C. Lopes

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Molecular and cellular mechanisms elucidating neurocognitive basis of functional impairments associated with intellectual disability in Down syndrome.

Mohammed Rachidi, M. Rachidi, C. Lopes, 2010, American journal on intellectual and developmental disabilities.

Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5.

A. Rosenthal, S. Taudien, J. Delabar, 2000, Genomics.

Virus-like particle formation in Drosophila melanogaster germ cells suggests a complex translational regulation of the retrotransposon cycle and new mechanisms inhibiting transposition

M. Rachidi, C. Lopes, R. Hellio, 2005, Cytogenetic and Genome Research.

Expression of the mnb (dyrk) protein in adult and embryonic mouse tissues.

J. Delabar, Z. Rahmani, M. Rachidi, 1998, Biochemical and biophysical research communications.

Dynamic expression pattern of Ca(2+)/calmodulin-dependent protein kinase II gene in the central nervous system of Drosophila throughout development.

J. Delabar, M. Rachidi, C. Lopes, 1999, Biochemical and biophysical research communications.

Characterization of the dCaMKII-GAL4 driver line whose expression is controlled by the Drosophila Ca2+/calmodulin-dependent protein kinase II promoter

Y. Nishida, H. Nakagoshi, M. Rachidi, 2002, Cell and Tissue Research.

Mental Retardation and Human Chromosome 21 Gene Overdosage: From Functional Genomics and Molecular Mechanisms Towards Prevention and Treatment of the Neuropathogenesis of Down Syndrome

M. Rachidi, C. Lopes, 2011 .

C21orf5, a new member of Dopey family involved in morphogenesis, could participate in neurological alterations and mental retardation in Down syndrome.

Mohammed Rachidi, J. Delabar, M. Rachidi, 2005, DNA research : an international journal for rapid publication of reports on genes and genomes.

Mental retardation in Down syndrome: From gene dosage imbalance to molecular and cellular mechanisms

M. Rachidi, C. Lopes, 2007, Neuroscience Research.

Differential transcription of Barhl1 homeobox gene in restricted functional domains of the central nervous system suggests a role in brain patterning

M. Rachidi, C. Lopes, 2006, International Journal of Developmental Neuroscience.

BARHL1 homeogene, the human ortholog of the mouse Barhl1 involved in cerebellum development, shows regional and cellular specificities in restricted domains of developing human central nervous system.

J. Delabar, M. Rachidi, C. Lopes, 2006, Biochemical and biophysical research communications.

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.

An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.

R. Mott, D. Nižetić, G. Zehetner, 1994, Human molecular genetics.

A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions

J. Delabar, M. Rachidi, C. Lopes, 2009, International Journal of Developmental Neuroscience.

C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome

J. Delabar, M. Rachidi, C. Lopes, 2005, Cytogenetic and Genome Research.

Mental retardation and associated neurological dysfunctions in Down syndrome: a consequence of dysregulation in critical chromosome 21 genes and associated molecular pathways.

M. Rachidi, C. Lopes, 2008, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development.

J M Delabar, B. Bloch, M. Yaspo, 1995, Proceedings of the National Academy of Sciences of the United States of America.

New cerebellar phenotypes in YAC transgenic mouse in vivo library of human Down syndrome critical region-1.

E. Rubin, Desmond J. Smith, J. Delabar, 2007, Biochemical and biophysical research communications.

The CASK/Lin-2 Drosophila homologue, Camguk, could play a role in epithelial patterning and in neuronal targeting.

J. Delabar, M. Rachidi, C. Lopes, 2001, Biochemical and biophysical research communications.

Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development

J. Delabar, M. Vekemans, M. Rachidi, 2000, Mechanisms of Development.

Developmentally regulated expression of mtprd, the murine ortholog of tprd, a gene from the Down syndrome chromosomal region 1

J. Delabar, M. Rachidi, C. Lopes, 1999, Mechanisms of Development.

Analysis of period circadian expression in the Drosophila head by in situ hybridization.

M. Rachidi, C. Lopes, F. Rouyer, 1997, Journal of neurogenetics.

Existence of two novel and non-sectorized clades of the giant clam Tridacna maxima in French Polynesia: implications for connectivity and origin

V. Berteaux-Lecellier, C. Lopes, G. Lecellier, 2014 .

Genetical analysis ofvisual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain inDrosophila melanogaster

M. Rachidi, C. Lopes, J. Bénichou, 2005, Genetica.

Genetical analysis of visual system disorganizer (vid), a new gene involved in normal development of eye and optic lobe of the brain in Drosophila melanogaster

M. Rachidi, C. Lopes, J. Bénichou, 2004, Genetica.

Spatial and temporal localization during embryonic and fetal human development of the transcription factor SIM2 in brain regions altered in Down syndrome

J. Delabar, M. Rachidi, C. Lopes, 2005, International Journal of Developmental Neuroscience.

The differentially expressed C21orf5 gene in the medial temporal-lobe system could play a role in mental retardation in Down syndrome and transgenic mice.

J. Delabar, M. Rachidi, C. Lopes, 2003, Biochemical and biophysical research communications.