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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - Elsevier
Background Mutations of MAGEL2 have been reported in patients presenting with autism,
and loss of MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental …
被引用次数：191 相关文章

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

H Meziane, F Schaller, S Bauer… - Biological …, 2015 - pubmed.ncbi.nlm.nih.gov
Background Mutations of MAGEL2 have been reported in patients presenting with autism,
and loss of MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental …

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.

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - psycnet.apa.org
Background: Mutations of MAGEL2 have been reported in patients presenting with autism,
and loss of MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental …

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

H Meziane, F Schaller, S Bauer… - Biological …, 2015 - biologicalpsychiatryjournal.com
Background Mutations of MAGEL2 have been reported in patients presenting with autism,
and loss of MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental …

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 …

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2014 - europepmc.org
Background Mutations of MAGEL2 have been reported in patients presenting with autism,
and loss of MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental …

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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - cir.nii.ac.jp
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 | CiNii Research …

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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - hal.science
Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of
MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental genetic …

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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - infona.pl
Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of
MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental genetic …

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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - amu.hal.science
Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of
MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental genetic …

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

H Meziane, F Schaller, S Bauer, C Villard… - Biological …, 2015 - hal.science
Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of
MAGEL2 is also associated with Prader-Willi syndrome, a neurodevelopmental genetic …