Miniou P[auth] - Search Results

Year	Number of Results
1992	1
1994	2
1995	2
1996	1
1997	5
1999	3
2000	1
2021	1
2022	1
2023	1
2024	0

1

Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice.

Bai Y, Treins C, Volpi VG, Scapin C, Ferri C, Mastrangelo R, Touvier T, Florio F, Bianchi F, Del Carro U, Baas FF, Wang D, Miniou P, Guedat P, Shy ME, D'Antonio M. Bai Y, et al. Among authors: miniou p. Mol Neurobiol. 2022 Jul;59(7):4159-4178. doi: 10.1007/s12035-022-02838-y. Epub 2022 Apr 30. Mol Neurobiol. 2022. PMID: 35501630 Free PMC article.

2

Therapeutic Development in Charcot Marie Tooth Type 1 Disease.

Miniou P, Fontes M. Miniou P, et al. Int J Mol Sci. 2021 Jun 23;22(13):6755. doi: 10.3390/ijms22136755. Int J Mol Sci. 2021. PMID: 34201736 Free PMC article. Review.

3

A Rat Model of Clinically Relevant Extracorporeal Circulation Develops Early Organ Dysfunctions.

Persello A, Souab F, Dupas T, Aillerie V, Bigot E, Denis M, Erraud A, Pelé T, Blangy-Letheule A, Miniou P, Guedat P, De Waard M, Abgueguen E, Rozec B, Lauzier B. Persello A, et al. Among authors: miniou p. Int J Mol Sci. 2023 Apr 16;24(8):7338. doi: 10.3390/ijms24087338. Int J Mol Sci. 2023. PMID: 37108501 Free PMC article.

4

Gene targeting restricted to mouse striated muscle lineage.

Miniou P, Tiziano D, Frugier T, Roblot N, Le Meur M, Melki J. Miniou P, et al. Nucleic Acids Res. 1999 Oct 1;27(19):e27. doi: 10.1093/nar/27.19.e27. Nucleic Acids Res. 1999. PMID: 10481039 Free PMC article.

5

Abnormal methylation does not prevent X inactivation in ICF patients.

Bourc'his D, Miniou P, Jeanpierre M, Molina Gomes D, Dupont J, De Saint-Basile G, Maraschio P, Tiepolo L, Viegas-Péquignot E. Bourc'his D, et al. Among authors: miniou p. Cytogenet Cell Genet. 1999;84(3-4):245-52. doi: 10.1159/000015269. Cytogenet Cell Genet. 1999. PMID: 10393442

6

Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy.

Frugier T, Tiziano FD, Cifuentes-Diaz C, Miniou P, Roblot N, Dierich A, Le Meur M, Melki J. Frugier T, et al. Among authors: miniou p. Hum Mol Genet. 2000 Mar 22;9(5):849-58. doi: 10.1093/hmg/9.5.849. Hum Mol Genet. 2000. PMID: 10749994

7

The promoters of the survival motor neuron gene (SMN) and its copy (SMNc) share common regulatory elements.

Echaniz-Laguna A, Miniou P, Bartholdi D, Melki J. Echaniz-Laguna A, et al. Among authors: miniou p. Am J Hum Genet. 1999 May;64(5):1365-70. doi: 10.1086/302372. Am J Hum Genet. 1999. PMID: 10205267 Free PMC article.

8

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease.

Bürglen L, Seroz T, Miniou P, Lefebvre S, Burlet P, Munnich A, Pequignot EV, Egly JM, Melki J. Bürglen L, et al. Among authors: miniou p. Am J Hum Genet. 1997 Jan;60(1):72-9. Am J Hum Genet. 1997. PMID: 8981949 Free PMC article.

9

Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.

Oliveira L, Miniou P, Viegas-Pequignot E, Rozet JM, Dollfus H, Pittler SJ. Oliveira L, et al. Among authors: miniou p. Genomics. 1994 Jul 15;22(2):478-81. doi: 10.1006/geno.1994.1415. Genomics. 1994. PMID: 7806240

10

Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH.

Marinoni JC, Roy R, Vermeulen W, Miniou P, Lutz Y, Weeda G, Seroz T, Gomez DM, Hoeijmakers JH, Egly JM. Marinoni JC, et al. Among authors: miniou p. EMBO J. 1997 Mar 3;16(5):1093-102. doi: 10.1093/emboj/16.5.1093. EMBO J. 1997. PMID: 9118947 Free PMC article.

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