Daniel Guerrier

Summary

Country: France

Publications

  1. ncbi Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
    Karine Morcel
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, IFR 140 GFAS, Faculte de Medecine, 2 avenue du Professeur Léon Bernard CS 34317, 35043 Rennes Cedex, France
    Orphanet J Rare Dis 6:9. 2011
  2. ncbi Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
    Karine Morcel
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, Universite de Rennes 1, IFR140 GFAS, Faculte de Medecine, Rennes, France
    Orphanet J Rare Dis 2:13. 2007
  3. ncbi Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)
    Agnes Burel
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, Groupe IPD, IFR140 GFAS, Faculte de Medecine, Rennes, France
    J Negat Results Biomed 5:4. 2006
  4. ncbi Inducible expression of beta defensins by human respiratory epithelial cells exposed to Aspergillus fumigatus organisms
    Ludmila Alekseeva
    UMR 956, INRA, AFSSA, ENVA, Maisons Alfort Cedex, France
    BMC Microbiol 9:33. 2009
  5. ncbi The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches
    Daniel Guerrier
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, Groupe IPD, IFR140 GFAS, Faculte de Medecine, Rennes, France
    J Negat Results Biomed 5:1. 2006
  6. ncbi Involvement of ZFPIP/Zfp462 in chromatin integrity and survival of P19 pluripotent cells
    Julie Masse
    UMR CNRS 6061, Institut of Génétique et Développement de Rennes IGDR, Faculte de Medecine, Universite de Rennes 1, Rennes, France
    Exp Cell Res 316:1190-201. 2010
  7. ncbi ZFPIP/Zfp462 is involved in P19 cell pluripotency and in their neuronal fate
    Julie Masse
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, Universite de Rennes 1, Campus Villejean, 2 Avenue du Professeur Leon Bernard, Rennes Cedex, France
    Exp Cell Res 317:1922-34. 2011
  8. ncbi Identification of a new type of PBX1 partner that contains zinc finger motifs and inhibits the binding of HOXA9-PBX1 to DNA
    Audrey Laurent
    UMR CNRS 6061, Genetique et Developpement, IFR 140, Faculte de Medecine, Universite de Rennes 1, Campus Villejean, 2 Avenue du Professeur Leon Bernard, CS34317, F 35043 Rennes Cedex, France
    Mech Dev 124:364-76. 2007
  9. ncbi The developing female genital tract: from genetics to epigenetics
    Julie Masse
    IGDR, UMR CNRS 6061, Genetique et Developpement, IFR 140, Faculte de Medecine, Universite de Rennes 1, France
    Int J Dev Biol 53:411-24. 2009
  10. ncbi Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother
    Claude Bendavid
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, IFR140 GFAS, Faculte de Medecine, 2, avenue du Profeseur Leon Bernard, Rennes 35043, France
    Eur J Med Genet 50:66-72. 2007

Collaborators

  • Christele Dubourg
  • Agnes Burel
  • K Morcel
  • Cedric Le Caignec
  • Isabelle Pellerin
  • Julie Masse
  • Stephane Deschamps
  • Audrey Laurent
  • Agnès Dintilhac
  • Tanguy Watrin
  • Réjane Bihan
  • Ludmila Alekseeva
  • Claude Bendavid
  • Claire Piquet-Pellorce
  • Justine Viet
  • Barbara Nicol
  • Virginie Tichanné-Seltzer
  • Adrien Cagna
  • Françoise Féménia
  • Mahdia Abdelouahab
  • Nadia Berkova
  • Armelle Baeza-Squiban
  • Dominique Huet
  • Rene Chermette
  • Jean Paul Latge
  • Isabelle Mouyna
  • Valérie Dupé
  • Josette Lucas
  • Jean Leveque
  • Veronique David
  • Isabelle Gicquel
  • Laurent Pasquier
  • Sylvie Odent
  • Catherine Henry
  • Francis Omilli
  • Georgette Bonnec
  • Héloise Bougerie

Detail Information

Publications12

  1. ncbi Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci
    Karine Morcel
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, IFR 140 GFAS, Faculte de Medecine, 2 avenue du Professeur Léon Bernard CS 34317, 35043 Rennes Cedex, France
    Orphanet J Rare Dis 6:9. 2011
    ..Its etiology remains poorly understood. Thus the phenotypic manifestations of MRKH and DGS overlap suggesting a possible genetic link. This would potentially have clinical consequences...
  2. ncbi Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
    Karine Morcel
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, Universite de Rennes 1, IFR140 GFAS, Faculte de Medecine, Rennes, France
    Orphanet J Rare Dis 2:13. 2007
    ..As psychological distress is very important in young women with MRKH, it is essential for the patients and their families to attend counseling before and throughout treatment...
  3. ncbi Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)
    Agnes Burel
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, Groupe IPD, IFR140 GFAS, Faculte de Medecine, Rennes, France
    J Negat Results Biomed 5:4. 2006
    ..This tends to show that HOX genes are not involved in MRKH syndrome. However it does not exclude that other mechanisms leading to HOX dysfunction may account for the syndrome...
  4. ncbi Inducible expression of beta defensins by human respiratory epithelial cells exposed to Aspergillus fumigatus organisms
    Ludmila Alekseeva
    UMR 956, INRA, AFSSA, ENVA, Maisons Alfort Cedex, France
    BMC Microbiol 9:33. 2009
    ..The role of the airway epithelium involves a complex interaction with the inhaled pathogen. Antimicrobial peptides with direct antifungal and chemotactic activities may boost antifungal immune response...
  5. ncbi The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches
    Daniel Guerrier
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, Groupe IPD, IFR140 GFAS, Faculte de Medecine, Rennes, France
    J Negat Results Biomed 5:1. 2006
    ..Expression and/or function defects of one or several HOX genes may account for this syndrome...
  6. ncbi Involvement of ZFPIP/Zfp462 in chromatin integrity and survival of P19 pluripotent cells
    Julie Masse
    UMR CNRS 6061, Institut of Génétique et Développement de Rennes IGDR, Faculte de Medecine, Universite de Rennes 1, Rennes, France
    Exp Cell Res 316:1190-201. 2010
    ..These data suggested an instrumental role of ZFPIP/Zfp462 in maintaining the chromatin structure of pluripotent cells...
  7. ncbi ZFPIP/Zfp462 is involved in P19 cell pluripotency and in their neuronal fate
    Julie Masse
    CNRS UMR 6061, Institut de Génétique et Développement de Rennes, Universite de Rennes 1, Campus Villejean, 2 Avenue du Professeur Leon Bernard, Rennes Cedex, France
    Exp Cell Res 317:1922-34. 2011
    ....
  8. ncbi Identification of a new type of PBX1 partner that contains zinc finger motifs and inhibits the binding of HOXA9-PBX1 to DNA
    Audrey Laurent
    UMR CNRS 6061, Genetique et Developpement, IFR 140, Faculte de Medecine, Universite de Rennes 1, Campus Villejean, 2 Avenue du Professeur Leon Bernard, CS34317, F 35043 Rennes Cedex, France
    Mech Dev 124:364-76. 2007
    ..We suggest that ZFPIP is a new type of PBX1 partner that could participate in PBX1 function during several developmental pathways...
  9. ncbi The developing female genital tract: from genetics to epigenetics
    Julie Masse
    IGDR, UMR CNRS 6061, Genetique et Developpement, IFR 140, Faculte de Medecine, Universite de Rennes 1, France
    Int J Dev Biol 53:411-24. 2009
    ....
  10. ncbi Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother
    Claude Bendavid
    CNRS UMR 6061, Genetique et Developpement, Universite de Rennes 1, IFR140 GFAS, Faculte de Medecine, 2, avenue du Profeseur Leon Bernard, Rennes 35043, France
    Eur J Med Genet 50:66-72. 2007
    ..The daughter presented isolated congenital aplasia of the uterus and vagina, the prime feature of the MRKH syndrome. This has not been described before in association with a 46,XX,del(4)(q34qter)...
  11. ncbi PBX1 intracellular localization is independent of MEIS1 in epithelial cells of the developing female genital tract
    Agnès Dintilhac
    UMR 6061, Genetique et Developpement, IFR 140, Universite de Rennes 1, Campus Villejean, Rennes, France
    Int J Dev Biol 49:851-8. 2005
    ..We thus provide evidence for a control of PBX1 intracellular distribution which is independent of MEINOX proteins, but is cell cycle correlated...
  12. ncbi A conserved non-homeodomain Hoxa9 isoform interacting with CBP is co-expressed with the 'typical' Hoxa9 protein during embryogenesis
    Agnès Dintilhac
    UMR 6061, Genetique et Developpement, IFR 97, Universite de Rennes 1, Campus Villejean, 2 Avenue du Professeur Leon Bernard, CS34317, F 35043 Rennes, France
    Gene Expr Patterns 4:215-22. 2004
    ..We further found that both isoforms are able to interact with CBP, suggesting a competition between Hoxa9 and Hoxa9T with this protein...