List of works - Francoise Watrin

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.

scientific article

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

scientific article published on 28 September 2010

Causes and consequences of gray matter heterotopia

scientific article published on 02 September 2014

Conservation and divergence of patterns of expression and lineage-specific transcripts in orthologues and paralogues of the mouse Hox-1.4 gene

scientific article published on 01 March 1993

Correct laminar positioning in the neocortex influences proper dendritic and synaptic development

article

Deletion of the mouse T-cell receptor beta gene enhancer blocks alphabeta T-cell development

scientific journal article

Differential expression of the proto-oncogenes c-abl and c-mos in developing mouse germ cells.

scientific article published in June 1993

Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.

scientific article

Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.

scientific article published on 13 February 2016

Expression of Homeobox Genes during Spermatogenesis ⬇️

scientific article published on January 1, 1991

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

scientific article published in December 2003

H19 acts as a trans regulator of the imprinted gene network controlling growth in mice

scientific journal article

List of cloned mouse genes with unique expression patterns during spermatogenesis

scientific article published on 01 January 1991

Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome

scientific article

Normotopic cortex is the major contributor to epilepsy in experimental double cortex.

scientific article published on 11 August 2014

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene

scientific journal article

Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model.

scientific article

Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia

scientific article published on 30 December 2018

Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences

scientific article

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

scientific journal article

The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene

scientific article

List of works by Francoise Watrin

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations.

A single postnatal injection of oxytocin rescues the lethal feeding behaviour in mouse newborns deficient for the imprinted Magel2 gene

Causes and consequences of gray matter heterotopia

Conservation and divergence of patterns of expression and lineage-specific transcripts in orthologues and paralogues of the mouse Hox-1.4 gene

Correct laminar positioning in the neocortex influences proper dendritic and synaptic development

Deletion of the mouse T-cell receptor beta gene enhancer blocks alphabeta T-cell development

Differential expression of the proto-oncogenes c-abl and c-mos in developing mouse germ cells.

Dynamic developmental regulation of the large non-coding RNA associated with the mouse 7C imprinted chromosomal region.

Epilepsy in young Tsc1(+/-) mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.

Expression of Homeobox Genes during Spermatogenesis ⬇️

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

H19 acts as a trans regulator of the imprinted gene network controlling growth in mice

List of cloned mouse genes with unique expression patterns during spermatogenesis

Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome

Normotopic cortex is the major contributor to epilepsy in experimental double cortex.

Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene

Selective suppression of excessive GluN2C expression rescues early epilepsy in a tuberous sclerosis murine model.

Spontaneous epileptiform activity in a rat model of bilateral subcortical band heterotopia

Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene