PubMed for id: 56006

Year	Number of Results
1996	1
2000	1
2001	1
2002	1
2003	1
2004	1
2005	1
2006	1
2009	1
2010	2
2011	3
2014	3
2015	2
2016	3
2017	1
2018	1
2019	5
2020	6
2021	6
2022	8
2023	2
2024	0

1

Identification of a novel compound heterozygous SMG9 variants in a Chinese family with heart and brain malformation syndrome using whole exome sequencing.

Yang Q, Qin Z, Zhang Q, Yi S, Yi S, Luo J. Yang Q, et al. BMC Med Genomics. 2022 Mar 23;15(1):67. doi: 10.1186/s12920-022-01217-9. BMC Med Genomics. 2022. PMID: 35321723 Free PMC article.

2

A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development.

Rahikkala E, Urpa L, Ghimire B, Topa H, Kurki MI, Koskela M, Airavaara M, Hämäläinen E, Pylkäs K, Körkkö J, Savolainen H, Suoranta A, Bertoli-Avella A, Rolfs A, Mattila P, Daly M, Palotie A, Pietiläinen O, Moilanen J, Kuismin O. Rahikkala E, et al. Eur J Hum Genet. 2022 May;30(5):619-627. doi: 10.1038/s41431-022-01046-5. Epub 2022 Jan 28. Eur J Hum Genet. 2022. PMID: 35087184 Free PMC article.

3

SMG9-deficiency syndrome caused by a homozygous missense variant: Expanding the genotypic and phenotypic spectrum of this developmental disorder.

Lemire G, MacDonald SK, Boycott KM. Lemire G, et al. Am J Med Genet A. 2020 Jul;182(7):1829-1831. doi: 10.1002/ajmg.a.61616. Epub 2020 May 15. Am J Med Genet A. 2020. PMID: 32412169 No abstract available.

4

Expanding the phenotypic and allelic spectrum of SMG8: Clinical observations reveal overlap with SMG9-associated disease trait.

Abdel-Salam GMH, Duan R, Abdel-Hamid MS, Sayed ISM, Jhangiani SN, Khan Z, Du H, Gibbs RA, Posey JE, Marafi D, Lupski JR. Abdel-Salam GMH, et al. Am J Med Genet A. 2022 Feb;188(2):648-657. doi: 10.1002/ajmg.a.62561. Epub 2021 Nov 10. Am J Med Genet A. 2022. PMID: 34761517

5

SMG9 drives ferroptosis by directly inhibiting GPX4 degradation.

Han L, Bai L, Fang X, Liu J, Kang R, Zhou D, Tang D, Dai E. Han L, et al. Biochem Biophys Res Commun. 2021 Aug 27;567:92-98. doi: 10.1016/j.bbrc.2021.06.038. Epub 2021 Jun 16. Biochem Biophys Res Commun. 2021. PMID: 34146907

6

MicroRNA 4651 regulates nonsense-mediated mRNA decay by targeting SMG9 mRNA.

Tan Y, Ma Z, Jin Y, Zong R, Wu J, Ren Z. Tan Y, et al. Gene. 2019 Jun 15;701:65-71. doi: 10.1016/j.gene.2019.03.031. Epub 2019 Mar 19. Gene. 2019. PMID: 30902786

7

Role of a tyrosine phosphorylation of SMG-9 in binding of SMG-9 to IQGAP and the NMD complex.

Takeda S, Fujimoto A, Yamauchi E, Hiyoshi M, Kido H, Watanabe T, Kaibuchi K, Ohta T, Konishi H. Takeda S, et al. Biochem Biophys Res Commun. 2011 Jun 24;410(1):29-33. doi: 10.1016/j.bbrc.2011.05.099. Epub 2011 May 24. Biochem Biophys Res Commun. 2011. PMID: 21640080

8

Structure of substrate-bound SMG1-8-9 kinase complex reveals molecular basis for phosphorylation specificity.

Langer LM, Gat Y, Bonneau F, Conti E. Langer LM, et al. Elife. 2020 May 29;9:e57127. doi: 10.7554/eLife.57127. Elife. 2020. PMID: 32469312 Free PMC article.

9

InsP₆ binding to PIKK kinases revealed by the cryo-EM structure of an SMG1-SMG8-SMG9 complex.

Gat Y, Schuller JM, Lingaraju M, Weyher E, Bonneau F, Strauss M, Murray PJ, Conti E. Gat Y, et al. Nat Struct Mol Biol. 2019 Dec;26(12):1089-1093. doi: 10.1038/s41594-019-0342-7. Epub 2019 Dec 2. Nat Struct Mol Biol. 2019. PMID: 31792449

10

Cryo-EM structure of SMG1-SMG8-SMG9 complex.

Zhu L, Li L, Qi Y, Yu Z, Xu Y. Zhu L, et al. Cell Res. 2019 Dec;29(12):1027-1034. doi: 10.1038/s41422-019-0255-3. Epub 2019 Nov 15. Cell Res. 2019. PMID: 31729466 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

45 results

Results by year