U. Lenk

发表

Summary A role for mammalian Ubc 6 homologues in ER-associated protein degradation

E. Hartmann, Helen Yu, R. Kopito, 2022 .

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis

A. Weindl, A. Ludolph, T. Meyer, 1995, Annals of neurology.

Carrier detection in DMD families with point mutations, using PCR-SSCP and direct sequencing

A. Speer, U. Lenk, R. Hanke, 1994, Neuromuscular Disorders.

Cell-Free Synthesis of Membrane Proteins on a Preparative Scale

V. Flockerzi, C. Fecher-Trost, R. Zimmermann, 2003 .

A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-wave.

C. Hübner, T. Voit, K. Oexle, 1996, Human molecular genetics.

Protein truncation test: Analysis of two novel point mutations at the carboxy‐terminus of the human dystrophin gene associated with mental retardation

M. Claustres, J. Demaille, S. Tuffery, 1995, Human mutation.

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients.

H. Thiele, H. Thiele, A. Speer, 1993, Human molecular genetics.

Endoplasmic reticulum-associated protein degradation.

T. Sommer, E. Jarosch, U. Lenk, 2003, International review of cytology.

Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin gene.

I. Grunewald, U Lenk, R Hanke, 1993, Journal of medical genetics.

Compartment-specific functions of the ubiquitin-proteasome pathway.

T. Sommer, E. Jarosch, U. Lenk, 2001, Reviews of physiology, biochemistry and pharmacology.

Ubiquitin-mediated Proteolysis of a Short-lived Regulatory Protein Depends on Its Cellular Localization*

T. Sommer, U. Lenk, 2000, The Journal of Biological Chemistry.

Four new polymorphisms in the human dystrophin gene from an Argentinian population

S. Baranzini, I. Szijan, A. Speer, 1997, Muscle & nerve.

A role for mammalian Ubc6 homologues in ER-associated protein degradation.

E. Hartmann, Helen Yu, R. Kopito, 2002, Journal of cell science.

Alternative splicing of dystrophin mRNA complicates carrier determination: report of a DMD family.

A. Speer, S. Demuth, U. Lenk, 1993, Journal of medical genetics.

Mental Retardation

J. Demaille, S. Tuffery, C. Coubes, 2005 .