M. Mattéi

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A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human.

A. Agulnik, M. Mitchell, J. Lerner, 1994, Human molecular genetics.

Evidence for allelism of the recessive insertional mutation add and the dominant mouse mutation extra-toes (Xt).

M. Mattéi, T. Pohl, U. Rüther, 1990, Development.

Molecular characterization of the mouse beta 3‐adrenergic receptor: relationship with the atypical receptor of adipocytes.

M. Mattéi, A. Strosberg, A. Strosberg, 1991, The EMBO journal.

Mapping the mouse X chromosome: possible symmetry in the location of a family of sequences on the mouse X and Y chromosomes.

D. Hatat, M. Mattéi, P. Avner, 1987, Development.

New gene in the homologous human 11q13–q14 and mouse 7F chromosomal regions

M. Mattéi, D. Birnbaum, V. Ollendorff, 2004, Mammalian Genome.

Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation

J. Gécz, M. Mattéi, C. Schwartz, 2002, Journal of medical genetics.

Prader-Willi syndrome: Diagnostic strategy with a cytogenetic and molecular approach

M. Mattéi, A. Moncla, P. Malzac, 1993, Neuromuscular Disorders.

Genomic structure and chromosomal localization of the mouse Hsf2 gene and promoter sequences.

M. Mattéi, M. Morange, V. Mezger, 1999, Gene.

Molecular aspects of sex determination in mice: an alternative model for the origin of the Sxr region.

C. Bishop, M. Mattéi, A. Weith, 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Juxtaposition of N‐myc and Igk through a reciprocal t(6;12) translocation in a mouse plasmacytoma

M. Mattéi, Yi-Song Wang, G. Klein, 1994 .

Molecular and cytogenetic evidence for the location of Tdy and Hya on the mouse Y chromosome short arm.

C. Bishop, M. Mattéi, M. Mattei, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Isolation and Characterization ofSuv39h2, a Second Histone H3 Methyltransferase Gene That Displays Testis-Specific Expression

M. Mattéi, H. Scherthan, D. O’Carroll, 2000, Molecular and Cellular Biology.

The mapping of the human 52-kD Ro/SSA autoantigen gene to human chromosome 11, and its polymorphisms.

M. Mattéi, P. Pontarotti, A. Fujisaku, 1993, American journal of human genetics.

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

M. Mitchell, M. Mattéi, N. Lévy, 2004, Journal of Medical Genetics.

Thyroid nuclear factor 1 (TTF‐1) contains a homeodomain and displays a novel DNA binding specificity.

M. Mattéi, R. Lauro, M. Mattei, 1990, The EMBO journal.

A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications.

M. Mattéi, M. Mattei, M. Lalande, 1998, Human molecular genetics.

Genetic control of diabetes progression.

M. Mattéi, C. Benoist, D. Mathis, 1997, Immunity.

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome.

M. Mattéi, A. Aurias, N. Philip, 1995, Human molecular genetics.

PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase

M. Mitchell, M. Mattéi, A. Mégarbané, 2006, Journal of Cell Science.

Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution.

M. Mitchell, M. Mattéi, N. Brockdorff, 1998, Human molecular genetics.

Clinical Heterogeneity in 16 Patients with inv dup 15 Chromosome: Cytogenetic and Molecular Studies, Search for an Imprinting Effect

M. Mattéi, M. Mattei, A. Moncla, 1996, European journal of human genetics : EJHG.

Evaluation of the genotoxic activity of paclitaxel by the in vitro micronucleus test in combination with fluorescent in situ hybridization of a DNA centromeric probe and the alkaline single cell gel electrophoresis technique (comet assay) in human T‐lymphocytes

M. Mattéi, T. Orsière, F. Duffaud, 1999, Environmental and molecular mutagenesis.

Programmed cell death is affected in the novel mouse mutant Fused toes (Ft).

M. Mattéi, B. Kyewski, M. Mattei, 1994, Development.

Complementary DNA characterization and chromosomal localization of a human gene related to the poliovirus receptor-encoding gene.

M. Mattéi, F. Birg, J. Gabert, 1995, Gene.

The human PRR2 gene, related to the human poliovirus receptor gene (PVR), is the true homolog of the murine MPH gene.

M. Mattéi, E. Devilard, P. Dubreuil, 1995, Gene.

Inactivation of an X-linked transgene in murine extraembryonic and adult tissues.

M. Mattéi, P. Avner, C. Stewart, 1993, Development.

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

M. Mattéi, C. Roberts, S. Halford, 1993, Human molecular genetics.

Intrachromosomal triplication for the distal part of chromosome 15q

M. Mattéi, J. Willig, M. Mattei, 2005, American journal of medical genetics. Part A.

RNF11 is a GGA protein cargo and acts as a molecular adaptor for GGA3 ubiquitination mediated by Itch

M. Mattéi, L. Castagnoli, G. Cesareni, 2014, Oncogene.

The characterization of the promoter of the gene encoding the p50 subunit of NF‐kappa B indicates that it participates in its own regulation.

P. Kourilsky, M. Mattéi, A. Israël, 1992, The EMBO journal.

Structure, mapping and expression of a growth factor inducible gene encoding a putative nuclear hormonal binding receptor.

M. Mattéi, M. Mattei, R. Bravo, 1989, The EMBO journal.

Identification and expression of the cDNA of KIN17, a zinc-finger gene located on mouse chromosome 2, encoding a new DNA-binding protein.

M. Mattéi, R. Benarous, E. Rouer, 1991, Nucleic acids research.

Chromosomal assignment and expression pattern of the murine Lasp-1 gene.

M. Mattéi, M. Mattei, V. Schreiber, 1998, Gene.

Genetic Analysis of the Fragile X-Mental Retardation Syndrome with Polymorphic DNA Markers

M. Mattéi, G. Camerino, B. Arveiler, 1986 .