A G1528C Hadha knock-in mouse model recapitulates aspects of human clinical phenotypes for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Gaston, Garen; Babcock, Shannon; Ryals, Renee; Elizondo, Gabriela; DeVine, Tiffany; Wafai, Dahlia; Packwood, William; Holden, Sarah; Raber, Jacob; Lindner, Jonathan R; Pennesi, Mark E; Harding, Cary O; Gillingham, Melanie B

Gaston, Garen; Babcock, Shannon; Ryals, Renee; Elizondo, Gabriela; DeVine, Tiffany; Wafai, Dahlia; Packwood, William; Holden, Sarah; Raber, Jacob; Lindner, Jonathan R; Pennesi, Mark E; Harding, Cary O; Gillingham, Melanie B.

Afiliação

Gaston G; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR, USA.
Babcock S; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR, USA.
Ryals R; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR, USA.
Elizondo G; Casey Eye Institute, Oregon Health and Science University, Portland, OR, USA.
DeVine T; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR, USA.
Wafai D; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, OR, USA.
Packwood W; Casey Eye Institute, Oregon Health and Science University, Portland, OR, USA.
Holden S; Knight Cardiovascular Institute, Oregon Health and Science University, Portland, OR, USA.
Raber J; Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, USA.
Lindner JR; Knight Cardiovascular Institute, Oregon Health and Science University, Portland, OR, USA.
Pennesi ME; Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, USA.
Harding CO; Departments of Neurology and Radiation Medicine, Oregon Health and Science University, Portland, OR, USA.
Gillingham MB; Division of Neuroscience, Oregon National Primate Research Center (ONPRC), Oregon Health and Science University, Portland, OR, USA.

Commun Biol ; 6(1): 890, 2023 08 29.

Article em En | MEDLINE | ID: mdl-37644104

Assuntos

Cardiomiopatias; Erros Inatos do Metabolismo Lipídico; Rabdomiólise; Humanos; Animais; Camundongos; Modelos Animais de Doenças; Cardiomiopatias/genética; Erros Inatos do Metabolismo Lipídico/genética; Rabdomiólise/genética; Subunidade alfa da Proteína Mitocondrial Trifuncional

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rabdomiólise / Erros Inatos do Metabolismo Lipídico / Cardiomiopatias Limite: Animals / Humans Idioma: En Revista: Commun Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

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