نتایج جستجو برای: ppargc1a

تعداد نتایج: 1119  

Journal: :Genetika 2022

PPARGC1A is involved in many metabolic processes including normal mitochondrial biogenesis, oxidation of glucose and lipids transport into skeletal muscles. Previous researches linked this polymorphism with the higher risk developing type 2 diabetes, syndrome obesity. The aim study was to investigate association Gly482Ser body mass index (BMI), fasting levels lipid profile Serbian adolescents. ...

2016
Emanuel Gasser Helge C. Johannssen Thomas Rülicke Hanns Ulrich Zeilhofer Markus Stoffel

Inactivation of transcription factor Foxa1 in mice results in neonatal mortality of unknown cause. Here, we report that ablation of Foxa1 causes impaired development and loss of the subthalamic nucleus (STN). Functional deficits in the STN have been implicated in the etiology of Huntington's and Parkinson's disease. We show that neuronal ablation by Synapsin1-Cre-mediated Foxa1 deletion is suff...

2015
Diana Moreira Vasco Rodrigues Maria Abengozar Luis Rivas Eduardo Rial Mireille Laforge Xiaoling Li Marc Foretz Benoit Viollet Jérôme Estaquier Anabela Cordeiro da Silva Ricardo Silvestre

Metabolic manipulation of host cells by intracellular pathogens is currently recognized to play an important role in the pathology of infection. Nevertheless, little information is available regarding mitochondrial energy metabolism in Leishmania infected macrophages. Here, we demonstrate that during L. infantum infection, macrophages switch from an early glycolytic metabolism to an oxidative p...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2010
Karolin H Nord Linda Magnusson Margareth Isaksson Jenny Nilsson Henrik Lilljebjörn Henryk A Domanski Lars-Gunnar Kindblom Nils Mandahl Fredrik Mertens

Hibernomas are benign tumors with morphological features resembling brown fat. They consistently display cytogenetic rearrangements, typically translocations, involving chromosome band 11q13. Here we demonstrate that these aberrations are associated with concomitant deletions of AIP and MEN1, tumor suppressor genes that are located 3 Mb apart and that underlie the hereditary syndromes pituitary...

2013
Arya Biragyn Jessica Bonzo Frank J. Gonzalez Elin Lehrmann Katarzyna Wejksza Catalina Lee-Chang Monica Bodogai Kevin Becker

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