Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gastón Calfa"'
Autor:
Leandro Champarini, Macarena Herrera, Matías Jávega, Aracely Naranjo Viteri, Rosana Crespo, Gastón Calfa, Claudia Hereñú
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S382-S383 (2023)
Externí odkaz:
https://doaj.org/article/9fa5f0cb46b34593883c267397fa1f14
Autor:
Agustina Cabral, Gimena Fernandez, María J. Tolosa, Ángeles Rey Moggia, Gastón Calfa, Pablo N. De Francesco, Mario Perello
Publikováno v:
Molecular Metabolism, Vol 32, Iss , Pp 69-84 (2020)
Objective: Arcuate nucleus (ARC) neurons producing Agouti-related peptide (AgRP) and neuropeptide Y (NPY; ARCAgRP/NPY neurons) are activated under energy-deficit states. ARCAgRP/NPY neurons innervate the hypothalamic paraventricular nucleus (PVH), an
Externí odkaz:
https://doaj.org/article/9a1d6614df2245d3b03ec96872e26138
Publikováno v:
Neuro endocrinology letters. 25(3)
Experimental autoimmune encephalomyelitis (EAE) was induced to investigate the levels of circulating total testosterone (TT) and the possible association of corticosterone with the steroid-producing capacity of the testes.We determined gonad weights,
Autor:
Jennifer Larimore, Pearl V Ryder, Kun-Yong Kim, L Alex Ambrose, Christopher Chapleau, Gaston Calfa, Christina Gross, Gary J Bassell, Lucas Pozzo-Miller, Yoland Smith, Konrad Talbot, In-Hyun Park, Victor Faundez
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e65069 (2013)
Clinical, epidemiological, and genetic evidence suggest overlapping pathogenic mechanisms between autism spectrum disorder (ASD) and schizophrenia. We tested this hypothesis by asking if mutations in the ASD gene MECP2 which cause Rett syndrome affec
Externí odkaz:
https://doaj.org/article/e5e9c45d4bc141f79c492ef9d2530021
Autor:
Christopher A. Chapleau, Elena Maria Boggio, Gaston Calfa, Alan K. Percy, Maurizio Giustetto, Lucas Pozzo-Miller
Publikováno v:
Neural Plasticity, Vol 2012 (2012)
Alterations in dendritic spines have been documented in numerous neurodevelopmental disorders, including Rett Syndrome (RTT). RTT, an X chromosome-linked disorder associated with mutations in MECP2, is the leading cause of intellectual disabilities
Externí odkaz:
https://doaj.org/article/f392644bc0b540778fd47b6cb9a52a61