PubMed for id: 4848

Year	Number of Results
2000	2
2002	1
2003	2
2004	3
2005	3
2006	3
2007	1
2008	1
2009	1
2010	4
2011	4
2012	2
2013	5
2014	2
2015	7
2016	4
2017	5
2018	4
2019	12
2020	5
2021	8
2022	8
2023	3
2024	0

1

Delineation of the clinical profile of CNOT2 haploinsufficiency and overview of the IDNADFS phenotype.

Niceta M, Pizzi S, Inzana F, Peron A, Bakhtiari S, Nizon M, Levy J, Mancini C, Cogné B, Radio FC, Agolini E, Cocciadiferro D, Novelli A, Salih MA, Recalcati MP, Arancio R, Besnard M, Tabet AC, Kruer MC, Priolo M, Dallapiccola B, Tartaglia M. Niceta M, et al. Clin Genet. 2023 Feb;103(2):156-166. doi: 10.1111/cge.14247. Epub 2022 Nov 24. Clin Genet. 2023. PMID: 36224108 Free PMC article.

2

CNOT2 haploinsufficiency in a 40-year-old man with intellectual disability, autism, and seizures.

Royer-Bertrand B, Cisarova K, Niel Bütschi F, Foletti G, Guinchat V, Tran C, Superti-Furga A, Good JM. Royer-Bertrand B, et al. Am J Med Genet A. 2021 Aug;185(8):2602-2606. doi: 10.1002/ajmg.a.62343. Epub 2021 May 21. Am J Med Genet A. 2021. PMID: 34018673 Review. No abstract available.

3

CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features.

Uehara T, Tsuchihashi T, Yamada M, Suzuki H, Takenouchi T, Kosaki K. Uehara T, et al. Am J Med Genet A. 2019 Dec;179(12):2506-2509. doi: 10.1002/ajmg.a.61356. Epub 2019 Sep 11. Am J Med Genet A. 2019. PMID: 31512373 Review. No abstract available.

4

CNOT2 facilitates dengue virus infection via negatively modulating IFN-Independent Non-Canonical JAK/STAT pathway.

Liu J, Yang L, Liu F, Li H, Tang W, Tong X, Zuo J. Liu J, et al. Biochem Biophys Res Commun. 2019 Jul 30;515(3):403-409. doi: 10.1016/j.bbrc.2019.05.083. Epub 2019 May 31. Biochem Biophys Res Commun. 2019. PMID: 31155293

5

A heterozygous, intragenic deletion of CNOT2 recapitulates the phenotype of 12q15 deletion syndrome.

Alesi V, Loddo S, Calì F, Orlando V, Genovese S, Ferretti D, Calacci C, Calvieri G, Falasca R, Ulgheri L, Drago F, Dallapiccola B, Baban A, Novelli A. Alesi V, et al. Am J Med Genet A. 2019 Aug;179(8):1615-1621. doi: 10.1002/ajmg.a.61217. Epub 2019 May 30. Am J Med Genet A. 2019. PMID: 31145527 Review.

6

CNOT2 as the critical gene for phenotypes of 12q15 microdeletion syndrome.

Uehara T, Takenouchi T, Yamaguchi Y, Daimon Y, Suzuki H, Sakaguchi Y, Kosaki K. Uehara T, et al. Am J Med Genet A. 2019 Apr;179(4):659-662. doi: 10.1002/ajmg.a.61068. Epub 2019 Feb 15. Am J Med Genet A. 2019. PMID: 30768759

7

The CCR4-NOT complex plays diverse roles in mRNA metabolism.

Denis CL, Chen J. Denis CL, et al. Prog Nucleic Acid Res Mol Biol. 2003;73:221-50. doi: 10.1016/s0079-6603(03)01007-9. Prog Nucleic Acid Res Mol Biol. 2003. PMID: 12882519 Review.

8

CCR4‑NOT transcription complex subunit 2 regulates TRAIL sensitivity in non‑small‑cell lung cancer cells via the STAT3 pathway.

Kim EO, Kang SE, Choi M, Rhee KJ, Yun M. Kim EO, et al. Int J Mol Med. 2020 Feb;45(2):324-332. doi: 10.3892/ijmm.2019.4425. Epub 2019 Dec 12. Int J Mol Med. 2020. PMID: 31894259 Free PMC article.

9

CNOT2 promotes proliferation and angiogenesis via VEGF signaling in MDA-MB-231 breast cancer cells.

Sohn EJ, Jung DB, Lee H, Han I, Lee J, Lee H, Kim SH. Sohn EJ, et al. Cancer Lett. 2018 Jan 1;412:88-98. doi: 10.1016/j.canlet.2017.09.052. Epub 2017 Oct 9. Cancer Lett. 2018. PMID: 29024811

10

CNOT2 promotes degradation of p62/SQSTM1 as a negative regulator in ATG5 dependent autophagy.

Jeong K, Kwon HY, Jeong MS, Sohn EJ, Kim SH. Jeong K, et al. Oncotarget. 2017 Jul 11;8(28):46034-46046. doi: 10.18632/oncotarget.17682. Oncotarget. 2017. PMID: 28537904 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

82 results

Results by year