Hovnanian A - Search Results

1

Correction to: Antisense-Mediated Splice Modulation to Reframe Transcripts.

Titeux M, Turczynski S, Pironon N, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. Methods Mol Biol. 2018;1828:E1. doi: 10.1007/978-1-4939-8651-4_37. Methods Mol Biol. 2018. PMID: 30488375

2

Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene.

Titeux M, Mazereeuw-Hautier J, Hadj-Rabia S, Prost C, Tonasso L, Fraitag S, de Prost Y, Hovnanian A, Bodemer C. Titeux M, et al. Among authors: hovnanian a. J Invest Dermatol. 2006 Apr;126(4):773-6. doi: 10.1038/sj.jid.5700154. J Invest Dermatol. 2006. PMID: 16439965 Free article.

3

Recessive dystrophic epidermolysis bullosa caused by COL7A1 hemizygosity and a missense mutation with complex effects on splicing.

Titeux M, Mejía JE, Mejlumian L, Bourthoumieu S, Mirval S, Tonasso L, Heller M, Prost-Squarcioni C, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. Hum Mutat. 2006 Mar;27(3):291-2. doi: 10.1002/humu.9406. Hum Mutat. 2006. PMID: 16470588

4

TLR3 deficiency in patients with herpes simplex encephalitis.

Zhang SY, Jouanguy E, Ugolini S, Smahi A, Elain G, Romero P, Segal D, Sancho-Shimizu V, Lorenzo L, Puel A, Picard C, Chapgier A, Plancoulaine S, Titeux M, Cognet C, von Bernuth H, Ku CL, Casrouge A, Zhang XX, Barreiro L, Leonard J, Hamilton C, Lebon P, Héron B, Vallée L, Quintana-Murci L, Hovnanian A, Rozenberg F, Vivier E, Geissmann F, Tardieu M, Abel L, Casanova JL. Zhang SY, et al. Among authors: hovnanian a. Science. 2007 Sep 14;317(5844):1522-7. doi: 10.1126/science.1139522. Science. 2007. PMID: 17872438

5

A frequent functional SNP in the MMP1 promoter is associated with higher disease severity in recessive dystrophic epidermolysis bullosa.

Titeux M, Pendaries V, Tonasso L, Décha A, Bodemer C, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. Hum Mutat. 2008 Feb;29(2):267-76. doi: 10.1002/humu.20647. Hum Mutat. 2008. PMID: 18030675

6

Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa.

Pendaries V, Gasc G, Titeux M, Leroux C, Vitezica ZG, Mejía JE, Décha A, Loiseau P, Bodemer C, Prost-Squarcioni C, Hovnanian A. Pendaries V, et al. Among authors: hovnanian a. Gene Ther. 2010 Jul;17(7):930-7. doi: 10.1038/gt.2010.36. Epub 2010 Apr 8. Gene Ther. 2010. PMID: 20376098

7

Gene therapy for recessive dystrophic epidermolysis bullosa.

Titeux M, Pendaries V, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. Dermatol Clin. 2010 Apr;28(2):361-6, xii. doi: 10.1016/j.det.2010.02.003. Dermatol Clin. 2010. PMID: 20447504 Review.

8

SIN retroviral vectors expressing COL7A1 under human promoters for ex vivo gene therapy of recessive dystrophic epidermolysis bullosa.

Titeux M, Pendaries V, Zanta-Boussif MA, Décha A, Pironon N, Tonasso L, Mejia JE, Brice A, Danos O, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. Mol Ther. 2010 Aug;18(8):1509-18. doi: 10.1038/mt.2010.91. Epub 2010 May 18. Mol Ther. 2010. PMID: 20485266 Free PMC article.

9

A new case of keratin 14 functional knockout causes severe recessive EBS and questions the haploinsufficiency model of Naegeli-Franceschetti-Jadassohn syndrome.

Titeux M, Décha A, Pironon N, Tonasso L, Gasc G, Mejía JE, Prost-Squarcioni C, Hovnanian A. Titeux M, et al. Among authors: hovnanian a. J Invest Dermatol. 2011 Oct;131(10):2131-3. doi: 10.1038/jid.2011.166. Epub 2011 Jul 7. J Invest Dermatol. 2011. PMID: 21734713 Free article. No abstract available.

10

siRNA-mediated allele-specific inhibition of mutant type VII collagen in dominant dystrophic epidermolysis bullosa.

Pendaries V, Gasc G, Titeux M, Tonasso L, Mejía JE, Hovnanian A. Pendaries V, et al. Among authors: hovnanian a. J Invest Dermatol. 2012 Jun;132(6):1741-3. doi: 10.1038/jid.2012.11. Epub 2012 Feb 16. J Invest Dermatol. 2012. PMID: 22336946 Free article. No abstract available.

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