Jansen G - Search Results

1

Presymptomatic diagnosis of myotonic dystrophy.

Brunner HG, Nillesen W, van Oost BA, Jansen G, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: jansen g. J Med Genet. 1992 Nov;29(11):780-4. doi: 10.1136/jmg.29.11.780. J Med Genet. 1992. PMID: 1453426 Free PMC article.

2

Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus.

Jansen G, Bächner D, Coerwinkel M, Wormskamp N, Hameister H, Wieringa B. Jansen G, et al. Hum Mol Genet. 1995 May;4(5):843-52. doi: 10.1093/hmg/4.5.843. Hum Mol Genet. 1995. PMID: 7633444 Free article.

3

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Jansen G, Willems P, Coerwinkel M, Nillesen W, Smeets H, Vits L, Höweler C, Brunner H, Wieringa B. Jansen G, et al. Am J Hum Genet. 1994 Apr;54(4):575-85. Am J Hum Genet. 1994. PMID: 8128954 Free PMC article.

4

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al. Brunner HG, et al. Among authors: jansen g. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

5

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues.

Jansen G, Bartolomei M, Kalscheuer V, Merkx G, Wormskamp N, Mariman E, Smeets D, Ropers HH, Wieringa B. Jansen G, et al. Hum Mol Genet. 1993 Aug;2(8):1221-7. doi: 10.1093/hmg/2.8.1221. Hum Mol Genet. 1993. PMID: 8401505

6

Brief report: reverse mutation in myotonic dystrophy.

Brunner HG, Jansen G, Nillesen W, Nelen MR, de Die CE, Höweler CJ, van Oost BA, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: jansen g. N Engl J Med. 1993 Feb 18;328(7):476-80. doi: 10.1056/NEJM199302183280705. N Engl J Med. 1993. PMID: 8421477 Free article. No abstract available.

7

Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) gene.

Jansen G, Coerwinkel-Driessen M, Nillesen W, Brunner H, Wieringa B. Jansen G, et al. Hum Mol Genet. 1993 Mar;2(3):333. doi: 10.1093/hmg/2.3.333. Hum Mol Genet. 1993. PMID: 8499928 No abstract available.

8

Constitutive and regulated modes of splicing produce six major myotonic dystrophy protein kinase (DMPK) isoforms with distinct properties.

Groenen PJ, Wansink DG, Coerwinkel M, van den Broek W, Jansen G, Wieringa B. Groenen PJ, et al. Among authors: jansen g. Hum Mol Genet. 2000 Mar 1;9(4):605-16. doi: 10.1093/hmg/9.4.605. Hum Mol Genet. 2000. PMID: 10699184

9

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C, et al. Shutler G, et al. Among authors: jansen g. Genomics. 1992 Jul;13(3):518-25. doi: 10.1016/0888-7543(92)90119-d. Genomics. 1992. PMID: 1639380

10

Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice.

Jansen G, Groenen PJ, Bächner D, Jap PH, Coerwinkel M, Oerlemans F, van den Broek W, Gohlsch B, Pette D, Plomp JJ, Molenaar PC, Nederhoff MG, van Echteld CJ, Dekker M, Berns A, Hameister H, Wieringa B. Jansen G, et al. Nat Genet. 1996 Jul;13(3):316-24. doi: 10.1038/ng0796-316. Nat Genet. 1996. PMID: 8673131 Free article.

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