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991.
Weiping HUANG Masashi NAGANO Sung-Sik KANG Yojiro YANAGAWA Yoshiyuki TAKAHASHI 《The Journal of reproduction and development》2014,60(1):9-13
The objective of this study was to clarify the effects of prematurational culture
(pre-IVM) supplemented with 3-isobutyl-1-methylxanthine (IBMX) on nuclear and cytoplasmic
maturation of in vitro-grown bovine oocytes. In experiment 1, oocytes (95
μm in diameter) derived from early antral follicles (0.5–1 mm in diameter) were cultured
for 12 days for in vitro growth (IVG). IVG oocytes with a normal
appearance were subjected to examinations of diameter and chromatin structure in the
germinal vesicle (GV) before IVM. In addition, percentages of metaphase II (M II) were
examined after IVM. Regardless of pre-IVM, the mean diameters of IVG oocytes were about
115 μm. The proportions of GV3 (50.0%) and M II stages (80.1%) of IVG oocytes with pre-IVM
were higher than those without pre-IVM (28.0 and 49.4%, respectively). In experiment 2,
the fertilizability and developmental competence of IVG oocytes were examined. Regardless
of pre-IVM, the normal fertilization rates of IVG oocytes were similar (around 70%) but
were lower than that of in vivo-grown oocytes (88.0%). Cleavage and
blastocyst rates of IVG oocytes with pre-IVM (63.0 and 26.1%, respectively) were higher
than those without pre-IVM (45.8 and 12.7%, respectively). The blastocyst rate based on
cleaved IVG oocytes with pre-IVM (41.7%) was similar to that of in
vivo-grown oocytes (48.7%), although the cleavage rate of IVG oocytes with
pre-IVM was lower than that of in vivo-grown oocytes. In conclusion,
pre-IVM with IBMX improved the maturational and developmental competences of IVG oocytes,
probably due to promotion of their chromatin transition and synchronization of meiotic
progression. 相似文献
992.
Yuki YAMAMOTO Yoshihiko KOBAYASHI Kiyoshi OKUDA 《The Journal of reproduction and development》2014,60(1):73-77
Isolated stromal cells from the ampullary and isthmic parts of bovine oviductal tissues
were cultured in monolayer and spheroid (cell aggregate) systems. Prostaglandin F2α (PGF)
plays a crucial role in oviductal contraction and is produced by oviductal epithelial
cells in cattle. Since stromal cells of many organs produce PGF, PGF production by bovine
oviductal stromal cells was investigated. After PGF synthesis was confirmed, the utility
of isolation and culture methods for oviductal stromal cells was evaluated by PGF
production in the present study. The homogeneity of the cells was > 99%. PGF production
of the cells was increased by tumor necrosis factor-α. The stromal cells aggregated and
formed a spheroid by the treatments with several reagents. PGF production was higher in
the spheroid culture than in the monolayer culture. The isolation and culture methods
described here will facilitate studies of the physiological function of bovine oviductal
stromal cells. 相似文献
993.
994.
In this study, the expressions of VEGF in dog follicles were detected by immunohistochemistry and the effects of VEGF treatment on the primordial to primary follicle transition and on subsequent follicle progression were examined using a dog ovary organ culture system. The frozen‐thawed canine ovarian follicles within slices of ovarian cortical tissue were cultured for 7 and 14 days in presence or absence of VEGF. After culture, the ovaries were fixed, sectioned, stained and counted for morphologic analysis. The results showed that VEGF was expressed in the theca cells of antral follicles and in the granulosa cells nearest the oocyte in preantral follicle but not in granulosa cells of primordial and primary follicles; however, the VEGF protein was expressed in CL. After in vitro culture, VEGF caused a decrease in the number of primordial follicles and concomitant increase in the number of primary follicles that showed growth initiation and reached the secondary and preantral stages of development after 7 and 14 days. Follicular viability was also improved in the presence of VEGF after 7 and 14 days in culture. In conclusion, treatment with VEGF was found to promote the activation of primordial follicle development that could provide an alternative approach to stimulate early follicle development in dogs. 相似文献
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998.
[目的]探讨添加不同浓度激素及其组合培养基对海南菜豆树芽诱导、增殖和生根的影响,为建立海南菜豆树组培快繁体系提供参考依据.[方法]以海南菜豆树幼嫩茎段为外植体,以MS为基本培养基,添加不同浓度6-BA及6-BA与NAA、IBA和NAA组合,进行诱导萌芽、增殖、生根培养研究,分析添加不同浓度激素及其组合的培养基对海南菜豆树组织培养的效果.[结果]海南菜豆树芽的诱导率随6-BA质量浓度的增加而提高,当6-BA质量浓度为4.0mg/L时,芽诱导率达100.0%,且长势良好;当6-BA质量浓度为3.5 mg/L、NAA质量浓度为0.2 mg/L时芽增殖率最高,增值系数达5.8;在生根培养中,当NAA质量浓度为0.2 mg/L、IBA质量浓度为0.3 mg/L时生根率最高,达76.0%.[结论]海南菜豆树最适芽诱导培养基为MS+6-BA 4.0 mg/L;增殖培养以MS+6-BA 3.5 mg/L +NAA 0.2 mg/L效果最好;生根培养以MS+IBA 0.3 mg/L +NAA 0.2 mg/L效果最佳. 相似文献
999.
针对大运河扬州段城市水系的特殊性,以科学发展观为指导,探讨了以生态和文化相结合对水环境进行修复和提升的理念。根据各水系特色,提出了对河床、驳岸、滨河绿化、沿岸历史遗存等进行修复与提升的建议,形成和谐统一的水环境人文生态景观,以解决城市发展带来的一些问题,改善城市人居环境,提升城市品位,彰显城市特色。 相似文献
1000.
以活菌数为检测指标,通过单因子和正交试验对淡紫拟青霉 E16液体发酵工艺进行优化。结果表明,淡紫拟青霉E16发酵最佳液体培养基配方为:白砂糖1.5%(质量分数,下同),大豆粉1%,磷酸二氢钾0.1%,硫酸锌0.01%;最佳发酵条件为:起始 pH 值6,500 mL 三角瓶装液量30%,接菌量5%,培养温度30℃,摇床转速150 r/min,培养时间4 d。在最佳发酵培养基和发酵条件下,淡紫拟青霉E16产生的活菌数为9.80×109 cfu/mL,较优化前提高近1个数量级。 相似文献