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101.
Identification of ten loci associated with height highlights new biological pathways in human growth 总被引:1,自引:0,他引:1
Lettre G Jackson AU Gieger C Schumacher FR Berndt SI Sanna S Eyheramendy S Voight BF Butler JL Guiducci C Illig T Hackett R Heid IM Jacobs KB Lyssenko V Uda M;Diabetes Genetics Initiative;FUSION;KORA;Prostate Lung Colorectal Ovarian Cancer Screening Trial;Nurses' Health Study;SardiNIA Boehnke M Chanock SJ Groop LC Hu FB Isomaa B Kraft P Peltonen L Salomaa V Schlessinger D Hunter DJ Hayes RB Abecasis GR Wichmann HE Mohlke KL Hirschhorn JN 《Nature genetics》2008,40(5):584-591
Height is a classic polygenic trait, reflecting the combined influence of multiple as-yet-undiscovered genetic factors. We carried out a meta-analysis of genome-wide association study data of height from 15,821 individuals at 2.2 million SNPs, and followed up the strongest findings in >10,000 subjects. Ten newly identified and two previously reported loci were strongly associated with variation in height (P values from 4 x 10(-7) to 8 x 10(-22)). Together, these 12 loci account for approximately 2% of the population variation in height. Individuals with < or =8 height-increasing alleles and > or =16 height-increasing alleles differ in height by approximately 3.5 cm. The newly identified loci, along with several additional loci with strongly suggestive associations, encompass both strong biological candidates and unexpected genes, and highlight several pathways (let-7 targets, chromatin remodeling proteins and Hedgehog signaling) as important regulators of human stature. These results expand the picture of the biological regulation of human height and of the genetic architecture of this classical complex trait. 相似文献
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Microtubules of the mitotic spindle form the structural basis for chromosome segregation. In metaphase, microtubules show high dynamic instability, which is thought to aid the 'search and capture' of chromosomes for bipolar alignment on the spindle. Microtubules suddenly become more stable at the onset of anaphase, but how this change in microtubule behaviour is regulated and how important it is for the ensuing chromosome segregation are unknown. Here we show that in the budding yeast Saccharomyces cerevisiae, activation of the phosphatase Cdc14 at anaphase onset is both necessary and sufficient for silencing microtubule dynamics. Cdc14 is activated by separase, the protease that triggers sister chromatid separation, linking the onset of anaphase to microtubule stabilization. If sister chromatids separate in the absence of Cdc14 activity, microtubules maintain high dynamic instability; this correlates with defects in both the movement of chromosomes to the spindle poles (anaphase A) and the elongation of the anaphase spindle (anaphase B). Cdc14 promotes localization of microtubule-stabilizing proteins to the anaphase spindle, and dephosphorylation of the kinetochore component Ask1 contributes to both the silencing of microtubule turnover and successful anaphase A. 相似文献
106.
Apolipoprotein-mediated pathways of lipid antigen presentation 总被引:1,自引:0,他引:1
van den Elzen P Garg S León L Brigl M Leadbetter EA Gumperz JE Dascher CC Cheng TY Sacks FM Illarionov PA Besra GS Kent SC Moody DB Brenner MB 《Nature》2005,437(7060):906-910
Peptide antigens are presented to T cells by major histocompatibility complex (MHC) molecules, with endogenous peptides presented by MHC class I and exogenous peptides presented by MHC class II. In contrast to the MHC system, CD1 molecules bind lipid antigens that are presented at the antigen-presenting cell (APC) surface to lipid antigen-reactive T cells. Because CD1 molecules survey endocytic compartments, it is self-evident that they encounter antigens from extracellular sources. However, the mechanisms of exogenous lipid antigen delivery to CD1-antigen-loading compartments are not known. Serum apolipoproteins are mediators of extracellular lipid transport for metabolic needs. Here we define the pathways mediating markedly efficient exogenous lipid antigen delivery by apolipoproteins to achieve T-cell activation. Apolipoprotein E binds lipid antigens and delivers them by receptor-mediated uptake into endosomal compartments containing CD1 in APCs. Apolipoprotein E mediates the presentation of serum-borne lipid antigens and can be secreted by APCs as a mechanism to survey the local environment to capture antigens or to transfer microbial lipids from infected cells to bystander APCs. Thus, the immune system has co-opted a component of lipid metabolism to develop immunological responses to lipid antigens. 相似文献
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Zusammenfassung Es wird die Synthese von Diazoacetyl-cholin-bromid beschrieben. Die Verbindung zeigt in verschiedenen biologischen Präparaten starke acetyl-cholin-ähnliche Wirkung; sie wird von Acetylcholinesterase etwa 1.6×104 mal langsamer als Acetylcholiniodid hydrolysiert. Die Photolyse gelingt mit Wellenlängen grösser als 315 nm. Das hauptsächliche Photolyseprodukt in Wasser ist Hydroxyacetyl-cholin-bromid. Es scheint — entsprechend dem stark elektronegativen Charakter der Trimethylammoniumgruppe — dieWolff'sche Umlagerung nur in untergeordnetem Masse einzutreten. Aufgrund dieser Befunde soll die Eignung der Verbindung zur Affinitätsmarkierung von Acetylcholinesterase, Cholinacetyltransferase und von Rezeptormolekeln untersucht werden. 相似文献
108.
H. Baker O. Frank S. H. Hutner S. Aaronson H. Ziffer H. Sobotka 《Cellular and molecular life sciences : CMLS》1962,18(5):224-226
Résumé Les auteurs ont étudié le mécanisme de la toxicité de la primidone (Mysoline) chez certains microorganismes. Ces recherches montrent que le métabolisme de l'acide folique est inhibé par le primidone et cela en trois étapes: (a) la réduction de l'acide folique en acide dihydrofolique, (b) le métabolisme des ptéridines nonconjugées et (c) la phosphorylation de la thymidine.
This work was aided by grants from the National Vitamin Foundation, National Association for Mental Health, American Cancer Society, and U.S. Public Health Service. We thank Dr.Th. Robitcher, Ayerst Laboratories, New York, for aid and gifts of primidone and Dr.E. Patterson of the American Cyanamid Co., Pearl River, New York, for the gifts of unconjugated pteridine. 相似文献
This work was aided by grants from the National Vitamin Foundation, National Association for Mental Health, American Cancer Society, and U.S. Public Health Service. We thank Dr.Th. Robitcher, Ayerst Laboratories, New York, for aid and gifts of primidone and Dr.E. Patterson of the American Cyanamid Co., Pearl River, New York, for the gifts of unconjugated pteridine. 相似文献
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Hoogenraad CC Koekkoek B Akhmanova A Krugers H Dortland B Miedema M van Alphen A Kistler WM Jaegle M Koutsourakis M Van Camp N Verhoye M van der Linden A Kaverina I Grosveld F De Zeeuw CI Galjart N 《Nature genetics》2002,32(1):116-127
Williams syndrome is a neurodevelopmental disorder caused by the hemizygous deletion of 1.6 Mb on human chromosome 7q11.23. This region comprises the gene CYLN2, encoding CLIP-115, a microtubule-binding protein of 115 kD. Using a gene-targeting approach, we provide evidence that mice with haploinsufficiency for Cyln2 have features reminiscent of Williams syndrome, including mild growth deficiency, brain abnormalities, hippocampal dysfunction and particular deficits in motor coordination. Absence of CLIP-115 also leads to increased levels of CLIP-170 (a closely related cytoplasmic linker protein) and dynactin at the tips of growing microtubules. This protein redistribution may affect dynein motor regulation and, together with the loss of CLIP-115-specific functions, underlie neurological alterations in Williams syndrome. 相似文献