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Planta Medica|February 6, 2015
Downregulation of microglial activation by achillolide AAnat Elmann, Alona Telerman, Sharon Mordechay, et al.
Plos Genetics|December 31, 2016
A Differentiation Transcription Factor Establishes Muscle-Specific Proteostasis in Caenorhabditis elegansYael Bar-Lavan, Netta Shemesh, Shiran Dror, et al.
International Journal of Molecular Sciences|November 13, 2021
The Effect of Sera from Children with Obstructive Sleep Apnea Syndrome (OSAS) on Human Cardiomyocytes Differentiated from Human Embryonic Stem CellsHen Haddad, Sharon Etzion, Tatiana Rabinski, et al.
American Journal of Human Genetics|August 19, 2007
Lethal contractural syndrome type 3 (LCCS3) is caused by a mutation in PIP5K1C, which encodes PIPKI gamma of the phophatidylinsitol pathwayGinat Narkis, Rivka Ofir, Daniella Landau, et al.
The Journal of Biological Chemistry|October 17, 2012
Novel evolutionary-conserved role for the activity-dependent neuroprotective protein (ADNP) family that is important for erythropoiesisEfrat Dresner, Anna Malishkevich, Carmit Arviv, et al.
Biological Research|June 22, 2023
Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compactionNataly Korover, Sharon Etzion, Alexander Cherniak, et al.
Phytochemistry|March 14, 2009
Methyl jasmonate induced accumulation of kalopanaxsaponin I in Nigella sativaMartin Scholz, Marta Lipinski, Marco Leupold, et al.
Planta Medica|June 26, 2010
African descents are more sensitive than European descents to the antitumor compounds α-hederin and kalopanaxsaponin IGeva Feller, Aleksandra Kugel, Dana Moonshine, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13Ginat Narkis, Daniella Landau, Esther Manor, et al.
American Journal of Human Genetics|April 29, 2008
Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQOrtal Barel, Zamir Shorer, Hagit Flusser, et al.
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