W. Roth

发表

Proteases involved in MHC dass II antigen presentation

J. Deussing, C. Peters, H. Ploegh, 1999, Immunological reviews.

Systems Biology Approaches to the Study of Biological Networks Underlying Alzheimer's Disease: Role of miRNAs.

Eugenio Fava, W. Roth, David Hecker, 2016, Methods in molecular biology.

Keratin 1 maintains skin integrity and participates in an inflammatory network in skin through interleukin-18

Joachim L. Schultze, Thomas Vogl, Johannes Roth, 2012, Journal of Cell Science.

Skin fragility and impaired desmosomal adhesion in mice lacking all keratins.

N. Schwarz, R. Leube, T. Magin, 2014, The Journal of investigative dermatology.

Cytokines as genetic modifiers in K5–/– mice and in human epidermolysis bullosa simplex

T. Magin, L. Bruckner-Tuderman, W. Roth, 2009, Human mutation.

Keratins mediate localization of hemidesmosomes and repress cell motility.

T. Magin, M. Lederer, S. Hüttelmaier, 2013, The Journal of investigative dermatology.

Human iPSC-derived brain endothelial microvessels in a multi-well format enable permeability screens of anti-inflammatory drugs

S. Kaushalya, S. Fengler, B. Kurkowsky, 2021, bioRxiv.

New roles for glial cell line-derived neurotrophic factor and neurturin: involvement in hair cycle control.

C. Peters, R. Paus, P. Welker, 2000, The American journal of pathology.

Gene Targeting of the Cysteine Peptidase Cathepsin H Impairs Lung Surfactant in Mice

J. Deussing, C. Peters, T. Reinheckel, 2011, PloS one.

Decreased intracellular degradation of insulin‐like growth factor binding protein‐3 in cathepsin L‐deficient fibroblasts

P. Saftig, T. Braulke, J. Scharf, 2002, FEBS letters.

Towards Specific Functions of Lysosomal Cysteine Peptidases: Phenotypes of Mice Deficient for Cathepsin B or Cathepsin L

J. Deussing, C. Peters, T. Reinheckel, 2001, Biological chemistry.

Mouse procathepsin E gene: molecular organisation and chromosomal localisation.

J. Deussing, C. Peters, J. Kay, 1998, Biochimica et biophysica acta.

Targeting the palm: a leap forward toward treatment of keratin disorders.

T. Magin, M. Hatzfeld, W. Roth, 2012, Journal of Investigative Dermatology.

FGF4, a direct target of LEF1 and Wnt signaling, can rescue the arrest of tooth organogenesis in Lef1(-/-) mice.

K. Kratochwil, R. Grosschedl, J. Galceran, 2002, Genes & development.

Role of cathepsin B in intracellular trypsinogen activation and the onset of acute pancreatitis.

H Lippert, J. Deussing, C. Peters, 2000, The Journal of clinical investigation.

Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrity.

O. Paul, P. Ruther, T. Magin, 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

Cathepsin L deficiency as molecular defect of furless: hyperproliferation of keratinocytes and pertubation of hair follicle cycling

J. Deussing, C. Peters, K. von Figura, 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Noggin is a mesenchymally derived stimulator of hair-follicle induction

Christoph Peters, Andrew P. McMahon, Wiebke Herzog, 1999, Nature Cell Biology.

Cathepsins B and D are dispensable for major histocompatibility complex class II-mediated antigen presentation.

J. Deussing, C. Peters, H. Ploegh, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Keratin function and regulation in tissue homeostasis and pathogenesis

T. Magin, M. Hatzfeld, M. Friedrich, 2012, Biomolecular concepts.

Cathepsin L: critical role in Ii degradation and CD4 T cell selection in the thymus.

A. Rudensky, J. Deussing, C. Peters, 1998, Science.

Dilated cardiomyopathy in mice deficient for the lysosomal cysteine peptidase cathepsin L

Christoph Peters, Günter Breithardt, Jörg Stypmann, 2002, Proceedings of the National Academy of Sciences of the United States of America.

PIASy-Deficient Mice Display Modest Defects in IFN and Wnt Signaling1

E. Kremmer, C. Turck, R. Grosschedl, 2004, The Journal of Immunology.

in IFN and Wnt Signaling PIASy-Deficient Mice Display Modest Defects

E. Kremmer, C. Turck, R. Grosschedl, 2004 .

Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 gene

C. Has, T. Magin, L. Bruckner-Tuderman, 2012, The British journal of dermatology.

Recruitment of RNA polymerase II cofactor PC4 to DNA damage sites

H. Leonhardt, M. C. Cardoso, M. Meisterernst, 2008, The Journal of cell biology.

Towards Specific Functions of Lysosomal Cysteine Peptidases: Phenotypes of Mice Deficient for Cathepsin Β or Cathepsin L

J. Deussing, C. Peters, T. Reinheckel, 2001 .