PubMed for id: 3376

Year	Number of Results
1991	1
1993	1
1994	3
1995	1
1996	2
1997	1
1998	2
1999	1
2000	3
2001	1
2002	1
2003	1
2004	2
2005	4
2006	1
2007	2
2008	4
2009	6
2010	7
2011	11
2012	9
2013	5
2014	10
2015	11
2016	9
2017	16
2018	21
2019	16
2020	18
2021	19
2022	33
2023	11
2024	1

1

New evidence for association of recessive IARS gene mutations with hepatopathy, hypotonia, intellectual disability and growth retardation.

Smigiel R, Biela M, Biernacka A, Stembalska A, Sasiadek M, Kosinska J, Rydzanicz M, Ploski R. Smigiel R, et al. Clin Genet. 2017 Dec;92(6):671-673. doi: 10.1111/cge.13080. Epub 2017 Oct 19. Clin Genet. 2017. PMID: 29052218 No abstract available.

2

Bi-allelic IARS mutations in a child with intra-uterine growth retardation, neonatal cholestasis, and mild developmental delay.

Orenstein N, Weiss K, Oprescu SN, Shapira R, Kidron D, Vanagaite-Basel L, Antonellis A, Muenke M. Orenstein N, et al. Clin Genet. 2017 Jun;91(6):913-917. doi: 10.1111/cge.12930. Epub 2017 Feb 22. Clin Genet. 2017. PMID: 27891590 Free PMC article.

3

Human isoleucyl-tRNA synthetase: sequence of the cDNA, alternative mRNA splicing, and the characteristics of an unusually long C-terminal extension.

Nichols RC, Raben N, Boerkoel CF, Plotz PH. Nichols RC, et al. Gene. 1995 Apr 3;155(2):299-304. doi: 10.1016/0378-1119(94)00634-5. Gene. 1995. PMID: 7721108

4

Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy.

Kopajtich R, Murayama K, Janecke AR, Haack TB, Breuer M, Knisely AS, Harting I, Ohashi T, Okazaki Y, Watanabe D, Tokuzawa Y, Kotzaeridou U, Kölker S, Sauer S, Carl M, Straub S, Entenmann A, Gizewski E, Feichtinger RG, Mayr JA, Lackner K, Strom TM, Meitinger T, Müller T, Ohtake A, Hoffmann GF, Prokisch H, Staufner C. Kopajtich R, et al. Am J Hum Genet. 2016 Aug 4;99(2):414-22. doi: 10.1016/j.ajhg.2016.05.027. Epub 2016 Jul 14. Am J Hum Genet. 2016. PMID: 27426735 Free PMC article.

5

Isoleucylation properties of native human mitochondrial tRNAIle and tRNAIle transcripts. Implications for cardiomyopathy-related point mutations (4269, 4317) in the tRNAIle gene.

Degoul F, Brulé H, Cepanec C, Helm M, Marsac C, Leroux J, Giegé R, Florentz C. Degoul F, et al. Hum Mol Genet. 1998 Mar;7(3):347-54. doi: 10.1093/hmg/7.3.347. Hum Mol Genet. 1998. PMID: 9466989

6

Interaction between human tRNA synthetases involves repeated sequence elements.

Rho SB, Lee KH, Kim JW, Shiba K, Jo YJ, Kim S. Rho SB, et al. Proc Natl Acad Sci U S A. 1996 Sep 17;93(19):10128-33. doi: 10.1073/pnas.93.19.10128. Proc Natl Acad Sci U S A. 1996. PMID: 8816763 Free PMC article.

7

Assignment of two human autoantigen genes-isoleucyl-tRNA synthetase locates to 9q21 and lysyl-tRNA synthetase locates to 16q23-q24.

Nichols RC, Blinder J, Pai SI, Ge Q, Targoff IN, Plotz PH, Liu P. Nichols RC, et al. Genomics. 1996 Aug 15;36(1):210-3. doi: 10.1006/geno.1996.0449. Genomics. 1996. PMID: 8812440 No abstract available.

8

Mouse Zac1, a transcriptional coactivator and repressor for nuclear receptors.

Huang SM, Stallcup MR. Huang SM, et al. Mol Cell Biol. 2000 Mar;20(5):1855-67. doi: 10.1128/MCB.20.5.1855-1867.2000. Mol Cell Biol. 2000. PMID: 10669760 Free PMC article.

9

A multifunctional repeated motif is present in human bifunctional tRNA synthetase.

Rho SB, Lee JS, Jeong EJ, Kim KS, Kim YG, Kim S. Rho SB, et al. J Biol Chem. 1998 May 1;273(18):11267-73. doi: 10.1074/jbc.273.18.11267. J Biol Chem. 1998. PMID: 9556618 Free article.

10

The bI4 group I intron binds directly to both its protein splicing partners, a tRNA synthetase and maturase, to facilitate RNA splicing activity.

Rho SB, Martinis SA. Rho SB, et al. RNA. 2000 Dec;6(12):1882-94. doi: 10.1017/s1355838200001254. RNA. 2000. PMID: 11142386 Free PMC article.

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