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排序方式: 共有169条查询结果,搜索用时 15 毫秒
41.
Luciano Vellón Félix Royo Rune Matthiesen José Torres-Fuenzalida Alicia Lorenti Luis A Parada 《BMC cell biology》2010,11(1):81
Background
Cell scattering is a physiological process executed by stem and progenitor cells during embryonic liver development and postnatal organ regeneration. Here, we investigated the genomic events occurring during this process induced by functional blockade of α5β1 integrin in liver progenitor cells. 相似文献42.
L. J. Royo A. Traoré H. H. Tambourá I. Álvarez A. Kaboré I. Fernández G. Ouédraogo-Sanou A. Toguyeni L. Sawadogo F. Goyache 《Animal genetics》2009,40(3):344-347
To date, no comprehensive study has been performed on mitochondrial genetic diversity of the West African goat. Here, we analysed a 481-bp fragment of the HVI region of 111 goats representing four native West African populations, namely the three main Burkina Faso breeds, zoo-farm kept Dwarf goats and endangered Spanish goat breeds used as the outgroup. Analyses gave 83 different haplotypes with 102 variable sites. Most haplotypes (65) were unique. Only three haplotypes were shared between populations. Haplotypes were assigned to cluster A except for H45 (belonging to the Spanish Bermeya goat) which was assigned to cluster C. amova analysis showed that divergence between groups (ΦCT ) was not statistically significant regardless of whether the partition in two hierarchical levels that was fitted included Spanish samples or not. The West African goat scenario shown here is consistent with that previously reported for the species: haplogroup A is predominant and has a very high haplotype diversity regardless of the geographic area or sampled breed. The large phenotypic differences observable between the West African Dwarf and Sahelian long-legged goat populations are not detectable with mitochondrial markers. Moreover, a previously suggested introgression of Sahelian goat southwards because of desertification could not be assessed using mtDNA information. 相似文献
43.
Evidence for factors regulating transfer cell-specific expression in maize endosperm 总被引:1,自引:0,他引:1
In maize, a layer of basal endosperm cells adjacent to the pedicel is modified for a function in solute transfer. Three genes specifically expressed in this region, termed the basal endosperm transfer layer (BETL-2 to -4), were isolated by differential hybridization. BETL-2 to -4 are coordinately expressed in early and mid-term endosperm development, but are absent at later stages. BETL-2 to -4 coding sequences all predict small (<100 amino acids), secreted, cysteine-rich polypeptides which lack close relatives in current database accessions. BETL-3 and BETL-1 display some sequence similarities with each other and to plant defensins. BETL-2 to -4 promoter regions were isolated and compared, revealing the presence of a promoter-proximal microsatellite repeat as the most highly conserved sequence element in each sequence. Electrophoretic mobility shift assays (EMSA) showed that specific BETL-2 to -4 promoter fragments competed for binding to the same DNA-binding activity in nuclear extracts prepared from maize endosperm. Although BETL-2 to -4 are only expressed in basal endosperm cells, the DNA-binding activities detected were of two types: distal endosperm-specific, or present in both basal and distal endosperm extracts. On the basis of these findings, a model to account for the coordinate regulation of BETL genes in endosperm cells is proposed. 相似文献
44.
Second-generation dendrimers have been prepared on solid phase by successive additions of branched polyproline building blocks starting from two different branching units anchored to the solid support. The preparation of Pro-rich building blocks was carried out by stepwise solid-phase synthesis and their iterative addition was performed by a convergent approach, also using solid-phase synthesis. cis-4-Amino-L-proline and imidazolidine-2-carboxylic acid were used as branching units due to their structural resemblance to proline. The optimized strategy allowed the target compounds to be obtained with high purities without the need for purification steps. 相似文献
45.
Huang L Zhao A Lew JL Zhang T Hrywna Y Thompson JR de Pedro N Royo I Blevins RA Peláez F Wright SD Cui J 《The Journal of biological chemistry》2003,278(51):51085-51090
The human multidrug resistance gene MDR3 encodes a P-glycoprotein that belongs to the ATP-binding cassette transporter family (ABCB4). MDR3 is a critical trans-locator for phospholipids across canalicular membranes of hepatocytes, evidenced by the fact that human MDR3 deficiencies result in progressive familial intrahepatic cholestasis type III. It has been reported previously that MDR3 expression is modulated by hormones, cellular stress, and xenobiotics. Here we show that the MDR3 gene is trans-activated by the farnesoid X receptor (FXR) via a direct binding of FXR/retinoid X receptor alpha heterodimers to a highly conserved inverted repeat element (a FXR response element) at the distal promoter (-1970 to -1958). In FXR trans-activation assays, both the endogenous FXR agonist chenodeoxycholate and the synthetic agonist GW4064 activated the MDR3 promoter. Deletion or mutation of this inverted repeat element abolished FXR-mediated MDR3 promoter activation. Consistent with these data, MDR3 mRNA was significantly induced by both chenodeoxycholate and GW4064 in primary human hepatocytes in time- and dose-dependent fashions. In conclusion, we demonstrate that MDR3 expression is directly up-regulated by FXR. These results, together with the previous report that the bile salt export pump is a direct FXR target, suggest that FXR coordinately controls secretion of bile salts and phospholipids. Results of this study further support the notion that FXR is a master regulator of lipid metabolism. 相似文献
46.
Synthesis and screening of a small library of proline-based biodendrimers for use as delivery agents
A small library of defined peptide dendrimers based on polyproline sequences was designed to demonstrate the feasibility of generating a new type of polymeric agent for therapeutic use. Structural modifications to dendrimer surfaces further enriched the diversity of the library. Data show that the prolinerich dendrimers can be internalized in human epithelial (HeLa) cells, demonstrating the importance of the dendrimeric motif. The promising results described herein suggest that controlled modification of the dendrimer surface should eventually yield proline dendrimers with therapeutic potential. 相似文献
47.
del Fresno M Fernández-Forner D Miralpeix M Segarra V Ryder H Royo M Albericio F 《Bioorganic & medicinal chemistry letters》2005,15(6):1659-1664
The synthesis and evaluation as tryptase inhibitors of a library of 2,5-diketopiperazine derivatives containing guanidine or amidine functional groups is reported. Among the compounds evaluated, derivatives 6{CG4-CG8} and 6{CG4-CG9} are the most active compounds and have marked selectivity towards tryptase in front of trypsin. 相似文献
48.
Seitz H Royo H Lin SP Youngson N Ferguson-Smith AC Cavaillé J 《Biological chemistry》2004,385(10):905-911
49.
I. Álvarez∗ A. Traoré∗ H. H. Tamboura A. Kaboré L. J. Royo I. Fernández 《Animal biotechnology》2013,24(2):47-57
A total of 123 sheep belonging to the Djallonké, Mossi, and Burkina-Sahel breeds, along with 41 Spanish Xalda sheep were genotyped for 27 microsatellites. The pair Djallonké-Mossi had the highest between breeds molecular coancestry. Admixture analysis informed on the parental role of the Burkina-Sahel and Djallonké breeds. The Mossi breed was a hybrid population nearer to the Djallonké breed. Only half of the Mossi individuals were correctly assigned to their breed. The Burkina-Sahel and Djallonké breeds can be considered ancestrally different genetic entities. Differentiation between the Djallonké and Mossi breeds may be due to introgression of Sahelian sheep. 相似文献
50.
Pemán J Cantón E Miñana JJ Florez JA Echeverria J Ortega DN Alarcón JM Fontanals D Sard BG Moreno BB Torroba L Ayats J Pérez MÁ Fernández MA Reus FS Natal IF García GR Ezpeleta G Martín-Mazuelos E Iglesias I Rezusta A de Ocariz IR Nieto AG;el Grupo de Estudio FUNGEMYCA 《Revista iberoamericana de micología》2011,28(2):91-99