Literature DB >> 18085261

Neurodevelopmental abnormalities in the brainstem of prenatal mice lacking the Prader-Willi syndrome gene Necdin.

Silvia Pagliardini1, Jun Rent, Rachel Wevrick, John J Greer.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2008        PMID： 18085261     DOI： 10.1007/978-0-387-73693-8_24

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


× No keyword cloud information.
  2 in total

1.  Necdin protects embryonic motoneurons from programmed cell death.

Authors:  Julianne Aebischer; Rachel Sturny; David Andrieu; Anne Rieusset; Fabienne Schaller; Sandrine Geib; Cédric Raoul; Françoise Muscatelli
Journal:  PLoS One       Date:  2011-09-02       Impact factor: 3.240

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

Authors:  Laura Caccialupi; Fabienne Schaller; Yuri Shvarev; Valéry Matarazzo; Nazim Kourdougli; Alessandra Bertoni; Clément Menuet; Nicolas Voituron; Evan Deneris; Patricia Gaspar; Laurent Bezin; Pascale Durbec; Gérard Hilaire; Françoise Muscatelli
Journal:  Elife       Date:  2017-10-31       Impact factor: 8.713
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.