N. Créau

发表

A High-resolution map of 1.6 Mb in the Down syndrome region: a new map between D21S55 and ETS2

C. Broeckhoven, D. Theophile, P. Sinet, 1995, Mammalian Genome.

Chromosome 21 KIR channels in brain development.

J M Delabar, J. Delabar, S. Thomas, 2003, Journal of neural transmission. Supplementum.

Isolation and analysis of chromosome 21 genes potentially involved in Down syndrome.

P. Sinet, P. Gosset, N. Créau, 1999, Journal of neural transmission. Supplementum.

Report and abstracts of the Sixth International Workshop on Human Chromosome 21 Mapping 1996. Cold Spring Harbor, New York, USA. May 6-8,1996.

John Quackenbush, R. Hubert, J. Korenberg, 1997, Cytogenetics and cell genetics.

Classification of variations of HSA21 gene expression in down syndrome lymphoblastoid cell lines : impact on disease phenotype

L. Personnaz, J. Rossier, L. Dauphinot, 2007 .

Chromosome 11pi, in Congenital Lactic Acidosis

B. Aral, N. Créau, G. Ait-Ghezala, 2006 .

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

Molecular and Cellular Alterations in Down Syndrome: Toward the Identification of Targets for Therapeutics

N. Créau, 2012, Neural plasticity.

Conservation of pericentromeric duplications of a 200-kb part of the human 21q22.1 region in primates

J. Delabar, M. Potier, M. Prieur, 1999, Cytogenetic and Genome Research.

Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.

S. Antonarakis, H. Lehrach, B. Korn, 1998, Genomics.

Developmental Defects in Trisomy 21 and Mouse Models

J. Delabar, N. Créau, Revital Aflalo-Rattenbac, 2006, TheScientificWorldJournal.

Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes.

J M Delabar, G Golfier, J Aubert, 2007, American journal of human genetics.

Construction of a 2.5-Mb integrated physical and gene map of distal 21q22.3.

S. Antonarakis, H. Scott, C. Brahe, 1998, Genomics.

Developmental molecular and functional cerebellar alterations induced by PCP4/PEP19 overexpression: Implications for Down syndrome

Y. Hérault, J. Bizot, M. Dierssen, 2014, Neurobiology of Disease.

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage

Y. Yanagawa, Y. Hérault, M. Dierssen, 2014, Neurobiology of Disease.

Report of the Fourth International Workshop on Human Chromosome 21.

A. Chakravarti, S. Antonarakis, D. Nižetić, 1993, Genomics.

Molecular Signatures of Cardiac Defects in Down Syndrome Lymphoblastoid Cell Lines Suggest Altered Ciliome and Hedgehog Pathways

A. Mégarbané, R. Touraine, L. Dauphinot, 2012, PloS one.

Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15)

D. Damotte, P. Gosset, C. Vayssettes, 2000, Mechanisms of Development.

A new inward rectifier potassium channel gene (KCNJ15) localized on chromosome 21 in the Down syndrome chromosome region 1 (DCR1).

H. Lehrach, B. Korn, P. Sinet, 1997, Genomics.

J. Delabar, N. Créau, E. Cabet, 2016, Brain Research.

Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models

Y. Hérault, J. Bizot, B. Delatour, 2015, Front. Behav. Neurosci..

Mutations in PDX1, the human lipoyl-containing component X of the pyruvate dehydrogenase-complex gene on chromosome 11p1, in congenital lactic acidosis.

F. Fouque, B. Aral, P. Kamoun, 1997, American journal of human genetics.

Mutations inPDX1,theHumanLipoyl-Containin g Component Xofthe Pyruvate DehydrogenaseComplex Geneon Chromosome 11pi, in Congenital Lactic Acidosis

B. Aral, N. Créau, G. Ait-Ghezala, 1997 .

Cloning of a rat-specific long PCP4/PEP19 isoform.

M. Scaturro, N. Créau, G. Schiera, 2007, International journal of molecular medicine.

Changing Paradigms in Down Syndrome: The First International Conference of the Trisomy 21 Research Society

M. Dierssen, J. Delabar, K. Gardiner, 2016, Molecular Syndromology.

PCP4 (PEP19) overexpression induces premature neuronal differentiation associated with Ca2+/Calmodulin‐Dependent kinase II‐δ activation in mouse models of down syndrome

Y. Hérault, C. Verney, N. Créau, 2011, The Journal of comparative neurology.

PCP4 is highly expressed in ectoderm and particularly in neuroectoderm derivatives during mouse embryogenesis.

C. Verney, C. Vayssettes, N. Créau, 2003, Gene expression patterns : GEP.