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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Published in:
Journal of Human Genetics, 2014, v. 59, n. 4, p. 216, doi. 10.1038/jhg.2014.4
By:
- Jellouli, Nadege Kammoun;
- Hadj Salem, Ikhlass;
- Ellouz, Emna;
- Kamoun, Zeineb;
- kamoun, Fatma;
- tlili, Abdelaziz;
- Kaabachi, Naziha;
- Triki, Chanez;
- Fakhfakh, Faiza
Publication type:
Article
Co-Culture of Human Bronchial Fibroblasts and CD4+ T Cells Increases Th17 Cytokine Signature.
Published in:
PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0081983
By:
- Loubaki, Lionel;
- Hadj-Salem, Ikhlass;
- Fakhfakh, Raouia;
- Jacques, Eric;
- Plante, Sophie;
- Boisvert, Marc;
- Aoudjit, Fawzi;
- Chakir, Jamila
Publication type:
Article
Molecular Characterization of X-Linked Adrenoleukodystrophy in a Tunisian Family: Identification of a Novel Missense Mutation in the ABCD1 Gene.
Published in:
Neurodegenerative Diseases, 2013, v. 12, n. 4, p. 207, doi. 10.1159/000346680
By:
- Kallabi, Fakhri;
- Hadj Salem, Ikhlass;
- Ben Salah, Ghada;
- Ben Turkia, Hadhami;
- Ben Chehida, amel;
- Tebib, Neji;
- Fakhfakh, Faiza;
- Kamoun, Hassen
Publication type:
Article
<italic>Retracted</italic>: Genotyping of Tunisian azoospermic men with Sertoli cell‐only and maturation arrest.
Published in:
Andrologia, 2018, v. 50, n. 4, p. 1, doi. 10.1111/j.1439-0272.2010.01088.x
By:
- Hadjkacem‐Loukil, Lobna;
- Hadj‐kacem, Hassen;
- Hadj Salem, Ikhlass;
- Bahloul, Ali;
- Fakhfakh, Faiza;
- Ayadi, Hammadi
Publication type:
Article
Impact of single-nucleotide polymorphisms at the TP53-binding and responsive promoter region of BCL2 gene in modulating the phenotypic variability of LGMD2C patients.
Published in:
Molecular Biology Reports, 2012, v. 39, n. 7, p. 7479, doi. 10.1007/s11033-012-1581-4
By:
- Hadj Salem, Ikhlass;
- Kamoun, Fatma;
- Louhichi, Nacim;
- Trigui, Moez;
- Triki, Chahnez;
- Fakhfakh, Faiza
Publication type:
Article

Found: 5

Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.

Co-Culture of Human Bronchial Fibroblasts and CD4+ T Cells Increases Th17 Cytokine Signature.

Molecular Characterization of X-Linked Adrenoleukodystrophy in a Tunisian Family: Identification of a Novel Missense Mutation in the ABCD1 Gene.

<italic>Retracted</italic>: Genotyping of Tunisian azoospermic men with Sertoli cell‐only and maturation arrest.

Impact of single-nucleotide polymorphisms at the TP53-binding and responsive promoter region of BCL2 gene in modulating the phenotypic variability of LGMD2C patients.