Showing results (1-10 of 11) with videos related to
Sort By:
Pageof 2
The Journal of Biological Chemistry|September 19, 2000
Ubiquitin-mediated proteolysis of a short-lived regulatory protein depends on its cellular localizationU Lenk, T SommerDiskussionsforum Medizinische Ethik|January 1, 1993
[Integration of medical responsibility]H Lenk, U LenkDer Anaesthesist|March 1, 1989
[Intra- and postoperative complications in infrarenal abdominal aortic aneurysms]H J Hartung, U LenkNeuromuscular Disorders : NMD|September 1, 1994
Carrier detection in DMD families with point mutations, using PCR-SSCP and direct sequencingU Lenk, R Hanke, A SpeerHuman Molecular Genetics|November 1, 1993
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patientsU Lenk, R Hanke, H Thiele, et al.Muscle & Nerve|October 28, 1997
Four new polymorphisms in the human dystrophin gene from an Argentinian populationS E Baranzini, U Lenk, I Szijan, et al.Journal of Medical Genetics|March 1, 1993
Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD familyU Lenk, S Demuth, U Kräft, et al.Journal of Medical Genetics|November 1, 1993
Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin geneU Lenk, R Hanke, U Kräft, et al.Human Mutation|January 1, 1995
Protein truncation test: analysis of two novel point mutations at the carboxy-terminus of the human dystrophin gene associated with mental retardationS Tuffery, U Lenk, R G Roberts, et al.Annals of Neurology|June 1, 1995
Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosisT Meyer, U Lenk, G Küther, et al.Pageof 2