Z. Chettouh

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Molecular Mapping of Twenty-Four Features of Down Syndrome on Chromosome 21

J. Delabar, Z. Rahmani, D. Theophile, 1993, European journal of human genetics : EJHG.

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

B. Delobel, M. Rethoré, Z. Chettouh, 1995, American journal of human genetics.

New chromosome 21 DNA markers isolated by pulsed field gel electrophoresis from an ETS2-containing Down syndrome chromosomal region

M. Yaspo, J. Delabar, Z. Rahmani, 1992, Human Genetics.

Dual origin of enteric neurons in vagal Schwann cell precursors and the sympathetic neural crest

C. Birchmeier, H. Enomoto, Z. Chettouh, 2017, Proceedings of the National Academy of Sciences.

No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.

J. Lejeune, M. Rethoré, D. Theophile, 1992, American journal of human genetics.

A medullary centre for lapping in mice

Evan R. Harrell, J. Poulet, A. Genovesio, 2021, Nature Communications.

Ancient origin of somatic and visceral neurons

E. Kandel, G. Fortin, Z. Chettouh, 2013, BMC Biology.

Centralization of the Deuterostome Nervous System Predates Chordates

M. Martindale, É. Röttinger, Z. Chettouh, 2009, Current Biology.

Taste bud formation depends on taste nerves

G. Consalez, Z. Chettouh, J. Brunet, 2019, eLife.

Parasympathetic ganglia derive from Schwann cell precursors

E. Coppola, Z. Chettouh, S. Dymecki, 2014, Science.

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

A. Aurias, J. Delabar, Z. Rahmani, 1989, Proceedings of the National Academy of Sciences of the United States of America.

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.

Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.

J. Delabar, Z. Rahmani, D. Theophile, 1994, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Direct electronic radioisotope detection yields improved gene dosage analysis.

J. Delabar, Z. Chettouh, P. Sinet, 1990, BioTechniques.

Down syndrome: a model for the study of Alzheimer’s disease and aging

J. Delabar, Z. Rahmani, Z. Chettouh, 1990 .

Gene-dosage mapping of 30 DNA markers on chromosome 21.

D. Patterson, J. Delabar, Z. Rahmani, 1992, Genomics.

Down Syndrome Critical Region Around D 21 S 55 On Proximal 21 q 22 . 3

A. Aurias, J. Delabar, Z. Rahmani, 2005 .

Down syndrome critical region around D21S55 on proximal 21q22.3.

A. Aurias, Z. Rahmani, Z. Chettouh, 2005, American journal of medical genetics. Supplement.

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.

J. Fermanian, Z. Rahmani, Z. Chettouh, 1990, American journal of human genetics.

Molecular mapping of the Down syndrome phenotype on chromosome 21.

J. Delabar, Z. Rahmani, D. Theophile, 1993, Progress in clinical and biological research.

The sacral autonomic outflow is sympathetic

W. Richardson, R. Vierstra, Z. Chettouh, 2016, Science.

An executive center for the intake of liquids

Evan R. Harrell, J. Poulet, A. Genovesio, 2021, bioRxiv.

Precraniate origin of cranial motoneurons.

J. Joly, R. de Rosa, C. Goridis, 2006, Proceedings of the National Academy of Sciences of the United States of America.

3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21.

J. Delabar, D. Theophile, Z. Chettouh, 1994, Genomics.

C21orf5, a novel human chromosome 21 gene, has a Caenorhabditis elegans ortholog (pad-1) required for embryonic patterning.

S. Antonarakis, N. Shimizu, J. Kudoh, 2000, Genomics.

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.