C. Ferenz

发表

Inhibition of ICE family proteases by baculovirus antiapoptotic protein p35.

J. Mankovich, S. Seshagiri, Lianfa Shi, 1995, Science.

Stimulation of murine hemopoietic colony formation by human IL-6.

R. Kriz, M. Ogawa, S. Clark, 1988, Journal of immunology.

Characterization and NH2-terminal amino acid sequence of natural human interleukin for DA cells: leukemia inhibitory factor. Differentiation inhibitory activity secreted by a T lymphoma cell line.

V. Praloran, H. Gascan, R. Hewick, 1989, The Journal of biological chemistry.

The beta-globin domain in immature chicken erythrocytes: enhanced solubility is coincident with histone hyperacetylation.

D. Nelson, D. Zhang, C. Ferenz, 1986, Nucleic acids research.

N-Butyrate incubation of immature chicken erythrocytes preferentially enhances the solubility of β^ chromatin

D. Nelson, C. Ferenz, 1985 .

The synthesis of biologically active pteroyloligo- 0L-glutamates (folic acid conjugates). Evaluation of ( 3 H)pteroylheptaglutamate for metabolic studies.

J. Meienhofer, C. Ferenz, H. A. Godwin, 1972, The Journal of biological chemistry.

Sequence similarity of phospholipase C with the non-catalytic region of src

R. Kriz, M. Stahl, K. Kelleher, 1988, Nature.

Cloning of cDNA for natural killer cell stimulatory factor, a heterodimeric cytokine with multiple biologic effects on T and natural killer cells.

R. Hewick, L. Fitz, M. Kobayashi, 1991, Journal of immunology.

Stability and Oligomeric Equilibria of Refolded Interleukin-1β Converting Enzyme*

J. Mankovich, R. Talanian, M. Hackett, 1996, The Journal of Biological Chemistry.

Characterization of peptide binding to the murine MHC class I H-2Kk molecule. Sequencing of the bound peptides and direct binding of synthetic peptides to isolated class I molecules.

E. Brown, R. Hewick, S. Herrmann, 1994, Journal of immunology.

Cloning and functional expression of a cDNA encoding the catalytic subunit of bovine enterokinase.

A. Rehemtulla, J. Mccoy, E. Lavallie, 1993, The Journal of biological chemistry.

Recombinant human macrophage colony-stimulating factor (M-CSF) requires subliminal concentrations of granulocyte/macrophage (GM)-CSF for optimal stimulation of human macrophage colony formation in vitro

B. Lange, D. Caracciolo, S. Clark, 1987, The Journal of experimental medicine.