G. Forrest

发表

A genomewide oscillation in transcription gates DNA replication and cell cycle.

D. Murray, R. Klevecz, J. Bolen, 2004, Proceedings of the National Academy of Sciences of the United States of America.

G. Forrest, B. Gonzalez, 2000, Chemico-biological interactions.

Human carbonyl reductase overexpression in the heart advances the development of doxorubicin-induced cardiotoxicity in transgenic mice.

X. Li, G. Forrest, J. Mann, 2000, Cancer research.

Protection against daunorubicin cytotoxicity by expression of a cloned human carbonyl reductase cDNA in K562 leukemia cells.

J. Doroshow, W. D. Kaplan, S. Akman, 1995, Cancer research.

Rat liver NAD(P)H:quinone oxidoreductase: cDNA expression and site-directed mutagenesis.

J. Doroshow, W. D. Kaplan, S. Akman, 1990, Biochemical and biophysical research communications.

Elevated DT-diaphorase activity and messenger RNA content in human non-small cell lung carcinoma: relationship to the response of lung tumor xenografts to mitomycin Cł.

A. Malkinson, A. Gazdar, P. Bunn, 1992, Cancer research.

Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region.

A. Chakravarti, S. Antonarakis, D. Avramopoulos, 1992, Genomics.

NAD(P)H:quinone oxidoreductase expression and mitomycin C resistance developed by human colon cancer HCT 116 cells.

S. Akman, G. Forrest, S. Pan, 1995, Cancer research.

Nad(P)H:Quinone oxidoreductase (DT‐Diaphorase) activity and mRNA content in normal and neoplastic mouse lung epithelia

A. Malkinson, D. Ross, D. Siegel, 1991, International journal of cancer.

Structural defects of T-even bacteriophages.

G. Forrest, D. Cummings, N. Couse, 1970, Advances in virus research.

In vitro metabolism of the phosphatidylinositol 3-kinase inhibitor, wortmannin, by carbonyl reductase.

M. Egorin, G. Forrest, S. Musser, 2004, Drug metabolism and disposition: the biological fate of chemicals.

Head Proteins from T-Even Bacteriophage

G. Forrest, D. Cummings, 1970, Journal of virology.

Induction of a human carbonyl reductase gene located on chromosome 21.

T. Mohandas, J. Doroshow, R. Paxton, 1990, Biochimica et biophysica acta.

Genomic sequence and expression of a cloned human carbonyl reductase gene with daunorubicin reductase activity.

J. Doroshow, W. D. Kaplan, S. Akman, 1991, Molecular pharmacology.

Synthesis of poly(adenosine diphosphate ribose) in synchronized Chinese hamster cells.

S. D. Gross, N. Berger, R. Klevecz, 1978, Experimental cell research.

5 – METABOLIC REGULATION IN THE CELL CYCLE

R. Klevecz, G. Forrest, 1977 .

REGULATION OF TUBULIN EXPRESSION THROUGH THE CELL CYCLE *

R. Klevecz, G. Forrest, 1975, Annals of the New York Academy of Sciences.

Sequencing of peR Products

G. Forrest, J. Mann, P. Szabó, 1996 .

Sequencing of PCR Products

G. Forrest, J. Mann, P. Szabó, 1996 .

The role of NAD(P)H: quinone oxidoreductase in mitomycin C- and porfiromycin-resistant HCT 116 human colon-cancer cells

Robin Johnson, S. Akman, G. Forrest, 2004, Cancer Chemotherapy and Pharmacology.

Cloning and expression of the cDNA encoding rabbit liver carbonyl reductase.

W. D. Kaplan, G. Forrest, B. Gonzalez, 1995, Gene.

Human carbonyl reductase (CBR) localized to band 21q22.1 by high-resolution fluorescence in situ hybridization displays gene dosage effects in trisomy 21 cells.

G. Forrest, B. Malfoy, N. Lemieux, 1993, Genomics.

Human Colon Cancer HCT 116 Cells

Li-Tai Hu, S. Akman, G. Forrest, 2006 .

Localization of four human chromosome 21 genes--SOD1, ETS2, IFNAR, and CBR--to two different chromosomes in the marsupial species Macropus eugenii.

J. Graves, M. Tymms, S. Brookes, 1992, Cytogenetics and cell genetics.

Synthesis and degradation of microtubule protein in synchronized Chinese hamster cells.

R. Klevecz, G. Forrest, 1972, The Journal of biological chemistry.

Tyrosyltubulin ligase and colchicine binding activity in synchronized Chinese hamster cells

R. Klevecz, G. Forrest, 1978, The Journal of cell biology.

Colchicine binding activity and tyrosyl tubulin ligase activity in normal and cystic fibrosis fibroblasts.

G. Forrest, 1981, Biochemical and biophysical research communications.

Head Proteins from T-Even Bacteriophages II. Physical and Chemical Characterization

G. Forrest, D. Cummings, 1971, Journal of virology.

A site-directed mutagenesis study at Lys-113 of NAD(P)H:quinone-acceptor oxidoreductase: an involvement of Lys-113 in the binding of the flavin adenine dinucleotide prosthetic group.

G. Forrest, G. Tedeschi, V. Massey, 1995, Archives of Biochemistry and Biophysics.

Nad(P)H:Quinone oxidoreductase (DT‐Diaphorase) activity and mRNA content in normal and neoplastic mouse lung epithelia

A. Malkinson, D. Siegel, G. Forrest, 1991, International journal of cancer.

Expression of rat liver NAD(P)H:quinone-acceptor oxidoreductase in Escherichia coli and mutagenesis in vitro at Arg-177.

G. Forrest, T. Lee, S. Chen, 1992, The Biochemical journal.

Antioxidant and xenobiotic-metabolizing enzyme gene expression in doxorubicin-resistant MCF-7 breast cancer cells.

J. Doroshow, S. Akman, G. Forrest, 1990, Cancer research.