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Dysregulated COMT Expression in Fragile X Syndrome.
Utami, Kagistia Hana; Yusof, Nur Amirah Binte Muhammed; Garcia-Miralles, Marta; Skotte, Niels Henning; Nama, Srikanth; Sampath, Prabha; Langley, Sarah R; Pouladi, Mahmoud A.
Afiliación
  • Utami KH; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore, 138648, Singapore.
  • Yusof NABM; Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
  • Garcia-Miralles M; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore, 138648, Singapore.
  • Skotte NH; Translational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore, 138648, Singapore.
  • Nama S; Department of Molecular Embryology, Medical Faculty, Institute of Anatomy and Cell Biology, Albert-Ludwigs-University Freiburg, 79104, Freiburg, Germany.
  • Sampath P; Proteomics Program, Novo Nordisk Foundation Center for Protein Research, Faculty of Health Sciences, University of Copenhagen, 2200, Copenhagen, Denmark.
  • Langley SR; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
  • Pouladi MA; Institute of Medical Biology, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore, 138648, Singapore.
Neuromolecular Med ; 25(4): 644-649, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37684514
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Catecol O-Metiltransferasa / Síndrome del Cromosoma X Frágil Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Neuromolecular Med Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Singapur
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Catecol O-Metiltransferasa / Síndrome del Cromosoma X Frágil Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Neuromolecular Med Asunto de la revista: BIOLOGIA MOLECULAR / NEUROLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Singapur