Gilgenkrantz H - Search Results

1

Additional case of female monozygotic twins discordant for the clinical manifestations of Duchenne muscular dystrophy due to opposite X-chromosome inactivation.

Abbadi N, Philippe C, Chery M, Gilgenkrantz H, Tome F, Collin H, Theau D, Recan D, Broux O, Fardeau M, et al. Abbadi N, et al. Among authors: gilgenkrantz h. Am J Med Genet. 1994 Aug 15;52(2):198-206. doi: 10.1002/ajmg.1320520215. Am J Med Genet. 1994. PMID: 7802009

2

[Molecular pathology of Duchenne and Becker muscular dystrophy].

Gilgenkrantz H, Chelly J, Récan D, Chafey P, Kaplan JC. Gilgenkrantz H, et al. C R Seances Soc Biol Fil. 1992;186(4):349-53. C R Seances Soc Biol Fil. 1992. PMID: 1301222 French.

3

Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies.

Chelly J, Gilgenkrantz H, Lambert M, Hamard G, Chafey P, Récan D, Katz P, de la Chapelle A, Koenig M, Ginjaar IB, et al. Chelly J, et al. Among authors: gilgenkrantz h. Cell. 1990 Dec 21;63(6):1239-48. doi: 10.1016/0092-8674(90)90419-f. Cell. 1990. PMID: 2261642

4

Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.

Chelly J, Gilgenkrantz H, Hugnot JP, Hamard G, Lambert M, Récan D, Akli S, Cometto M, Kahn A, Kaplan JC. Chelly J, et al. Among authors: gilgenkrantz h. J Clin Invest. 1991 Oct;88(4):1161-6. doi: 10.1172/JCI115417. J Clin Invest. 1991. PMID: 1918370 Free PMC article.

5

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.

Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Among authors: gilgenkrantz h. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.

6

Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies.

Gilgenkrantz H, Chelly J, Lambert M, Récan D, Barbot JC, van Ommen GJ, Kaplan JC. Gilgenkrantz H, et al. Genomics. 1989 Oct;5(3):574-80. doi: 10.1016/0888-7543(89)90025-6. Genomics. 1989. PMID: 2613240

7

Long-term correction of mouse dystrophic degeneration by adenovirus-mediated transfer of a minidystrophin gene.

Vincent N, Ragot T, Gilgenkrantz H, Couton D, Chafey P, Grégoire A, Briand P, Kaplan JC, Kahn A, Perricaudet M. Vincent N, et al. Among authors: gilgenkrantz h. Nat Genet. 1993 Oct;5(2):130-4. doi: 10.1038/ng1093-130. Nat Genet. 1993. PMID: 8252038

8

Striking conservation of the brain-specific region of the dystrophin gene.

Hugnot JP, Gilgenkrantz H, Jeanpierre M, Chelly J, Kaplan JC, Kahn A. Hugnot JP, et al. Among authors: gilgenkrantz h. Mamm Genome. 1993;4(7):393-6. doi: 10.1007/BF00360592. Mamm Genome. 1993. PMID: 8358174 No abstract available.

9

Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues.

Hugnot JP, Gilgenkrantz H, Vincent N, Chafey P, Morris GE, Monaco AP, Berwald-Netter Y, Koulakoff A, Kaplan JC, Kahn A, et al. Hugnot JP, et al. Among authors: gilgenkrantz h. Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7506-10. doi: 10.1073/pnas.89.16.7506. Proc Natl Acad Sci U S A. 1992. PMID: 1380160 Free PMC article.

10

Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice.

Ragot T, Vincent N, Chafey P, Vigne E, Gilgenkrantz H, Couton D, Cartaud J, Briand P, Kaplan JC, Perricaudet M, et al. Ragot T, et al. Among authors: gilgenkrantz h. Nature. 1993 Feb 18;361(6413):647-50. doi: 10.1038/361647a0. Nature. 1993. PMID: 8437625

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