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Marie-Geneviève Mattei

Marie-Geneviève Mattei

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Genetics and Molecular Biology
France
2024

D-Index & Metrics

Genetics

D-Index
105
Citations
33700
World Ranking
632
National Ranking
14

Research.com Recognitions

  • 2024 - Research.com Genetics and Molecular Biology in France Leader Award

Overview

Marie-Geneviève Mattei is affiliated with Inserm in France. Their academic profile indicates a research career based primarily within this institution, suggesting involvement in biomedical or health-related scientific studies, given Inserm's focus as a French public research organization dedicated to human health.

No detailed list of recent publications is available, and no specific research papers have been documented. Similarly, there are no records of frequent co-authors or publication venues, which limits the insight into collaborative networks or preferred journals for disseminating research findings.

Their research fields, subfields, and main topics of study have not been provided, leaving the precise areas of scientific inquiry unspecified. Likewise, there are no book publications recorded under their name or any noted awards, which suggests that publicly available data on accolades or extended academic contributions such as monographs are not present.

The absence of information about recent papers or main study topics indicates either an early-stage research profile or a low public footprint in widely indexed academic databases. Given the sole confirmed institutional affiliation, it may be assumed that their work is grounded within the framework of Inserm's biomedical research programs.

Best Publications

  • A new member of the immunoglobulin superfamily--CTLA-4.

    Jean-François Brunet;François Denizot;Marie-Françoise Luciani;Magali Roux-Dosseto;Magali Roux-Dosseto

  • CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene.

    E Rouvier;M F Luciani;M G Mattéi;F Denizot

  • Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

    Brendan Lee;Maurice Godfrey;Emilia Vitale;Hisae Hori

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

    S Guazzi;M Price;M De Felice;G Damante

  • CTLA-4 and CD28 activated lymphocyte molecules are closely related in both mouse and human as to sequence, message expression, gene structure, and chromosomal location.

    K Harper;C Balzano;E Rouvier;M G Mattéi

  • A Novel Lysosome-Associated Membrane Glycoprotein, DC-LAMP, Induced upon DC Maturation, Is Transiently Expressed in MHC Class II Compartment

    B de Saint-Vis;J Vincent;S Vandenabeele;B Vanbervliet

  • A New Member of the Rho Family, Rnd1, Promotes Disassembly of Actin Filament Structures and Loss of Cell Adhesion

    Catherine D. Nobes;Inger Lauritzen;Marie-Geneviève Mattei;Sonia Paris

  • Isolation of a YAC clone covering a cluster of nine S100 genes on human chromosome 1q21: rationale for a new nomenclature of the S100 calcium-binding protein family

    Beat W. Schäfer;Roland Wicki;Dieter Engelkamp;Marie-geneviève Mattei

  • The chemokine TECK is expressed by thymic and intestinal epithelial cells and attracts double- and single-positive thymocytes expressing the TECK receptor CCR9

    Marc-André Wurbel;Jean-Marc Philippe;Catherine Nguyen;Genevieve Victorero

  • A novel, secreted form of human ADAM 12 (meltrin alpha) provokes myogenesis in vivo

    Brent J. Gilpin;Frosty Loechel;Marie-Geneviève Mattei;Eva Engvall

  • Human Ig superfamily CTLA-4 gene: chromosomal localization and identity of protein sequence between murine and human CTLA-4 cytoplasmic domains.

    Piona Dariavach;Marie-Geneviève Mattéi;Pierre Golstein;Marie-Paule Lefranc

  • A mouse model for hereditary thyroid dysgenesis and cleft palate

    Mario De Felice;Catherine Ovitt;Elio Biffali;Alina Rodriguez-Mallon

  • Regional expression of the homeobox gene Nkx-2.2 in the developing mammalian forebrain

    M. Price;D. Lazzaro;T. Pohl;M. G. Mattei

  • Identification and Characterization of a Novel Siglec, Siglec-7, Expressed by Human Natural Killer Cells and Monocytes

    Gavin Nicoll;Jian Ni;Ding Liu;Paul Klenerman

  • SRPX2 mutations in disorders of language cortex and cognition

    Patrice Roll;Gabrielle Rudolf;Sandrine Pereira;Barbara Royer

  • kappa-Opioid receptor in humans: cDNA and genomic cloning, chromosomal assignment, functional expression, pharmacology, and expression pattern in the central nervous system

    Frederic Simonin;Claire Gaveriaux-Ruff;Katia Befort;Hans Matthes

  • Insensitivity to anti-müllerian hormone due to a mutation in the human anti-müllerian hormone receptor.

    S. Imbeaud;E. Faure;I. Lamarre;M.-G. Mattei

  • Cloning, Chromosomal Mapping, and Expression of a Novel Human Secretory Phospholipase A2

    Lionel Cupillard;Kamen Koumanov;Marie-Geneviève Mattéi;Michel Lazdunski

  • Identification of Four Novel Human Genes Amplified and Overexpressed in Breast Carcinoma and Localized to the q11-q21.3 Region of Chromosome 17

    C. Tomasetto;C. Régnier;C. Moog-Lutz;M.G. Mattei

  • The lung amiloride-sensitive Na+ channel: biophysical properties, pharmacology, ontogenesis, and molecular cloning

    Nicolas Voilley;Eric Lingueglia;Guy Champigny;Marie-Genevieve Mattei

Frequent Co-Authors

Pierre Golstein
Pierre Golstein Aix-Marseille University
Bernard Malissen
Bernard Malissen Aix-Marseille University
Michel Lazdunski
Michel Lazdunski Centre national de la recherche scientifique, CNRS
Serge Lebecque
Serge Lebecque Claude Bernard University Lyon 1
Marie-Christine Rio
Marie-Christine Rio Grenoble Alpes University
Patrick Charnay
Patrick Charnay École Normale Supérieure
Claude Kedinger
Claude Kedinger University of Strasbourg
Jean-François Brunet
Jean-François Brunet École Normale Supérieure
Beat W. Schäfer
Beat W. Schäfer University of Zurich

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