M. Fondanèche

发表

Regulation of natural cytotoxicity by the adaptor SAP and the Src-related kinase Fyn

A. Fischer, S. Latour, A. Veillette, 2005, The Journal of experimental medicine.

Novel mutations in the RFXANK gene: RFX complex containing in-vitro-generated RFXANK mutant binds the promoter without transactivating MHC II

A. Fischer, F. Deist, W. Wiszniewski, 2003, Immunogenetics.

Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product

A. Fischer, S. Latour, B. Pasquier, 2005, The Journal of experimental medicine.

Immunohistochemical and biochemical study of a cathepsin B-like proteinase in human colonic cancers.

M. Pagano, P. Burtin, D. Keppler, 1988, Cancer research.

Lymphoid cells in lymph nodes and peripheral blood of patients with squamous cell carcinoma of the head and neck

P. Burtin, M. Fondanèche, P. Quan, 2004, Journal of Cancer Research and Clinical Oncology.

Leucocyte-migration-inhibition test in patients with colorectal cancer: clinicopathological correlations.

P. Burtin, C. Pinset, M. Fondanèche, 1978, British Journal of Cancer.

Limited proteolysis of tumor cells increases their plasmin‐binding ability

P. Burtin, M. Fondanèche, M. Camacho, 1989, FEBS letters.

The presence of plasmin receptors on three mammary carcinoma MCF‐7 sublines

P. Burtin, M. Bracke, M. Fondanèche, 1990, International journal of cancer.

Receptor for plasmin on human carcinoma cells.

P. Burtin, M. Fondanèche, P. Burtin, 1988, Journal of the National Cancer Institute.

Cernunnos, a Novel Nonhomologous End-Joining Factor, Is Mutated in Human Immunodeficiency with Microcephaly

A. Fischer, F. Deist, A. Plebani, 2006, Cell.

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B

K. Schwarz, W. Reith, W. Wiszniewski, 2000, Immunogenetics.

Two complementation groups account for most cases of inherited MHC class II deficiency.

M. Rols, C. Griscelli, A. Fischer, 1994, Human molecular genetics.

Alterations in expression and synthesis of glycolipid antigens in human colonic tumor cell lines.

P. Burtin, M. Fondanèche, V. Liepkalns, 1985, Cancer research.

Presence of NCA (nonspecific cross-reacting antigen) in the cells of the human granulocyte series.

G. Flandrin, P. Burtin, M. Fondanèche, 1980, Blood cells.

Characterization of the nonspecific cross-reacting antigen (NCA) in human monocytes.

P. Burtin, M. Fondanèche, 1981, Clinical immunology and immunopathology.

CEA and non‐specific cross‐reacting antigen (NCA) in medullary carcinomas of the thyroid

P. Burtin, M. Fondanèche, C. Calmettes, 1979, International journal of cancer.

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

F. Rieux-Laucat, A. Fischer, F. Deist, 2006, Nature.

lymphoproliferative disease gene sap Impaired Ig class switch in mice deficient for the X-linked

Zhao-Qi Wang, S. Latour, M. Fondanèche, 2013 .

Impaired Ig class switch in mice deficient for the X-linked lymphoproliferative disease gene Sap.

S. Tavtigian, Zhao-Qi Wang, S. Latour, 2005, Blood.

A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection

S. Dorman, A. Fischer, R. Döffinger, 1999, Nature Genetics.

Partial interferon-gamma receptor 1 deficiency in a child with tuberculoid bacillus Calmette-Guérin infection and a sibling with clinical tuberculosis.

J. Casanova, R. Schreiber, M. Levin, 1997, The Journal of clinical investigation.

In a novel form of IFN-gamma receptor 1 deficiency, cell surface receptors fail to bind IFN-gamma.

R. Döffinger, J. Casanova, J. Emile, 2000, The Journal of clinical investigation.

Partial interferon-gamma receptor signaling chain deficiency in a patient with bacille Calmette-Guérin and Mycobacterium abscessus infection.

S. Pestka, R. Döffinger, J. Casanova, 2000, The Journal of infectious diseases.

Mutation in the Class II trans-Activator Leading to a Mild Immunodeficiency1

N. Brousse, W. Wiszniewski, G. Barbieri, 2001, The Journal of Immunology.

Genetic and molecular definition of complementation group D in MHC class II deficiency.

W. Reith, B. Mach, W. Wiszniewski, 1998, Human molecular genetics.

Solubilization of the plasmin receptor from human carcinoma cells.

P. Burtin, M. Fondanèche, 1990, Biochemical and biophysical research communications.

Three novel mutations of the CIITA gene in MHC class II-deficient patients with a severe immunodeficiency

Dominique Charron, Capucine Picard, A. Fischer, 2002, Immunogenetics.

A causative relationship between mutant IFNgR1 alleles and impaired cellular response to IFNgamma in a compound heterozygous child.

A. Fischer, J. Casanova, R. Schreiber, 1998, American journal of human genetics.

A study of gastrointestinal cancer‐associated antigen (GICA) in human fetal organs

H. Raux, H. Koprowski, P. Burtin, 1983, International journal of cancer.

Erratum: Mutation in the class II trans-activator leading to a mild immunodeficiency (The Journal of Immunology (2001) 167 (1787-1794))

A. Fischer, F. Deist, N. Brousse, 2002 .

Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product

A. Fischer, S. Latour, B. Pasquier, 2005, The Journal of experimental medicine.

Regulation of natural cytotoxicity by the adaptor SAP and the Src-related kinase Fyn

A. Fischer, S. Latour, A. Veillette, 2005, The Journal of experimental medicine.