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31.
古尔班通古特沙漠钠猪毛菜种子异型性及其萌发行为研究   总被引:1,自引:0,他引:1  
王梦茹  魏岩 《草业学报》2019,28(3):85-92
钠猪毛菜在我国仅分布在新疆,具有很强的抗干旱和抗盐碱能力。研究钠猪毛菜不同类型种子形态及其萌发特性,结果表明,钠猪毛菜产生3种类型的种子,其形态特征、萌发特性均有显著差异。A型种子绿色,圆形,着生方式为横生,直径为(1.294±0.089) mm,百粒重(90.71±0.42) mg,花被背部有翅状附属物;B型种子红色,圆形,着生方式为直立,直径为(1.166±0.069) mm,百粒重(85.52±0.49) mg,花被背部有短/无翅状附属物;C型种子黄色,圆形,着生方式为直立,直径为(1.044±0.062) mm,百粒重(83.84±0.31) mg,花被背部无翅状附属物。A型种子在5 ℃/15 ℃、10 ℃/20 ℃、 15 ℃/25 ℃、 20 ℃/30 ℃、 25 ℃/35 ℃(光/暗=12 h/12 h)变温条件下萌发率均>92%,B型种子在5种变温条件下萌发率<60%,为非深度生理休眠,低温层积2周后可打破休眠;C型种子在5种变温条件下萌发率<5.3%,为深度生理休眠,划破种皮可打破休眠。浓度低于0.2 mol·L-1的NaCl溶液对A型种子萌发的影响不大,但从0.8 mol·L-1起,萌发率随着浓度增高而降低,直至为零,将在0.05~4.00 mol·L-1NaCl溶液中处理的A型种子转移至蒸馏水后,仍有一定的恢复萌发率。苞片延缓A型种子吸胀,影响种子的最终萌发率,去除苞片可显著提高种子的萌发率。通过研究钠猪毛菜种子异型性及其萌发行为,为揭示其生态适应机制提供科学依据,并为新疆荒漠地区生态建设提供基础资料。  相似文献   
32.
Resource polymorphism may play an important role in the process of speciation. The Arctic char (Salvelinus alpinus) exhibits great phenotypic and genetic diversity across its range, making it an ideal species for studies of resource polymorphism and divergence. Here, we investigated genetic variation at 11 microsatellite loci among 287 Arctic char from five isolated yet proximate postglacial lakes in south‐western Alaska that were previously examined for resource polymorphism. Significant differences in pairwise FST were detected among all lakes (range from 0.05 to 0.28, all < 0.02). In one lake (Lower Tazimina Lake), we found evidence for two genetic groups of char and for significant differences in the distribution of microsatellite variability among at least two of the three previously described body size morphotypes (‘large’‐, ‘medium’‐, and ‘small’‐bodied char; maximum FST = 0.09; differences in admixture proportions). We also found a significant association between genetic admixture proportions and gill raker counts among body size morphs (r = ?0.73, < 0.001). Our data represent the first record of genetically distinct sympatric morphs of Arctic char in Alaska and provide further evidence that differences in morphology associated with feeding (gill rakers) and growth trajectories reflect niche diversification and promote genetic divergence in Holarctic populations of Arctic char.  相似文献   
33.
棉花单核苷酸多态性标记研究进展   总被引:1,自引:0,他引:1  
单核苷酸多态性标记已在农作物研究中得到广泛应用并取得重大进展。为了便利棉花SNP(Single nucleotide polymorphism)标记的研究和应用,介绍了利用基因芯片、简化基因组测序、重测序等在棉花中开发SNP标记的方法 ,综述了SNP标记在棉花遗传图谱构建、数量位点的定位和分子标记辅助育种、基因组测序以及系统进化等研究中的应用。并对异源四倍体棉花中SNP标记开发时,同源序列位点和部分同源序列位点上的SNP标记辨别问题进行了系统探讨,对其快捷的开发、检测方式和在数量基因定位中的应用前景进行了展望。  相似文献   
34.
We analyzed the nuclear ribosomal internal transcribed spacer (ITS) 1 and ITS2 sequences for Bangladesh isolates of Ascaridia galli, and we determined that the sequences were unreliable as molecular markers for distinguishing A. galli from other Ascaridia species, because the sequences showed high identity with that of A. columbae. However, the ITS1 sequences were available for designing PCR primers distinguishable between Ascaridia galli and Heterakis spp. Bangladesh isolates of A. galli constituted a monophyletic clade along with other geographical isolates in the cytochrome c oxidase subunit I (COI) phylogenetic tree, however, we could not clarify the phylogenetic relationships between A. galli and other Ascaridia spp., because their available sequences in GenBank were very few. The developed PCR method using DNA from A. galli and Heterakis spp. eggs would enable differential diagnosis of the individual infections in the future.  相似文献   
35.
试验旨在研究肌肉生长抑制素(myostatin,MSTN)基因多态性及其对东佛里生羊生长性状的影响。从324只东佛里生羊全血中提取DNA,对MSTN基因外显子序列和非翻译区(untranslated region,UTR)序列进行PCR扩增,采用一代测序技术鉴定单核苷酸多态性(single nucleotide polymorphism,SNP)位点,分析不同位点的遗传多态性,并将不同基因型与东佛里生羊的生长性状进行关联分析。结果显示,在东佛里生羊MSTN基因外显子中未检测到突变;在3'-UTR区的272 bp处存在G→A单碱基突变,该位点只检测到AG和AA基因型,且AA基因型频率高于AG基因型;在5'-UTR区的176 bp处存在C→A突变,该位点只检测到CC和AC基因型,且CC基因型频率高于AC基因型。遗传多样性参数分析结果表明,东佛里生羊群体MSTN基因3'-UTR-272和5'-UTR-176位点的纯合度分别为0.827和0.887,杂合度分别为0.173和0.113,2个位点的多态性均较低(PIC<0.25),其群体基因型分布均符合哈代-温伯格平衡(P>0.05)。关联分析发现,3'-UTR-272位点AG基因型体斜长显著高于AA基因型(P<0.05),5'-UTR-176位点CC基因型胸围显著高于AC基因型(P<0.05),其余指标均无显著差异(P>0.05)。综上,东佛里生羊MSTN基因3'-UTR和5'-UTR突变位点可作为其目标性状选育的分子标记。  相似文献   
36.
为探究寡腺苷酸合成酶1(oligoadenylate synthase 1,OAS1)基因多态性与松辽黑猪繁殖性状的关联性,试验选取130头松辽黑猪母猪为研究对象,利用Sanger直接测序法测序查找OAS1基因外显子1~8的SNP位点,使用SPSS 19.0软件分析OAS1基因SNP位点与松辽黑猪繁殖性状的关联性。结果显示,在松辽黑猪OAS1基因外显子2、3和6上共检测到33个突变位点;其中在外显子2的110 bp处存在1个SNP位点(G110C),存在3种基因型:GG、GC和CC;在外显子3的176 bp处存在1个SNP位点(C176T),存在3种基因型:CC、CT和TT;在外显子6的145 bp处存在1个SNP位点(C145T),存在3种基因型:CC、CA和AA;在166 bp处存在1个SNP位点(G166A),存在3种基因型:GG、GA和AA;在206 bp处存在1个SNP位点(A206G),存在3种基因型:AA、AG和GG。卡方适合性检验结果显示,松辽黑猪OAS1基因G110C突变位点符合Hardy-Weinberg平衡状态,C176T、C145A、G166A和G206A位点均偏离Hardy-Weinberg平衡状态。群体遗传参数分析结果显示,各SNPs位点遗传杂合度均位于中等水平,为中度多态(0.25<PIC<0.5)。关联分析结果发现,G110C位点GC基因型个体总产仔数、产活仔数和断奶仔猪数均显著高于GG基因型个体(P<0.05);C176T位点CT基因型个体断奶仔猪数显著高于CC基因型个体(P<0.05);C145T位点CC基因型个体总产仔数和产活仔数均显著高于AA基因型个体(P<0.05);G166A位点GA基因型个体断奶仔猪数显著高于GG基因型个体(P<0.05);A206G位点GG基因型个体总产仔数和产活仔数显著高于AA基因型个体(P<0.05)。结果表明,OAS1基因外显子区存在突变位点,对松辽黑猪部分繁殖性状有显著性影响。  相似文献   
37.
The paper was aimed to investigate the polymorphism of copy number variation (CNV) in different pig breeds.Three CNV regions of CNVR91,CNVR92 and CNVR143 were chosen from the porcine SNP60 chip genotyping results.The polymorphisms of three CNVs were determined by Real-time quantitative PCR method,taking five pig breeds as samples,including Yorkshire pig,Xiang pig,Kele pig,Nuogu pig and Rongchang pig breeds.The results showed that the dominant status of CNVR91 was loss in Xiang pig,while it was normal in other four pig breeds.The major type of CNVR92 was deletion in Xiang pig,Yorkshire pig,Kele pig and Rongchang pig breeds,with a high normal percent in Nuogu pig.For CNVR143,the dominant event was gain in Xiang pig and Nuogu pig breeds,but it was not diverse in other three pig breeds.These results indicated that three CNV regions emerged with polymorphism in five pig breeds,which might have effects on gene expression in CNV regions and physiological function by dosage effect especially in Xiang pig,Nuogu pig and Kele pig breeds.  相似文献   
38.
This study was aimed to understand the characteristics of length polymorphism with repeat sequence of keratin associated protein 1 (KAP1) family genes in yak. KAP1 family genes of yak and cattle were sequenced, and compared with sheep KAP1 family gene sequences. The results showed that cattle KAP1 family genes were located in chromosome 19, according to location of sheep KAP1 family genes in the chromosome and similarity with cattle KAP1 family genes, renaming the cattle KAP1 family (according to the gene location of chromosome) B2D, B2A, KAP1-1 and B2C genes into KAP1-4, KAP1-1, KAP1-2 and KAP1-3 gene, respectively. KAP1 family genes in the 3'and 5' flank were highly conserved, the difference between family genes mainly in the the repeat sequence region, which yak KAP1 to KAP4 genes were found 30 bp length polymorphism. There were B(CCQTS)A1(CCQPT) repeat sequence and a new repeat sequence C(SIQTS). The results indicated that the repeat sequence was the key of the polymorphism of KAP1 family genes, which might be relate to combination with keratin protein.  相似文献   
39.
Using target and reference fattened steer populations, the performance of genotype imputation using lower‐density marker panels in Japanese Black cattle was evaluated. Population imputation was performed using BEAGLE software. Genotype information for approximately 40 000 single nucleotide polymorphism (SNP) markers by Illumina BovineSNP50 BeadChip was available, and imputation accuracy was assessed based on the average concordance rates of the genotypes, varying equally spaced SNP densities, and the number of individuals in the reference population. Two additional statistics were also calculated as indicators of imputation performance. The concordance rates tended to be lower for SNPs with greater minor allele frequencies, or those located near the ends of the chromosomes. Longer autosomes yielded greater imputation accuracies than shorter ones. When SNPs were selected based on linkage disequilibrium information, relative imputation accuracy was slightly improved. When 3000 and 10 000 equally spaced SNPs were used, the imputation accuracies were greater than 90% and approximately 97%, respectively. These results indicate that combining genotyping using a lower‐density SNP chip with genotype imputation based on a population of individuals genotyped using a higher‐density SNP chip is a cost‐effective and valid approach for genomic prediction.  相似文献   
40.
Mouse Double Minute‐2 (MDM2) is an ubiquitin ligase which is overexpressed or its promoter polymorphism has been reported in different tumours. The objective of this study was to examine the MDM2 protein expression and its promoter polymorphism in some canine tumours. Twenty specimens were collected from 20 dogs with 15 mammary gland carcinomas, 3 lymphomas, 1 transmissible venereal tumour and 1 trichoblastoma. Samples were analysed immunohistochemically using human antibody against MDM2 protein. PCR and DNA sequencing were carried out to identify MDM2 promoter polymorphism. MDM2 gene was expressed in 13 of 20 samples including 11 mammary carcinomas, 1 lymphoma and 1 trichoblastoma. We found 94% homology between canine and human sequences. Four mutations including G169C, A177G, G291T and A177G were identified in different types of breast carcinomas. An extra p53 response element was found in a mixed mammary carcinoma.  相似文献   
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