Van Ommen GJ - Search Results

1

Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization.

Rosenberg C, Navajas L, Vagenas DF, Bakker E, Vainzof M, Passos-Bueno MR, Takata RI, Van Ommen GJ, Zatz M, Den Dunnen JT. Rosenberg C, et al. Among authors: van ommen gj. Neuromuscul Disord. 1998 Oct;8(7):447-52. doi: 10.1016/s0960-8966(98)00050-9. Neuromuscul Disord. 1998. PMID: 9829273

2

Point mutation screening for 16 exons of the dystrophin gene by multiplex single-strand conformation polymorphism analysis.

Kneppers AL, Deutz-Terlouw PP, den Dunnen JT, van Ommen GJ, Bakker E. Kneppers AL, et al. Among authors: van ommen gj. Hum Mutat. 1995;5(3):235-42. doi: 10.1002/humu.1380050308. Hum Mutat. 1995. PMID: 7599634

3

Protein truncation test (PTT) to rapidly screen the DMD gene for translation terminating mutations.

Roest PA, Roberts RG, van der Tuijn AC, Heikoop JC, van Ommen GJ, den Dunnen JT. Roest PA, et al. Among authors: van der tuijn ac, van ommen gj. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):391-4. doi: 10.1016/0960-8966(93)90083-v. Neuromuscul Disord. 1993. PMID: 8186681

4

Application of in vitro Myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteins.

Roest PA, van der Tuijn AC, Ginjaar HB, Hoeben RC, Hoger-Vorst FB, Bakker E, den Dunnen JT, van Ommen GJ. Roest PA, et al. Among authors: van der tuijn ac, van ommen gj. Neuromuscul Disord. 1996 May;6(3):195-202. doi: 10.1016/0960-8966(96)00006-5. Neuromuscul Disord. 1996. PMID: 8784808

5

Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence risk.

Passos-Bueno MR, Bakker E, Kneppers AL, Takata RI, Rapaport D, den Dunnen JT, Zatz M, van Ommen GJ. Passos-Bueno MR, et al. Among authors: van ommen gj. Am J Hum Genet. 1992 Nov;51(5):1150-5. Am J Hum Genet. 1992. PMID: 1415256 Free PMC article.

6

Mapping of dystrophin brain promoter: a deletion of this region is compatible with normal intellect.

den Dunnen JT, Casula L, Makover A, Bakker B, Yaffe D, Nudel U, van Ommen GJ. den Dunnen JT, et al. Among authors: van ommen gj. Neuromuscul Disord. 1991;1(5):327-31. doi: 10.1016/0960-8966(91)90118-c. Neuromuscul Disord. 1991. PMID: 1822342

7

Detection of truncated dystrophin in fetal DMD myotubes.

Ginjaar IB, Bakker E, den Dunnen JT, Wessels A, van Paassen MM, Kloosterman MD, Zubrzycka-Gaarn EE, Fischbeck KH, Moorman AF, van Ommen GJ. Ginjaar IB, et al. Among authors: van ommen gj, van paassen mm. Adv Exp Med Biol. 1990;280:17-23. doi: 10.1007/978-1-4684-5865-7_4. Adv Exp Med Biol. 1990. PMID: 2248137

8

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

Blonden LA, den Dunnen JT, van Paassen HM, Wapenaar MC, Grootscholten PM, Ginjaar HB, Bakker E, Pearson PL, van Ommen GJ. Blonden LA, et al. Among authors: van paassen hm, van ommen gj. Nucleic Acids Res. 1989 Jul 25;17(14):5611-21. doi: 10.1093/nar/17.14.5611. Nucleic Acids Res. 1989. PMID: 2569720 Free PMC article.

9

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LA, Ginjaar HB, Wapenaar MC, van Paassen HM, van Broeckhoven C, Pearson PL, van Ommen GJ. Den Dunnen JT, et al. Among authors: van paassen hm, van ommen gj, van broeckhoven c. Am J Hum Genet. 1989 Dec;45(6):835-47. Am J Hum Genet. 1989. PMID: 2573997 Free PMC article.

10

The DMD gene analysed by field inversion gel electrophoresis.

den Dunnen JT, Bakker E, van Ommen GJ, Pearson PL. den Dunnen JT, et al. Among authors: van ommen gj. Br Med Bull. 1989 Jul;45(3):644-58. doi: 10.1093/oxfordjournals.bmb.a072350. Br Med Bull. 1989. PMID: 2597987

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