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961.
Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice. 总被引:11,自引:0,他引:11
Michael G Anderson Richard S Smith Norman L Hawes Adriana Zabaleta Bo Chang Janey L Wiggs Simon W M John 《Nature genetics》2002,30(1):81-85
Pigmentary glaucoma is a significant cause of human blindness. Abnormally liberated iris pigment and cell debris enter the ocular drainage structures, leading to increased intraocular pressure (IOP) and glaucoma. DBA/2J (D2) mice develop a form of pigmentary glaucoma involving iris pigment dispersion (IPD) and iris stromal atrophy (ISA). Using high-resolution mapping techniques, sequencing and functional genetic tests, we show that IPD and ISA result from mutations in related genes encoding melanosomal proteins. IPD is caused by a premature stop codon mutation in the Gpnmb (GpnmbR150X) gene, as proved by the occurrence of IPD only in D2 mice that are homozygous with respect to GpnmbR150X; otherwise, similar D2 mice that are not homozygous for GpnmbR150X do not develop IPD. ISA is caused by the recessive Tyrp1b mutant allele and rescued by the transgenic introduction of wildtype Tyrp1. We hypothesize that IPD and ISA alter melanosomes, allowing toxic intermediates of pigment production to leak from melanosomes, causing iris disease and subsequent pigmentary glaucoma. This is supported by the rescue of IPD and ISA in D2 eyes with substantially decreased pigment production. These data indicate that pigment production and mutant melanosomal protein genes may contribute to human pigmentary glaucoma. The fact that hypopigmentation profoundly alleviates the D2 disease indicates that therapeutic strategies designed to decrease pigment production may be beneficial in human pigmentary glaucoma. 相似文献
962.
高应变速率超塑性铝基材料的研究现状与展望 总被引:2,自引:0,他引:2
高应变速率超塑性是一个涉及先进制造技术和超细晶块体材料的高科技前沿研究领域 美国SuperformAluminium公司采用超塑成形技术使轿车重量减轻了一半 ,大大降低了油耗与排放 ,因此高应变速率超塑性铝基材料的研究对于今后有效地利用地球资源和减少地球环境污染具有重要的现实意义 应变速率太低和成本太高是今后超塑性先进制造技术和超细晶块体材料大规模实用化进程中必须解决的关键问题 本文综述了国内外超塑性铝基复合材料和铝合金的制备、性能及变形机理的研究现状 ,指出了加快铸造法低成本制备高应变速率超塑性铝合金研究的迫切性 ,并展望了该材料在 2 1世纪的应用前景 相似文献
963.
块体纳米材料的研究现状与发展思路 总被引:3,自引:0,他引:3
块体纳米材料的制备技术及性能研究 ,是当前纳米材料领域内的一个热点 块体纳米材料具有奇异的结构和特殊性能 ,其在力学、电学、光学和磁学等方面发生了巨大的变化 文中较为详细地介绍了国内外块状纳米材料的制备技术 针对块体纳米材料加工过程中存在热稳定性及致密性等两个主要问题进行了探讨 ,提出了通过加入第二相微粒、强烈塑性加工措施来改善块体纳米材料的热稳定性 ;采用烧结、挤压辅助工艺来提高块体纳米材料的致密性的方案 相似文献
964.
为获得眼镜王蛇(Ophiophagus hannah,简称Oh)蛇毒α-神经毒素(α-NT)的基因序列,依据眼镜蛇科不同毒蛇种类来源的α-NT基因有较高的同源性,设计1对上下游引物,为克服引物带来模糊扩增,在蛋白编码部分再设计1对上下游特异引物,用Nacleospin RNA Kit法从3条活眼镜王蛇毒腺中提取mRNA,以3′端引物合成的cDNA作为模板进行PCR扩增反应,测定产物的核苷酸序列,得到全长474bp的眼镜王蛇cDNA基因核苷酸序列。该核苷酸序列的信号肽与眼镜蛇树属Pseudonnaja textilis(Pt)、海蛇Laticauda semifasciata(Ls)100%同源,与眼镜蛇南洋亚种Naja sputatrix (Ns)、银环蛇(Bungarus multicinctus)(Bm)96.8%同源;蛋白密码部分有83.3%与Ns、79.2%与Pt、76.4%与Ls、74.1%与Bm同源。信号肽后紧接着的72个氨基酸有90.3%与已发现的眼镜王蛇毒长链α-NT Toxin a同源,大约有73.6%与Toxin b、69.7%与Oh-4、66.7%与Oh-5、56.9%与Oh-6A和6B同源,并与α-银环蛇毒素54.2%同源。说明新发现的眼镜王蛇cDNA是一条长链α-NT基因。 相似文献
965.
Altruistic punishment in humans. 总被引:66,自引:0,他引:66
Human cooperation is an evolutionary puzzle. Unlike other creatures, people frequently cooperate with genetically unrelated strangers, often in large groups, with people they will never meet again, and when reputation gains are small or absent. These patterns of cooperation cannot be explained by the nepotistic motives associated with the evolutionary theory of kin selection and the selfish motives associated with signalling theory or the theory of reciprocal altruism. Here we show experimentally that the altruistic punishment of defectors is a key motive for the explanation of cooperation. Altruistic punishment means that individuals punish, although the punishment is costly for them and yields no material gain. We show that cooperation flourishes if altruistic punishment is possible, and breaks down if it is ruled out. The evidence indicates that negative emotions towards defectors are the proximate mechanism behind altruistic punishment. These results suggest that future study of the evolution of human cooperation should include a strong focus on explaining altruistic punishment. 相似文献
966.
Sox9 induces testis development in XX transgenic mice. 总被引:18,自引:0,他引:18
Mutations in SOX9 are associated with male-to-female sex reversal in humans. To analyze Sox9 function during sex determination, we ectopically expressed this gene in XX gonads. Here, we show that Sox9 is sufficient to induce testis formation in mice, indicating that it can substitute for the sex-determining gene Sry. 相似文献
967.
968.
L Feliubadaló M Font J Purroy F Rousaud X Estivill V Nunes E Golomb M Centola I Aksentijevich Y Kreiss B Goldman M Pras D L Kastner E Pras P Gasparini L Bisceglia E Beccia M Gallucci L de Sanctis A Ponzone G F Rizzoni L Zelante M T Bassi A L George M Manzoni A De Grandi M Riboni J K Endsley A Ballabio G Borsani N Reig E Fernández R Estévez M Pineda D Torrents M Camps J Lloberas A Zorzano M Palacín 《Nature genetics》1999,23(1):52-57
969.
A I den Hollander J B ten Brink Y J de Kok S van Soest L I van den Born M A van Driel D J van de Pol A M Payne S S Bhattacharya U Kellner C B Hoyng A Westerveld H G Brunner E M Bleeker-Wagemakers A F Deutman J R Heckenlively F P Cremers A A Bergen 《Nature genetics》1999,23(2):217-221
Retinitis pigmentosa (RP) comprises a clinically and genetically heterogeneous group of diseases that afflicts approximately 1.5 million people worldwide. Affected individuals suffer from a progressive degeneration of the photoreceptors, eventually resulting in severe visual impairment. To isolate candidate genes for chorioretinal diseases, we cloned cDNAs specifically or preferentially expressed in the human retina and the retinal pigment epithelium (RPE) through a novel suppression subtractive hybridization (SSH) method. One of these cDNAs (RET3C11) mapped to chromosome 1q31-q32.1, a region harbouring a gene involved in a severe form of autosomal recessive RP characterized by a typical preservation of the para-arteriolar RPE (RP12; ref. 3). The full-length cDNA encodes an extracellular protein with 19 EGF-like domains, 3 laminin A G-like domains and a C-type lectin domain. This protein is homologous to the Drosophila melanogaster protein crumbs (CRB), and denoted CRB1 (crumbs homologue 1). In ten unrelated RP patients with preserved para-arteriolar RPE, we identified a homozygous AluY insertion disrupting the ORF, five homozygous missense mutations and four compound heterozygous mutations in CRB1. The similarity to CRB suggests a role for CRB1 in cell-cell interaction and possibly in the maintenance of cell polarity in the retina. The distinct RPE abnormalities observed in RP12 patients suggest that CRB1 mutations trigger a novel mechanism of photoreceptor degeneration. 相似文献
970.
把区间算法与正割算法相结合,给出了一种新的区间正割算法.并证明了其收敛性与Newton法相比,具有收敛快,误差小的优点,算例证明了其有效性. 相似文献