N Jenkins

发表

Glycosylation of recombinant proteins: problems and prospects.

N Jenkins, E M Curling, N. Jenkins, 1994, Enzyme and microbial technology.

Recombinant human interferon-gamma. Differences in glycosylation and proteolytic processing lead to heterogeneity in batch culture.

K. Gull, A. Bull, A. Baines, 1990, The Biochemical journal.

High-resolution separation of recombinant human interferon-gamma glycoforms by micellar electrokinetic capillary chromatography.

R B Freedman, M Hoare, N Jenkins, 1994, Analytical biochemistry.

Constraints on the transport and glycosylation of recombinant IFN-gamma in Chinese hamster ovary and insect cells.

D. James, A. Bull, A. Baines, 1999, Biotechnology and bioengineering.

The effect of the dilution rate on CHO cell physiology and recombinant interferon‐γ production in glucose‐limited chemostat culture

A. Bull, A. Baines, P. Strange, 1993, Biotechnology and bioengineering.

Glucose‐limited chemostat culture of chinese hamster ovary cells producing recombinant human interferon‐γ

A. Bull, A. Baines, P. Strange, 1992, Biotechnology and bioengineering.

Sialylation of human IgG-Fc carbohydrate by transfected rat alpha2,6-sialyltransferase.

R. Jefferis, J. Lund, P. Camilleri, 2001, Biochemical and biophysical research communications.

N‐glycans of recombinant human interferon‐γ change during batch culture of chinese hamster ovary cells

A. Bull, A. Baines, P. Strange, 1995 .

A new Chinese hamster ovary cell line expressing alpha2,6-sialyltransferase used as universal host for the production of human-like sialylated recombinant glycoproteins.

G. Distefano, L. Monaco, A. Bragonzi, 2000, Biochimica et biophysica acta.