Eisenbarth I - Search Results

1

Toward a survey of somatic mutation of the NF1 gene in benign neurofibromas of patients with neurofibromatosis type 1.

Eisenbarth I, Beyer K, Krone W, Assum G. Eisenbarth I, et al. Am J Hum Genet. 2000 Feb;66(2):393-401. doi: 10.1086/302747. Am J Hum Genet. 2000. PMID: 10677298 Free PMC article.

2

Somatic NF1 mutation spectra in a family with neurofibromatosis type 1: toward a theory of genetic modifiers.

Wiest V, Eisenbarth I, Schmegner C, Krone W, Assum G. Wiest V, et al. Among authors: eisenbarth i. Hum Mutat. 2003 Dec;22(6):423-7. doi: 10.1002/humu.10272. Hum Mutat. 2003. PMID: 14635100

3

Analysis of an alternatively spliced exon of the neurofibromatosis type 1 gene in cultured melanocytes from patients with neurofibromatosis 1.

Eisenbarth I, Hoffmeyer S, Kaufmann D, Assum G, Krone W. Eisenbarth I, et al. Arch Dermatol Res. 1995;287(5):413-6. doi: 10.1007/BF00373420. Arch Dermatol Res. 1995. PMID: 7625848

4

Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene.

Däschner K, Assum G, Eisenbarth I, Krone W, Hoffmeyer S, Wortmann S, Heymer B, Kehrer-Sawatzki H. Däschner K, et al. Among authors: eisenbarth i. Biochem Biophys Res Commun. 1997 May 19;234(2):346-50. doi: 10.1006/bbrc.1997.6645. Biochem Biophys Res Commun. 1997. PMID: 9177273

5

Evidence for the presence of the second allele of the neurofibromatosis type 1 gene in melanocytes derived from café au laitmacules of NF1 patients.

Eisenbarth I, Assum G, Kaufmann D, Krone W. Eisenbarth I, et al. Biochem Biophys Res Commun. 1997 Aug 8;237(1):138-41. doi: 10.1006/bbrc.1997.7097. Biochem Biophys Res Commun. 1997. PMID: 9266845

6

An isochore transition in the NF1 gene region coincides with a switch in the extent of linkage disequilibrium.

Eisenbarth I, Vogel G, Krone W, Vogel W, Assum G. Eisenbarth I, et al. Am J Hum Genet. 2000 Oct;67(4):873-80. doi: 10.1086/303085. Epub 2000 Sep 6. Am J Hum Genet. 2000. PMID: 10978227 Free PMC article.

7

Ras-GTP regulation is not altered in cultured melanocytes with reduced levels of neurofibromin derived from patients with neurofibromatosis 1 (NF1).

Griesser J, Kaufmann D, Eisenbarth I, Bäuerle C, Krone W. Griesser J, et al. Among authors: eisenbarth i. Biol Chem Hoppe Seyler. 1995 Feb;376(2):91-101. doi: 10.1515/bchm3.1995.376.2.91. Biol Chem Hoppe Seyler. 1995. PMID: 7794530

8

Long-range sequence composition mirrors linkage disequilibrium pattern in a 1.13 Mb region of human chromosome 22.

Eisenbarth I, Striebel AM, Moschgath E, Vogel W, Assum G. Eisenbarth I, et al. Hum Mol Genet. 2001 Nov 15;10(24):2833-9. doi: 10.1093/hmg/10.24.2833. Hum Mol Genet. 2001. PMID: 11734548

9

Mapping of members of the low-copy-number repetitive DNA sequence family chAB4 within the p arms of human acrocentric chromosomes: characterization of Robertsonian translocations.

Kehrer-Sawatzki H, Wöhr G, Schempp W, Eisenbarth I, Barbi G, Assum G. Kehrer-Sawatzki H, et al. Among authors: eisenbarth i. Chromosome Res. 1998 Sep;6(6):429-35. doi: 10.1023/a:1009287223826. Chromosome Res. 1998. PMID: 9865780

10

Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22.

Eisenbarth I, König-Greger D, Wöhr G, Kehrer-Sawatzki H, Assum G. Eisenbarth I, et al. Chromosome Res. 1999;7(1):65-9. doi: 10.1023/a:1009279412797. Chromosome Res. 1999. PMID: 10219734

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