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1.
为探究春小麦品种对氮肥的响应特征,采用盆栽方式,选用来自埃及的Egypt1和Egypt2、来自我国天津的津强6号和津强11号4个春小麦品种,设不施氮(B1)、施尿素1g/盆(B2)和施尿素1.5g/盆(B3)3个施氮处理,于小麦成熟期测定植株性状、产量和籽粒蛋白质及其组分含量。结果表明,Egypt2的穗长、穗粒数、小穗数、千粒重、产量均高于津强6号,但津强6号的籽粒总蛋白、清蛋白、醇溶蛋白和谷蛋白含量最高;随着拔节期施氮量的增加,小麦穗粒数、千粒重、产量、蛋白质及其组分含量均逐渐增高,其中B3处理最高;不同处理组合中,施氮量较高处理下Egypt2的千粒重和产量最高,施氮量较高的津强6号的籽粒总蛋白质及其组分含量最高,拔节期施氮量增多,有利于提高小麦产量、总蛋白质及其组分含量。由此可知,不同品种中,Egypt2的产量最高,津强6号的总蛋白质含量最高;合理施氮肥可以提高小麦的产量和品质,施尿素1.5g/盆的氮肥处理小麦生长最好。品种和施氮量对小麦的产量和品质有较大影响。  相似文献   
2.
为了探究施氮量和播种量对新选育大麦[2011(07)814]鲜叶产量和品质的影响,采用二因素4水平裂区试验设计,研究4个施氮量(N1:150kg/hm2,N2:180kg/hm2,N3:210kg/hm2,N4:240kg/hm2)和4个播种量(S1:375万粒/hm2,S2:450万粒/hm2,S3:525万粒/hm2,S4:600万粒/hm2)对大麦孕穗期鲜叶产量、叶绿素含量(SPAD值)、旗叶面积、蛋白质和微量元素含量的影响。结果表明,施氮量、播种量及二者的互作效应对大麦孕穗期鲜叶产量、SPAD值、旗叶面积、蛋白质和微量元素含量的影响均达到显著(P<0.05)或极显著(P<0.01)水平;随施氮量和播种量的增加,大麦孕穗期鲜叶产量、旗叶面积、SPAD值、蛋白质和微量元素含量均呈先增加后降低的趋势,在N2S3或N3S2处理组合下达到峰值;N2S3处理组合鲜叶产量、SPAD值、旗叶面积和蛋白质含量较N1S1处理组合分别提高了102.70%、16.09%、86.39%和33.31%,N2S3处理组合Fe(295mg/kg)、Mn(76.59mg/kg)、Cu(8.10mg/kg)、Zn(30.94mg/kg)元素含量显著高于其他处理组合。因此,在甘肃省河西地区种植大麦[2011(07)814]获取鲜叶时,根据土壤肥力情况建议一次性施氮量180~210kg/hm2以及播种量450万~525万粒/hm2,不仅能增加大麦鲜叶产量、SPAD值和旗叶面积,而且有利于提高鲜叶蛋白质和微量元素含量。  相似文献   
3.
蛋白质是食品加工中的重要原料,其乳化性对食品品质非常重要。本文综述了通过物理改性、化学改性、生物酶法改性、基因工程改性及复合改性等方法技术来提高食品蛋白质的乳化功能性,并为今后食品蛋白质加工过程中利用改性方法来提高乳化性提供一定理论基础和新的思路。  相似文献   
4.
本试验旨在研究奶牛采食前后瘤胃中短链脂肪酸(SCFA)浓度的变化及其吸收相关蛋白表达量的差异。试验选用3头体重(720±30)kg且装有瘘管的健康荷斯坦牛(动物伦理审查编号为SXAU-EAW-2019-C002013),采食精粗比为40:60的日粮(10kg),试验预试期10d,于第11天饲喂前开始取样,采用气相色谱法检测奶牛采食前(0 h)和采食后(1、2、3、4、5、6、7、8 h)瘤胃液中SCFA浓度;并采用荧光定量PCR方法检测瘤胃上皮组织中与SCFA吸收相关的蛋白表达量。结果表明:在采食后1 h奶牛瘤胃中SCFA浓度最高(P<0.05);在采食后一段时间内(2~5h)与SCFA吸收相关蛋白表达量上调(P<0.05),AE2、MCT1基因表达量均在5 h最高,PAT1、NHE3基因表达量均在4 h最高,MCT4基因表达量在4、5、6h均较高,NHE1基因表达量在2h达到最高;AE2、MCT1、MCT4、NHE1基因表达量与SCFA浓度负相关或正相关(P<0.05),AE2、MCT1、MCT4基因表达量与瘤胃内pH正相关(P<0.05)。以上结果初步揭示,在采食后一定时间内,瘤胃中与SCFA吸收相关蛋白表达受SCFA浓度和pH的调节。  相似文献   
5.

Background

Monitoring urine protein:creatinine ratios (UPC ) in dogs with protein‐losing nephropathy (PLN ) is challenging because of day‐to‐day variation in UPC results.

Hypothesis/Objectives

Determine whether single, averaged, or pooled samples from PLN dogs receiving medical treatment yield comparable UPC s, regardless of degree of proteinuria.

Animals

Twenty‐five client‐owned PLN dogs receiving medical treatment.

Methods

UPC ratios were prospectively measured in each dog utilizing 3 methods: single in‐hospital sample (day 3), average sample (days 1–3), and pooled sample (equal pooling of urine from days 1–3). Bland‐Altman analysis was performed to evaluate agreement between methods for all dogs, as well as in subgroups of dogs (UPC ≤4 or UPC >4).

Results

For all dogs, Bland‐Altman log‐transformed 95% limits of agreement were ?0.07–0.18 (single versus pooled UPC ), ?0.06–0.16 (single versus average UPC ), and ?0.06–0.04 (pooled versus average UPC ). For dogs with UPC ≤4, Bland‐Altman 95% limits of agreement were ?0.42–0.82 (single versus pooled UPC ), ?0.38–0.76 (single versus average UPC ), and ?0.27–0.25 (pooled versus average UPC ). For dogs with UPC >4, Bland‐Altman 95% limits of agreement were ?0.17–2.4 (single versus pooled UPC ), ?0.40–2.2 (single versus average UPC ), and ?0.85–0.43 (pooled versus average UPC ).

Conclusions and Clinical Importance

UPC ratios from all methods were comparable in PLN dogs receiving medical treatment. In PLN dogs with UPC >4, more variability between methods exists likely because of higher in‐hospital results, but whether this finding is clinically relevant is unknown.
  相似文献   
6.
AIM: To investigate the effect of flavonoids from stem and leaf of Scutellaria baicalonsis Georgi (SSF) on paired helical filament (PHF) abnormality and the regulatory mechanism of protein phosphatase (PP) in rats' brain induced by okadaic acid (OA). METHODS: Male Sprague-Dawley (SD) rats were microinjected with OA (200 ng/kg) by the lateral ventricle to establish a memory impairment model. Morris water maze was used to screen the memory impairment model. The successful model rats were continuous intragastric infusion (ig) SSF for 36 days. The relative protein expression of PHF, PP1, PP2A-Cα, PP2A-Cβ, PP2CA and PP2CB in the rat cerebral cortex and hippocampus were detected by Western blot. GinKgo biloba leaf flavonoids (GLF) were used as positive control drug. RESULTS: Compared with the sham-operated rats, the relative protein expression of PHF in the cerebral cortex and hippocampus and PP1 in cortex of model rats were significantly increased (P<0.01), and the protein expression of PP2A-Cα, PP2A-Cβ in the cerebral cortex and hippocampus and PP2CB in the hippocampus were decreased (P<0.05), while the relative protein expression of PP2CA and PP2CB in the cortex were significantly increased (P<0.01). SSF reversed the abnormality in the protein expression of PHF, PP2A-Cα and PP2A-Cβ in rat cortex and hippocampus and PP1 in rat cortex induced by OA (P<0.01), which had no significant effect on the relative protein expression of PP2CA and PP2CB. GLF also showed similar results to SSF. CONCLUSION: SSF significantly reduces the abnormal formation of PHF in rats' brain induced by OA, which may be related to the regulation of PP1, PP2A-Cα and PP2A-Cβ expression, but not with PP2CA and PP2CB expression.  相似文献   
7.
AIM: To investigate the expression and roles of family with sequence similarity 3, member C (FAM3C) in oral squamous-cell carcinoma cells. METHODS: The mRNA and protein expression levels of FAM3C in dysplastic oral keratinocyte (DOK) and oral squamous-cell carcinoma WSU-HN6 cells were detected by RT-qPCR and Western blot. The WSU-HN6 cells were treated with siFAM3C or FAM3C antibody. After 24, 48 and 72 h, the viability of WSU-HN6 cells was measured by CCK-8 assay, and the activation of protein kinase B (Akt) was detected by Western blot. Adenovirus was used to mediate over-expression of FAM3C in the DOK cells. The DOK cell viability was measured by CCK-8 assay after adenovirus infection for 24, 48 and 72 h, and the activation of Akt was detected by Western blot. RESULTS: Compared with the DOK cells, the mRNA and protein levels of FAM3C were significantly increased in the WSU-HN6 cells (P<0.05). The viability of WSU-HN6 cells transfected with siFAM3C was significantly inhibited at 48 h and 72 h (P<0.05). siFAM3C treatment inhibited the activation of Akt (P<0.05). FAM3C antibody treatment also suppressed the viability of the WSU-HN6 cells at 48 h and 72 h and the activation of Akt (P<0.05). Over-expression of FAM3C in the DOK cells promoted the cell viability at 48 h and 72 h and activated Akt (P<0.05). CONCLUSION: FAM3C might promote oral squamous-cell carcinoma cell growth by activating Akt.  相似文献   
8.
根据目标性状有的放矢的选配杂交亲本是提高优异品质组成品种的选择效率的基本前提。本研究对东北三省102份大豆种质资源的蛋白、氨基酸组分、油份及脂肪酸组分进行测定,通过遗传多样性、主成分和聚类分析,对其进行表型鉴定及基因型分类以综合评价种质品质特性。结果表明:东北三省大豆种质油份及脂肪酸组分变异较丰富,遗传多样性程度较高。根据主成分分析筛选到9个主成分进行聚类分析,通过聚类分析将供试种质资源分为5类。第I类群蛋白含量较高、油份含量偏低,第II类群蛋白、油份含量均居中,第III类群油份含量较高、蛋白含量偏低,第IV类群高油,第V类群高蛋白,类群间的氨基酸、脂肪酸组分各有差异。需根据育种目标在群体间选配亲本,以提高品质育种的效率。  相似文献   
9.
Four sets of durum samples were used in this study to further understand the interrelationships among hard vitreous kernels (HVK), protein content, and pigment concentration, with a focus on the interaction and synergistic effects of protein content and vitreousness on durum quality. HVK level increases with higher protein content in the range of 9.5–12.5%, but this relationship is less evident in durum samples with high protein content (12.5–14.5%). Both protein content and kernel vitreousness can significantly affect durum milling quality. White starchy kernels (WSK) in low protein durum have a very detrimental impact on milling and pasta processing quality, but high protein content can mitigate the adverse impact of WSK on durum quality. Although protein content plays a dominant role, higher HVK might contribute positively to pasta firmness. There was no significant difference in yellow pigment content between HVK and WSK. However, pigment loss from semolina to dough was higher for WSK than HVK. Despite the difference in protein content, HVK and WSK have little difference in gluten strength. The monomeric protein was preferentially accumulated in HVK. The glutenin proteins of HVK and WSK were similar in the ratios of 1Bx/1By and HMW/LMW-GS.  相似文献   
10.
本研究以克隆所得杜仲(Eucommia ulmoides)EuGT2基因为基础,利用基因重组技术构建原核表达载体pMCSG19-EuGT2。重组载体转化到E.coli Rosetta(DE3)中,用0.05 mmol/L异丙基β-D-硫代半乳糖苷(IPTG)在37℃下诱导6 h。使用镍-亚氨基二乙酸(Ni-IDA)亲和层析柱进行纯化,并用15%十二烷基硫酸钠-聚丙烯酰胺(SDS-PAGE)凝胶电泳进行检测。研究结果表明,杜仲EuGT2基因在E.coli Rosetta(DE3)中得到成功表达,重组蛋白表达形式为部分包涵体、部分可溶性蛋白。经SDS-PAGE凝胶电泳检测,在相对分子质量约56 kD处有1条特异性蛋白条带,经质谱鉴定该特异性蛋白条带确为杜仲EuGT2蛋白。以上研究结果为后续研究杜仲糖基转移酶的功能提供了科学依据。  相似文献   
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