Similar articles for PMID: 23030649

Year	Number of Results
1993	2
2001	2
2003	1
2006	3
2007	1
2009	1
2010	1
2011	3
2012	8
2013	8
2014	4
2015	1
2016	2
2019	2
2020	1
2024	0

1

Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population.

Baklouti-Gargouri S, Ghorbel M, Chamkha I, Mkaouar-Rebai E, Sellami A, Chakroun N, Fakhfakh F, Ammar-Keskes L. Baklouti-Gargouri S, et al. Genet Test Mol Biomarkers. 2012 Nov;16(11):1298-302. doi: 10.1089/gtmb.2012.0052. Epub 2012 Oct 2. Genet Test Mol Biomarkers. 2012. PMID: 23030649

2

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.

Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, Fakhfakh F, Ammar-Keskes L. Baklouti-Gargouri S, et al. Mol Biol Rep. 2013 Aug;40(8):4705-12. doi: 10.1007/s11033-013-2566-7. Epub 2013 May 6. Mol Biol Rep. 2013. PMID: 23645088

3

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men.

Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, Fakhfakh F, Ammar-Keskes L. Baklouti-Gargouri S, et al. Mol Reprod Dev. 2013 Jul;80(7):581-7. doi: 10.1002/mrd.22197. Epub 2013 Jun 17. Mol Reprod Dev. 2013. PMID: 23712756

4

Two novel mutations in COII and tRNA(His) mitochondrial genes in asthenozoospermic infertiles men.

Siwar BG, Myriam G, Afif BM, Emna MR, Nozha C, Afifa S, Faiza F, Leila AK. Siwar BG, et al. Biochem Biophys Res Commun. 2014 Jul 18;450(1):610-5. doi: 10.1016/j.bbrc.2014.06.020. Epub 2014 Jun 12. Biochem Biophys Res Commun. 2014. PMID: 24931671

5

Identification of a novel m.9588G > a missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men.

Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, Fakhfakh F, Ammar-Keskes L. Baklouti-Gargouri S, et al. J Assist Reprod Genet. 2014 May;31(5):595-600. doi: 10.1007/s10815-014-0187-2. Epub 2014 Feb 19. J Assist Reprod Genet. 2014. PMID: 24550096 Free PMC article.

6

Molecular-clinical correlation in a family with a novel heteroplasmic Leigh syndrome missense mutation in the mitochondrial cytochrome c oxidase III gene.

Mkaouar-Rebai E, Ellouze E, Chamkha I, Kammoun F, Triki C, Fakhfakh F. Mkaouar-Rebai E, et al. J Child Neurol. 2011 Jan;26(1):12-20. doi: 10.1177/0883073810371227. Epub 2010 Jun 4. J Child Neurol. 2011. PMID: 20525945

7

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.

Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F. Tabebi M, et al. Biochem Biophys Res Commun. 2015 Apr 10;459(3):353-60. doi: 10.1016/j.bbrc.2015.01.151. Epub 2015 Feb 19. Biochem Biophys Res Commun. 2015. PMID: 25701779

8

LRPPRC mutation suppresses cytochrome oxidase activity by altering mitochondrial RNA transcript stability in a mouse model.

Xu F, Addis JB, Cameron JM, Robinson BH. Xu F, et al. Biochem J. 2012 Jan 1;441(1):275-83. doi: 10.1042/BJ20110985. Biochem J. 2012. PMID: 21880015

9

Sperm mitochondrial DNA 15bp deletion of cytochrome c oxidase subunit III is significantly associated with human male infertility in Pakistan.

Mughal IA, Irfan A, Hameed A, Jahan S. Mughal IA, et al. J Pak Med Assoc. 2016 Jan;66(1):3-7. J Pak Med Assoc. 2016. PMID: 26712170

10

A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss.

Mkaouar-Rebai E, Chamkha I, Kammoun T, Alila-Fersi O, Aloulou H, Hachicha M, Fakhfakh F. Mkaouar-Rebai E, et al. Biochem Biophys Res Commun. 2013 Jan 11;430(2):585-91. doi: 10.1016/j.bbrc.2012.11.109. Epub 2012 Dec 5. Biochem Biophys Res Commun. 2013. PMID: 23219819

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