Itani OA - Search Results

1

Longevity Genes Revealed by Integrative Analysis of Isoform-Specific daf-16/FoxO Mutants of Caenorhabditis elegans.

Chen AT, Guo C, Itani OA, Budaitis BG, Williams TW, Hopkins CE, McEachin RC, Pande M, Grant AR, Yoshina S, Mitani S, Hu PJ. Chen AT, et al. Among authors: itani oa. Genetics. 2015 Oct;201(2):613-29. doi: 10.1534/genetics.115.177998. Epub 2015 Jul 27. Genetics. 2015. PMID: 26219299 Free PMC article.

2

Chromoanasynthetic Genomic Rearrangement Identified in a N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Screen in Caenorhabditis elegans.

Itani OA, Flibotte S, Dumas KJ, Moerman DG, Hu PJ. Itani OA, et al. G3 (Bethesda). 2015 Dec 1;6(2):351-6. doi: 10.1534/g3.115.024257. G3 (Bethesda). 2015. PMID: 26628482 Free PMC article.

3

N-Ethyl-N-Nitrosourea (ENU) Mutagenesis Reveals an Intronic Residue Critical for Caenorhabditis elegans 3' Splice Site Function in Vivo.

Itani OA, Flibotte S, Dumas KJ, Guo C, Blumenthal T, Hu PJ. Itani OA, et al. G3 (Bethesda). 2016 Jun 1;6(6):1751-6. doi: 10.1534/g3.116.028662. G3 (Bethesda). 2016. PMID: 27172199 Free PMC article.

4

Requirement for translocon-associated protein (TRAP) α in insulin biogenesis.

Li X, Itani OA, Haataja L, Dumas KJ, Yang J, Cha J, Flibotte S, Shih HJ, Delaney CE, Xu J, Qi L, Arvan P, Liu M, Hu PJ. Li X, et al. Among authors: itani oa. Sci Adv. 2019 Dec 4;5(12):eaax0292. doi: 10.1126/sciadv.aax0292. eCollection 2019 Dec. Sci Adv. 2019. PMID: 31840061 Free PMC article.

5

Daf-16 mediated repression of cytosolic ribosomal protein genes facilitates a hypoxia sensitive to hypoxia resistant transformation in long-lived germline mutants.

Hemphill C, Pylarinou-Sinclair E, Itani O, Scott B, Crowder CM, Van Gilst MR. Hemphill C, et al. PLoS Genet. 2022 May 27;18(5):e1009672. doi: 10.1371/journal.pgen.1009672. eCollection 2022 May. PLoS Genet. 2022. PMID: 35622856 Free PMC article.

6

Functional analysis of a de novo variant in the neurodevelopment and generalized epilepsy disease gene NBEA.

Boulin T, Itani O, El Mouridi S, Leclercq-Blondel A, Gendrel M, Macnamara E, Soldatos A, Murphy JL, Gorman MP, Lindsey A, Shimada S, Turner D, Silverman GA, Baldridge D; Undiagnosed Diseases Network; Malicdan MC, Schedl T, Pak SC. Boulin T, et al. Mol Genet Metab. 2021 Sep-Oct;134(1-2):195-202. doi: 10.1016/j.ymgme.2021.07.013. Epub 2021 Aug 9. Mol Genet Metab. 2021. PMID: 34412939 Free PMC article.

7

Coordinate Regulation of Ribosome and tRNA Biogenesis Controls Hypoxic Injury and Translation.

Itani OA, Zhong X, Tang X, Scott BA, Yan JY, Flibotte S, Lim Y, Hsieh AC, Bruce JE, Van Gilst M, Crowder CM. Itani OA, et al. Curr Biol. 2021 Jan 11;31(1):128-137.e5. doi: 10.1016/j.cub.2020.10.001. Epub 2020 Nov 5. Curr Biol. 2021. PMID: 33157031 Free PMC article.

8

Ageing and hypoxia cause protein aggregation in mitochondria.

Kaufman DM, Wu X, Scott BA, Itani OA, Van Gilst MR, Bruce JE, Crowder CM. Kaufman DM, et al. Among authors: itani oa. Cell Death Differ. 2017 Oct;24(10):1730-1738. doi: 10.1038/cdd.2017.101. Epub 2017 Jun 23. Cell Death Differ. 2017. PMID: 28644434 Free PMC article.

9

Familial ossicular malformations: case report and review of literature.

Higashi K, Yamakawa K, Itani O, Togawa K. Higashi K, et al. Am J Med Genet. 1987 Nov;28(3):655-9. doi: 10.1002/ajmg.1320280313. Am J Med Genet. 1987. PMID: 3322009 Review.

10

[The middle and inner ear findings of the earpits-deafness syndrome].

Higashi K, Itani O, Inoue S, Yoshida M. Higashi K, et al. Nihon Jibiinkoka Gakkai Kaiho. 1983 Jun 20;86(6):666-70. Nihon Jibiinkoka Gakkai Kaiho. 1983. PMID: 6620004 Japanese. No abstract available.

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