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ANXA1 with Anti-Inflammatory Properties Might Contribute to Parkinsonism.
Darvish, Hossein; Azcona, Luis J; Taghavi, Shaghayegh; Firouzabadi, Saghar Ghasemi; Tafakhori, Abbas; Alehabib, Elham; Mohajerani, Fatemeh; Zardadi, Safoura; Paisán-Ruiz, Coro.
Afiliação
  • Darvish H; Neuroscience Research Center, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
  • Azcona LJ; Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Taghavi S; Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Firouzabadi SG; Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Tafakhori A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
  • Alehabib E; Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
  • Mohajerani F; Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Zardadi S; Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
  • Paisán-Ruiz C; Department of Biology, School of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Ann Neurol ; 90(2): 319-323, 2021 08.
Article em En | MEDLINE | ID: mdl-34180078
ABSTRACT
We here describe the identification of a novel variant in the anti-inflammatory Annexin A1 protein likely to be the cause of disease in two siblings with autosomal recessive parkinsonism. The disease-segregating variant was ascertained through a combination of homozygosity mapping and whole genome sequencing and was shown to impair phagocytosis in zebrafish mutant embryos. The highly conserved variant, absent in healthy individuals and public SNP databases, affected a functional domain of the protein with neuroprotective properties. This study supports the hypothesis that damaged microglia might lead to impairments in the clearance of accumulated and aggregated proteins resulting in parkinsonism. ANN NEUROL 2021;90319-323.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Anexinas / Transtornos Parkinsonianos Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Anexinas / Transtornos Parkinsonianos Idioma: En Ano de publicação: 2021 Tipo de documento: Article