I. Eisenbarth

发表

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

Verena Wiest, I. Eisenbarth, C. Schmegner, 2003, Human mutation.

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

W Krone, W. Vogel, I. Eisenbarth, 2000, American journal of human genetics.

Characterization of an Alphoid Subfamily Located Near P-arm Sequences on Human Chromosome 22

H. Kehrer-Sawatzki, I. Eisenbarth, G. Assum, 2004, Chromosome Research.

Cultured Epidermal Melanocytes from Patients with Neurofibromatosis 1 (Recklinghausen’s Disease): a Cell Culture Model for Neurofibromatosis 1

I. Eisenbarth, D. Kaufmann, S. Wiandt, 1993 .

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

I. Eisenbarth, W. Krone, D. Kaufmann, 1995, Biological chemistry Hoppe-Seyler.

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

I. Eisenbarth, W. Krone, G. Assum, 2000, American journal of human genetics.

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

I. Eisenbarth, W. Krone, G. Assum, 1997, Biochemical and biophysical research communications.

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.

H. Kehrer-Sawatzki, I. Eisenbarth, W. Krone, 1997, Biochemical and biophysical research communications.

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

I. Eisenbarth, G. Assum, W. Vogel, 2001, Human molecular genetics.

Investigations of neurofibromin expression in the skin of patients with NF 1 (neurofibromatosis type 1)

I. Eisenbarth, W. Krone, G. Assum, 1994 .

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

H. Kehrer-Sawatzki, I. Eisenbarth, G. Assum, 1998, Chromosome Research.

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

I. Eisenbarth, W. Krone, G. Assum, 2004, Archives of Dermatological Research.

Description of Three New Alleles at the D1S80 (MCT118) Locus

I. Eisenbarth, W. Krone, G. Assum, 1999 .