Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis

Emeline F. Nandrot, Éric Dufour, Alexandra Provost, +13

Neurobiology of Disease

Knockout MouseHomozygous DeletionSignal TransductionMolecular PhysiologyCell Regulation +11

Organization of the Gene (RHCE) Encoding the Human Blood Group RhCcEe Antigens and Characterization of the Promoter Region

Baya Chérif‐Zahar, Caroline Le Van Kim, Christelle Rouillac, +3

Genomics

ImmunogeneticsTranscriptional RegulationPromoter RegionProtein ExpressionGenetics +7

Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes

Christelle Rouillac, Yves Colin, NC Hughes-Jones, +4

Blood

Rearrangements of the blood group RhD gene associated with the DVI category phenotype

Caroline Le Van Kim, Christelle Rouillac, DJ van Rhenen, +4

Blood

Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes

Christelle Rouillac, Pierre Gane, J.-P. Cartron, +3

Blood

Spatial and Temporal Expression of the Cystathionine β-Synthase Gene During Early Human Development

I. Quéré, Véronique Paul, Christelle Rouillac, +7

Biochemical and Biophysical Research Communications

Developmental BiologyDevelopmental GeneticsEarly Human DevelopmentTemporal ExpressionEmbryonic Development +5

Leu110Pro substitution in the RhD polypeptide is responsible for the D^VII category blood group phenotype

Christelle Rouillac, Caroline Le Van Kim, Marylise Beolet, +2

American Journal of Hematology

HistocompatibilityGeneticsGenetic EpidemiologyImmunologyPathology +18

Insulin-like 4 (INSL4) gene expression in human embryonic and trophoblastic tissues

Anne Laurent, Christelle Rouillac, Anne‐Lise Delezoide, +5

Molecular Reproduction and Development

Lack of G blood group antigen in D^IIIb erythrocytes is associated with segmental DNA exchange between RH genes

Christelle Rouillac, Caroline Le Van Kim, Antoine Blancher, +3

British Journal of Haematology

HistocompatibilityImmunohematologyGeneticsImmunologyBlood Cell +17

Mapping of a Congenital Microcoria Locus to 13q31-q32

Christelle Rouillac, Olivier Roche, Dominique Marchant, +9

The American Journal of Human Genetics

Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics +4