Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Silvia Menkes"'
Autor:
Probal Banerjee, Vitaliy Lasiychuk, Andrew Mancuso, Daniel J. Kerr, Lovena David, David Salame, Rodina Sadek, Youstina Soliman, Bishoy Gerges, Silvia Menkes, Alexandra Marsillo, Aheli Chatterjee
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1867:166048
Fragile X Syndrome (FXS) is an inherited developmental disorder caused by the non-expression of the Fmr1 gene. FXS is associated with abnormal social and anxiety behavior that is more prominent among males. Given that oxytocin (OXT) regulates both so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fccda4d85370a20cdcb6ed9b3e997a8e
https://doi.org/10.1016/j.bbadis.2020.166048
https://doi.org/10.1016/j.bbadis.2020.166048
Autor:
Probal Banerjee, Silvia Menkes, Alexandra Marsillo, Guang Y. Wen, Abha Chauhan, Tatyana Budylin, Sara R. Guariglia, Andrzej Wieraszko, Rodina Sadek, Daniel P. McCloskey, Daniel J. Kerr
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862:1755-1765
Type IV ATPases are putative aminophospholipid translocases (APLTs), more commonly known as flippases. A pronounced induction of the flippase Atp8a1 was observed in post-mortem tissue homogenates from the hippocampus and temporal lobe of juvenile aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df58895b156e19559406829ee5e47d1e
https://doi.org/10.1016/j.bbadis.2016.06.005
https://doi.org/10.1016/j.bbadis.2016.06.005