N. Wedemeyer

发表

Mutagenic effect of low energy neutrons on human chromosome 11

W. Göhde, H. J. Brede, E. Severin, 2003, International journal of radiation biology.

IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse Chromosome 5

H. Himmelbauer, H. Lehrach, E. Wanker, 2009, Mammalian Genome.

Keratinocytes Exposed to Ultraviolet Radiation Reveal Three Down-regulated Genes with Potential Function in Differentiation and Cell Cycle Control

W. Göhde, W. Köhnlein, N. Wedemeyer, 2000, Radiation research.

Flow cytometric quantification of competitive reverse transcription-PCR products.

W. Göhde, N. Wedemeyer, T. Pötter, 2002, Clinical chemistry.

YAC contigs of the Rab1 and wobbler (wr) spinal muscular atrophy gene region on proximal mouse chromosome 11 and of the homologous region on human chromosome 2p.

A. Lengeling, H. Jockusch, K. Baer, 1996, Genomics.

Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23.

H. Himmelbauer, H. Lehrach, E. Wanker, 1997, Genomics.

Homology between human Chromosome 2p13.3 and the wobbler critical region on mouse Chromosome 11: comparative high-resolution mapping of STS and EST loci on YAC/BAC contigs

A. Lengeling, H. Jockusch, K. Baer, 1998, Mammalian Genome.

Quantification of PCR products using microparticles and flow cytometry.

W. Göhde, U. Cassens, N. Wedemeyer, 2004, Annales de biologie clinique.

Flow cytometry: an ‘old’ tool for novel applications in medical genetics

N Wedemeyer, T Pötter, N. Wedemeyer, 2001, Clinical genetics.

Flow cytometric analysis of reverse transcription-PCR products: quantification of p21(WAF1/CIP1) and proliferating cell nuclear antigen mRNA.

W. Göhde, N. Wedemeyer, T. Pötter, 2000, Clinical chemistry.

Identification of a deletion hotspot on distal mouse chromosome 4 by YAC fingerprinting.

W. Göhde, W. Köhnlein, N. Wedemeyer, 2001, Mutation research.

Conservation of the 3′‐untranslated region of the Rab1a gene in amniote vertebrates: exceptional structure in marsupials and possible role for posttranscriptional regulation

D. Evers, H. Jockusch, D. Eberhard, 2000, FEBS letters.

Scientific Proceedings Second International Symposium on Cytostatic Drug Resistance

R. Pieters, K. Sikora, W. Siegert, 1991, Journal of Cancer Research and Clinical Oncology.

Integrated radiation hybrid map of human chromosome 2p13: possible involvement of dynactin in neuromuscular diseases.

A. Lengeling, H. Jockusch, M. Ronsiek, 1997, Genomics.

The mouse Clc1/myotonia gene: ETn insertion, a variable AATC repeat, and PCR diagnosis of alleles

H. Jockusch, M. Gronemeier, V. Schnülle, 1997, Mammalian Genome.

Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2.

H. Himmelbauer, H. Lehrach, E. Wanker, 1998, Genomics.

SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates.

H. Lehrach, E. Wanker, E. Scherzinger, 1998, Molecular cell.

Evidence for predictive validity of blood assays to evaluate individual radiosensitivity.

N. Willich, W. Göhde, B. Greve, 2006, International journal of radiation oncology, biology, physics.

The gene for cytoplasmatic malate dehydrogenase, Mor2, is closely linked to the wobbler spinal muscular atrophy gene (wr)

H. Jockusch, C. Wiegand, N. Wedemeyer, 1996, Mammalian Genome.

YAC Contigs of the Rab 1 and wobbler ( wr ) Spinal Muscular Atrophy Gene Region on Proximal Mouse Chromosome 11 and of the Homologous Region on Human Chromosome 2 p

A. Lengeling, H. Jockusch, K. Baer, 1996 .

Frequency of CD59 mutations induced in human-hamster hybrid A(L) cells by low-dose X-irradiation.

W. Göhde, B. Greve, E. Severin, 2001, Mutation research.