van Ommen GJ - Search Results

1

Different localization of dystrophin in developing and adult human skeletal muscle.

Wessels A, Ginjaar IB, Moorman AF, van Ommen GJ. Wessels A, et al. Among authors: van ommen gj. Muscle Nerve. 1991 Jan;14(1):1-7. doi: 10.1002/mus.880140102. Muscle Nerve. 1991. PMID: 1992292

2

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

3

Dystrophin expression in the developing conduction system of the human heart.

Ginjaar IB, Virágh S, Markman MW, van Ommen GJ, Moorman AF. Ginjaar IB, et al. Among authors: van ommen gj. Microsc Res Tech. 1995 Apr 15;30(6):458-68. doi: 10.1002/jemt.1070300603. Microsc Res Tech. 1995. PMID: 7599357

4

Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophy.

Ginjaar IB, Bakker E, van Paassen MM, den Dunnen JT, Wessels A, Zubrzycka-Gaarn EE, Moorman AF, van Ommen GJ. Ginjaar IB, et al. Among authors: van ommen gj, van paassen mm. J Med Genet. 1991 Aug;28(8):505-10. doi: 10.1136/jmg.28.8.505. J Med Genet. 1991. PMID: 1920366 Free PMC article.

5

Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD.

Roest PA, Bout M, van der Tuijn AC, Ginjaar IB, Bakker E, Hogervorst FB, van Ommen GJ, den Dunnen JT. Roest PA, et al. Among authors: van der tuijn ac, van ommen gj. J Med Genet. 1996 Nov;33(11):935-9. doi: 10.1136/jmg.33.11.935. J Med Genet. 1996. PMID: 8950674 Free PMC article.

6

The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

van Essen AJ, Kneppers AL, van der Hout AH, Scheffer H, Ginjaar IB, ten Kate LP, van Ommen GJ, Buys CH, Bakker E. van Essen AJ, et al. Among authors: van der hout ah, van ommen gj. J Med Genet. 1997 Oct;34(10):805-12. doi: 10.1136/jmg.34.10.805. J Med Genet. 1997. PMID: 9350811 Free PMC article.

7

Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells.

van Deutekom JC, Bremmer-Bout M, Janson AA, Ginjaar IB, Baas F, den Dunnen JT, van Ommen GJ. van Deutekom JC, et al. Among authors: van ommen gj. Hum Mol Genet. 2001 Jul 15;10(15):1547-54. doi: 10.1093/hmg/10.15.1547. Hum Mol Genet. 2001. PMID: 11468272

8

Monoclonal antibodies for dystrophin analysis. Epitope mapping and improved binding to SDS-treated muscle sections.

Nguyen TM, Ginjaar IB, van Ommen GJ, Morris GE. Nguyen TM, et al. Among authors: van ommen gj. Biochem J. 1992 Dec 1;288 ( Pt 2)(Pt 2):663-8. doi: 10.1042/bj2880663. Biochem J. 1992. PMID: 1281410 Free PMC article.

9

Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopes.

Ginjaar HB, van Paassen HB, den Dunnen JT, Man NT, Morris GE, Moorman AF, van Ommen GJ. Ginjaar HB, et al. Among authors: van paassen hb, van ommen gj. FEBS Lett. 1992 Aug 24;308(3):293-7. doi: 10.1016/0014-5793(92)81296-x. FEBS Lett. 1992. PMID: 1380469 Free article.

10

Monoclonal antibody evidence for structural similarities between the central rod regions of actinin and dystrophin.

Nguyen TM, Ellis JM, Ginjaar IB, van Paassen MM, van Ommen GJ, Moorman AF, Cartwright AJ, Morris GE. Nguyen TM, et al. Among authors: van ommen gj, van paassen mm. FEBS Lett. 1990 Oct 15;272(1-2):109-12. doi: 10.1016/0014-5793(90)80460-z. FEBS Lett. 1990. PMID: 1699800 Free article.

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