PubMed for id: 92609

Year	Number of Results
1999	1
2002	2
2003	2
2004	4
2005	3
2007	1
2008	1
2009	1
2010	4
2011	11
2012	11
2013	10
2014	9
2015	11
2016	12
2017	12
2018	24
2019	22
2020	18
2021	15
2022	25
2023	12
2024	1

1

Complete resolution of epileptic spasms with vigabatrin in a patient with 3-methylglutaconic aciduria caused by TIMM50 gene mutation.

Mir A, Hadab S, Sammak M, Alhazmi R, Housawi Y, Bashir S. Mir A, et al. Clin Genet. 2020 Jul;98(1):102-103. doi: 10.1111/cge.13763. Epub 2020 May 5. Clin Genet. 2020. PMID: 32369862 No abstract available.

2

Mutations in TIMM50 cause severe mitochondrial dysfunction by targeting key aspects of mitochondrial physiology.

Tort F, Ugarteburu O, Texidó L, Gea-Sorlí S, García-Villoria J, Ferrer-Cortès X, Arias Á, Matalonga L, Gort L, Ferrer I, Guitart-Mampel M, Garrabou G, Vaz FM, Pristoupilova A, Rodríguez MIE, Beltran S, Cardellach F, Wanders RJ, Fillat C, García-Silva MT, Ribes A. Tort F, et al. Hum Mutat. 2019 Oct;40(10):1700-1712. doi: 10.1002/humu.23779. Epub 2019 May 17. Hum Mutat. 2019. PMID: 31058414

3

TIMM50 promotes tumor progression via ERK signaling and predicts poor prognosis of non-small cell lung cancer patients.

Zhang X, Han S, Zhou H, Cai L, Li J, Liu N, Liu Y, Wang L, Fan C, Li A, Miao Y. Zhang X, et al. Mol Carcinog. 2019 May;58(5):767-776. doi: 10.1002/mc.22969. Epub 2019 Jan 22. Mol Carcinog. 2019. PMID: 30604908

4

Inner Mitochondrial Translocase Tim50 Is Central in Adrenal and Testicular Steroid Synthesis.

Bose HS, Gebrail F, Marshall B, Perry EW, Whittal RM. Bose HS, et al. Mol Cell Biol. 2018 Dec 11;39(1):e00484-18. doi: 10.1128/MCB.00484-18. Print 2019 Jan 1. Mol Cell Biol. 2018. PMID: 30348838 Free PMC article.

5

Mutations in TIMM50 compromise cell survival in OxPhos-dependent metabolic conditions.

Reyes A, Melchionda L, Burlina A, Robinson AJ, Ghezzi D, Zeviani M. Reyes A, et al. EMBO Mol Med. 2018 Oct;10(10):e8698. doi: 10.15252/emmm.201708698. EMBO Mol Med. 2018. PMID: 30190335 Free PMC article.

6

Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutations.

Shahrour MA, Staretz-Chacham O, Dayan D, Stephen J, Weech A, Damseh N, Pri Chen H, Edvardson S, Mazaheri S, Saada A; NISC Intramural Sequencing; Hershkovitz E, Shaag A, Huizing M, Abu-Libdeh B, Gahl WA, Azem A, Anikster Y, Vilboux T, Elpeleg O, Malicdan MC. Shahrour MA, et al. Clin Genet. 2017 May;91(5):690-696. doi: 10.1111/cge.12855. Epub 2016 Oct 12. Clin Genet. 2017. PMID: 27573165 Free PMC article.

7

Loss of TIM50 suppresses proliferation and induces apoptosis in breast cancer.

Gao SP, Sun HF, Jiang HL, Li LD, Hu X, Xu XE, Jin W. Gao SP, et al. Tumour Biol. 2016 Jan;37(1):1279-87. doi: 10.1007/s13277-015-3878-0. Epub 2015 Aug 20. Tumour Biol. 2016. PMID: 26289846

8

Interaction of divalent metal ions with human translocase of inner membrane of mitochondria Tim50.

Zhang Y, Deng H, Zhang X, Li SJ. Zhang Y, et al. Biochem Biophys Res Commun. 2012 Nov 23;428(3):365-70. doi: 10.1016/j.bbrc.2012.10.060. Epub 2012 Oct 23. Biochem Biophys Res Commun. 2012. PMID: 23098911

9

Interaction of presequence with human translocase of the inner membrane of mitochondria Tim50.

Zhang Y, Deng H, Zhao Q, Li SJ. Zhang Y, et al. J Phys Chem B. 2012 Mar 8;116(9):2990-8. doi: 10.1021/jp2108279. Epub 2012 Feb 27. J Phys Chem B. 2012. PMID: 22335443

10

Expression and structural characterization of human translocase of inner membrane of mitochondria Tim50.

Zhang Y, Xu Y, Zhao Q, Ji Z, Li Q, Li SJ. Zhang Y, et al. Protein Expr Purif. 2011 Nov;80(1):130-7. doi: 10.1016/j.pep.2011.06.012. Epub 2011 Jun 30. Protein Expr Purif. 2011. PMID: 21742040

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