GPCR voltage dependence controls neuronal plasticity and behavior von Rozenfeld, Eyal, Tauber, Merav, Ben-Chaim, Yair, Parnas, Moshe

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Differential Role for a Defined Lateral Horn Neuron Subset in Naïve Odor Valence in Drosophila von Lerner, Hadas, Rozenfeld, Eyal, Rozenman, Bar, Huetteroth, Wolf, Parnas, Moshe

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Olfactory stimuli and moonwalker SEZ neurons can drive backward locomotion in Drosophila von Israel, Shai, Rozenfeld, Eyal, Weber, Denise, Huetteroth, Wolf, Parnas, Moshe

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Muscarinic Modulation of Antennal Lobe GABAergic Local Neurons Shapes Odor Coding and Behavior von Rozenfeld, Eyal, Lerner, Hadas, Parnas, Moshe

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Inhibitory muscarinic acetylcholine receptors enhance aversive olfactory learning in adult Drosophila von Bielopolski, Noa, Amin, Hoger, Apostolopoulou, Anthi A, Rozenfeld, Eyal, Lerner, Hadas, Huetteroth, Wolf, Lin, Andrew C, Parnas, Moshe

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Neuronal circuit mechanisms of competitive interaction between action-based and coincidence learning von Rozenfeld, Eyal, Parnas, Moshe

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A highly conserved A-to-I RNA editing event within the glutamate-gated chloride channel GluClα is necessary for olfactory-based behaviors in Drosophila von Zak, Hila, Rozenfeld, Eyal, Levi, Mali, Deng, Patricia, Gorelick, David, Pozeilov, Hadar, Israel, Shai, Paas, Yoav, Paas, Yoav, Li, Jin Billy, Parnas, Moshe, Shohat-Ophir, Galit

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Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping von Beryozkin, Avigail, Zelinger, Lina, Bandah-Rozenfeld, Dikla, Shevach, Elia, Harel, Anat, Storm, Tim, Sagi, Michal, Eli, Dalia, Merin, Saul, Banin, Eyal, Sharon, Dror

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A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews von Zelinger, Lina, Banin, Eyal, Obolensky, Alexey, Mizrahi-Meissonnier, Liliana, Beryozkin, Avigail, Bandah-Rozenfeld, Dikla, Frenkel, Shahar, Ben-Yosef, Tamar, Merin, Saul, Schwartz, Sharon B., Cideciyan, Artur V., Jacobson, Samuel G., Sharon, Dror

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Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa von Bandah-Rozenfeld, Dikla, Mizrahi-Meissonnier, Liliana, Farhy, Chen, Obolensky, Alexey, Chowers, Itay, Pe'er, Jacob, Merin, Saul, Ben-Yosef, Tamar, Ashery-Padan, Ruth, Banin, Eyal, Sharon, Dror

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Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations von Beryozkin, Avigail, Zelinger, Lina, Bandah-Rozenfeld, Dikla, Harel, Anat, Strom, Tim A, Merin, Saul, Chowers, Itay, Banin, Eyal, Sharon, Dror

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Short-term outcomes in low birth weight infants following antenatal exposure to betamethasone versus dexamethasone von ROZENFELD BAR-LEV, Michal R, MAAYAN-METZGER, Ayala, MATOK, Ilan, HEYMAN, Zahava, SIVAN, Eyal, KUINT, Jacob

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SYSTEMS AND METHODS FOR IDENTIFYING IMAGES CONTAINING INDICATORS OF A CELIAC-LIKE DISEASE von Rozenfeld, Stas, Dekel, Eyal, Elharar, Almog

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SYSTEMS AND METHODS FOR IDENTIFYING IMAGES CONTAINING INDICATORS OF A CELIAC-LIKE DISEASE von DEKEL, Eyal, ROZENFELD, Stas, ELHARAR, Almog

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SYSTEMS AND METHODS FOR IDENTIFYING IMAGES CONTAINING INDICATORS OF A CELIAC-LIKE DISEASE von DEKEL, Eyal, ROZENFELD, Stas, ELHARAR, Almog

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