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1.
Chem Commun (Camb) ; 56(1): 125-128, 2020 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-31793952

RESUMO

We compare the ability of a prototypical dicarboxylic acid and its fluorinated analogue to act as molecular building blocks for the formation of self-assembled monolayers. Whilst fluorination is found to prevent homomolecular self-assembly, it greatly increases the ability of the carboxylic acid to act as a hydrogen bond donor for the formation of bimolecular networks.


Assuntos
Fluorbenzenos/química , Ácidos Ftálicos/química , Piridinas/química , Triazinas/química , Halogenação , Ligação de Hidrogênio
2.
Int J Pediatr Otorhinolaryngol ; 98: 59-63, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28583505

RESUMO

INTRODUCTION: Branchio-oto-renal (BOR) syndrome is an autosomal dominant genetic disorder characterized by second branchial arch anomalies, hearing impairment, and renal malformations. Pathogenic mutations have been discovered in several genes such as EYA1, SIX5, and SIX1. However, nearly half of those affected reveal no pathogenic variant by traditional genetic testing. METHODS AND MATERIALS: Whole Exome sequencing and/or Sanger sequencing performed in 10 unrelated families from Turkey, Iran, Ecuador, and USA with BOR syndrome in this study. RESULTS: We identified causative DNA variants in six families including novel c.525delT, c.979T > C, and c.1768delG and a previously reported c.1779A > T variants in EYA1. Two large heterozygous deletions involving EYA1 were detected in additional two families. Whole exome sequencing did not reveal a causative variant in the remaining four families. CONCLUSIONS: A variety of DNA changes including large deletions underlie BOR syndrome in different populations, which can be detected with comprehensive genetic testing.


Assuntos
Síndrome Brânquio-Otorrenal/genética , Peptídeos e Proteínas de Sinalização Intracelular/genética , Proteínas Nucleares/genética , Proteínas Tirosina Fosfatases/genética , Adulto , Pré-Escolar , Equador , Feminino , Humanos , Irã (Geográfico) , Masculino , Mutação , Linhagem , Análise de Sequência de DNA , Turquia , Estados Unidos
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