Puymirat J - Search Results

1

Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles.

Vilquin JT, Guérette B, Puymirat J, Yaffe D, Tomé FM, Fardeau M, Fiszman M, Schwartz K, Tremblay JP. Vilquin JT, et al. Among authors: puymirat j. Gene Ther. 1999 May;6(5):792-800. doi: 10.1038/sj.gt.3300889. Gene Ther. 1999. PMID: 10505103

2

Transplantation of human myoblasts in SCID mice as a potential muscular model for myotonic dystrophy.

Skuk D, Furling D, Bouchard JP, Goulet M, Roy B, Lacroix Y, Vilquin JT, Tremblay JP, Puymirat J. Skuk D, et al. Among authors: puymirat j. J Neuropathol Exp Neurol. 1999 Sep;58(9):921-31. doi: 10.1097/00005072-199909000-00003. J Neuropathol Exp Neurol. 1999. PMID: 10499435

3

Increased granzyme B mRNA after alloincompatible myoblast transplantation.

Guérette B, Roy R, Tremblay M, Asselin I, Kinoshita I, Puymirat J, Tremblay JP. Guérette B, et al. Among authors: puymirat j. Transplantation. 1995 Nov 15;60(9):1011-6. Transplantation. 1995. PMID: 7491674

4

Increase in the proliferative capacity of human myoblasts by using the T antigen under the vimentin promoter control.

Deschênes I, Chahine M, Tremblay J, Paulin D, Puymirat J. Deschênes I, et al. Among authors: puymirat j. Muscle Nerve. 1997 Apr;20(4):437-45. doi: 10.1002/(sici)1097-4598(199704)20:4<437::aid-mus6>3.0.co;2-b. Muscle Nerve. 1997. PMID: 9121501

5

Viral vector producing antisense RNA restores myotonic dystrophy myoblast functions.

Furling D, Doucet G, Langlois MA, Timchenko L, Belanger E, Cossette L, Puymirat J. Furling D, et al. Among authors: puymirat j. Gene Ther. 2003 May;10(9):795-802. doi: 10.1038/sj.gt.3301955. Gene Ther. 2003. PMID: 12704419

6

Enhanced Delivery of Ligand-Conjugated Antisense Oligonucleotides (C16-HA-ASO) Targeting Dystrophia Myotonica Protein Kinase Transcripts for the Treatment of Myotonic Dystrophy Type 1.

Ait Benichou S, Jauvin D, De Serres-Bérard T, Bennett F, Rigo F, Gourdon G, Boutjdir M, Chahine M, Puymirat J. Ait Benichou S, et al. Among authors: puymirat j. Hum Gene Ther. 2022 Aug;33(15-16):810-820. doi: 10.1089/hum.2022.069. Hum Gene Ther. 2022. PMID: 35794764

7

Translating the genomics revolution: the need for an international gene therapy consortium for monogenic diseases.

Tremblay JP, Xiao X, Aartsma-Rus A, Barbas C, Blau HM, Bogdanove AJ, Boycott K, Braun S, Breakefield XO, Bueren JA, Buschmann M, Byrne BJ, Calos M, Cathomen T, Chamberlain J, Chuah M, Cornetta K, Davies KE, Dickson JG, Duchateau P, Flotte TR, Gaudet D, Gersbach CA, Gilbert R, Glorioso J, Herzog RW, High KA, Huang W, Huard J, Joung JK, Liu D, Liu D, Lochmüller H, Lustig L, Martens J, Massie B, Mavilio F, Mendell JR, Nathwani A, Ponder K, Porteus M, Puymirat J, Samulski J, Takeda S, Thrasher A, VandenDriessche T, Wei Y, Wilson JM, Wilton SD, Wolfe JH, Gao G. Tremblay JP, et al. Among authors: puymirat j. Mol Ther. 2013 Feb;21(2):266-8. doi: 10.1038/mt.2013.4. Mol Ther. 2013. PMID: 23369965 Free PMC article. No abstract available.

8

Hammerhead ribozyme-mediated destruction of nuclear foci in myotonic dystrophy myoblasts.

Langlois MA, Lee NS, Rossi JJ, Puymirat J. Langlois MA, et al. Among authors: puymirat j. Mol Ther. 2003 May;7(5 Pt 1):670-80. doi: 10.1016/s1525-0016(03)00068-6. Mol Ther. 2003. PMID: 12718910 Free article.

9

Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1.

Ait Benichou S, Jauvin D, De Serres-Bérard T, Pierre M, Ling KK, Bennett CF, Rigo F, Gourdon G, Chahine M, Puymirat J. Ait Benichou S, et al. Among authors: puymirat j. Gene Ther. 2022 Dec;29(12):698-709. doi: 10.1038/s41434-022-00316-7. Epub 2022 Jan 25. Gene Ther. 2022. PMID: 35075265 Free PMC article.

10

RNA based gene therapy for dominantly inherited diseases.

Pelletier R, Caron SO, Puymirat J. Pelletier R, et al. Among authors: puymirat j. Curr Gene Ther. 2006 Feb;6(1):131-46. doi: 10.2174/156652306775515592. Curr Gene Ther. 2006. PMID: 16475951 Review.

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