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Items: 7

1.

An RNA decay factor wears a new coat: UPF3B modulates translation termination.

Gao Z, Wilkinson M.

F1000Res. 2017 Dec 20;6:2159. doi: 10.12688/f1000research.12704.1. eCollection 2017. Review.

2.

A Upf3b-mutant mouse model with behavioral and neurogenesis defects.

Huang L, Shum EY, Jones SH, Lou CH, Dumdie J, Kim H, Roberts AJ, Jolly LA, Espinoza JL, Skarbrevik DM, Phan MH, Cook-Andersen H, Swerdlow NR, Gecz J, Wilkinson MF.

Mol Psychiatry. 2017 Sep 26. doi: 10.1038/mp.2017.173. [Epub ahead of print]

3.

Full UPF3B function is critical for neuronal differentiation of neural stem cells.

Alrahbeni T, Sartor F, Anderson J, Miedzybrodzka Z, McCaig C, Müller B.

Mol Brain. 2015 May 27;8:33. doi: 10.1186/s13041-015-0122-1.

4.

The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.

Jolly LA, Homan CC, Jacob R, Barry S, Gecz J.

Hum Mol Genet. 2013 Dec 1;22(23):4673-87. doi: 10.1093/hmg/ddt315. Epub 2013 Jul 2.

PMID:
23821644
5.

An EJC factor RBM8a regulates anxiety behaviors.

Alachkar A, Jiang D, Harrison M, Zhou Y, Chen G, Mao Y.

Curr Mol Med. 2013 Jul;13(6):887-99.

PMID:
23638902
6.

A nonconservative amino acid change in the UPF3B gene in a patient with schizophrenia.

Szyszka P, Sharp SI, Dedman A, Gurling HM, McQuillin A.

Psychiatr Genet. 2012 Jun;22(3):150-1. doi: 10.1097/YPG.0b013e32834accbe. No abstract available.

PMID:
21862950
7.

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

Addington AM, Gauthier J, Piton A, Hamdan FF, Raymond A, Gogtay N, Miller R, Tossell J, Bakalar J, Inoff-Germain G, Gochman P, Long R, Rapoport JL, Rouleau GA.

Mol Psychiatry. 2011 Mar;16(3):238-9. doi: 10.1038/mp.2010.59. Epub 2010 May 18. No abstract available. Erratum in: Mol Psychiatry. 2012 Apr;17(4):468. Germain, G [corrected to Inoff-Germain, G].

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