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1.
刘玉记 《佛山科学技术学院学报(自然科学版)》1994,(6)
在齿轮图.的每个齿的齿顶分别加上 m_1,m_2,…,m_n,条悬挂边后构成的图称为齿顶边星图,记为,(m_1,m_2,…,m_n).本文给出了、(m_1,m_2…,m_n)的优美标号,从而证明了.(m_1,m_2,…,m_n)是优美图;当m_1=m_2=…,m_n=k 时,(k,k,…k)即为 k 顶边星图,于是解决了“所有的 k 顶边星图都是优美图”这一猜想. 相似文献
2.
刘玉记 《内蒙古民族大学学报(自然科学版)》1994,(2)
本文研究Pell方程x ̄2─2y ̄2=1与y ̄2─DZ ̄2=4的公解的问题,完整地证明了当D无平方因子且至多含三个不同奇素因子时,除开(x,y,z)=(17,12,2).(D=35);(x,y,z)=(19601,13860.26).(D=29×41×239)外无其它非平凡解.这个结果加强了Mahanty ̄[1]和陈建华 ̄[2]的结论. 相似文献
3.
研究了不同培养基及外植体条件下麝香石竹玻璃苗的诱导形成及玻璃苗部分生理特性。本文研究认为:麝香石竹玻璃的形成是培养基和外植体因素相互作用的结果,培养基极端的水分环境可能是导致玻璃苗形成的外在原因。 相似文献
4.
The genome sequence and structure of rice chromosome 1 总被引:2,自引:0,他引:2
Sasaki T Matsumoto T Yamamoto K Sakata K Baba T Katayose Y Wu J Niimura Y Cheng Z Nagamura Y Antonio BA Kanamori H Hosokawa S Masukawa M Arikawa K Chiden Y Hayashi M Okamoto M Ando T Aoki H Arita K Hamada M Harada C Hijishita S Honda M Ichikawa Y Idonuma A Iijima M Ikeda M Ikeno M Ito S Ito T Ito Y Ito Y Iwabuchi A Kamiya K Karasawa W Katagiri S Kikuta A Kobayashi N Kono I Machita K Maehara T Mizuno H Mizubayashi T Mukai Y Nagasaki H Nakashima M Nakama Y Nakamichi Y Nakamura M Namiki N 《Nature》2002,420(6913):312-316
The rice species Oryza sativa is considered to be a model plant because of its small genome size, extensive genetic map, relative ease of transformation and synteny with other cereal crops. Here we report the essentially complete sequence of chromosome 1, the longest chromosome in the rice genome. We summarize characteristics of the chromosome structure and the biological insight gained from the sequence. The analysis of 43.3 megabases (Mb) of non-overlapping sequence reveals 6,756 protein coding genes, of which 3,161 show homology to proteins of Arabidopsis thaliana, another model plant. About 30% (2,073) of the genes have been functionally categorized. Rice chromosome 1 is (G + C)-rich, especially in its coding regions, and is characterized by several gene families that are dispersed or arranged in tandem repeats. Comparison with a draft sequence indicates the importance of a high-quality finished sequence. 相似文献
5.
Summary The eggs of a sea hare,Aplysia kurodai, contained antibacterial factors which probably play a role in the defense of eggs against bacterial infection. The active factors were composed of several heat-labile proteins, unrelated to lysozyme, and were produced in the albumen gland. 相似文献
6.
C. Kitada M. Fujino Y. Kamiya A. Sakurai S. Tamura N. Takahashi E. Tsuchiya K. Abe S. Fukui 《Cellular and molecular life sciences : CMLS》1979,35(10):1275-1276
Summary The inducing factor of mating tube formation ofRhodosporidium turuloides, named rhodotorucine A (H-Tyr-Pro-Glu-Ile-Ser-Trp-Thr-Arg-Asn-Gly-Cys(S-farnesyl)-OH), has been synthesized to confirm the structure proposed for the natural lipopeptide. The synthetic S-farnesyl undecapeptide has identical Rf values on TLC using several different solvents, and also the same biological activity as the natural hormone.Acknowledgments. We wish to express our thanks to Drs E. Ohmura, M. Nishikawa and M. Yoneda of Takeda Chemical Industries and Dr I. Banno of Institute for Fermentation, Osaka, for their encouragement throughout this work. 相似文献
7.
Birth of parthenogenetic mice that can develop to adulthood 总被引:1,自引:0,他引:1
Only mammals have relinquished parthenogenesis, a means of producing descendants solely from maternal germ cells. Mouse parthenogenetic embryos die by day 10 of gestation. Bi-parental reproduction is necessary because of parent-specific epigenetic modification of the genome during gametogenesis. This leads to unequal expression of imprinted genes from the maternal and paternal alleles. However, there is no direct evidence that genomic imprinting is the only barrier to parthenogenetic development. Here we show the development of a viable parthenogenetic mouse individual from a reconstructed oocyte containing two haploid sets of maternal genome, derived from non-growing and fully grown oocytes. This development was made possible by the appropriate expression of the Igf2 and H19 genes with other imprinted genes, using mutant mice with a 13-kilobase deletion in the H19 gene as non-growing oocytes donors. This full-term development is associated with a marked reduction in aberrantly expressed genes. The parthenote developed to adulthood with the ability to reproduce offspring. These results suggest that paternal imprinting prevents parthenogenesis, ensuring that the paternal contribution is obligatory for the descendant. 相似文献
8.
Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer 总被引:29,自引:0,他引:29
Suzuki H Watkins DN Jair KW Schuebel KE Markowitz SD Chen WD Pretlow TP Yang B Akiyama Y Van Engeland M Toyota M Tokino T Hinoda Y Imai K Herman JG Baylin SB 《Nature genetics》2004,36(4):417-422
Aberrant WNT pathway signaling is an early progression event in 90% of colorectal cancers. It occurs through mutations mainly of APC and less often of CTNNB1 (encoding beta-catenin) or AXIN2 (encoding axin-2, also known as conductin). These mutations allow ligand-independent WNT signaling that culminates in abnormal accumulation of free beta-catenin in the nucleus. We previously identified frequent promoter hypermethylation and gene silencing of the genes encoding secreted frizzled-related proteins (SFRPs) in colorectal cancer. SFRPs possess a domain similar to one in the WNT-receptor frizzled proteins and can inhibit WNT receptor binding to downregulate pathway signaling during development. Here we show that restoration of SFRP function in colorectal cancer cells attenuates WNT signaling even in the presence of downstream mutations. We also show that the epigenetic loss of SFRP function occurs early in colorectal cancer progression and may thus provide constitutive WNT signaling that is required to complement downstream mutations in the evolution of colorectal cancer. 相似文献
9.
BMP signaling inhibits intestinal stem cell self-renewal through suppression of Wnt-beta-catenin signaling 总被引:21,自引:0,他引:21
He XC Zhang J Tong WG Tawfik O Ross J Scoville DH Tian Q Zeng X He X Wiedemann LM Mishina Y Li L 《Nature genetics》2004,36(10):1117-1121
In humans, mutations in BMPR1A, SMAD4 and PTEN are responsible for juvenile polyposis syndrome, juvenile intestinal polyposis and Cowden disease, respectively. The development of polyposis is a common feature of these diseases, suggesting that there is an association between BMP and PTEN pathways. The mechanistic link between BMP and PTEN pathways and the related etiology of juvenile polyposis is unresolved. Here we show that conditional inactivation of Bmpr1a in mice disturbs homeostasis of intestinal epithelial regeneration with an expansion of the stem and progenitor cell populations, eventually leading to intestinal polyposis resembling human juvenile polyposis syndrome. We show that BMP signaling suppresses Wnt signaling to ensure a balanced control of stem cell self-renewal. Mechanistically, PTEN, through phosphatidylinosital-3 kinase-Akt, mediates the convergence of the BMP and Wnt pathways on control of beta-catenin. Thus, BMP signaling may control the duplication of intestinal stem cells, thereby preventing crypt fission and the subsequent increase in crypt number. 相似文献
10.
Free fatty acids regulate insulin secretion from pancreatic beta cells through GPR40 总被引:32,自引:0,他引:32
Itoh Y Kawamata Y Harada M Kobayashi M Fujii R Fukusumi S Ogi K Hosoya M Tanaka Y Uejima H Tanaka H Maruyama M Satoh R Okubo S Kizawa H Komatsu H Matsumura F Noguchi Y Shinohara T Hinuma S Fujisawa Y Fujino M 《Nature》2003,422(6928):173-176
Diabetes, a disease in which carbohydrate and lipid metabolism are regulated improperly by insulin, is a serious worldwide health issue. Insulin is secreted from pancreatic beta cells in response to elevated plasma glucose, with various factors modifying its secretion. Free fatty acids (FFAs) provide an important energy source as nutrients, and they also act as signalling molecules in various cellular processes, including insulin secretion. Although FFAs are thought to promote insulin secretion in an acute phase, this mechanism is not clearly understood. Here we show that a G-protein-coupled receptor, GPR40, which is abundantly expressed in the pancreas, functions as a receptor for long-chain FFAs. Furthermore, we show that long-chain FFAs amplify glucose-stimulated insulin secretion from pancreatic beta cells by activating GPR40. Our results indicate that GPR40 agonists and/or antagonists show potential for the development of new anti-diabetic drugs. 相似文献