Werner Leistner

Nearby Stop Codons in Exons of the Neurofibromatosis Type 1 Gene Are Disparate Splice Effectors

Sven Hoffmeyer, Peter Nürnberg, Heide Ritter et al. · The American Journal of Human Genetics · 1998 · 50 citations · Full text

Stop Codons, Neurogenomics, Genetic Disorder +8

Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences11Accession numbers and URLs for data in this article are as follows: Online Mendelian Inheritance in Man: http://www.ncbi.nlm.nih.gov/omim. For TSC1 (MIM 191100) and TSC2 (MIM 191092). The Human Gene Mutation Data Base, Cardiff (HGMD): http://www.uwcm.acuk/uwcm/mg. For TSC1 120735 and for TSC2 120466. TSC Variation Database: http://www.expmed.bwh.harvard.edu/projects/tsc_database. GenBank: http://www.ncbi.nlm.nih.gov/Genbank. For TSC2 cDNA X75621 and TSC2 complete genomic sequence AC005600.

Karin Mayer, Wolfgang G. Ballhausen, Werner Leistner et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2000 · 49 citations

Aberrant splicing in several human tumors in the tumor suppressor genes neurofibromatosis type 1, neurofibromatosis type 2, and tuberous sclerosis 2.

Dieter Kaufmann, Werner Leistner, Petra Kruse et al. · PubMed · 2002 · 33 citations

Aberrant Splicing, Rna Splicing, Pathology +16

The N-terminal splice product NF1-10a-2 of the NF1 gene codes for a transmembrane segment

Dieter Kaufmann, Ralf Müller-Xing, Oliver Kenner et al. · Biochemical and Biophysical Research Communications · 2002 · 23 citations

Natural Sciences, Genetics, Gene Structure +9