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1.
Nanomaterials (Basel) ; 11(1)2021 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-33467610

RESUMO

Trace amounts of Co3O4 modified TiO2 nanorod arrays were successfully fabricated through the photochemical deposition method without adding any nocuous reagents. The Co3O4/TiO2 nanorod arrays fabricated in acid solution had the highest photo-electrochemical activity. We elaborated on the mechanism of Co3O4-TiO2 fabricated in different pH value solutions. The Co3O4-TiO2 had a more remarkable photo-electrochemical performance than the pure TiO2 nanorod arrays owing to the heterojunction between Co3O4 and TiO2. The degradation of methylene blue and hydroquinone was selected as the model reactions to evaluate the photo-electrochemical performance of Co3O4-TiO2 nanorod arrays. The Co3O4/TiO2 nanorod arrays had great potential in waste water treatment.

2.
IET Syst Biol ; 9(4): 164-71, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26243833

RESUMO

Poplar, as a model species for forestry research, has many excellent characteristics. Studies on functional genes have provided the foundation, at the molecular level, for improving genetic traits and cultivating elite lines. Although studies on functional genes have been performed for many years, large amounts of experimental data remain scattered across various reports and have not been unified via comprehensive statistical analysis. This problem can be addressed by employing bioinformatic methodology and technology to gather and organise data to construct a Poplar Functional Gene Database, containing data on 207 poplar functional genes. As an example, the authors investigated genes of Populus euphratica involved in the response to salt stress. Four small cDNA libraries were constructed and treated with 300 mM NaCl or pure water for 6 and 24 h. Using high-throughput sequencing, they identified conserved and novel miRNAs that were differentially expressed. Target genes were next predicted and detailed functional information derived using the Gene Ontology database and Kyoto Encyclopedia of Genes and Genomes pathway analysis. This information provides a primary visual schema allowing us to understand the dynamics of the regulatory gene network responding to salt stress in Populus.


Assuntos
Bases de Dados Genéticas , Genoma de Planta/genética , Modelos Genéticos , Proteínas de Plantas/genética , Populus/genética , Plantas Tolerantes a Sal/genética , Mapeamento Cromossômico/métodos , Simulação por Computador , Genômica/métodos
3.
Nat Commun ; 5: 5696, 2014 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-25526346

RESUMO

Intrahepatic cholangiocarcinoma (ICC) is a fatal primary liver cancer (PLC) that affects 5-10% of all PLCs. Here we sequence tumour and matching control sample pairs of a large cohort of 103 ICC patients in China, resulting in the identification of an ICC-specific somatic mutational signature that is associated with liver inflammation, fibrosis and cirrhosis. We further uncover 25 significantly mutated genes including eight potential driver genes (TP53, KRAS, IDH1, PTEN, ARID1A, EPPK1, ECE2 and FYN). We find that TP53-defective ICC patients are more likely to be HBsAg-seropositive, whereas mutations in the oncogene KRAS are nearly exclusively found in HBsAg-seronegative ICC patients. Three pathways (Ras/phosphatidylinositol-4,5-bisphosphate 3-kinase signalling, p53/cell cycle signalling and transforming growth factor-ß/Smad signalling), genes important for epigenetic regulation and oxidative phosphorylation are substantially affected in ICC. We reveal mutations in this study that may be valuable for designing further studies, better diagnosis and effective therapies.


Assuntos
Neoplasias dos Ductos Biliares/genética , Colangiocarcinoma/genética , Neoplasias Hepáticas/genética , Mutação , Adulto , Idoso , Ductos Biliares Intra-Hepáticos , China , Estudos de Coortes , Feminino , Regulação Neoplásica da Expressão Gênica , Humanos , Isocitrato Desidrogenase/genética , Masculino , Pessoa de Meia-Idade , PTEN Fosfo-Hidrolase/genética , Proteínas Proto-Oncogênicas/genética , Proteínas Proto-Oncogênicas p21(ras) , Proteína Supressora de Tumor p53/genética , Proteínas ras/genética
4.
BMC Genomics ; 15: 440, 2014 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-24906389

RESUMO

BACKGROUND: Evidence based on genomic sequences is urgently needed to confirm the phylogenetic relationship between Mesorhizobium strain MAFF303099 and M. huakuii. To define underlying causes for the rather striking difference in host specificity between M. huakuii strain 7653R and MAFF303099, several probable determinants also require comparison at the genomic level. An improved understanding of mobile genetic elements that can be integrated into the main chromosomes of Mesorhizobium to form genomic islands would enrich our knowledge of how genome dynamics may contribute to Mesorhizobium evolution in general. RESULTS: In this study, we sequenced the complete genome of 7653R and compared it with five other Mesorhizobium genomes. Genomes of 7653R and MAFF303099 were found to share a large set of orthologs and, most importantly, a conserved chromosomal backbone and even larger perfectly conserved synteny blocks. We also identified candidate molecular differences responsible for the different host specificities of these two strains. Finally, we reconstructed an ancestral Mesorhizobium genomic island that has evolved into diverse forms in different Mesorhizobium species. CONCLUSIONS: Our ortholog and synteny analyses firmly establish MAFF303099 as a strain of M. huakuii. Differences in nodulation factors and secretion systems T3SS, T4SS, and T6SS may be responsible for the unique host specificities of 7653R and MAFF303099 strains. The plasmids of 7653R may have arisen by excision of the original genomic island from the 7653R chromosome.


Assuntos
Genoma Bacteriano , Mesorhizobium/genética , Evolução Molecular , Especificidade de Hospedeiro , Mesorhizobium/classificação , Mesorhizobium/fisiologia , Dados de Sequência Molecular , Filogenia , Fenômenos Fisiológicos Vegetais , Plantas/microbiologia , Análise de Sequência de DNA , Simbiose
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