Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Caroline E Laverriere"'
Autor:
Caitrín M Coffey, Patricia A Solleveld, Joyce Fang, Antonia K Roberts, Sung-Kook Hong, Igor B Dawid, Caroline E Laverriere, Eric Glasgow
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53991 (2013)
Fetal Alcohol Spectrum Disorders (FASD) are a collection of disorders resulting from fetal ethanol exposure, which causes a wide range of physical, neurological and behavioral deficits including heightened susceptibility for alcoholism and addictive
Externí odkaz:
https://doaj.org/article/da5c117bacc04e5f8271b1ae10e9878a
Autor:
Emma D. Spikol, Caroline E. Laverriere, Maya Robnett, Gabriela Carter, Erin Wolfe, Eric Glasgow
Publikováno v:
Diseases, Vol 4, Iss 1, p 13 (2016)
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder characterized by an insatiable appetite, leading to chronic overeating and obesity. Additional features include short stature, intellectual disability, behavioral problems and
Externí odkaz:
https://doaj.org/article/8f883440ab8547df92f6ed57830f80c8
Autor:
Maya Robnett, Emma D. Spikol, Gabriela Carter, Caroline E. Laverriere, Erin M Wolfe, Eric Glasgow
Publikováno v:
Diseases, Vol 4, Iss 1, p 13 (2016)
Diseases
Diseases
Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder characterized by an insatiable appetite, leading to chronic overeating and obesity. Additional features include short stature, intellectual disability, behavioral problems and
Autor:
Igor B. Dawid, Caroline E. Laverriere, Caitrín M. Coffey, Eric Glasgow, Joyce Fang, Patricia A. Solleveld, Antonia K. Roberts, Sung-Kook Hong
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53991 (2013)
PLoS ONE
PLoS ONE
Background: Fetal Alcohol Spectrum Disorders (FASD) are a collection of disorders resulting from fetal ethanol exposure, which causes a wide range of physical, neurological and behavioral deficits including heightened susceptibility for alcoholism an
Autor:
Encarna Guillén-Navarro, Ann Nordgren, Agne Liedén, Ronnie Wright, Chiara Pantaleoni, María Juliana Ballesta-Martínez, Philippe M. Campeau, Meriel McEntagart, Katherine E. Schertz, Céline Pebrel-Richard, Silvia Annunziata, Megan Thomas, Peter E. Clayton, Cristina Hernando, Catherine Sarret, Paul R. Kasher, Bronwyn Kerr, Tiziana Granata, Jennifer L. Eaton, Caroline E. Laverriere, Francesca L. Sciacca, Eric Glasgow, Adam Jackson, Olaya Villa-Marcos, Siddharth Banka
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
American Journal of Human Genetics, 2016, 98 (2), pp.363-372. ⟨10.1016/j.ajhg.2015.12.014⟩
Genetic studies of intellectual disability and identification of monogenic causes of obesity in humans have made immense contribution toward the understanding of the brain and control of body mass. The leptin > melanocortin > SIM1 pathway is dysregul