 | 29篇 |
1996年 | 21篇 |
1995年 | 26篇 |
1994年 | 16篇 |
1993年 | 27篇 |
1992年 | 38篇 |
1991年 | 16篇 |
1990年 | 17篇 |
1989年 | 33篇 |
1988年 | 16篇 |
1987年 | 16篇 |
1986年 | 19篇 |
1985年 | 23篇 |
1984年 | 27篇 |
1983年 | 15篇 |
1982年 | 10篇 |
1981年 | 17篇 |
1980年 | 21篇 |
1979年 | 18篇 |
1978年 | 11篇 |
1977年 | 16篇 |
1976年 | 14篇 |
1975年 | 15篇 |
1974年 | 10篇 |
1973年 | 12篇 |
1970年 | 5篇 |
排序方式: 共有2451条查询结果,搜索用时 390 毫秒
931.
Activation mechanism of Gi and Go by reactive oxygen species. 总被引:2,自引:0,他引:2
Motohiro Nishida Kevin L Schey Shuichi Takagahara Kenji Kontani Toshiaki Katada Yasuteru Urano Tetsuo Nagano Taku Nagao Hitoshi Kurose 《The Journal of biological chemistry》2002,277(11):9036-9042
Reactive oxygen species are proposed to work as intracellular mediators. One of their target proteins is the alpha subunit of heterotrimeric GTP-binding proteins (Galpha(i) and Galpha(o)), leading to activation. H(2)O(2) is one of the reactive oxygen species and activates purified Galpha(i2). However, the activation requires the presence of Fe(2+), suggesting that H(2)O(2) is converted to more reactive species such as c*OH. The analysis with mass spectrometry shows that seven cysteine residues (Cys(66), Cys(112), Cys(140), Cys(255), Cys(287), Cys(326), and Cys(352)) of Galpha(i2) are modified by the treatment with *OH. Among these cysteine residues, Cys(66), Cys(112), Cys(140), Cys(255), and Cys(352) are not involved in *OH-induced activation of Galpha(i2). Although the modification of Cys(287) but not Cys(326) is required for subunit dissociation, the modification of both Cys(287) and Cys(326) is necessary for the activation of Galpha(i2) as determined by pertussis toxin-catalyzed ADP-ribosylation, conformation-dependent change of trypsin digestion pattern or guanosine 5'-3-O-(thio)triphosphate binding. Wild type Galpha(i2) but not Cys(287)- or Cys(326)-substituted mutants are activated by UV light, singlet oxygen, superoxide anion, and nitric oxide, indicating that these oxidative stresses activate Galpha(i2) by the mechanism similar to *OH-induced activation. Because Cys(287) exists only in G(i) family, this study explains the selective activation of G(i)/G(o) by oxidative stresses. 相似文献
932.
Izumi Suzuma Kiyoshi Suzuma Kohjiro Ueki Yasuaki Hata Edward P Feener George L King Lloyd Paul Aiello 《The Journal of biological chemistry》2002,277(2):1047-1057
Stretch-induced expression of vascular endothelial growth factor (VEGF) is thought to be important in mediating the exacerbation of diabetic retinopathy by systemic hypertension. However, the mechanisms underlying stretch-induced VEGF expression are not fully understood. We present novel findings demonstrating that stretch-induced VEGF expression in retinal capillary pericytes is mediated by phosphatidylinositol (PI) 3-kinase and protein kinase C (PKC)-zeta but is not mediated by ERK1/2, classical/novel isoforms of PKC, Akt, or Ras despite their activation by stretch. Cardiac profile cyclic stretch at 60 cpm increased VEGF mRNA expression in a time- and magnitude-dependent manner without altering mRNA stability. Stretch increased ERK1/2 phosphorylation, PI 3-kinase activity, Akt phosphorylation, and PKC-zeta activity. Signaling pathways were explored using inhibitors of PKC, MEK1/2, and PI 3-kinase; adenovirus-mediated overexpression of ERK, PKC-alpha, PKC-delta, PKC-zeta, and Akt; and dominant negative (DN) mutants of ERK, PKC-zeta, Ras, PI 3-kinase and Akt. Although stretch activated ERK1/2 through a Ras- and PKC classical/novel isoform-dependent pathway, these pathways were not responsible for stretch-induced VEGF expression. Overexpression of DN ERK and Ras had no effect on VEGF expression in these cells. In contrast, DN PI 3-kinase as well as pharmacologic inhibitors of PI 3-kinase blocked stretch-induced VEGF expression. Although stretch-induced PI 3-kinase activation increased both Akt phosphorylation and activity of PKC-zeta, VEGF expression was dependent on PKC-zeta but not Akt. In addition, PKC-zeta did not mediate stretch-induced ERK1/2 activation. These results suggest that stretch-induced expression of VEGF involves a novel mechanism dependent upon PI 3-kinase-mediated activation of PKC-zeta that is independent of stretch-induced activation of ERK1/2, classical/novel PKC isoforms, Ras, or Akt. This mechanism may play a role in the well documented association of concomitant hypertension with clinical exacerbation of neovascularization and vascular permeability. 相似文献
933.
934.
935.
Atsushi Miyagawa Hidehiro Kurosawa Toshiyuki Watanabe Tetsuo Koyama Daiyo Terunuma Koji Matsuoka 《Carbohydrate polymers》2004,57(4):441-450
As an artificial ligand, a glycoconjugate polymer carrying carbohydrate moiety of lactosyl ceramide or globotriaosyl ceramide (Gb3) was synthesized. Gb3 is known as the receptor of Shiga toxin-producing Escherichia coli O157: H7. The preparation of the glycoconjugate polymer initially involves the construction of the carbohydrate moiety of Gb3 derivative which has n-pentenyl group as polymerizable group. In addition, the n-pentenyl group of the Gb3 derivative was modified and different polymerizable groups such as acrylamide group were introduced at ω-position of the aglycon. Radical polymerization of the synthesized glycosyl monomers with or without acrylamide proceeded smoothly in water using ammonium persulfate and N, N, N′, N′-tetramethylethylenediamine as usual initiator system and gave water-soluble glycoconjugate polymers having various polymer compositions. These polymers have the potential to neutralize Shiga toxin by reason of cluster effect and multivalency. 相似文献
936.
A mutation in the serum and glucocorticoid-inducible kinase-like kinase (Sgkl) gene is associated with defective hair growth in mice. 总被引:2,自引:0,他引:2
Kentaro Masujin Taro Okada Takehito Tsuji Yoshiyuki Ishii Kaoru Takano Junichiro Matsuda Atsuo Ogura Tetsuo Kunieda 《DNA research》2004,11(6):371-379
YPC is a mutant mouse strain with defective hair growth characterized by thin, short hairs and poorly developed hair bulbs and dermal papillae. To identify the gene associated with the phenotype, we performed genome-wide linkage analysis using 1010 backcross progeny and 123 microsatellite markers covering all chromosomes. The mutant locus (ypc) was mapped to a 0.2-cM region in the proximal part of mouse chromosome 1. This 0.2-cM region corresponds to a 450-kb region of genome sequence that contains two genes with known functions and five ESTs or predicted genes with unknown functions. Sequence analysis revealed a single C-to-A nucleotide substitution at nucleotide 1382 in the Sgkl gene, causing a nonsense mutation at codon 461. Sgkl encodes serum and glucocorticoid-inducible kinase-like kinase (SGKL), which belongs to a subfamily of serine/threonine protein kinases and has been suggested to have a role downstream of lipid signals produced by activation of phosphoinositide 3-kinase (PI3K). In the mutant SGKL, a serine residue in the C-terminal end of the protein (Ser486), which is indispensable for activation of SGKL upon phosphorylation, is abolished by premature termination. Specific expression of the Sgkl gene in the inner root sheath of growing hair follicles was also identified by in situ hybridization. Therefore, we concluded that the nucleotide substitution in the Sgkl gene is the causative mutation for defective hair growth in the ypc mutant mouse and that the signaling pathway involving SGKL plays an essential role in mammalian hair development. 相似文献
937.
Extremely small animals including fishes have been reported with discussion of the causes and consequences of their miniaturization.
Here we demonstrate, for the first time, very early (i.e., 23–60 days old and 42–67 days old) sexual maturity in two groups
of gobioid fishes (Schindleria and Paedogobius, respectively) in warm water, based on the otolith increments. The generation time of Schindleria is the shortest known among vertebrates under natural conditions. We discuss the occurrence and evolutionary significance
of the progenesis found in gobioid fishes.
Received: September 27, 2001 / Revised: January 26, 2002 / Accepted: February 20, 2002 相似文献
938.
The chemical synthesis and binding affinity to the EGF receptor of the EGF-like domain of heparin-binding EGF-like growth factor (HB-EGF). 总被引:3,自引:0,他引:3
Song Yub Shin Tetsuo Yokoyama Takato Takenouchi Eisuke Munekata 《Journal of peptide science》2003,9(4):244-250
Heparin-binding EGF-like growth factor (HB-EGF), which belongs to the EGF-family of growth factors, was isolated from the conditioned medium of macrophage-like cells. To investigate the effect of N- and C-terminal residues of the EGF-like domain of HB-EGF in the binding affinity to the EGF receptor on A431 cell. We synthesized HB-EGF(44-86) corresponding to the EGF-like domain of HB-EGF and its N- or C-terminal truncated peptides. Thermolytic digestion demonstrated three disulfide bond pairings of the EGF-like domain in HB-EGF is consistent with that of human-EGF and human-TGF-alpha. HB-EGF(44-86) showed high binding affinity to EGF-receptor, like human-EGF. The truncation of the C-terminal Leu86 residue from HB-EGF(44-86), HB-EGF(45-86) or HB-EGF(46-86) caused a drastic reduction in the binding affinity to the EGF receptor. These results suggest that the EGF-like domain of HB-EGF plays an important role in the binding to the EGF receptor, and its C-terminal Leu86 residue is necessary for binding with the EGF-receptor. In addition, the deletion of the two N-terminal residues (Asp44-Pro45) from HB-EGF(44-86) caused a 10-fold decrease in relative binding affinity to the EGF receptor. This indicates that the two N-terminal residues of the EGF-like domain of HB-EGF are necessary for its optimal binding affinity to the EGF receptor. 相似文献
939.
940.
Tetsuo Endo Satoshi Koizumi Kazuhiko Tabata Shingo Kakita Akio Ozaki 《Carbohydrate research》2001,330(4)
α-Neup5Ac-(2→6)-
-GalpNAc, the carbohydrate portion of sialyl–Tn epitope of the tumor-associated carbohydrate antigen, was prepared by a whole-cell reaction through the combination of recombinant Escherichia coli strains and Corynebacterium ammoniagenes. Two recombinant E. coli strains overexpressed the CMP-Neup5Ac biosynthetic genes and the α-(2→6)-sialyltransferase gene of Photobacterium damsela. C. ammoniagenes contributed to the production of UTP from orotic acid. α-Neup5Ac-(2→6)-
-GalpNAc was accumulated at 87 mM (45 g/L) after a 25-h reaction starting from orotic acid, N-acetylneuraminic acid, and 2-acetamide-2-deoxy-
-galactose. 相似文献