Similar articles for PMID: 27448789

Year	Number of Results
1998	1
2001	2
2002	2
2003	3
2004	7
2005	1
2006	1
2007	3
2008	4
2009	3
2010	7
2011	6
2012	9
2013	6
2014	4
2015	8
2016	11
2017	9
2018	8
2019	16
2020	14
2021	16
2022	14
2023	18
2024	0

1

Mutations in TFAM, encoding mitochondrial transcription factor A, cause neonatal liver failure associated with mtDNA depletion.

Stiles AR, Simon MT, Stover A, Eftekharian S, Khanlou N, Wang HL, Magaki S, Lee H, Partynski K, Dorrani N, Chang R, Martinez-Agosto JA, Abdenur JE. Stiles AR, et al. Mol Genet Metab. 2016 Sep;119(1-2):91-9. doi: 10.1016/j.ymgme.2016.07.001. Epub 2016 Jul 4. Mol Genet Metab. 2016. PMID: 27448789

2

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss.

Ullah F, Rauf W, Khan K, Khan S, Bell KM, de Oliveira VC, Tariq M, Bakhshalizadeh S, Touraine P, Katsanis N, Sinclair A, He S, Tucker EJ, Baig SM, Davis EE. Ullah F, et al. Hum Genet. 2021 Dec;140(12):1733-1751. doi: 10.1007/s00439-021-02380-2. Epub 2021 Oct 13. Hum Genet. 2021. PMID: 34647195

3

High levels of TFAM repress mammalian mitochondrial DNA transcription in vivo.

Bonekamp NA, Jiang M, Motori E, Garcia Villegas R, Koolmeister C, Atanassov I, Mesaros A, Park CB, Larsson NG. Bonekamp NA, et al. Life Sci Alliance. 2021 Aug 30;4(11):e202101034. doi: 10.26508/lsa.202101034. Print 2021 Nov. Life Sci Alliance. 2021. PMID: 34462320 Free PMC article.

4

Overexpression of mitochondrial transcription factor a ameliorates mitochondrial deficiencies and cardiac failure after myocardial infarction.

Ikeuchi M, Matsusaka H, Kang D, Matsushima S, Ide T, Kubota T, Fujiwara T, Hamasaki N, Takeshita A, Sunagawa K, Tsutsui H. Ikeuchi M, et al. Circulation. 2005 Aug 2;112(5):683-90. doi: 10.1161/CIRCULATIONAHA.104.524835. Epub 2005 Jul 25. Circulation. 2005. PMID: 16043643

5

Mitochondrial transcription factor A regulates mitochondrial transcription initiation, DNA packaging, and genome copy number.

Campbell CT, Kolesar JE, Kaufman BA. Campbell CT, et al. Biochim Biophys Acta. 2012 Sep-Oct;1819(9-10):921-9. doi: 10.1016/j.bbagrm.2012.03.002. Epub 2012 Mar 21. Biochim Biophys Acta. 2012. PMID: 22465614 Review.

6

The TFAM-to-mtDNA ratio defines inner-cellular nucleoid populations with distinct activity levels.

Brüser C, Keller-Findeisen J, Jakobs S. Brüser C, et al. Cell Rep. 2021 Nov 23;37(8):110000. doi: 10.1016/j.celrep.2021.110000. Cell Rep. 2021. PMID: 34818548 Free article.

7

Metabolic Reprogramming in Response to Alterations of Mitochondrial DNA and Mitochondrial Dysfunction in Gastric Adenocarcinoma.

Chang TC, Lee HT, Pan SC, Cho SH, Cheng C, Ou LH, Lin CI, Lin CS, Wei YH. Chang TC, et al. Int J Mol Sci. 2022 Feb 6;23(3):1857. doi: 10.3390/ijms23031857. Int J Mol Sci. 2022. PMID: 35163779 Free PMC article.

8

MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations.

El-Hattab AW, Li FY, Schmitt E, Zhang S, Craigen WJ, Wong LJ. El-Hattab AW, et al. Mol Genet Metab. 2010 Mar;99(3):300-8. doi: 10.1016/j.ymgme.2009.10.003. Epub 2009 Oct 13. Mol Genet Metab. 2010. PMID: 20074988

9

Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options.

El-Hattab AW, Scaglia F. El-Hattab AW, et al. Neurotherapeutics. 2013 Apr;10(2):186-98. doi: 10.1007/s13311-013-0177-6. Neurotherapeutics. 2013. PMID: 23385875 Free PMC article. Review.

10

Failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers of chronic obstructive pulmonary disease locomotor muscle.

Konokhova Y, Spendiff S, Jagoe RT, Aare S, Kapchinsky S, MacMillan NJ, Rozakis P, Picard M, Aubertin-Leheudre M, Pion CH, Bourbeau J, Hepple RT, Taivassalo T. Konokhova Y, et al. Skelet Muscle. 2016 Feb 18;6:10. doi: 10.1186/s13395-016-0083-9. eCollection 2016. Skelet Muscle. 2016. PMID: 26893822 Free PMC article.

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