Similar articles for PMID: 10075708

Year	Number of Results
1988	1
1992	2
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1995	2
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1997	7
1998	6
1999	2
2000	9
2001	8
2002	6
2003	5
2004	3
2005	6
2006	2
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2011	2
2012	4
2014	1
2015	1
2016	1
2017	1
2019	2
2020	2
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2022	5
2024	0

1

Genes for the human mitochondrial trifunctional protein alpha- and beta-subunits are divergently transcribed from a common promoter region.

Orii KE, Orii KO, Souri M, Orii T, Kondo N, Hashimoto T, Aoyama T. Orii KE, et al. J Biol Chem. 1999 Mar 19;274(12):8077-84. doi: 10.1074/jbc.274.12.8077. J Biol Chem. 1999. PMID: 10075708 Free article.

2

Fluorescence in situ hybridization mapping of the alpha and beta subunits (HADHA and HADHB) of human mitochondrial fatty acid beta-oxidation multienzyme complex to 2p23 and their evolution.

Aoyama T, Wakui K, Orii KE, Hashimoto T, Fukushima Y. Aoyama T, et al. Cytogenet Cell Genet. 1997;79(3-4):221-4. doi: 10.1159/000134727. Cytogenet Cell Genet. 1997. PMID: 9605857

3

Genomic and mutational analysis of the mitochondrial trifunctional protein beta-subunit (HADHB) gene in patients with trifunctional protein deficiency.

Orii KE, Aoyama T, Wakui K, Fukushima Y, Miyajima H, Yamaguchi S, Orii T, Kondo N, Hashimoto T. Orii KE, et al. Hum Mol Genet. 1997 Aug;6(8):1215-24. doi: 10.1093/hmg/6.8.1215. Hum Mol Genet. 1997. PMID: 9259266

4

Comprehensive cDNA study and quantitative analysis of mutant HADHA and HADHB transcripts in a French cohort of 52 patients with mitochondrial trifunctional protein deficiency.

Boutron A, Acquaviva C, Vianey-Saban C, de Lonlay P, de Baulny HO, Guffon N, Dobbelaere D, Feillet F, Labarthe F, Lamireau D, Cano A, de Villemeur TB, Munnich A, Saudubray JM, Rabier D, Rigal O, Brivet M. Boutron A, et al. Mol Genet Metab. 2011 Aug;103(4):341-8. doi: 10.1016/j.ymgme.2011.04.006. Epub 2011 Apr 19. Mol Genet Metab. 2011. PMID: 21549624

5

Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB gene.

Das AM, Illsinger S, Lücke T, Hartmann H, Ruiter JP, Steuerwald U, Waterham HR, Duran M, Wanders RJ. Das AM, et al. Clin Chem. 2006 Mar;52(3):530-4. doi: 10.1373/clinchem.2005.062000. Epub 2006 Jan 19. Clin Chem. 2006. PMID: 16423905

6

Analysis of a family with mitochondrial trifunctional protein deficiency caused by HADHA gene mutations.

Yang J, Yuan D, Tan X, Zeng Y, Tang N, Chen D, Tan J, Cai R, Huang J, Yan T. Yang J, et al. Mol Med Rep. 2022 Feb;25(2):47. doi: 10.3892/mmr.2021.12563. Epub 2021 Dec 8. Mol Med Rep. 2022. PMID: 34878152 Free PMC article.

7

A patient with mitochondrial trifunctional protein deficiency due to the mutations in the HADHB gene showed recurrent myalgia since early childhood and was diagnosed in adolescence.

Yagi M, Lee T, Awano H, Tsuji M, Tajima G, Kobayashi H, Hasegawa Y, Yamaguchi S, Takeshima Y, Matsuo M. Yagi M, et al. Mol Genet Metab. 2011 Dec;104(4):556-9. doi: 10.1016/j.ymgme.2011.09.025. Epub 2011 Sep 28. Mol Genet Metab. 2011. PMID: 22000755

8

Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies.

Fletcher AL, Pennesi ME, Harding CO, Weleber RG, Gillingham MB. Fletcher AL, et al. Mol Genet Metab. 2012 May;106(1):18-24. doi: 10.1016/j.ymgme.2012.02.015. Epub 2012 Mar 8. Mol Genet Metab. 2012. PMID: 22459206 Free PMC article. Review.

9

E2F mediates induction of the Sp1-controlled promoter of the human DNA polymerase epsilon B-subunit gene POLE2.

Huang D, Jokela M, Tuusa J, Skog S, Poikonen K, Syväoja JE. Huang D, et al. Nucleic Acids Res. 2001 Jul 1;29(13):2810-21. doi: 10.1093/nar/29.13.2810. Nucleic Acids Res. 2001. PMID: 11433027 Free PMC article.

10

Mitochondrial trifunctional protein deficiency in human cultured fibroblasts: effects of bezafibrate.

Djouadi F, Habarou F, Le Bachelier C, Ferdinandusse S, Schlemmer D, Benoist JF, Boutron A, Andresen BS, Visser G, de Lonlay P, Olpin S, Fukao T, Yamaguchi S, Strauss AW, Wanders RJ, Bastin J. Djouadi F, et al. J Inherit Metab Dis. 2016 Jan;39(1):47-58. doi: 10.1007/s10545-015-9871-3. Epub 2015 Jun 25. J Inherit Metab Dis. 2016. PMID: 26109258 Free article.

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