D. Godelaine

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The dolichol pathway of protein glycosylation in rat liver. Stimulation by GTP of the incorporation of N-acetylglucosamine in endogenous lipids and proteins of rough microsomes treated with pyrophosphate.

A. Amar‐Costesec, M. Wibo, D. Godelaine, 1979, European journal of biochemistry.

LAGE‐1, a new gene with tumor specificity

L. Michaux, T. Boon, E. De Plaen, 1998, International journal of cancer.

MAGE-A1 interacts with adaptor SKIP and the deacetylase HDAC1 to repress transcription.

T. Boon, Rachel Deplus, F. Fuks, 2004, Nucleic acids research.

Restoring the association of the T cell receptor with CD8 reverses anergy in human tumor-infiltrating lymphocytes.

P. Courtoy, T. Boon, P. van der Smissen, 2008, Immunity.

The tum− antigens P91A and P198 derive from proteins located in the cytosolic compartment of cells

A. Dautry‐Varsat, A. van Pel, A. Amar‐Costesec, 1993, European journal of immunology.

A new tumor-specific antigen encoded by MAGE-C2 and presented to cytolytic T lymphocytes by HLA-B44

B. Neyns, F. Brasseur, T. Boon, 2007, Cancer Immunology, Immunotherapy.

A reversible functional defect of CD8+ T lymphocytes involving loss of tetramer labeling

P. Bruggen, T. Boon, D. Colau, 2002, European journal of immunology.

Vaccination of a Melanoma Patient with Mature Dendritic Cells Pulsed with MAGE-3 Peptides Triggers the Activity of Nonvaccine Anti-Tumor Cells1

B. Neyns, F. Brasseur, T. Boon, 2008, The Journal of Immunology.

last antigenic stimulation CD45RA on human CD8 T cells is sensitive to the time elapsed since the

P. Bruggen, T. Boon, D. Godelaine, 2008 .

CD45RA on human CD8 T cells is sensitive to the time elapsed since the last antigenic stimulation.

T. Boon, P. van der Bruggen, A. van Pel, 2006, Blood.

Identification and characterization of the tumor‐specific P1A gene product

B. Eynde, A. Amar‐Costesec, D. Godelaine, 1994, Biology of the cell.

Coalescence of microsomal vesicles from rat liver: a phenomenon occurring in parallel with enhancement of the glycosylation activity during incubation of stripped rough microsomes with GTP

J. Paiement, D. Godelaine, H. Beaufay, 1980, The Journal of cell biology.

Analytical study of microsomes and isolated subcellular membranes from rat liver VIII. Subfractionation of preparations enriched with plasma membranes, outer mitochondrial membranes, or Golgi complex membranes

A. Amar‐Costesec, D. Thinès-Sempoux, M. Wibo, 1981, The Journal of cell biology.

Cytolytic T-cell responses of cancer patients vaccinated with a MAGE antigen.

P. Coulie, T. Connerotte, T. Boon, 2002, Immunological reviews.

Alteration of membrane barrier in stripped rough microsomes from rat liver on incubation with GTP: its relevance to the stimulation by this nucleotide of the dolichol pathway for protein glycosylation

M. Wibo, D. Godelaine, H. Beaufay, 1983, The Journal of cell biology.

Genes encoding tumor-specific antigens are expressed in human myeloma cells.

F. Brasseur, M. André, T. Boon, 1999, Blood.

Anti-Tumor Cells Peptides Triggers the Activity of Nonvaccine Mature Dendritic Cells Pulsed with MAGE-3 Vaccination of a Melanoma Patient with Boon and Danièle Godelaine

B. Neyns, F. Brasseur, P. Bruggen, 2008 .

Polyclonal CTL Responses Observed in Melanoma Patients Vaccinated with Dendritic Cells Pulsed with a MAGE-3.A1 Peptide 1

P. Coulie, G. Schuler, T. Boon, 2003, The Journal of Immunology.

Peptide Dendritic Cells Pulsed with a MAGE-3 . A 1 Melanoma Patients Vaccinated with Polyclonal CTL Responses Observed in

P. Coulie, G. Schuler, T. Boon, 2003 .

Monoclonal antibody 57B stains tumor tissues that express gene MAGE‐A4

P. Coulie, F. Brasseur, E. Marbaix, 2000, International journal of cancer.

Myeloma Cells Genes Encoding Tumor-Specific Antigens Are Expressed in Human

F. Brasseur, T. Boon, C. Doyen, 2013 .

Quantitative assay and subcellular distribution of enzymes acting on dolichyl phosphate in rat liver

A. Amar‐Costesec, D. Godelaine, H. Beaufay, 1981, The Journal of cell biology.

Processing of the carbohydrate units of thyroglobulin.

R. Spiro, M. Spiro, D. Godelaine, 1981, The Journal of biological chemistry.

Mutations of the beta2-microglobulin gene result in a lack of HLA class I molecules on melanoma cells of two patients immunized with MAGE peptides.

F. Brasseur, M. R. Oliva, T. Boon, 1998, Tissue antigens.

Immune Suppression in Tumors as a Surmountable Obstacle to Clinical Efficacy of Cancer Vaccines

P. van der Bruggen, D. Godelaine, N. Demotte, 2011, Cancers.

The IL-9 receptor gene (IL9R): genomic structure, chromosomal localization in the pseudoautosomal region of the long arm of the sex chromosomes, and identification of IL9R pseudogenes at 9qter, 10pter, 16pter, and 18pter.

J. Vermeesch, K. Arden, D. Higgs, 1995, Genomics.

Functions of Anti-MAGE T-cells induced in melanoma patients under different vaccination modalities.

E. Tartour, P. Coulie, T. Connerotte, 2008, Cancer research.

Identification of a naturally processed HLA-A*02:01-restricted CTL epitope from the human tumor-associated antigen Nectin-4

D. Olive, P. Coulie, D. Colau, 2016, Cancer Immunology, Immunotherapy.

Cytolytic T‐cell responses of cancer patients vaccinated with a MAGE antigen

P. Coulie, T. Connerotte, T. Boon, 2002 .

Phase 1/2 study of subcutaneous and intradermal immunization with a recombinant MAGE‐3 protein in patients with detectable metastatic melanoma

A. Eggermont, B. Dréno, F. Brasseur, 2005, International journal of cancer.

A major secretory defect of tumour-infiltrating T lymphocytes due to galectin impairing LFA-1-mediated synapse completion

S. Valitutti, P. van der Bruggen, D. Godelaine, 2016, Nature Communications.

The tumor protein MAGE-1 is located in the cytosol of human melanoma cells.

E. Stockert, P. van der Bruggen, A. Amar‐Costesec, 1994, Biochemical and biophysical research communications.

Structure, chromosomal location, and expression pattern of three mouse genes homologous to the human MAGE genes.

O. de Backer, R. Brasseur, P. Avner, 1995, Genomics.

Expression of gene MAGE-A4 in Reed-Sternberg cells.

L. Xerri, D. Olive, P. Coulie, 2000, Blood.

The dolichol pathway of protein glycosylation in rat liver. Evidence that GTP promotes transformation of endogenous dolichyl phosphate into dolichylpyrophosphoryl-N-acetylglucosamine in stripped rough microsomes.

D. Godelaine, H. Beaufay, 1983, European journal of biochemistry.

Incorporation of N-acetylglucosamine into endogenous acceptors of rough microsomes from rat liver: stimulation by GTP after treatment with pyrophosphate.

M. Wibo, D. Godelaine, H. Beaufay, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Presentation of mouse tum− P91A antigen from chimeric proteins with different subcellular localizations by class I molecules of the major histocompatibility complex

A. van Pel, D. Godelaine, H. Beaufay, 1993, European journal of immunology.

Functions of Anti-MAGE T-cells induced in melanoma patients under different vaccination modalities.

E. Tartour, P. Coulie, T. Connerotte, 2008, Cancer Research.

Comparative Study of the Effect of Various Fibres on the Secretion of Plasminogen Activator by Murine Peritoneal Macrophages

D. Godelaine, H. Beaufay, 1989 .

Coalescence of microsomal vesicles from rat liver: a phenomenon occurring in parallel with enhancement of the glycosylation activity during incubation of stripped rough microsomes with GTP

Gerardo J. Ramírez-Nava, M. Luna-Gutiérrez, B. Ocampo-García, 1980, The Journal of cell biology.

A. Amar‐Costesec, D. Thinès-Sempoux, M. Wibo, 1981, The Journal of cell biology.

The dolichol pathway of protein glycosylation in rat liver. Incorporation of mannose into endogenous lipids and proteins of rough microsomes.

M. Wibo, D. Godelaine, H. Beaufay, 1979, European journal of biochemistry.