Schwemmle S - Search Results

1

Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stability.

Wöhrle D, Kennerknecht I, Wolf M, Enders H, Schwemmle S, Steinbach P. Wöhrle D, et al. Among authors: schwemmle s. Hum Mol Genet. 1995 Jul;4(7):1147-53. doi: 10.1093/hmg/4.7.1147. Hum Mol Genet. 1995. PMID: 8528201

2

Characterization of FMR1 promoter elements by in vivo-footprinting analysis.

Schwemmle S, de Graaff E, Deissler H, Gläser D, Wöhrle D, Kennerknecht I, Just W, Oostra BA, Döerfler W, Vogel W, Steinbach P. Schwemmle S, et al. Am J Hum Genet. 1997 Jun;60(6):1354-62. doi: 10.1086/515456. Am J Hum Genet. 1997. PMID: 9199556 Free PMC article.

3

The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat.

Steinbach P, Gläser D, Vogel W, Wolf M, Schwemmle S. Steinbach P, et al. Among authors: schwemmle s. Am J Hum Genet. 1998 Feb;62(2):278-85. doi: 10.1086/301711. Am J Hum Genet. 1998. PMID: 9463318 Free PMC article.

4

DNA methylation and triplet repeat stability: new proposals addressing actual questions on the CGG repeat of fragile X syndrome.

Wöhrle D, Schwemmle S, Steinbach P. Wöhrle D, et al. Among authors: schwemmle s. Am J Med Genet. 1996 Aug 9;64(2):266-7. doi: 10.1002/ajmg.1320640202. Am J Med Genet. 1996. PMID: 8844061 No abstract available.

5

XX-agonadism in a fetus with multiple dysraphic lesions: a new syndrome.

Kennerknecht I, Mattfeldt T, Paulus W, Nitsch C, Negri G, Barbi G, Just W, Schwemmle S, Vogel W. Kennerknecht I, et al. Among authors: schwemmle s. Am J Med Genet. 1997 Jun 27;70(4):413-4. Am J Med Genet. 1997. PMID: 9182784

6

X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation.

Preis W, Barbi G, Liptay S, Kennerknecht I, Schwemmle S, Pohlandt F. Preis W, et al. Among authors: schwemmle s. Am J Med Genet. 1996 Jan 11;61(2):117-21. doi: 10.1002/(SICI)1096-8628(19960111)61:2<117::AID-AJMG2>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8669435

7

How does inactivation change timing of replication in the human X chromosome?

Schwemmle S, Mehnert K, Vogel W. Schwemmle S, et al. Hum Genet. 1989 Aug;83(1):26-32. doi: 10.1007/BF00274142. Hum Genet. 1989. PMID: 2767677

8

In vivo footprinting analysis of the FMR1 gene: proposals concerning gene regulation in high-functioning males.

Schwemmle S. Schwemmle S. Am J Med Genet. 1999 May 28;84(3):266-7. Am J Med Genet. 1999. PMID: 10331604 No abstract available.

9

Developmental and tissue-specific expression of the Q5k gene.

Schwemmle S, Bevec D, Brem G, Urban MB, Baeuerle PA, Weiss EH. Schwemmle S, et al. Immunogenetics. 1991;34(1):28-38. doi: 10.1007/BF00212309. Immunogenetics. 1991. PMID: 1713191 Free article.

10

Organization of the AKR Qa region: structure of a divergent class I sequence, Q5k.

Weiss EH, Bevec D, Messer G, Schwemmle S, Grosshaus C, Steinmetz M, Schmidt W. Weiss EH, et al. Among authors: schwemmle s. J Immunogenet. 1989 Aug-Oct;16(4-5):283-90. doi: 10.1111/j.1744-313x.1989.tb00474.x. J Immunogenet. 1989. PMID: 2639903

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