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virginie-haushalter

DR. Virginie Haushalter

Post-Doctoral student

 

Role in the project: Studies of mouse models

haushalv@igbmc.fr

Institute of Genetics and and Molecular and Cellular Biology, IGBMC
CNRS UMR 7104 – Inserm U 964 – 1 rue Laurent Fries – BP 10142

DESCRIPTION

I am working at IGBMC as a post-doctoral student and my project objectives are to combine complementary research approaches in developmental biology especially via the study of animal models and bioinformatics to improve the understanding of etiopathogenic mechanisms involved in oral development, focusing on palatogenesis, odontogenesis and their anomalies.

In parallel I teach developmental biology, but also biochemistry and biotechnology within the University of Strasbourg.

PUBLICATIONS

RSK2 is a modulator of craniofacial development.

Laugel-Haushalter V, Paschaki M, Pilgram C, Langer A, Kuntz T, Demassue J, Morkmued S, Choquet P, Constantinesco A, Bornert F, Schmittbuhl M, Pannetier S, Dolle P, Hanauer A, Bloch-Zupan A
PLoS One. 2014 Jan 8;9(1)

Molars and incisors : show your microarray IDs.

Laugel-Haushalter V, Paschaki M, Thibault-Carpentier C, Dembele D, Dollé P, Bloch-Zupan A
BMC Res Notes. 2013 Mar 26;6:113.

A possible cranio-oro-facial phenotype in Cockayne syndrome.

Bloch-Zupan A, Rousseaux M, Laugel V, Schmittbuhl M, Mathis R, Desforges E, Koob M, Zaloszyc A, Dollfus H, Laugel V.
Orphanet J Rare Dis. 2013 Jan 14;8(1):9.

From the transcription of genes involved in ectodermal dysplasias to the understanding of associated dental anomalies.

Laugel-Haushalter V, Langer A, Marrie J, Fraulob V, Schuhbaur B, Koch-Phillips M, Dollé P, Bloch-Zupan A.
Mol Syndromol. 2012 Oct;3(4):158-68. doi: 10.1159/000342833. Epub 2012 Sep 27.
Read the article : http://www.ncbi.nlm.nih.gov/pubmed/23239958

Homozygosity mapping and candidate prioritization identify mutations, missed by whole-exome sequencing, in SMOC2, causing major dental developmental defects.

Bloch-Zupan A, Jamet X, Etard C, Laugel V, Muller J, Geoffroy V, Strauss JP, Pelletier V, Marion V, Poch O, Strahle U, Stoetzel C, Dollfus H.
Am J Hum Genet. 2011 Dec 9;89(6):773-81.
Read the article : http://www.ncbi.nlm.nih.gov/pubmed/22152679

KEYWORDS

  • Dental anomalies
  • Mice
  • Syndromes