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11.
Tirichine L Sandal N Madsen LH Radutoiu S Albrektsen AS Sato S Asamizu E Tabata S Stougaard J 《Science (New York, N.Y.)》2007,315(5808):104-107
Legume root nodules originate from differentiated cortical cells that reenter the cell cycle and form organ primordia. We show that perception of the phytohormone cytokinin is a key element in this switch. Mutation of a Lotus japonicus cytokinin receptor gene leads to spontaneous development of root nodules in the absence of rhizobia or rhizobial signal molecules. The mutant histidine kinase receptor has cytokinin-independent activity and activates an Escherichia coli two-component phosphorelay system in vivo. Mutant analysis shows that cytokinin signaling is required for cell divisions that initiate nodule development and defines an autoregulated process where cytokinin induction of nodule stem cells is controlled by shoots. 相似文献
12.
Changelian PS Flanagan ME Ball DJ Kent CR Magnuson KS Martin WH Rizzuti BJ Sawyer PS Perry BD Brissette WH McCurdy SP Kudlacz EM Conklyn MJ Elliott EA Koslov ER Fisher MB Strelevitz TJ Yoon K Whipple DA Sun J Munchhof MJ Doty JL Casavant JM Blumenkopf TA Hines M Brown MF Lillie BM Subramanyam C Shang-Poa C Milici AJ Beckius GE Moyer JD Su C Woodworth TG Gaweco AS Beals CR Littman BH Fisher DA Smith JF Zagouras P Magna HA Saltarelli MJ Johnson KS Nelms LF Des Etages SG Hayes LS Kawabata TT 《Science (New York, N.Y.)》2003,302(5646):875-878
Because of its requirement for signaling by multiple cytokines, Janus kinase 3 (JAK3) is an excellent target for clinical immunosuppression. We report the development of a specific, orally active inhibitor of JAK3, CP-690,550, that significantly prolonged survival in a murine model of heart transplantation and in cynomolgus monkeys receiving kidney transplants. CP-690,550 treatment was not associated with hypertension, hyperlipidemia, or lymphoproliferative disease. On the basis of these preclinical results, we believe JAK3 blockade by CP-690,550 has potential for therapeutically desirable immunosuppression in human organ transplantation and in other clinical settings. 相似文献
13.
Hideki ASAI Noboru HAYASHI Naoharu TAKAI Yoshihisa YOSHIMURA Yutaka NAKAMURA Hiroomi YOKOTA Kazumi KITA 《Animal Science Journal》2005,76(1):51-54
In the present study, the daily excretion of potassium (K) in urine (urinary K(UK)) was estimated from a 6 h urine sample using urinary creatinine (UC) as the index substance. All urine was collected from six pregnant Holstein cows at 6 h intervals for 24 h on 3 days of the 4th, 2nd and final week before the expected date of parturition. In total, 72 6 h urine samples were obtained. Daily UC excretion (mg/day per kg bodyweight (BW)) was almost the same for the three sampling days. Daily UC excretion varied among cows from 22.1 to 24.3 mg/day per kg BW with a mean of 22.8 mg/day per kg BW with no significant difference. Thus, daily UC excretion was confirmed to be constant throughout the prepartum period with no differences among individuals. The concentration ratios of K to creatinine ((UK mg/dL)/(UC mg/dL) (UK/UC)) correlated strongly to the hourly K excretions (mg/h per kg BW) (r = 0.952, P < 0.01) in the 6 h urine samples. The differences in the UK/UC ratio between sampling periods were not significant within each cow. Therefore, daily UK excretion (mg/day) can be estimated using the equation: daily UK excretion (mg/day) = daily UC excretion (mg/day per kg BW) × BW (kg) × 6 h urine sample UK/UC, where daily UC excretion can be a given value. 相似文献
14.
We investigated the physicochemical properties of the thermal gel of water‐washed pork meat (WWM) in the presence of the soluble fraction of porcine sarcoplasmic protein (SP) obtained with ammonium sulfate at 75 percent saturation. Two precipitated fractions of SP were obtained at 0–50 percent and 50–75 percent saturation, named SP‐f1 and SP‐f2, respectively, and the soluble fraction obtained at 75 percent saturation, SP‐f3, was used. Sodium dodecyl sulfate‐polyacrylamide gel electrophoresis showed that SP‐f3 contained mainly glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH), while SP‐f1 and SP‐f2 had other SPs such as phosphorylase b, enolase, actin and phosphoglycerate mutase. The gel strength of WWM was greater when SP‐f3 rather than one of various animal proteins such as bovine plasma (BP), egg white, or whey protein isolates (WPI), was added and SP‐f3 had a gel‐enhancing effect as good as that of polyphosphate (PP). The gel strength of WWM with added SP‐f3 increased significantly with NaCl at 0.15 mol/L or more, but not in the absence of NaCl (0 mol/L). The effect of SP‐f3 was evident at neutral pH and maximum gel strength was obtained at a pH above 6.0. Differential scanning calorimetric (DSC) analysis showed that an endothermic peak corresponding to myosin heads in WWM shifted to a lower temperature with the addition of SP‐f3, as in the case of PP, though there was no such shift in the presence of other animal proteins (BP, egg white and WPI), suggesting that SP‐f3 increases the gel strength of WWM through the dissociation of actomyosin similar to PP. Scanning electron microscopy (SEM) revealed wall‐like structures among the protein strands in the WWM gel matrix in the presence of SP‐f3. The results of DSC and SEM indicated that the formation of a gel network in meat products is reinforced with GAPDH in SP after the interaction between GAPDH and myofibrillar protein. 相似文献
15.
Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs 总被引:5,自引:0,他引:5
Erika Varkonyi-Gasic Rongmei Wu Marion Wood Eric F Walton Roger P Hellens 《Plant methods》2007,3(1):12
MicroRNAs (miRNAs) are a class of small non-coding RNAs with a critical role in development and environmental responses. Efficient
and reliable detection of miRNAs is an essential step towards understanding their roles in specific cells and tissues. However,
gel-based assays currently used to detect miRNAs are very limited in terms of throughput, sensitivity and specificity. Here
we provide protocols for detection and quantification of miRNAs by RT-PCR. We describe an end-point and real-time looped RT-PCR
procedure and demonstrate detection of miRNAs from as little as 20 pg of plant tissue total RNA and from total RNA isolated
from as little as 0.1 μl of phloem sap. In addition, we have developed an alternative real-time PCR assay that can further
improve specificity when detecting low abundant miRNAs. Using this assay, we have demonstrated that miRNAs are differentially
expressed in the phloem sap and the surrounding vascular tissue. This method enables fast, sensitive and specific miRNA expression
profiling and is suitable for facilitation of high-throughput detection and quantification of miRNA expression. 相似文献
16.
Jun-ichi WAKAMATSU Juichi UEMURA Hiroko ODAGIRI Jun OKUI Nobutaka HAYASHI Shoji HIOKI Takanori NISHIMURA Akihito HATTORI 《Animal Science Journal》2009,80(2):198-205
Zinc protoporphyrin IX (ZPP) is a characteristic red pigment in meat products that are manufactured without the addition of a curing agent such as nitrate or nitrite. To examine the effects of impurities such as mineral components in sea salt on the formation of ZPP, we manufactured Parmatype dry-cured hams that were salted with refined salt or sea salt and examined the involvement of oxidation-reduction potential (ORP) in the formation of ZPP. The content of ZPP was increased drastically after 40 weeks. Microscopic observation showed strong fluorescence caused by ZPP muscle fiber after 40 weeks. Conversely, heme content varied considerably during processing. ORP increased during processing. However, there was no obvious difference between ham salted with refined salt and that salted with sea salt. Therefore, it was concluded that impurities in sea salt were not involved in the formation of ZPP. 相似文献
17.
Kazuhiro WATANABE Kotaro HAYASHI Saku KIJIMA Chie NONAKA Kazuaki YAMAZOE 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2015,77(10):1323-1325
In this study, scaling, polishing and daily tooth brushing were performed in 20 beagle
dogs, and the number of oral bacteria was determined using a bacterial counter. The dogs
were randomized into the scaling (S), scaling + polishing (SP), scaling + tooth daily
brushing (SB) and scaling + polishing + tooth daily brushing (SPB) groups. Samples were
collected from the buccal surface of the maxillary fourth premolars of the dogs
immediately after scaling and every week thereafter from weeks 1 to 8. Throughout the
study, the number of bacteria was significantly lower in the SB and SPB groups compared
with the S group. The findings suggest that daily tooth brushing inhibited oral bacterial
growth in the dogs. 相似文献
18.
de Medeiros Erika Valente Lima Neyla Thayná de Sousa Lima José Romualdo Pinto Kedma Maria Silva da Costa Diogo Paes Franco Junior Cícero Luiz Souza Rodolfo Marcondes Silva Hammecker Claude 《Phytoparasitica》2021,49(4):713-726
Phytoparasitica - The current agricultural scenario faces a range of challenges, with phytosanitary ones being paramount. In most cases, plant diseases are treated with chemicals; however, they... 相似文献
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