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61.
Johannes F. Scheid Christopher O. Barnes Basak Eraslan Andrew Hudak Jennifer R. Keeffe Lisa A. Cosimi Eric M. Brown Frauke Muecksch Yiska Weisblum Shuting Zhang Toni Delorey Ann E. Woolley Fadi Ghantous Sung-Moo Park Devan Phillips Betsabeh Tusi Kathryn E. Huey-Tubman Alexander A. Cohen Ramnik J. Xavier 《Cell》2021,184(12):3205-3221.e24
62.
Xuan He Abishek Chandrashekar Roland Zahn Frank Wegmann Jingyou Yu Noe B. Mercado Katherine McMahan Amanda J. Martinot Cesar Piedra-Mora Sidney Beecy Sarah Ducat Ronnie Chamanza Sietske Rosendahl Huber Marjolein van Heerden Leslie van der Fits Erica N. Borducchi Michelle Lifton Jinyan Liu Dan H. Barouch 《Cell》2021,184(13):3467-3473.e11
63.
《Biocatalysis and Biotransformation》2013,31(1-4):329-341
The reduction of six derivatives of benzaldehyde, α,α,α-trifluorotolualdehyde, nitrobenzaldehyde, anisaldehyde, fluorobenzaldehyde, tolualdehyde, chlorobenzaldehyde, each of which was substituted in the ortho-, meta- and para-positions, was investigated in whole cell yeast biotransformations conducted in non-conventional media. Correlation between hydrophobic (π) and electronic (σ) parameters of the substituent of the substrate and biocatalytic activity in organic solvent media (hexane containing 2% v/v water) was evaluated. While catalytic activity in general decreased as the substituent hydrophobicity (π) increased, the trend was more pronounced for ortho- substituents compared to meta- and para-. When the electronic parameters (σ) of the meta- and para- substituents were correlated with the catalytic activity, the opposite was observed, namely the catalytic activity increased as the electronic parameter of the substituent increased. This observation was similar for meta- and para- substituents.Preliminary studies on the relationships between solvent and substrate polarity on the one hand and catalytic activity on the other are also presented and discussed. 相似文献
64.
Hyang Jee Su-Hyung Lee Jun-Won Park Bo-Ram Lee Ki-Taek Nam Dae-Yong Kim 《BMB reports》2013,46(1):25-30
Gap junctions and their structural proteins, connexins (Cxs), have been implicated in carcinogenesis. To explore the involvement of Cx32 in gastric carcinogenesis, immunochemical analysis of Cx32 and proliferation marker Ki67 using tissue-microarrayed human gastric cancer and normal tissues was performed. In addition, after Cx32 overexpression in the human gastric cancer cell line AGS, cell proliferation, cell cycle analyses, and p21Cip1 and p27Kip1 expression levels were examined by bromodeoxyuridine assay,
flow cytometry, real-time RT-PCR, and western blotting. Immunohistochemical study noted a strong inverse correlation between Cx32 and Ki67 expression pattern as well as their
location. In vitro, overexpression of Cx32 in AGS cells inhibited cell proliferation significantly. G1 arrest, up-regulation of cell cycle-regulatory proteins p21Cip1 and p27Kip1 was also found at both mRNA and protein levels. Taken together, Cx32 plays some roles in gastric cancer development by inhibiting gastric cancer cell proliferation through cell cycle arrest and cell cycle regulatory proteins. [BMB Reports 2013; 46(1): 25-30] 相似文献
65.
66.
After E. coli cells (WP2 and WP2uvrA) were treated with chemical mutagens (methyl methanesulfonate, MMS; N-methyl-N-nitrosourea, MNU; 4-nitroquinoline 1-oxide, 4NQO) in 1/15 M phosphate buffer, the mutability of the treated cells plated on a D2O-agar plate was compared with that plated on an ordinary H2O-agar plate. The mutation frequency decreased more or less on the D2O-agar plate. The D2O-substitution effects, as termed by the relative mutation frequencies (MFD2O/MFH2O), are 0.92 for MMS, 0.29 for MNU, and 0.42 for 4NQO in WP2, and 0.68 for MMS, 0.49 for MNU, and 0.16 for 4NQO in WP2uvrA. The D2O effect seemed to be partly related to the function of the uvrA gene-associated products. The pH dependence of mutability was discussed in connection with the D2O-substitution effect. 相似文献
67.
Résumé L'ultrastructure générale des cellules K endométriales est semblable chez l'Homme, le Rat et le Singe. Mais les granulations des cellules K humaines sont plus variées que dans ces deux dernières espèces et ont certains aspects suggérant une fonction catabolique.Etant donné cet aspect catabolique et l'existence connue d'une activité phosphatasique acide de ces cellules contenant de la relaxine, les auteurs suggèrent que les cellules K pourraient être des cellules sécrétantes en involution et ques les cellules sécrétant activement la relaxine pourraient avoir un aspect morphologique quelque peu différent de celui des cellules K.
Ultrastructure of the normal human endometriumIII. The endometrial granular stroma cells
Summary The general ultrastructure of endometrial granular stroma cells is similar in man, rat, and monkey. But the granulations of human granular stroma cells are more various than in these two last species and have some aspects suggesting a catabolic function.With respect to this catabolic aspect and the previously shown acid-phosphatase activity of these relaxin-containing cells the authors suggest that the granular stroma cells could be involutive secretory cells and that the active relaxin-secretory cells may have some different morphological aspect.相似文献
68.
In this work we describe not previously explored binding studies on the reversible interaction of benzoxaborole with ligands of medical and pharmaceutical interest such as nucleosidic drugs gemcitabine and capecitabine, as well as the hydrophobic chemotherapeutic doxorubicin. We include functional derivatives of benzoxaborole such as a near infrared fluorescent boronolectine, Cy-Bx, The dynamic covalent interaction in physiological conditions was assessed by spectroscopic techniques yielding moderate to high binding affinities. The cytotoxic activity of the drugs upon conjugation to the boronolectins was evaluated revealing significant influence of the bioconjugation status on the cellular viability. The availability of the conjugate for cellular uptake and localization in the model cancer cell line HeLa was assessed by fluorescence imaging. Benzoxaborole and the fluorescent boronolectin Cy-Bx, proved to be versatile conjugation tools for 1,2 and 1,3-diol containing pharmacophores as well as bioisosteric forms such as 1,2-hydroxyamino, envisioning these small boronolectins as components in systems for drug release with tracking capability. 相似文献
69.
Takeshi Kawamura Noriyuki Kuroda Yuko Kimura Eliada Lazoura Noriko Okada Hidechika Okada 《Biochemical genetics》2001,39(1-2):33-42
We examined embryonic carcinoma (EC) cells for a potential prototype molecule of C3, the third component of complement. PCR primers, corresponding to the base sequence derived from the C3 cDNA of several species, were used for PCR amplification of the EC cell cDNA. All the PCR products obtained had the same sequence and showed no sequence homology to C3. Subsequently, cDNA clones were isolated from a mouse liver cDNA library using the PCR product as a probe. Unexpectedly, neither the base sequence of the cDNA clones nor the amino acid sequence deduced from the cDNA showed homology to C3, although partial homology was observed to a number of sequences from EST databases. We designated this new clone NCU-G1. Northern hybridization experiments revealed that NCU-G1 is expressed constitutively not only in the mouse fetus but also in various mouse tissues, and is most abundant in the kidney cortex. 相似文献
70.
J. Denry Sato Hui-Ting Gao Yoshiaki Kayada Myles C. Cabot Gordon H. Sato Tetsuji Okamoto Clement J. Welsh 《In vitro cellular & developmental biology. Plant》1988,24(12):1223-1228
Summary The proximate cholesterol precursors lathosterol, 7-dehydrocholesterol and desmosterol supported the growth of NS-1 and X63
mouse myeloma cells. These cells and X63.653 cells are cholesterol auxotrophs, yet each was able to convert [3H]lathosterol to [3H]cholesterol. These results are consistent with the conclusion that cholesterol auxotrophy in these myeloma cells is due
to a deficiency in 3-ketosteroid reductase activity. The steroid hormones testosterone, progesserone and hydrocortisone could
not replace cholesterol as a medium supplement. These results provide a greater understanding of the cholesterol auxotrophy
characteristic of cell lines clonally-derived from the MOPC 21 myeloma tumor, and they provide a rational basis for the use
of sterols in defined culture medium for mouse myeloma cells.
This work was supported by National Institute of Health grants CA40294 and CA37589 to G. H. Sato and by a grant from RJR nabisco
Inc.
Editor's Statement These results help identify the defect in myeloma cells leading to cholesterol auxotrophy. The use of these
cells in hybridoma derivation adds practical utility to a detailed appreciation of cholesterol metabolism in these cultures. 相似文献