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131.
132.
An evolutionarily conserved P‐subfamily pentatricopeptide repeat protein is required to splice the plastid ndhA transcript in the moss Physcomitrella patens and Arabidopsis thaliana 下载免费PDF全文
133.
Nokihara Kiyoshi Nagawa Yoshinobu Hong Seon-Pyo Nakanishi Hiroshi 《International journal of peptide research and therapeutics》1997,4(3):141-146
Summary Peptide chain assembly is now routinely performed by the use of automated synthesizers, although purification and characterization
of large peptides still requires knowledge and experience. Structural biology has recently become closely involved in molecular
recognition studies that often require the analysis of relatively large peptides using high-resolution NMR spectroscopy, for
which synthesis of high-quality peptides in 5–10 mg amounts is of prime importance. The present study describes a solid-phase
synthesis of a 7 kDa peptide related to the recently characterized ethylene-responsive element binding protein of tobacco,
which is the conserved sequence among these proteins. The rapid and efficient preparation was carried out through a single
coupling in combination with a single HPLC separation step. Assembly was performed in 63 h. Different coupling chemistries
were employed and compared, involving benzotriazol-1-yloxy-tris(pyrrolidino)phosphonium hexafluorophosphate, 1-hydroxy-7-azabenzotriazole
and/or the recently introduced reagent,N-[(dimethylamino)-1H-1,2,3-triazolo[4,5-b]pyridin-1-ylmethylene]-N-methylmethanaminium hexafluorophosphateN-oxide. After each synthesis, purified material was characterized by mass spectrometry, sequencing and enzymatic mapping and
shown to contain a high proportion of the desired peptide. 相似文献
134.
Cell Wall Peptidoglycan Mutants of Escherichia coli K-12: Existence of Two Clusters of Genes, mra and mrb, for Cell Wall Peptidoglycan Biosynthesis 总被引:32,自引:23,他引:9 下载免费PDF全文
Tokichi Miyakawa Hiroshi Matsuzawa Michio Matsuhashi Yoshinobu Sugino 《Journal of bacteriology》1972,112(2):950-958
Temperature-sensitive mutants of Escherichia coli K-12 which cannot form cell wall peptidoglycan at 42 C were isolated. The thermosensitive steps were characterized biochemically, and the genes coding the enzymes of peptidoglycan synthesis were mapped. These genes were in two clusters: one group, located at about 1.5 min between leu and azi, was designated as mra (murein a); the second group, located at about 77.5 min close to argH and metB, was designated as mrb (murein b, with the order metB-argH-mrb). No simple relations were found between the gene location and the order or localization of enzymes involved in the sequence of reactions of cell wall peptidoglycan biosynthesis. 相似文献
135.
A blue violet pigment was isolated in a crystalline state from the flowers ofPlatycodon grandiflorum A. DC. by the use of neutral solvents. The absorption spectrum of this pigment in buffer solution (pH 4.5) was almost identical with that of an intact tissue. The essential component of this pigment is platyconin, i.e., delphinidin 3-dicaffeoylrutinosido-5-glucoside. 相似文献
136.
Kita K Watanabe T Ohsaka K Hayashi H Kubota Y Nagashima Y Aoki I Taniguchi H Noce T Inoue K Miki H Ogonuki N Tanaka H Ogura A Ogawa T 《Biology of reproduction》2007,76(2):211-217
Testicular germ cell transplantation into the seminiferous tubules is at present the only way to induce spermatogenesis from a given source of spermatogonial stem cells. Here we show an alternative method that harnesses the self-organizing ability of testicular somatic cells. The testicular cells of embryonic or neonatal mice or rats and of newborn pigs were dissociated into single cells. Each of them reorganized into a tubular structure following implantation into the subcutis of immunodeficient mice. When mouse germline stem (GS) cells derived from spermatogonial stem cells and expanded in culture were intermingled with testicular cells of rodents, they were integrated in the reconstituted tubules and differentiated beyond meiosis into spermatids. Normal offspring were produced by the microinjection of those spermatids into oocytes. This method could be applicable to various mammalian species and useful for producing functional gametes from GS cells in a xenoectopic environment. 相似文献
137.
Masahiro Fukaya Kanta Ibuchi Takeyuki Sugawara Makoto Itakura Akiko Ito Tomoko Shiroshima Yoshinobu Hara Hirotsugu Okamoto Frédéric Luton Hiroyuki Sakagami 《Traffic (Copenhagen, Denmark)》2024,25(5):e12936
Endosomal trafficking of TrkA is a critical process for nerve growth factor (NGF)-dependent neuronal cell survival and differentiation. The small GTPase ADP-ribosylation factor 6 (Arf6) is implicated in NGF-dependent processes in PC12 cells through endosomal trafficking and actin cytoskeleton reorganization. However, the regulatory mechanism for Arf6 in NGF signaling is largely unknown. In this study, we demonstrated that EFA6A, an Arf6-specific guanine nucleotide exchange factor, was abundantly expressed in PC12 cells and that knockdown of EFA6A significantly inhibited NGF-dependent Arf6 activation, TrkA recycling from early endosomes to the cell surface, prolonged ERK1/2 phosphorylation, and neurite outgrowth. We also demonstrated that EFA6A forms a protein complex with TrkA through its N-terminal region, thereby enhancing its catalytic activity for Arf6. Similarly, we demonstrated that EFA6A forms a protein complex with TrkA in cultured dorsal root ganglion (DRG) neurons. Furthermore, cultured DRG neurons from EFA6A knockout mice exhibited disturbed NGF-dependent TrkA trafficking compared with wild-type neurons. These findings provide the first evidence for EFA6A as a key regulator of NGF-dependent TrkA trafficking and signaling. 相似文献
138.
Yoshio Goshima Tadashi Kawakami Hideaki Hori Yoshinobu Sugiyama Shuichi Takasawa Yoko Hashimoto Masako Kagoshima-Maezono Toshifumi Takenaka Yoshimi Misu Stephen M. Strittmatter 《Developmental neurobiology》1997,33(3):316-328
Chick collapsin-1, a member of the semaphorin family, has been implicated in axonal pathfinding as a repulsive guidance cue. Collapsin-1 induces growth cone collapse via a pathway which may include CRMP-62 and heterotrimeric G proteins. CRMP-62 protein is related to UNC-33, a nematode neuronal protein required for appropriately directed axonal extension. Mutations in unc-33 affect neural microtubules, the basic cytoskeletal elements for axoplasmic transport. Using computer-assisted video-enhanced differential interference contrast microscopy, we now demonstrate that collapsin-1 potently promotes axoplasmic transport. Collapsin-1 doubles the number of antero- and retrograde-transported organelles but not their velocity. Collapsin-1 decreases the number of stationary organelles, suggesting that the fraction of time during which a particle is moving is increased. Collapsin-1-stimulated transport occurs by a mechanism distinct from that causing growth cone collapse. Pertussis toxin (PTX) but not its B oligomer blocks collapsin-induced growth cone collapse. The holotoxin does not affect collapsin-stimulated axoplasmic transport. Mastoparan and a myelin protein NI-35 induce PTX-sensitive growth cone collapse but do not stimulate axoplasmic transport. These results provide evidence that collapsin has a unique property to activate axonal vesicular transport systems. There are at least two distinct pathways through which collapsin exerts its actions in developing neurons. © 1997 John Wiley & Sons, Inc. J Neurobiol 33: 316–328, 1997 相似文献
139.
Temporal and spatial changes in gene expression,metabolite accumulation and phytohormone content in rice seedlings grown under drought stress conditions 下载免费PDF全文
Daisuke Todaka Yu Zhao Takuya Yoshida Madoka Kudo Satoshi Kidokoro Junya Mizoi Ken‐Suke Kodaira Yumiko Takebayashi Mikiko Kojima Hitoshi Sakakibara Kiminori Toyooka Mayuko Sato Alisdair R. Fernie Kazuo Shinozaki Kazuko Yamaguchi‐Shinozaki 《The Plant journal : for cell and molecular biology》2017,90(1):61-78
140.
Bacteriorhodopsin (bR) is the prototype of an integral membrane protein with seven membrane-spanning α-helices and serves as a model of the G-protein-coupled drug receptors. This study is aimed at reaching a greater understanding of the role of amine local anesthetic cations on the proton transport in the bR protein, and furthermore, the functional role of “the cation” in the proton pumping mechanism. The effect of the amine anesthetic cations on the proton pump in the bR blue membrane was compared with those by divalent (Ca2+, Mg2+ and Mn2+) and monovalent metal cations (Li+, Na+, K+ and Cs+), which are essential for the correct functioning of the proton pumping of the bR protein. The results suggest that the interacting site of the divalent cation to the bR membrane may differ from that of the monovalent metal cation. The electric current profile of the bR blue membrane in the presence of the amine anesthetic cations was biphasic, involving the generation and inhibition of the proton pumping activity in a concentration-dependent manner. The extent of the regeneration of the proton pump by the additives increased in the order of monovalent metal cation<monovalent amine anesthetic cation<divalent metal cation. We found that organic cations such as the amine anesthetics can also regenerate the proton pump in the bR protein. The inhibition of proton transport in the bR protein by the anesthetic cations was elucidated using the wild type, the E204Q and the D96N mutated bRs. The hydrophobic interaction of the amine anesthetics with the bR protein plays an important part in inhibiting the bR proton pump. 相似文献