Your browser doesn't support javascript.
loading
Humanin gene expression in fibroblast of Down syndrome subjects.
Salemi, Michele; Ridolfo, Federico; Salluzzo, Maria Grazia; Cannarrella, Rossella; Giambirtone, Mariaconcetta; Caniglia, Salvatore; Tirolo, Cataldo; Ferri, Raffaele; Romano, Corrado.
Afiliação
  • Salemi M; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Ridolfo F; UOSD of Clinical Pathology, ASUR Marche -AV2, Hospital of Senigallia, Senigallia, Italy.
  • Salluzzo MG; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Cannarrella R; Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy.
  • Giambirtone M; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Caniglia S; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Tirolo C; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Ferri R; Oasi Research Institute-IRCCS, Troina (EN), Italy.
  • Romano C; Oasi Research Institute-IRCCS, Troina (EN), Italy.
Int J Med Sci ; 17(3): 320-324, 2020.
Article em En | MEDLINE | ID: mdl-32132866
ABSTRACT
Down syndrome (DS) is characterized by trisomy of chromosome 21 and peculiar phenotype. Humanin (HN) is a mitochondrial short 24-residue polypeptide whit anti-apoptotic and neuroprotective effects. In this study we evaluated HN protein expression and HN mRNA levels in cultured fibroblasts from DS patients and normal controls. Our results obtained by immunocytochemistry, western-blot and qRT-PCR analysis show a significant HN up-regulation in DS patients. These results confirm previous studies and suggest a role for HN may in the DS phenotype.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Expressão Gênica / Síndrome de Down Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Expressão Gênica / Síndrome de Down Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article