全文获取类型
收费全文 | 720篇 |
免费 | 14篇 |
国内免费 | 21篇 |
出版年
2023年 | 4篇 |
2022年 | 7篇 |
2021年 | 11篇 |
2020年 | 16篇 |
2019年 | 13篇 |
2018年 | 5篇 |
2017年 | 11篇 |
2016年 | 8篇 |
2015年 | 13篇 |
2014年 | 18篇 |
2013年 | 20篇 |
2012年 | 14篇 |
2011年 | 19篇 |
2010年 | 22篇 |
2009年 | 28篇 |
2008年 | 36篇 |
2007年 | 31篇 |
2006年 | 46篇 |
2005年 | 42篇 |
2004年 | 39篇 |
2003年 | 31篇 |
2002年 | 26篇 |
2001年 | 30篇 |
2000年 | 28篇 |
1999年 | 22篇 |
1998年 | 17篇 |
1997年 | 14篇 |
1996年 | 18篇 |
1995年 | 10篇 |
1994年 | 12篇 |
1993年 | 22篇 |
1992年 | 14篇 |
1991年 | 17篇 |
1990年 | 19篇 |
1989年 | 7篇 |
1988年 | 8篇 |
1987年 | 6篇 |
1985年 | 12篇 |
1984年 | 9篇 |
1983年 | 1篇 |
1981年 | 4篇 |
1980年 | 4篇 |
1979年 | 3篇 |
1978年 | 3篇 |
1977年 | 5篇 |
1976年 | 3篇 |
1973年 | 1篇 |
1971年 | 2篇 |
1970年 | 1篇 |
1967年 | 1篇 |
排序方式: 共有755条查询结果,搜索用时 187 毫秒
1.
V. G. Borkhvardt 《Russian Journal of Developmental Biology》2000,31(3):154-161
The development of the fin and limb buds involves a balance of centrifugal (active) and centripetal (passive) mechanical forces,
the first of which acts to move the walls of these structures away from each other and the second of which holds them together.
When the volume of the mesodermal core increases, the generated force meets with the resistance of the basal membrane, and
as a result, the limb bud has a tendency to acquire a cylindrical shape. Collagen fibers, individual mesenchymal cells, and
their groups hold together the dorsal and the ventral wall of the limb bud, prevent the movement of these walls away from
each other, and in this way direct bud growth along the proximodistal and the anteroposterior axes. The balance of the forces
which stretch the ectodermal layer and those which constrain it has also been observed in the development of other body parts. 相似文献
2.
Sara Basconsuelo Herminda Reinoso Eugenia Lorenzo Rubén Bottini 《Plant Growth Regulation》1995,16(2):113-119
Morphological studies were carried out with peach flower buds collected monthly in 1989 and 1990, from two months before leaf fall (7 March) until two to three weeks before bloom (7/8 August). Chilled (2–4°C for 30 days) and unchilled buds were exposed to 20 to 25°C, 100% RH and continuous light. Gibberellin A3 (3 ng or 30 ng) was applied to some of the non-chilled cuttings at three days intervals. Then, 12, 19, and 26 days after they were planted, the buds were sampled and processed for histological studies. Cultured flower buds (chilled or unchilled) had accelerated anther and gynoecium morphogenesis after 12 days under controlled conditions, compared to buds processed immediately after collection from the field. Chilling treatment augmented the bud culture effect, while Gibberellin A3 applications to the excised buds retarded bud morphogenesis to a stage comparable to that of buds collected directly from the field. This, suggests that the comparatively high levels of Gibberellin A1/3 we previously found in mid winter [15, 18] could be at least one of the factors that controls floral bud dormancy by retarding anther and gynoecium development. 相似文献
3.
Large numbers of European ash have died in Poland in all age classes during the last ten years. The characteristic symptom occurring on shoots of planted and self‐sown seedlings was bark necroses starting from the shoot apex, necrotic buds, or leaf and twig scars. The results showed that in the bud tissue of cold acclimated European ash extracellular and intracellular ice formation occurred at approximately ?9 and ?32°C, respectively. In deacclimated plants in spring water supercooling is limited by the heterogenous ice nucleation temperature and consequently the cold tolerance is ?9 to ?4°C for bud tissues and ?13 to ?9°C for shoots. Isolations of fungi were performed from dead buds and from necroses occurring on the main stem. Alternaria alternata, Fusarium lateritium and Phomopsis scobina were among the fungi occurring in both these organs at frequencies of more than 7%. Cylindrocarpon heteronemum, Diplodia mutila and Tubercularia vulgaris from necroses were only isolated in frequencies; 3.3, 1.2 and 5.4%, respectively. It seems likely that freezing injury is the inciting factor, which combined with fungal colonization manifests itself as fatal damage to European ash buds and shoots. 相似文献
4.
Rachel E. Pieterse 《Plant Cell, Tissue and Organ Culture》1989,19(2):175-179
Immature embryos of apricot (Prunus armeniaca L.) cv. Royal with a PF index of 25–100 were used to regenerate plants in vitro using two methods. In the first case, callus was initiated on MS medium with 4.5 M 2, 4-D plus 0.44 M BA and regeneration of shoots from the callus occurred on MS medium with 4.4 M BA plus 1.0 M 2, 4-D. In the second case, adventitious buds were directly regenerated from the cotyledons on MS medium with 4.4 M BA plus 1.0 M 2, 4-D.Abbreviations BA
6-benzyladenine
- IBA
dole-3-butyric acid
- NAA
-naphthylacetic acid
- 2, 4-D
2, 4-dichlorophenoxyacetic acid
- PF
(embryo length/seed length) x 100 相似文献
5.
Summary Axillary bud expiants from South Pacific (Solomon Islands) taro, Colocasia esculenta var. esculenta cv. Akalomamale (Araceae) cultured on a modified Murashige-Skoog medium containing 1 mg NAA 1–1 and TE formed callus and produced multiple plantlets. Explants died if NAA was present at levels lower than 0.1 mg 1–1. BA was not required and may have been inhibitory. Plantlets developed faster and became larger following transfer to a hormone-free medium two weeks after the start of culture. Fully grown plants were established in a potting mix and are growing well in a greenhouse.Abbreviations BA
benzyladenine
- BM
basal medium
- Ca
Colocasia esculenta var. antiquorum
- Ce
Colocasia esculenta var. esculenta
- Ck
cytokinin(s)
- CW
coconut water
- HSMSM
half strength Murashige Skoog macroelements
- HSMS
half strength Murashige and Skoog medium
- IM
initial medium(ia)
- MS
Murashige and Skoog medium
- NAA
naphthaleneacetic acid
- SM
second medium
- TE
taro corm extract
- UCI
University of California, Irvine 相似文献
6.
Nicola J. Atkinson H. John Newbury Brian V. Ford-Lloyd 《Plant Cell, Tissue and Organ Culture》1991,27(1):77-79
A broadly applicable method for the successful induction of root systems in a number of cultivars of A. majus has been determined. This involves a double filter-paper bridge with a liquid medium for root induction and allows the transfer of culture-grown plantlets to a glasshouse environment with minimal disturbance to the plant as a whole. 100% survival of transferred plantlets has been achieved with the inclusion of a few simple precautions upon shoot transfer and during the initial stages of plant establishment in vivo. 相似文献
7.
Micropropagation of the actinorhizal plant Comptonia peregrina of the Myricaceae was achieved successfully by the induction of root buds in excised root culture with cytokinin (1.0 M benzyladenine). Excised root segments with initiated root buds were subcultured in Woody Plant Medium (WPM) lacking growth regulators, developing extensive callus which subsequently gave rise to multiple adventitious buds. Shoot elongation was facilitated by transfer of calluses to more aerated conditions. Root initiation was induced on shoots by brief treatment with auxin (<1 M indolebutyric acid) and transfer to WPM for plantlet development. Controlled light and aeration in liquid medium were critical conditions for successful micropropagation. 相似文献
8.
Roderick A. Drew 《Plant Cell, Tissue and Organ Culture》1991,26(1):23-27
Cultivar E23, an F1 hybrid of P. edulis and P. edulis f. flavicarpa is usually propagated by shoot-tip grafting. Various media were tested to evaluate the potential of E23 for in vitro propagation. Adult tissue was difficult to culture and did not respond to media containing low (<10 µM) concentrations of growth regulators. Growth of adult buds on intact stem sections was promoted by 1 week of dark incubation on MS basal medium plus 150 µM 2iP, 200 µM adenine sulphate and 17.1 µM IAA (3 mg l–1), and further developed into shoots on MS medium plus 4.9 µM 2iP (1 mg l–1) and 5.7 µM IAA (1 mg l–1). By contrast, juvenile shoots of E23, and Passiflora species: edulis f. flavicarpa, edulis, alata, caerulea, mollissima, coccinea, herbertiana and suberosa grew rapidly on MS medium plus 10 µM kinetin and 5 µM IAA. Rapid multiplication was achieved on MS plus 20 µM BA, 10 µM kinetin, 5 µM IAA, and roots initiated on MS plus 5 µM IAA.Abbreviations IAA
indole-3-acetic acid
- 2iP
N6-iso pentenyl adenine
- BA
N6-benzyl adenine 相似文献
9.
J. A. McComb 《Plant Cell, Tissue and Organ Culture》1985,4(2):151-158
The number of plants in the gazetted rare species Stylidium coroniforme was increased through micropropagation. A method was first developed using the common species S. brunonianum. It was found that for both species, rapid propagation could be obtained by excising shoots from sterile seedlings and inducing shoot proliferation on Murashige and Skoog medium supplemented with 1 M BAP. Rooting was achieved using 1 M IBA and over 100 plants of each species were successfully established in soil. Leaf pieces could also be used to initiate cultures. In media with 20–25 M BAP and 1–5 M IBA, leaf pieces of S. brunonianum, S. piliferum, S. caricifolium and S. crassifolium produced adventitious buds, thus providing another method of micropropagation. 相似文献
10.
Michael Marcotrigiano Susan P. McGlew Grant Hackett Bindu Chawla 《Plant Cell, Tissue and Organ Culture》1996,44(3):195-199
A method for shoot regeneration from leaf explants in two cultivars of cranberry (Vaccinium macrocarpon Ait.) is described. Modified Anderson's medium supplemented with combinations of thidiazuron (TDZ) with or without 1 M NAA (-naphthaleneacetic acid) was used to optimize shoot regeneration. The effect of light or dark incubation was also determined. Maximum regeneration was obtained in the light in the presence of 10 M TDZ and 1 M NAA. While this medium was suitable for leaf explants obtained from shoot cultures, regeneration did not occur from leaves collected from greenhouse-grown plants. Elongation of the regenerated shoot tips did not occur until explants were transferred to growth regulator-free medium at which time only a minority of shoots elongated. Elongated shoots could be dissected away from leaf tissue, rooted easily, and acclimitized to ambient conditions.Abbreviations NAA
-naphthaleneacetic acid
- TDZ
1-phenyl-3-(1,2,3-thiadiazol-5-yl) urea 相似文献