Mbarka Bchetnia - Search Results

Year	Number of Results
2008	2
2009	3
2010	1
2011	1
2012	2
2013	3
2014	2
2015	2
2016	1
2020	3
2021	1
2022	4
2024	1

1

Genetic burden linked to founder effects in Saguenay-Lac-Saint-Jean illustrates the importance of genetic screening test availability.

Bchetnia M, Bouchard L, Mathieu J, Campeau PM, Morin C, Brisson D, Laberge AM, Vézina H, Gaudet D, Laprise C. Bchetnia M, et al. J Med Genet. 2021 Oct;58(10):653-665. doi: 10.1136/jmedgenet-2021-107809. Epub 2021 Apr 28. J Med Genet. 2021. PMID: 33910931 Free PMC article. Review.

2

Expression signature of the Leigh syndrome French-Canadian type.

Bchetnia M, Tardif J, Morin C, Laprise C. Bchetnia M, et al. Mol Genet Metab Rep. 2022 Feb 5;30:100847. doi: 10.1016/j.ymgmr.2022.100847. eCollection 2022 Mar. Mol Genet Metab Rep. 2022. PMID: 35242578 Free PMC article.

3

Allele-Specific Inactivation of an Autosomal Dominant Epidermolysis Bullosa Simplex Mutation Using CRISPR-Cas9.

Bchetnia M, Dionne Gagné R, Powell J, Morin C, McCuaig C, Dupérée A, Germain L, Tremblay JP, Laprise C. Bchetnia M, et al. CRISPR J. 2022 Aug;5(4):586-597. doi: 10.1089/crispr.2021.0132. Epub 2022 Jul 21. CRISPR J. 2022. PMID: 35862015

4

Generation of three induced pluripotent stem cell lines (UQACi003-A, UQACi004-A, and UQACi006-A) from three patients with KRT5 epidermolysis bullosa simplex mutations.

Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Morin C, Dupérée A, Gros-Louis F, Laprise C. Bchetnia M, et al. Stem Cell Res. 2022 Apr;60:102726. doi: 10.1016/j.scr.2022.102726. Epub 2022 Feb 25. Stem Cell Res. 2022. PMID: 35247839 Free article.

5

Expression signature of epidermolysis bullosa simplex.

Bchetnia M, Tremblay ML, Leclerc G, Dupérée A, Powell J, McCuaig C, Morin C, Legendre-Guillemin V, Laprise C. Bchetnia M, et al. Hum Genet. 2012 Mar;131(3):393-406. doi: 10.1007/s00439-011-1077-7. Epub 2011 Aug 30. Hum Genet. 2012. PMID: 21877134

6

Generation of two induced pluripotent stem cell lines (UQACi002-A and UQACi005-A) from two patients with KRT14 epidermolysis bullosa simplex mutations.

Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Morin C, Dupérée A, Gros-Louis F, Laprise C. Bchetnia M, et al. Stem Cell Res. 2022 May;61:102750. doi: 10.1016/j.scr.2022.102750. Epub 2022 Mar 14. Stem Cell Res. 2022. PMID: 35334406 Free article.

7

Reduction in keratin aggregates in epidermolysis bullosa simplex keratinocytes after pretreatment with trimethylamine N-oxide.

Bchetnia M, Lacroix J, Farez T, Larouche M, Powell J, McCuaig C, Dupéré A, Morin C, Legendre-Guillemin V, Laprise C. Bchetnia M, et al. Exp Dermatol. 2016 Mar;25(3):229-30. doi: 10.1111/exd.12821. Epub 2015 Sep 15. Exp Dermatol. 2016. PMID: 26264477 No abstract available.

8

New mutations of Darier disease in Tunisian patients.

Bchetnia M, Benmously R, Ben Brick AS, Charfeddine C, Ben Ameur Y, Fajraoui M, Debbiche A, Ben Ayed M, Mokni M, Fenniche S, Mokhtar I, Abdelhak S. Bchetnia M, et al. Arch Dermatol Res. 2009 Sep;301(8):615-9. doi: 10.1007/s00403-009-0963-5. Epub 2009 Jun 2. Arch Dermatol Res. 2009. PMID: 19488774

9

Generation of a human induced pluripotent stem cell line (UQACi001-A) from a severe epidermolysis bullosa simplex patient with the heterozygous mutation p.R125S in the KRT14 gene.

Bchetnia M, Martineau L, Racine V, Powell J, McCuaig C, Puymirat J, Laprise C. Bchetnia M, et al. Stem Cell Res. 2020 Apr;44:101748. doi: 10.1016/j.scr.2020.101748. Epub 2020 Mar 6. Stem Cell Res. 2020. PMID: 32179493 Free article.

10

Cancer Spheroids Embedded in Tissue-Engineered Skin Substitutes: A New Method to Study Tumorigenicity In Vivo.

Barbier MA, Ferland K, De Koninck H, Doucet EJ, Dubourget L, Kim M, Cattier B, Morissette A, Bchetnia M, Larouche D, Kim DH, St-Jean G, Germain L. Barbier MA, et al. Among authors: bchetnia m. Int J Mol Sci. 2024 Jan 26;25(3):1513. doi: 10.3390/ijms25031513. Int J Mol Sci. 2024. PMID: 38338792 Free PMC article.

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