C. Schlüter

发表

Modulation of lipopolysaccharide-induced production of tumor necrosis factor, interleukin 1, and interleukin 6 by synthetic precursor Ia of lipid A.

J. Gerdes, H. Flad, Ming-Hai Wang, 1992, FEMS microbiology immunology.

Endotoxin activates human vascular smooth muscle cells despite lack of expression of CD14 mRNA or endogenous membrane CD14

M. Ernst, H. Flad, H. Loppnow, 1995, Infection and immunity.

Species-specific assessment of Mycobacterium leprae in skin biopsies by in situ hybridization and polymerase chain reaction.

J. Gerdes, M. Ernst, M. Duchrow, 1992, Laboratory investigation; a journal of technical methods and pathology.

New Ki-67-equivalent murine monoclonal antibodies (MIB 1-3) generated against bacterially expressed parts of the Ki-67 cDNA containing three 62 base pair repetitive elements encoding for the Ki-67 epitope.

J. Gerdes, M. Duchrow, H. Flad, 1993, Laboratory investigation; a journal of technical methods and pathology.

Genomic organization, sequence, and transcriptional regulation of the human eotaxin gene.

C. Schlüter, J. Schröder, E. Christophers, 1997, Biochemical and biophysical research communications.

Tumor necrosis factor and lymphotoxin gene expression in human tumor cell lines.

P. Scheurich, K. Pfizenmaier, C. Schlüter, 1988, Cancer research.

Noncytocidal Mechanisms of Action of Tumor Necrosis Factor-α on Human Tumor Cells: Enhancement of HLA Gene Expression Synergistic with Interferon-γ*

P. Scheurich, K. Pfizenmaier, C. Schlüter, 1986 .

An examination of the immune system of the duck (Anas platyrhynchos) for factors resembling some defined mammalian cytokines.

J. Gerdes, G. Srivastava, H. Flad, 1993, Developmental and comparative immunology.

TumorNecrosis Factor a andLymphotoxin Production inHodgkin's Disease

W. Feist, C. Schlüter, T. Diamantstein, 1990 .

Increased eotaxin-mRNA expression in non-atopic and atopic nasal polyps: comparison to RANTES and MCP-3 expression.

J. Meyer, C. Schlüter, J. Schröder, 1997, Rhinology.

Genomic organization, sequence analysis and transcriptional regulation of the human MCP-4 chemokine gene (SCYA13) in dermal fibroblasts: a comparison to other eosinophilic beta-chemokines.

C. Schlüter, J. Schröder, E. Christophers, 1999, Biochemical and biophysical research communications.

Tumor necrosis factor alpha and lymphotoxin production in Hodgkin's disease.

D. Jones, H. Flad, A. Ulmer, 1990, The American journal of pathology.

Tumor Necrosis Factor α and Lymphotoxin Production in Hodgkin's Disease

J. Gerdes, D. Jones, H. Flad, 1990 .

Human dermal fibroblasts express eotaxin: molecular cloning, mRNA expression, and identification of eotaxin sequence variants.

C. Schlüter, J. Schröder, E. Christophers, 1996, Biochemical and biophysical research communications.

Noncytocidal mechanisms of action of tumor necrosis factor-alpha on human tumor cells: enhancement of HLA gene expression synergistic with interferon-gamma.

P. Scheurich, K. Pfizenmaier, C. Schlüter, 1986, Immunobiology.

Cell proliferation-associated nuclear antigen defined by antibody Ki-67: a new kind of cell cycle-maintaining proteins.

M. Kubbutat, J. Gerdes, M. Duchrow, 1995, Archivum immunologiae et therapiae experimentalis.

The cell proliferation-associated antigen of antibody Ki-67: a very large, ubiquitous nuclear protein with numerous repeated elements, representing a new kind of cell cycle-maintaining proteins

J. Gerdes, M. Duchrow, H. Flad, 1993, The Journal of cell biology.

Assessment of mycobacterial DNA in cells and tissues of mycobacterial and sarcoid lesions.

H. Magnussen, J. Gerdes, M. Schlaak, 1996, American journal of respiratory and critical care medicine.

The proliferation‐associated Ki‐67 protein: definition in molecular terms

J. Gerdes, M. Duchrow, C. Schlüter, 1994, Cell proliferation.

The CXC receptor 2 is overexpressed in psoriatic epidermis.

M. Sticherling, C. Schlüter, E. Christophers, 1998, The Journal of investigative dermatology.

Molecular characterization of the gene locus of the human cell proliferation‐associated nuclear protein defined by monoclonal antibody Ki‐67

J. Gerdes, M. Duchrow, H. Flad, 1996, Cell proliferation.

Tumor necrosis factor enhances HLA-A,B,C and HLA-DR gene expression in human tumor cells.

P. Scheurich, K. Pfizenmaier, C. Schlüter, 1987, Journal of immunology.

Assignment of the human Ki-67 gene (MKI67) to 10q25−qter

J. Gerdes, M. Duchrow, C. Fonatsch, 1991 .

New antiserum against Ki-67 antigen suitable for double immunostaining of paraffin wax sections.

J. Gerdes, M. Duchrow, C. Schlüter, 1993, Journal of clinical pathology.

Pentoxifylline: a potent inhibitor of IL-2 and IFN-gamma biosynthesis and BCG-induced cytotoxicity.

K. Toellner, M. Ernst, M. Duchrow, 1993, Immunology.

Mycobacterium leprae DNA content, cellular and cytokine patterns in skin lesions of leprosy patients undergoing multidrug therapy (MDT).

J. Gerdes, M. Duchrow, H. Flad, 1994, Immunobiology.

Detection of Mycobacterium leprae by three-primer PCR.

J. Gerdes, M. Duchrow, H. Flad, 1994, Immunobiology.

Tumor necrosis factor inhibits MYC expression in HL-60 cells at the level of mRNA transcription.

K. Pfizenmaier, C. Schlüter, M. Krönke, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Epitope analysis of antibodies recognising the cell proliferation associated nuclear antigen previously defined by the antibody Ki-67 (Ki-67 protein).

M. Kubbutat, J. Gerdes, M. Duchrow, 1994, Journal of clinical pathology.

Tumor necrosis factor-induced changes of gene expression in U937 cells. Differentiation-dependent plasticity of the responsive state.

P. Scheurich, K. Pfizenmaier, C. Schlüter, 1988, Journal of immunology.

The use of reverse transcription polymerase chain reaction to analyse large numbers of mRNA species from a single cell.

J. Gerdes, K. Toellner, L. Trümper, 1996, Journal of immunological methods.

An improved method for the species‐specific assessment of mycobacteria in routinely formalin‐fixed and paraffin‐embedded tissues

J. Gerdes, S. Rüsch-Gerdes, M. Duchrow, 1995, The Journal of pathology.