IGBMC : Institut de la Génétique et de la Biologie Moléculaire et Cellulaire

• Chercheurs

  Agnès BLOCH-ZUPAN

  Pascal DOLLE

  Wojciech KREZEL

  Karen NIEDERREITHER

• Post-Doctorants

  Supawich MORKMUED

  Anna PODLESNY

• Doctorants

  Lucile CATHIARD

  Marion CIANCIA

  Joanna SOBSKA

• Ingénieurs & Techniciens

  Valérie FRAULOB

  Brigitte SCHUHBAUR

• Collaborateur Occasionnel

  Bartlomiej STANCZYKIEWICZ

Biologie du développement et cellules souches

Rôle de l'acide rétinoïque dans le développement de la souris

Publications

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• Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathway

  Zullo A., Iaconis D., Barra A., Cantone A., Messaddeq N., Capasso G., Dolle P., Igarashi P., Franco B.

  Hum Mol Genet 15 juillet 2010;19:2792-803.

• Retinoid x receptor gamma control of affective behaviors involves dopaminergic signaling in mice

  Krzyzosiak A., Szyszka-Niagolov M., Wietrzych M., Gobaille S., Muramatsu S., Krezel W.

  Neuron 24 juin 2010;66:908-20.

• Early mouse caudal development relies on crosstalk between retinoic acid, Shh and Fgf signalling pathways

  Ribes V., Le Roux I., Rhinn M., Schuhbaur B., Dolle P.

  Development Feb 2009;136:665-76.

• Genetic disruption of CYP26B1 severely affects development of neural crest derived head structures, but does not compromise hindbrain patterning

  Maclean G., Dolle P., Petkovich M.

  Dev Dyn Mar 2009;238:732-45.

• Truncation of the catalytic domain of the cylindromatosis tumor suppressor impairs lung maturation

  Trompouki E., Tsagaratou A., Kosmidis S.K., Dolle P., Qian J., Kontoyiannis D.L., Cardoso W.V., Mosialos G.

  Neoplasia May 2009;11:469-76.

• Oral health of children with intractable epilepsy attending the UK National Centre for Young People with Epilepsy

  Percival T., Aylett S.E., Pool F., Bloch-Zupan A., Roberts G.J., Lucas V.S.

  Eur Arch Paediatr Dent Mar 2009;10:19-24.

• Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta

  Parry D.A., Mighell A.J., El-Sayed W., Shore R.C., Jalili I.K., Dollfus H., Bloch-Zupan A., Carlos R., Carr I.M., Downey L.M., Blain K.M., Mansfield D.C., Shahrabi M., Heidari M., Aref P., Abbasi M., Michaelides M., Moore A.T., Kirkham J., Inglehearn C.F.

  Am J Hum Genet Feb 2009;84:266-73.

• Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

  Reibel A., Maniere M.C., Clauss F., Droz D., Alembik Y., Mornet E., Bloch-Zupan A.

  Orphanet J Rare Dis 2009;4:6.