O'Brien WT - Search Results

1

Male-specific alterations in structure of isolation call sequences of mouse pups with 16p11.2 deletion.

Agarwalla S, Arroyo NS, Long NE, O'Brien WT, Abel T, Bandyopadhyay S. Agarwalla S, et al. Genes Brain Behav. 2020 Sep;19(7):e12681. doi: 10.1111/gbb.12681. Epub 2020 Jul 6. Genes Brain Behav. 2020. PMID: 32558237 Free PMC article.

2

An open-source toolbox for automated phenotyping of mice in behavioral tasks.

Patel TP, Gullotti DM, Hernandez P, O'Brien WT, Capehart BP, Morrison B 3rd, Bass C, Eberwine JE, Abel T, Meaney DF. Patel TP, et al. Front Behav Neurosci. 2014 Oct 8;8:349. doi: 10.3389/fnbeh.2014.00349. eCollection 2014. Front Behav Neurosci. 2014. PMID: 25339878 Free PMC article.

3

Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism.

Angelakos CC, Watson AJ, O'Brien WT, Krainock KS, Nickl-Jockschat T, Abel T. Angelakos CC, et al. Autism Res. 2017 Apr;10(4):572-584. doi: 10.1002/aur.1707. Epub 2016 Oct 14. Autism Res. 2017. PMID: 27739237 Free PMC article.

4

Male-specific deficits in natural reward learning in a mouse model of neurodevelopmental disorders.

Grissom NM, McKee SE, Schoch H, Bowman N, Havekes R, O'Brien WT, Mahrt E, Siegel S, Commons K, Portfors C, Nickl-Jockschat T, Reyes TM, Abel T. Grissom NM, et al. Mol Psychiatry. 2018 Mar;23(3):544-555. doi: 10.1038/mp.2017.184. Epub 2017 Oct 17. Mol Psychiatry. 2018. PMID: 29038598 Free PMC article.

5

Comprehensive Behavioral Phenotyping of a 16p11.2 Del Mouse Model for Neurodevelopmental Disorders.

Lynch JF 3rd, Ferri SL, Angelakos C, Schoch H, Nickl-Jockschat T, Gonzalez A, O'Brien WT, Abel T. Lynch JF 3rd, et al. Autism Res. 2020 Oct;13(10):1670-1684. doi: 10.1002/aur.2357. Epub 2020 Aug 28. Autism Res. 2020. PMID: 32857907 Free PMC article.

6

Towards Preclinical Validation of Arbaclofen (R-baclofen) Treatment for 16p11.2 Deletion Syndrome.

Gundersen BB, O'Brien WT, Schaffler MD, Schultz MN, Tsukahara T, Lorenzo SM, Nalesso V, Luo Clayton AH, Abel T, Crawley JN, Datta SR, Herault Y. Gundersen BB, et al. Among authors: o brien wt. bioRxiv [Preprint]. 2023 Sep 14:2023.05.01.538987. doi: 10.1101/2023.05.01.538987. bioRxiv. 2023. PMID: 37745360 Free PMC article. Preprint.

7

Regulation of glycogen synthase kinase-3 in patients with affective disorders.

O'Brien WT, Klein PS. O'Brien WT, et al. Biol Psychiatry. 2007 Jan 15;61(2):139-41. doi: 10.1016/j.biopsych.2006.11.008. Biol Psychiatry. 2007. PMID: 17223440 Free PMC article. No abstract available.

8

The role of mTORC1 activation in seizure-induced exacerbation of Alzheimer's disease.

Gourmaud S, Stewart DA, Irwin DJ, Roberts N, Barbour AJ, Eberwine G, O'Brien WT, Vassar R, Talos DM, Jensen FE. Gourmaud S, et al. Brain. 2022 Mar 29;145(1):324-339. doi: 10.1093/brain/awab268. Brain. 2022. PMID: 34264340 Free PMC article.

9

Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and mice.

Nair D, Diaz-Rosado A, Varella-Branco E, Ramos I, Black A, Angireddy R, Park J, Murali S, Yoon A, Ciesielski B, O'Brien WT, Passos-Bueno MR, Bhoj E. Nair D, et al. Am J Med Genet A. 2023 Oct;191(10):2508-2517. doi: 10.1002/ajmg.a.63320. Epub 2023 Jun 23. Am J Med Genet A. 2023. PMID: 37353954 Free PMC article.

10

Glycogen synthase kinase-3 is essential for β-arrestin-2 complex formation and lithium-sensitive behaviors in mice.

O'Brien WT, Huang J, Buccafusca R, Garskof J, Valvezan AJ, Berry GT, Klein PS. O'Brien WT, et al. J Clin Invest. 2011 Sep;121(9):3756-62. doi: 10.1172/JCI45194. Epub 2011 Aug 8. J Clin Invest. 2011. PMID: 21821916 Free PMC article.

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