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1.
Huang  Xing-Qi  Wang  Lin-Juan  Kong  Meng-Juan  Huang  Na  Liu  Xin-Ya  Liang  Han-Yu  Zhang  Jia-Xin  Lu  Shan 《Protoplasma》2021,258(2):371-378

Chloroplasts are semi-autonomous organelles, with more than 95% of their proteins encoded by the nuclear genome. The chloroplast-to-nucleus retrograde signals are critical for the nucleus to coordinate its gene expression for optimizing or repairing chloroplast functions in response to changing environments. In chloroplasts, the pentatricopeptide-repeat protein GENOMES UNCOUPLED 1 (GUN1) is a master switch that senses aberrant physiological states, such as the photooxidative stress induced by norflurazon (NF) treatment, and represses the expression of photosynthesis-associated nuclear genes (PhANGs). However, it is largely unknown how the retrograde signal is transmitted beyond GUN1. In this study, a protein GUN1-INTERACTING PROTEIN 1 (GIP1), encoded by At3g53630, was identified to interact with GUN1 by different approaches. We demonstrated that GIP1 has both cytosol and chloroplast localizations, and its abundance in chloroplasts is enhanced by NF treatment with the presence of GUN1. Our results suggest that GIP1 and GUN1 may function antagonistically in the retrograde signaling pathway.

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2.
The continuously arising of SARS-CoV-2 variants has been posting a great threat to public health safety globally, from B.1.17 (Alpha), B.1.351 (Beta), P.1 (Gamma), B.1.617.2 (Delta) to B.1.1.529 (Omicron). The emerging or reemerging of the SARS-CoV-2 variants of concern is calling for the constant monitoring of their epidemics, pathogenicity and immune escape. In this study, we aimed to characterize replication and pathogenicity of the Alpha and Delta variant strains isolated from patients infected in Laos. The amino acid mutations within the spike fragment of the isolates were determined via sequencing. The more efficient replication of the Alpha and Delta isolates was documented than the prototyped SARS-CoV-2 in Calu-3 and Caco-2 cells, while such features were not observed in Huh-7, Vero E6 and HPA-3 cells. We utilized both animal models of human ACE2 (hACE2) transgenic mice and hamsters to evaluate the pathogenesis of the isolates. The Alpha and Delta can replicate well in multiple organs and cause moderate to severe lung pathology in these animals. In conclusion, the spike protein of the isolated Alpha and Delta variant strains was characterized, and the replication and pathogenicity of the strains in the cells and animal models were also evaluated.  相似文献   
3.
豚鼠耳蜗中ATP对一氧化氮/环磷酸鸟苷途径的激活作用   总被引:2,自引:0,他引:2  
Zhao LD  Li YL  Li N  Li XQ 《生理学报》2003,55(6):658-662
实验研究了豚鼠耳蜗中ATP和一氧化氮/环磷酸鸟苷途径(nitric oxide/cyclic guanosine monophosphate,NO/cGMP pathway)的关系。将40只耳廓反射灵敏的健康白色豚鼠随机分为5组,分别对其离体的耳蜗即刻灌流人工外淋巴基础液(artificial perilymph basic solution,APBS)以及溶于人工外淋巴基础液的ATP、一氧化氮合酶抑制剂左旋-N^G-硝基精氨酸(L-N^G-nitroarginine,L-NNA) ATP、可溶性鸟苷酸环化酶抑制剂1H-[1,2,4]草酸重氮[4,3-a]喹恶啉(1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one,ODQ) ATP和A-23187(Ca^2 载体),收集耳蜗组织标本,利用放射免疫方法测定耳蜗组织中的cGMP的平均含量,比较各组之间耳蜗组织cGMF平均含量的差异。试验结果显示,向刚离体的耳蜗中灌流ATP和A-23187可以引起耳蜗组织中的cGMP含量升高,而灌流L-NNA和ODQ则可以抑制ATP所引起的耳蜗组织中cGMP含量的升高,提示在耳蜗组织中ATP可以通过升高细胞内Ca^2 浓度的作用而激活NO/cGMF途径。从本实验结果可以提出假说:耳蜗中ATP从神经末梢释放,通过提高细胞内Ca^2 的浓度,有激活NO/cGMP途径的作用,而NO/cGMP又能对ATP进行负反馈调节,两者共同调节耳蜗的生理功能,在耳蜗中存在ATP/Ca^2 -NO/cGMP通路。  相似文献   
4.
美洲商陆核基因组抗病毒蛋白基因的克隆及序列分析   总被引:1,自引:0,他引:1  
通过PCR扩增,从美洲商陆(Phytolacaamericana)核基因组中克隆了商陆抗病毒蛋白基因,序列分析表明,该基因含885个核苷酸,与已报道的序列比较,核苷酸同源性为99.3%。  相似文献   
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6.
云南疣粒野生稻幼穗一步成苗培养与植株再生   总被引:1,自引:0,他引:1  
1植物名称疣粒野生稻(Oryza meyeriana Baill.),云南类型。2材料类别幼穗(0.3~4.0 cm)。3培养条件云南疣粒野生稻的幼穗培养采用一次成苗分化培养基(1)为MS 6-BA 2.5 mg·L~(-1)(单位下  相似文献   
7.
8.
1 植物名称 疣粒野生稻(Oryza meyeriana Baill.),云南类型。  相似文献   
9.
从水稻中克隆了一个在稻属植物中高度保守和组成型表达的丝氨酸􊄯苏氨酸蛋白激酶基因(OsSTK)。该基因包含两个外显子和一个114 bp 的小内含子序列, 预测编码一个419 个氨基酸的蛋白质。该基因推导的氨基酸序列与其它已知序列的一致性均低于52%。利用从不同种和类型的野生稻克隆的部分该基因序列构建的系统树与野生稻的分类和进化关系相一致。OSPK N-端拥有一段富含丝氨酸、碱性氨基酸和带电荷氨基酸的特异性导肽序列, 其中包含“GDGDGDGDG”短重复序列。由于该基因蛋白激酶结构域中的VIb , VIII 和XI 亚结构域中同时具有酪氨酸蛋白激酶和丝氨酸􊄯苏氨酸蛋白激酶的特性, 推测该基因可能同时具有催化酪氨酸和丝氨酸、苏氨酸磷酸化的双重功能。  相似文献   
10.
A cytoplasmic serine􊄯thronine protein kinase gene (OsSTK), had been cloned from Oryza genus. It was found high conservative and constitutive expression in Oryza. OsSTK gene had two exons, separated by 114 bp short intron. The open reading frame of OsSTK gene that predicted encoded a 419 amino acids protein . The amino acid sequence of OsSTK had low identities ( less than 53% ) with any other known protein kinase . The phylogenetic tree based on the partial DNA sequences of OsSTK from different species and types of wild rice and cultivated rice, was close to the taxation system ofrice . Interestingly , OsSTK had a serine, including basic amino acids and charged amino acids abundant polypeptide with a “GDGDGDGDG”sequence at N- terminal that had not been found in any other genes. OsSTK may play dual specificity that phosphorylates both serine􊄯thronine and tyrosone, because the amino acids module of VIb , VIII and XI catalytic domain have both the serine􊄯thronine and tyrosine kinase characters .  相似文献   
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