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1.
Nanomaterials (Basel) ; 12(21)2022 Oct 29.
Artigo em Inglês | MEDLINE | ID: mdl-36364601

RESUMO

Single-walled carbon nanotube (SWCNT)/TiO2 hybrids were synthesized using 1,10-bis(decyloxy)decane-core PAMAM dendrimer as a molecular glue. Upon photoirradiation of a water dispersion of SWCNT/TiO2 hybrids with visible light (λ > 422 nm), the hydrogen evolution reaction proceeded at a rate of 0.95 mmol/h·g in the presence of a sacrificial agent (1-benzyl-1,4-dihydronicotinamide, BNAH). External quantum yields (EQYs) of the hydrogen production reaction photosensitized by (6,5), (7,5), and (8,3) tubes were estimated to be 5.5%, 3.6%, and 2.2%, respectively, using monochromatic lights corresponding to their E22 absorptions (570 nm, 650 nm, and 680 nm). This order of EQYs (i.e., (6,5) > (7,5) > (8,3)SWCNTs) exhibited the dependence on the C2 energy level of SWCNT for EQY and proved the hot electron extraction pathway.

2.
Sci Rep ; 11(1): 21815, 2021 11 08.
Artigo em Inglês | MEDLINE | ID: mdl-34750413

RESUMO

Biliary atresia (BA) is a progressive inflammation and fibrosis of the biliary tree characterized by the obstruction of bile flow, which results in liver failure, scarring and cirrhosis. This study aimed to explore the elusive aetiology of BA by conducting whole exome sequencing for 41 children with BA and their parents (35 trios, including 1 family with 2 BA-diagnosed children and 5 child-mother cases). We exclusively identified and validated a total of 28 variants (17 X-linked, 6 de novo and 5 homozygous) in 25 candidate genes from our BA cohort. These variants were among the 10% most deleterious and had a low minor allele frequency against the employed databases: Kinh Vietnamese (KHV), GnomAD and 1000 Genome Project. Interestingly, AMER1, INVS and OCRL variants were found in unrelated probands and were first reported in a BA cohort. Liver specimens and blood samples showed identical variants, suggesting that somatic variants were unlikely to occur during morphogenesis. Consistent with earlier attempts, this study implicated genetic heterogeneity and non-Mendelian inheritance of BA.


Assuntos
Atresia Biliar/genética , Proteínas Adaptadoras de Transdução de Sinal/genética , Estudos de Coortes , Feminino , Frequência do Gene , Genes Recessivos , Genes Ligados ao Cromossomo X , Estudos de Associação Genética , Marcadores Genéticos , Predisposição Genética para Doença , Variação Genética , Humanos , Lactente , Recém-Nascido , Masculino , Monoéster Fosfórico Hidrolases/genética , Fatores de Transcrição/genética , Proteínas Supressoras de Tumor/genética , Vietnã , Sequenciamento do Exoma
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