Dysregulated COMT Expression in Fragile X Syndrome-Reference-Cited by-同舟云学术

Dysregulated COMT Expression in Fragile X Syndrome

Published:2023-09-08 Issue:4 Volume:25 Page:644-649
ISSN:1535-1084
Container-title:NeuroMolecular Medicine
language:en
Short-container-title:Neuromol Med

Author:

Utami Kagistia Hana,Yusof Nur Amirah Binte Muhammed,Garcia-Miralles Marta,Skotte Niels Henning,Nama Srikanth,Sampath Prabha,Langley Sarah R.,Pouladi Mahmoud A.

Funder

FRAXA Research Foundation

Michael Smith Health Research BC

BC Children's Hospital

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology,Molecular Medicine

Link

https://link.springer.com/content/pdf/10.1007/s12017-023-08754-1.pdf

Reference25 articles.

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3. Babovic, D., O’Tuathaigh, C. M., O’Sullivan, G. J., Clifford, J. J., Tighe, O., Croke, D. T., et al. (2007). Exploratory and habituation phenotype of heterozygous and homozygous COMT knockout mice. Behavioural Brain Research, 183(2), 236–239.

4. Bowers, M. E., Buzzell, G. A., Salo, V., Troller-Renfree, S. V., Hodgkinson, C. A., Goldman, D., et al. (2020). Relations between catechol-O-methyltransferase Val158Met genotype and inhibitory control development in childhood. Developmental Psychobiology, 62(2), 181–190.

5. Craddock, N., Owen, M. J., & O’Donovan, M. C. (2006). The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: Evidence and lessons. Molecular Psychiatry, 11(5), 446–458.

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