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151.
Role of hippocampal M1 and M4 muscarinic receptor subtypes in memory consolidation in the rat 总被引:9,自引:0,他引:9
Ferreira AR Fürstenau L Blanco C Kornisiuk E Sánchez G Daroit D Castro e Silva M Cerveñansky C Jerusalinsky D Quillfeldt JA 《Pharmacology, biochemistry, and behavior》2003,74(2):411-415
Muscarinic receptors in the hippocampus are relevant to learning and memory, but the role of each subtype is poorly understood. Muscarinic toxins (MTs) from Dendroaspis snakes venom are selective for muscarinic receptor subtypes. MT2, a selective agonist for M(1) receptors, given into the hippocampus immediately after training, improved memory consolidation of an inhibitory avoidance task in rats, whereas the antagonist pirenzepine was amnestic, supporting a facilitatory role of M(1) receptors. Instead, MT3, a selective antagonist at M(4) receptors, caused amnesia. Neither M(1) nor M(4) receptor appeared involved in habituation to a new environment. Thus, our results suggest that memory consolidation of an inhibitory avoidance task in the rat involves the participation of both M(1) and M(4) hippocampal receptors, with a positive modulatory role. 相似文献
152.
G Bronzetti E Morichetti C Della Croce R Del Carratore L Giromini A Galli 《Mutagenesis》1990,5(3):293-295
Ammonium metavanadate was studied for its ability to induce mitotic gene conversion and reverse point mutation in the D7 strain of Saccharomyces cerevisiae. Metavanadate increased the convertant and revertant frequencies; the highest activity was observed without metabolic activation. This indicated that the S9 hepatic fraction and yeast cells in logarithmic phase (and containing a high level of cytochrome P450) biotransform vanadate, probably reducing it to vanadyl. In addition, the effect of ammonium metavanadate on the hepatic monooxygenase system was studied in mice by measuring the level of cytochrome P450 and determining the activities of aminopyrine N-demethylase, p-nitroanisole O-demethylase and 7-ethoxycoumarin O-deethylase in mouse liver microsomal fraction. The results indicated that this compound reduced mono-oxygenase activity and also the level of cytochrome P450. 相似文献
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154.
Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms. 下载免费PDF全文
Moira Crosier Luigi Viggiano Jane Guy Doriana Misceo Robert Stones Wenbin Wei Tom Hearn Mario Ventura Nicoletta Archidiacono Mariano Rocchi Michael S Jackson 《Genome research》2002,12(1):67-80
KIAA0187 is a gene of unknown function that maps to 10q11 and has been subject to recent duplication events. Here we analyze 18 human paralogs of this gene and show that paralogs of exons 14-23 were formed through satellite-associated pericentromeric-directed duplication, whereas paralogs of exons 1-9 were created via chromosome-specific satellite-independent duplications. In silico, Northern, and RT-PCR analyses indicate that nine paralogs are transcribed, including four in which KIAA0187 exons are spliced onto novel sequences. Despite this, no new genes appear to have been created by these events. The chromosome 10 paralogs map to 10q11, 10q22, 10q23.1, and 10q23.3, forming part of a complex family of chromosome-specific repeats that includes GLUD1, Cathepsin L, and KIAA1099 pseudogenes. Phylogenetic analyses and comparative FISH indicates that the 10q23.1 and 10q23.3 repeats were created in 10q11 and relocated by a paracentric inversion 13 to 27 Myr ago. Furthermore, the most recent duplications, involving the KIAA1099 pseudogenes, have largely been confined to 10q11. These results indicate a simple model for the evolution of this repeat family, involving multiple rounds of centromere-proximal duplication and dispersal through intrachromosomal rearrangement. However, more complex events must be invoked to account for high sequence identity between some paralogs. 相似文献
155.
Tiranti Valeria; Munaro Monica; Sandona Doriana; Lamantea Eleonora; Rimoldi Marco; DiDonato Stefano; Bisson Roberto; Zeviani Massimo 《Human molecular genetics》1995,4(11):2017-2023
Defects of the respiratory chain carrying out oxidative phosphorylation(OXPHOS) are the biochemical hallmark of human mitochondrialdisorders. Faulty OXPHOS can be due to mutations in either nuclearor mitochondrial genes, that are involved in the synthesis ofindividual respiratory subunits or in their post-translationalcontrol. The most common mitochondrial disorder of infancy andchildhood is Leigh's syndrome, a severe encephalopathy, oftenassociated with a defect of cytochrome c oxidase (COX). In orderto demonstrate which genome is primarily involved in COX-deficient(COX())-Leigh's syndrome, we generated two lines of transmitochondrialcybrids. The first was obtained by fusing nuclear DNA-less cytoplastsderived from normal fibroblasts, with mitochondrial DNA-less(rho°) transformant fibroblasts derived from a patient withCOX()-Leigh's syndrome. The second cybrid line was obtainedby fusing rho° cells derived from 143B.TK human osteosarcomacells, with cytoplasts derived from the same patient. The firstcybrid line showed a specific and severe COX(-) phenotype, whilein the second all the respiratory chain complexes, includingCOX, were normal. These results indicate that the COX defectin our patient is due to a mutation of a nuclear gene. The useof cybrids obtained from customized, patient-derivedrho° cells can have wide applications in the identificationof respiratory chain defects originated by nuclear DNAencodedmutations, and in the study of nuclear DNA-mitochondrial DNAinteractions. 相似文献
156.
Andrea S Melani Doriana Zanchetta Natalino Barbato Piersante Sestini Cristina Cinti Piero Aldo Canessa Stefano Aiolfi Margherita Neri 《Annals of allergy, asthma & immunology》2004,93(5):439-446
BACKGROUND: Pressurized metered-dose inhalers (pMDIs) are often poorly used, but little information is available concerning use of the newer dry powder inhalers (DPIs). OBJECTIVE: To estimate the inhalation technique and variables associated with the misuse of pMDIs and newer DPIs in clinical practice. METHODS: A multicenter, observational survey was used to evaluate the inhalation technique in 1,404 experienced outpatients aged 15 to 88 years affected mostly by asthma (47%) and chronic obstructive pulmonary disease (39%). A total of 1,056 patients were using pMDIs, 190 in conjunction with a large volume spacer (LVS); regarding DPIs, 230 patients were using the Aerolizer Inhaler, 524 were using the Turbuhaler, and 475 were using the Diskus. In each center, a trained observer recorded patients' inhalation techniques for each inhaler used against a standardized step-by-step checklist. RESULTS: Twenty-four percent and 3% of patients used pMDIs poorly, alone or with an add-on LVS, respectively. Failure to correctly perform essential steps for reliable lung delivery with the Aerolizer Inhaler, Turbuhaler, and Diskus was found in 17%, 23%, and 24% of patients, respectively. There was no difference in most variables correlated with poor inhalation between patients using pMDIs and those using DPIs. CONCLUSIONS: The use of DPIs is associated with a similar percentage of inadequate inhalation technique as the use of pMDIs in clinical practice. The addition of an LVS to a pMDI and education from health care personnel, rather than simply changing inhalers, represent the best strategies for minimizing poor inhalation technique. 相似文献
157.
Chun‐An Chen Emeline Crutcher Harinder Gill Tanya N. Nelson Laurie A. Robak Marjolijn C. J. Jongmans Rolph Pfundt Chitra Prasad Roberta A. Berard Madeleine Fannemel Eirik Frengen Doriana Misceo Keri Ramsey Yaping Yang Christian P. Schaaf Xia Wang 《Human mutation》2020,41(10):1738-1744
Congenital heart defects and skeletal malformations syndrome (CHDSKM) is a rare autosomal dominant disorder characterized by congenital heart disease, skeletal abnormalities, and failure to thrive. CHDSKM is caused by germline mutations in ABL1. To date, three variants have been in association with CHDSKM. In this study, we describe three de novo missense variants, c.407C>T (p.Thr136Met), c.746C>T (p.Pro249Leu), and c.1573G>A (p.Val525Met), and one recurrent variant, c.1066G>A (p.Ala356Thr), in six patients, thereby expanding the phenotypic spectrum of CHDSKM to include hearing impairment, lipodystrophy‐like features, renal hypoplasia, and distinct ocular abnormalities. Functional investigation of the three novel variants showed an increased ABL1 kinase activity. The cardiac findings in additional patients with p.Ala356Thr contribute to the accumulating evidence that patients carrying either one of the recurrent variants, p.Tyr245Cys and p.Ala356Thr, have a high incidence of cardiac abnormalities. The phenotypic expansion has implications for the clinical diagnosis of CHDSKM in patients with germline ABL1 variants. 相似文献
158.
Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B 下载免费PDF全文
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