Your browser doesn't support javascript.
loading
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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-37684514
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Catecol O-Metiltransferase / Síndrome do Cromossomo X Frágil Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Neuromolecular Med Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Catecol O-Metiltransferase / Síndrome do Cromossomo X Frágil Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Neuromolecular Med Ano de publicação: 2023 Tipo de documento: Article