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Search Results - Lenartowicz, Ewelina M.
Search Results - Lenartowicz, Ewelina M.
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PRDM12 Is Transcriptionally Active and Required for Nociceptor Function Throughout Life
by
Kokotović, Tomislav
,
Langeslag, Michiel
,
Lenartowicz, Ewelina M
,
Manion, John
,
Fell, Christopher W
,
Alehabib, Elham
,
Tafakhori, Abbas
,
Darvish, Hossein
,
Bellefroid, Eric J
,
Neely, G Gregory
,
Kress, Michaela
,
Penninger, Josef M
,
Nagy, Vanja
Published in
Frontiers in molecular neuroscience
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Transcription factor mesenchyme homeobox protein 2 (MEOX2) modulates nociceptor function
by
Kokotović, Tomislav
,
Lenartowicz, Ewelina M.
,
Langeslag, Michiel
,
Ciotu, Cosmin I.
,
Fell, Christopher W.
,
Scaramuzza, Angelica
,
Fischer, Michael J. M.
,
Kress, Michaela
,
Penninger, Josef M.
,
Nagy, Vanja
Published in
The FEBS journal
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Microglial activation in the rat brain following chronic antipsychotic treatment at clinically relevant doses
by
Cotel, Marie-Caroline
,
Lenartowicz, Ewelina M
,
Natesan, Sridhar
,
Modo, Michel M
,
Cooper, Jonathan D
,
Williams, Steven C.R
,
Kapur, Shitij
,
Vernon, Anthony C
Published in
European neuropsychopharmacology
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Intravenous high-dose enzyme replacement therapy with recombinant palmitoyl–protein thioesterase reduces visceral lysosomal storage and modestly prolongs survival in a preclinical...
by
Hu, Jie
,
Lu, Jui-Yun
,
Wong, Andrew M.S.
,
Hynan, Linda S.
,
Birnbaum, Shari G.
,
Yilmaz, Denis S.
,
Streit, Barbara M.
,
Lenartowicz, Ewelina M.
,
Thompson, Thomas C.M.
,
Cooper, Jonathan D.
,
Hofmann, Sandra L.
Published in
Molecular genetics and metabolism
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HACE1 deficiency leads to structural and functional neurodevelopmental defects
by
Nagy, Vanja
,
Hollstein, Ronja
,
Pai, Tsung-Pin
,
Herde, Michel K
,
Buphamalai, Pisanu
,
Moeseneder, Paul
,
Lenartowicz, Ewelina
,
Kavirayani, Anoop
,
Korenke, Georg Christoph
,
Kozieradzki, Ivona
,
Nitsch, Roberto
,
Cicvaric, Ana
,
Monje Quiroga, Francisco J
,
Deardorff, Matthew A
,
Bedoukian, Emma C
,
Li, Yun
,
Yigit, Gökhan
,
Menche, Jörg
,
Perçin, E Ferda
,
Wollnik, Bernd
,
Henneberger, Christian
,
Kaiser, Frank J
,
Penninger, Josef M
Published in
Neurology. Genetics
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