Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ewelina Lenartowicz"'
Autor:
Frank J. Kaiser, Emma Bedoukian, Roberto Nitsch, Georg Christoph Korenke, Bernd Wollnik, Michel K. Herde, Josef M. Penninger, Yun Li, Anoop Kavirayani, Ana Cicvaric, Ronja Hollstein, Paul Moeseneder, Christian Henneberger, Ewelina Lenartowicz, Gökhan Yigit, Vanja Nagy, Tsung-Pin Pai, Matthew A. Deardorff, Francisco Quiroga, E. Ferda Percin, Pisanu Buphamalai, Jörg Menche, Ivona Kozieradzki
Publikováno v:
Neurology / Genetics 5(3), e330 (2019). doi:10.1212/NXG.0000000000000330
Neurology: Genetics
Neurology: Genetics
ObjectiveWe aim to characterize the causality and molecular and functional underpinnings of HACE1 deficiency in a mouse model of a recessive neurodevelopmental syndrome called spastic paraplegia and psychomotor retardation with or without seizures (S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4354958f847d8df47dd78439d7e4f3f
http://resolver.sub.uni-goettingen.de/purl?gs-1/16714
http://resolver.sub.uni-goettingen.de/purl?gs-1/16714
Autor:
Maria Dadabhoy, Marie Caroline Cotel, Ewelina Lenartowicz, Sridhar Natesan, Anthony C. Vernon
Publikováno v:
Schizophrenia Bulletin
Background Positron emission tomography (PET) using radiolabeled ligands selective for the 18 kDa translocator protein (TSPO) is the most widely used technique to assess putative neuroimmune abnormalities in vivo. However, the results of TSPO PET in