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TBK1 haploinsufficiency results in changes in the K63-ubiquitination profiles in brain and fibroblasts from affected and presymptomatic mutation carriers.
Khoshnood, Behzad; Ullgren, Abbe; Laffita-Mesa, Jose; Öijerstedt, Linn; Patra, Kalicharan; Nennesmo, Inger; Graff, Caroline.
Afiliação
  • Khoshnood B; Division for Neurogeriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden. behzad.khoshnood@ki.se.
  • Ullgren A; Unit for Hereditary Dementias, Karolinska University Hospital Solna, Stockholm, Sweden. behzad.khoshnood@ki.se.
  • Laffita-Mesa J; Swedish FTD Initiative, Stockholm, Sweden. behzad.khoshnood@ki.se.
  • Öijerstedt L; Division for Neurogeriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
  • Patra K; Unit for Hereditary Dementias, Karolinska University Hospital Solna, Stockholm, Sweden.
  • Nennesmo I; Swedish FTD Initiative, Stockholm, Sweden.
  • Graff C; Division for Neurogeriatrics, Centre for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
J Neurol ; 269(6): 3037-3049, 2022 Jun.
Article em En | MEDLINE | ID: mdl-34800171
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doenças Neurodegenerativas / Demência Frontotemporal / Esclerose Lateral Amiotrófica Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: J Neurol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia