Wöhrle D - Search Results

1

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications.

Sudbrak R, Wieczorek G, Nuber UA, Mann W, Kirchner R, Erdogan F, Brown CJ, Wöhrle D, Sterk P, Kalscheuer VM, Berger W, Lehrach H, Ropers HH. Sudbrak R, et al. Among authors: wohrle d. Hum Mol Genet. 2001 Jan 1;10(1):77-83. doi: 10.1093/hmg/10.1.77. Hum Mol Genet. 2001. PMID: 11136717

2

The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene.

Geerkens C, Vetter U, Just W, Fedarko NS, Fisher LW, Young MF, Termine JD, Robey PG, Wöhrle D, Vogel W. Geerkens C, et al. Among authors: wohrle d. Hum Genet. 1995 Jul;96(1):44-52. doi: 10.1007/BF00214185. Hum Genet. 1995. PMID: 7607653

3

A human pseudoautosomal gene, ADP/ATP translocase, escapes X-inactivation whereas a homologue on Xq is subject to X-inactivation.

Schiebel K, Weiss B, Wöhrle D, Rappold G. Schiebel K, et al. Among authors: wohrle d. Nat Genet. 1993 Jan;3(1):82-7. doi: 10.1038/ng0193-82. Nat Genet. 1993. PMID: 8490661

4

Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue.

Wöhrle D, Fryns JP, Steinbach P. Wöhrle D, et al. Hum Genet. 1990 Oct;85(6):659-65. doi: 10.1007/BF00193594. Hum Genet. 1990. PMID: 2227957

5

Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells.

Wöhrle D, Salat U, Hameister H, Vogel W, Steinbach P. Wöhrle D, et al. Am J Hum Genet. 2001 Sep;69(3):504-15. doi: 10.1086/322739. Epub 2001 Jul 13. Am J Hum Genet. 2001. PMID: 11462172 Free PMC article.

6

Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation.

Wöhrle D, Steinbach P. Wöhrle D, et al. Hum Genet. 1991 Aug;87(4):421-4. doi: 10.1007/BF00197160. Hum Genet. 1991. PMID: 1715307

7

Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad.

Bächner D, Manca A, Steinbach P, Wöhrle D, Just W, Vogel W, Hameister H, Poustka A. Bächner D, et al. Among authors: wohrle d. Hum Mol Genet. 1993 Dec;2(12):2043-50. doi: 10.1093/hmg/2.12.2043. Hum Mol Genet. 1993. PMID: 8111372

8

A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome.

Wöhrle D, Kotzot D, Hirst MC, Manca A, Korn B, Schmidt A, Barbi G, Rott HD, Poustka A, Davies KE, et al. Wöhrle D, et al. Am J Hum Genet. 1992 Aug;51(2):299-306. Am J Hum Genet. 1992. PMID: 1642231 Free PMC article.

9

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families.

Steinbach P, Wöhrle D, Tariverdian G, Kennerknecht I, Barbi G, Edlinger H, Enders H, Götz-Sothmann M, Heilbronner H, Hosenfeld D, et al. Steinbach P, et al. Among authors: wohrle d. Hum Genet. 1993 Nov;92(5):491-8. doi: 10.1007/BF00216457. Hum Genet. 1993. PMID: 7902319

10

Heterozygous expression of X-linked chondrodysplasia punctata. Complex chromosome aberration including deletion of MIC2 and STS.

Wöhrle D, Barbi G, Schulz W, Steinbach P. Wöhrle D, et al. Hum Genet. 1990 Dec;86(2):215-8. doi: 10.1007/BF00197708. Hum Genet. 1990. PMID: 2265834

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