List of works - Françoise Muscatelli

A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression

scientific article published on 01 May 1992

A novel putative receptor protein tyrosine kinase of the met family

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

ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs

scientific article

Activation of Akt/FKHR in the medulla oblongata contributes to spontaneous respiratory recovery after incomplete spinal cord injury in adult rats

scientific article published on 27 May 2014

An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism

scientific article published on 20 November 2014

BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2

scientific article

Breathing deficits of the Prader-Willi syndrome

scientific article published on 31 March 2009

Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder

scientific article published on 18 October 2006

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

scientific article published on 01 July 2001

Correction of vasopressin deficit in the lateral septum ameliorates social deficits of mouse autism model

scientific article published on 24 November 2020

Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.

scientific article published on 20 February 2008

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

scientific article published in December 2000

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

scientific article

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

Functional consequences of necdin nucleocytoplasmic localization.

scientific article published on 19 March 2012

Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism

article

Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamily

scientific article (publication date: September 1992)

Inactivation of Socs3 in the hypothalamus enhances the hindbrain response to endogenous satiety signals via oxytocin signaling

scientific article published in November 2012

Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids

scientific article published on January 1, 1992

Isolation of the human Xp21 glycerol kinase gene by positional cloning

scientific article

Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localization

scientific article

Mutations and phenotype in isolated glycerol kinase deficiency

scientific article

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

scientific article

NRAGE, a p75NTR adaptor protein, is required for developmental apoptosis in vivo.

scientific article published on 05 September 2008

Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.

scientific article published on 12 December 2013

Necdin gene, respiratory disturbances and Prader-Willi syndrome.

scientific article

Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation

scientific article

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

scientific article

Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.

scientific article published on 31 October 2017

Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders

scientific article

Oxytocin Signaling in the Early Life of Mammals: Link to Neurodevelopmental Disorders Associated with ASD.

scientific article published on 16 August 2017

Physical mapping of an Xq-proximal interstitial duplication in a male

scientific article published on 01 March 1992

Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome

scientific article published on 01 February 1993

Prader-Willi syndrome as a model of human hyperphagia.

scientific article published on 07 April 2014

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

scientific article published on 29 June 2004

Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

scientific article

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

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

scientific article

The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader-Willi Syndrome

scientific article published on 18 January 2017

The high-affinity interleukin 8 receptor gene (IL8RA) maps to the 2q33-q36 region of the human genome: cloning of a pseudogene (IL8RBP) for the low-affinity receptor

scientific article

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

scientific article

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero

scientific article published on 5 July 2013

Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins

scientific article

Wired for eating: how is an active feeding circuitry established in the postnatal brain?

scientific article published on 19 July 2018

List of works by Françoise Muscatelli

A male with two contiguous inactivation centers on a single X chromosome: study of X inactivation and XIST expression

A novel putative receptor protein tyrosine kinase of the met family

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

ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs

Activation of Akt/FKHR in the medulla oblongata contributes to spontaneous respiratory recovery after incomplete spinal cord injury in adult rats

An Early Postnatal Oxytocin Treatment Prevents Social and Learning Deficits in Adult Mice Deficient for Magel2, a Gene Involved in Prader-Willi Syndrome and Autism

BMX, a novel nonreceptor tyrosine kinase gene of the BTK/ITK/TEC/TXK family located in chromosome Xp22.2

Breathing deficits of the Prader-Willi syndrome

Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder

Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15

Correction of vasopressin deficit in the lateral septum ameliorates social deficits of mouse autism model

Cross-cultural comparisons of obesity and growth in Prader-Willi syndrome.

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

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

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

Functional consequences of necdin nucleocytoplasmic localization.

Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism

Homologous chromosomal locations of the four genes for inter-alpha-inhibitor and pre-alpha-inhibitor family in human and mouse: assignment of the ancestral gene for the lipocalin superfamily

Inactivation of Socs3 in the hypothalamus enhances the hindbrain response to endogenous satiety signals via oxytocin signaling

Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids

Isolation of the human Xp21 glycerol kinase gene by positional cloning

Mouse 5-hydroxytryptamine5A and 5-hydroxytryptamine5B receptors define a new family of serotonin receptors: cloning, functional expression, and chromosomal localization

Mutations and phenotype in isolated glycerol kinase deficiency

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism

NRAGE, a p75NTR adaptor protein, is required for developmental apoptosis in vivo.

Natural breaking of the maternal silence at the mouse and human imprinted Prader-Willi locus: A whisper with functional consequences.

Necdin gene, respiratory disturbances and Prader-Willi syndrome.

Necdin mediates skeletal muscle regeneration by promoting myoblast survival and differentiation

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

Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome.

Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders

Oxytocin Signaling in the Early Life of Mammals: Link to Neurodevelopmental Disorders Associated with ASD.

Physical mapping of an Xq-proximal interstitial duplication in a male

Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome

Prader-Willi syndrome as a model of human hyperphagia.

Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn.

Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

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

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

The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader-Willi Syndrome

The high-affinity interleukin 8 receptor gene (IL8RA) maps to the 2q33-q36 region of the human genome: cloning of a pseudogene (IL8RBP) for the low-affinity receptor

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero

Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins

Wired for eating: how is an active feeding circuitry established in the postnatal brain?