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2016
Mark Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
Mkaouar-Rebai, Emna ; Felhi, Rahma ; Tabebi, Mouna ; Alila-Fersi, Olfa ; Chamkha, Imen ^LU ; Maalej, Marwa ; Ammar, Marwa ; Kammoun, Fatma ; Keskes, Leila and Hachicha, Mongia , et al. (2016) In Biochemical and Biophysical Research Communications 473(2). p.85-578
- Contribution to journal › Article
2014
Mark A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
Maalej, M ; Mkaouar-Rebai, E ; Mnif, M ; Mezghani, N ; Ben Ayed, I ; Chamkha, I ^LU ; Abid, M and Fakhfakh, F (2014) In Pathologie Biologie 62(1). p.8-41
- Contribution to journal › Article
Mark A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy
Mkaouar-Rebai, Emna ; Ben Mahmoud, Afif ; Chamkha, Imen ^LU ; Chabchoub, Imen ; Kammoun, Thouraya ; Hachicha, Mongia and Fakhfakh, Faiza (2014) In Mitochondrial DNA 25(5). p.9-394
- Contribution to journal › Article
Mark Platelets release mitochondria serving as substrate for bactericidal group IIA-secreted phospholipase A2 to promote inflammation
Boudreau, Luc H ; Duchez, Anne-Claire ; Cloutier, Nathalie ; Soulet, Denis ^LU ; Martin, Nicolas ; Bollinger, James ; Paré, Alexandre ; Rousseau, Matthieu ; Naika, Gajendra S and Lévesque, Tania , et al. (2014) In Blood 124(14). p.83-2173
- Contribution to journal › Article
2013
Mark Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Mezghani, Najla ; Ben Ayed, Imen and Fakhfakh, Faiza (2013) In Mitochondrial DNA 24(3). p.78-163
- Contribution to journal › Article
2012
Mark Evolutionary history of the genus Trisopterus
Gonzalez, Elena G ; Cunha, Regina L ; Sevilla, Rafael G ; Ghanavi, Hamid R ^LU ; Krey, Grigorios and Bautista, José M (2012) In Molecular Phylogenetics and Evolution 62(3). p.1013-1018
- Contribution to journal › Article
2011
Mark A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions
Ayed, Imen Ben ; Chamkha, Imen ^LU ; Mkaouar-Rebai, Emna ; Kammoun, Thouraya ; Mezghani, Najla ; Chabchoub, Imen ; Aloulou, Hajer ; Hachicha, Mongia and Fakhfakh, Faiza (2011) In Biochemical and Biophysical Research Communications 411(2). p.6-381
- Contribution to journal › Article
Mark A novel m.3395A>G missense mutation in the mitochondrial ND1 gene associated with the new tRNA(Ile) m.4316A>G mutation in a patient with hypertrophic cardiomyopathy and profound hearing loss
Chamkha, Imen ^LU ; Mkaouar-Rebai, Emna ; Aloulou, Hajer ; Chabchoub, Imen ; Kifagi, Chamseddine ^LU ; Fendri-Kriaa, Nourhene ; Kammoun, Thouraya ; Hachicha, Mongia and Fakhfakh, Faiza (2011) In Biochemical and Biophysical Research Communications 404(1). p.10-504
- Contribution to journal › Article
2010
Mark A case of Kearns-Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Kammoun, Thouraya ; Chabchoub, Imen ; Aloulou, Hajer ; Fendri, Nourhene ; Hachicha, Mongia and Fakhfakh, Faiza (2010) In Mitochondrion 10(5). p.55-449
- Contribution to journal › Article
Mark A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder
Mkaouar-Rebai, Emna ; Kammoun, Fatma ; Chamkha, Imen ^LU ; Kammoun, Nadège ; Hsairi, Ines ; Triki, Chahnez and Fakhfakh, Faiza (2010) In Journal of Child Neurology 25(6). p.5-770
- Contribution to journal › Article