Wieringa B - Search Results

1

Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.

van den Hurk JA, Hendriks W, van de Pol DJ, Oerlemans F, Jaissle G, Rüther K, Kohler K, Hartmann J, Zrenner E, van Bokhoven H, Wieringa B, Ropers HH, Cremers FP. van den Hurk JA, et al. Among authors: wieringa b. Hum Mol Genet. 1997 Jun;6(6):851-8. doi: 10.1093/hmg/6.6.851. Hum Mol Genet. 1997. PMID: 9175730 Free article.

2

An animal model for Norrie disease (ND): gene targeting of the mouse ND gene.

Berger W, van de Pol D, Bächner D, Oerlemans F, Winkens H, Hameister H, Wieringa B, Hendriks W, Ropers HH. Berger W, et al. Among authors: wieringa b. Hum Mol Genet. 1996 Jan;5(1):51-9. doi: 10.1093/hmg/5.1.51. Hum Mol Genet. 1996. PMID: 8789439 Free article.

3

Cloning of the breakpoints of a deletion associated with choroidermia.

Cremers FP, Brunsmann F, Berger W, van Kerkhoff EP, van de Pol TJ, Wieringa B, Pawlowitzki IH, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Hum Genet. 1990 Nov;86(1):61-4. doi: 10.1007/BF00205174. Hum Genet. 1990. PMID: 1979308

4

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B, et al. Cremers FP, et al. Among authors: wieringa b. Am J Hum Genet. 1990 Oct;47(4):622-8. Am J Hum Genet. 1990. PMID: 2220804 Free PMC article.

5

Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing.

van den Hurk JA, van de Pol TJ, Molloy CM, Brunsmann F, Rüther K, Zrenner E, Pinckers AJ, Pawlowitzki IH, Bleeker-Wagemakers EM, Wieringa B, et al. van den Hurk JA, et al. Among authors: wieringa b. Am J Hum Genet. 1992 Jun;50(6):1195-202. Am J Hum Genet. 1992. PMID: 1598901 Free PMC article.

6

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. Among authors: wieringa b. Hum Mol Genet. 1993 Aug;2(8):1221-7. doi: 10.1093/hmg/2.8.1221. Hum Mol Genet. 1993. PMID: 8401505

7

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: wieringa b. 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.

8

Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.

van de Pol TJ, Cremers FP, Brohet RM, Wieringa B, Ropers HH. van de Pol TJ, et al. Among authors: wieringa b. Nucleic Acids Res. 1990 Feb 25;18(4):725-31. doi: 10.1093/nar/18.4.725. Nucleic Acids Res. 1990. PMID: 1969148 Free PMC article.

9

Cloning of a gene that is rearranged in patients with choroideraemia.

Cremers FP, van de Pol DJ, van Kerkhoff LP, Wieringa B, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Nature. 1990 Oct 18;347(6294):674-7. doi: 10.1038/347674a0. Nature. 1990. PMID: 2215697

10

The recombinant DNA revolution: implications for diagnosis and prevention of inherited disease.

Ropers HH, Wieringa B. Ropers HH, et al. Among authors: wieringa b. Eur J Obstet Gynecol Reprod Biol. 1989 Jul;32(1):15-23. doi: 10.1016/0028-2243(89)90119-6. Eur J Obstet Gynecol Reprod Biol. 1989. PMID: 2569992 Review.

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