Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Nutrition/Eating Disorders"'
Publikováno v:
School Library Journal. Oct 2008 Curriculum Connections, Vol. 54, p46-47. 2p.
Autor:
Henry, Robin1
Publikováno v:
School Library Journal. Apr2008, Vol. 54 Issue 4, p161-162. 2p.
Publikováno v:
Library Media Connection. Mar/Apr2010, Vol. 28 Issue 5, p78-78. 1/7p.
Autor:
Glantz, Shelley sglantz@linworthpublishing.com
Publikováno v:
Library Media Connection. Apr/May2008, Vol. 26 Issue 7, p81-81. 1/9p.
Autor:
Henry, Robin1
Publikováno v:
School Library Journal. May2011, Vol. 57 Issue 5, p140-140. 1/6p.
Autor:
Fabicon, Joanna K.1
Publikováno v:
School Library Journal. Mar2010, Vol. 56 Issue 3, p175-175. 1/6p.
Publikováno v:
PLoS ONE, Vol 5, Iss 11, p e13825 (2010)
PLoS ONE
PLoS ONE
Background The OLETF rat is an animal model of early onset hyperphagia induced obesity, presenting multiple pre-obese characteristics during the suckling period. In the present study, we used a cross-fostering strategy to assess whether interactions
Autor:
Alfredo Csibi, Serge A. Leibovitch, Sabrina Batonnet-Pichon, Marie Pierre Leibovitch, Karen Cornille, Julie Lagirand-Cantaloube
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2009, 4 (3), 11 p. ⟨10.1371/journal.pone.0004973⟩
Plos One 3 (4), 11 p.. (2009)
PLoS ONE, Vol 4, Iss 3, p e4973 (2009)
PLoS ONE, Public Library of Science, 2009, 4 (3), 11 p. ⟨10.1371/journal.pone.0004973⟩
Plos One 3 (4), 11 p.. (2009)
PLoS ONE, Vol 4, Iss 3, p e4973 (2009)
International audience; Ubiquitin ligase Atrogin1/Muscle Atrophy F-box (MAFbx) up-regulation is required for skeletal muscle atrophy but substrates and function during the atrophic process are poorly known. The transcription factor MyoD controls myog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99782de8bba13564b54c7b4e8d8fd2ba
https://hal.inrae.fr/hal-02660231
https://hal.inrae.fr/hal-02660231
Autor:
Nicola M. Solomon, Shengwen Zhang, Uta Francke, Feng Ding, Sally A. Camper, Hong Hua Li, Pinchas Cohen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 3, Iss 3, p e1709 (2008)
PLoS ONE, Vol 3, Iss 3, p e1709 (2008)
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity. After initial severe hypotonia, PWS children become hyperphagic and morbidly obese, if intake is not restricted. Short stature with abnormal growth hormone secretion, hypogonadism,