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Indian J Hum Genet ; 2013 July-Sept ;19 (3): 291-292
Artigo em Inglês | IMSEAR | ID: sea-156572

RESUMO

BACKGROUND: Hemoglobin (Hb) D Punjab disorder is a congenital hemoglobinopathy described in India. It is a disorder due to defect in beta-globin gene. MATERIALS AND METHODS: Here, the author assesses the possibility of U7.623 gene therapy for Hb D Punjab disorder. A standard bioinformatic analysis to study the effect of co-expression between nucleic acid sequence for human Hb D Punjab beta-globin chain and U7.623 was performed. RESULT: It can be seen that fully recovery of Hb function and biological process can be derived via gene ontology study. CONCLUSION: Here, there is a rationale to use U7 small nuclear ribonucleic acid as a possible tool for gene therapy in Hb D Punjab disorder.


Assuntos
Biologia Computacional/métodos , Terapia Genética/métodos , Terapia Genética/uso terapêutico , Hemoglobinas Anormais/epidemiologia , Hemoglobinas Anormais/genética , Hemoglobinas Anormais/terapia , Humanos , PubMed , Ribonucleoproteína Nuclear Pequena U7
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