Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice

por Mercer, Rebecca E., Wevrick, Rachel
Publicado 2009

Leptin signaling defects in a mouse model of Prader-Willi syndrome: An orphan genetic obesity syndrome no more?

por Colmers, William F., Wevrick, Rachel
Publicado 2013

Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis

por Carias, K. Vanessa, Wevrick, Rachel
Publicado 2019

Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells

por Devos, Julia, Weselake, Sara V, Wevrick, Rachel
Publicado 2011

A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues

por Chibuk, Thea K, Bischof, Jocelyn M, Wevrick, Rachel
Publicado 2001

The N-terminal domain of the Schaaf–Yang syndrome protein MAGEL2 likely has a role in RNA metabolism

por Sanderson, Matthea R., Fahlman, Richard P., Wevrick, Rachel
Publicado 2021

A MAGEL2-deubiquitinase complex modulates the ubiquitination of circadian rhythm protein CRY1

por Carias, K. Vanessa, Zoeteman, Mercedes, Seewald, Abigail, Sanderson, Matthea R., Bischof, Jocelyn M., Wevrick, Rachel
Publicado 2020

Magel2 Is Required for Leptin-Mediated Depolarization of POMC Neurons in the Hypothalamic Arcuate Nucleus in Mice

por Mercer, Rebecca E., Michaelson, Sheldon D., Chee, Melissa J. S., Atallah, Tanya A., Wevrick, Rachel, Colmers, William F.
Publicado 2013

Hypothalamic AAV-BDNF gene therapy improves metabolic function and behavior in the Magel2-null mouse model of Prader-Willi syndrome

por Queen, Nicholas J., Zou, Xunchang, Anderson, Jacqueline M., Huang, Wei, Appana, Bhavya, Komatineni, Suraj, Wevrick, Rachel, Cao, Lei
Publicado 2022

The Smc5/Smc6/MAGE Complex Confers Resistance to Caffeine and Genotoxic Stress in Drosophila melanogaster

por Li, Xiao, Zhuo, Ran, Tiong, Stanley, Di Cara, Francesca, King-Jones, Kirst, Hughes, Sarah C., Campbell, Shelagh D., Wevrick, Rachel
Publicado 2013

ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison

por Barclay, Sarah F., Rand, Casey M., Nguyen, Lisa, Wilson, Richard J. A., Wevrick, Rachel, Gibson, William T., Bech-Hansen, N. Torben, Weese-Mayer, Debra E.
Publicado 2018

Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences

por Rieusset, Anne, Schaller, Fabienne, Unmehopa, Unga, Matarazzo, Valery, Watrin, Françoise, Linke, Matthias, Georges, Beatrice, Bischof, Jocelyn, Dijkstra, Femke, Bloemsma, Monique, Corby, Severine, Michel, François J., Wevrick, Rachel, Zechner, Ulrich, Swaab, Dick, Dudley, Keith, Bezin, Laurent, Muscatelli, Françoise
Publicado 2013

Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader–Willi syndrome

por Knani, Ibrahim, Earley, Brian J., Udi, Shiran, Nemirovski, Alina, Hadar, Rivka, Gammal, Asaad, Cinar, Resat, Hirsch, Harry J., Pollak, Yehuda, Gross, Itai, Eldar-Geva, Talia, Reyes-Capo, Daniela P., Han, Joan C., Haqq, Andrea M., Gross-Tsur, Varda, Wevrick, Rachel, Tam, Joseph
Publicado 2016

Regulation of autism-relevant behaviors by cerebellar–prefrontal cortical circuits

por Kelly, Elyza, Meng, Fantao, Fujita, Hirofumi, Morgado, Felipe, Kazemi, Yasaman, Rice, Laura C., Ren, Chongyu, Escamilla, Christine Ochoa, Gibson, Jennifer M., Sajadi, Sanaz, Pendry, Robert J., Tan, Tommy, Ellegood, Jacob, Basson, M. Albert, Blakely, Randy D., Dindot, Scott V., Golzio, Christelle, Hahn, Maureen K., Katsanis, Nicholas, Robins, Diane M., Silverman, Jill L., Singh, Karun K., Wevrick, Rachel, Taylor, Margot J., Hammill, Christopher, Anagnostou, Evdokia, Pfeiffer, Brad E., Stoodley, Catherine J., Lerch, Jason P., du Lac, Sascha, Tsai, Peter T.
Publicado 2020