Publications by authors named "Inbal Lasry"

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USP1 deubiquitinates Akt to inhibit PI3K-Akt-FoxO signaling in muscle during prolonged starvation.
Dana Goldbraikh, Danielle Neufeld, Yara Eid-Mutlak, Inbal Lasry, Jennifer E Gilda

EMBO Rep· April 2020

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Folic Acid Impairs the Uptake of 5-Methyltetrahydrofolate in Human Umbilical Vascular Endothelial Cells.
Desiree Smith, Jacqueline Hornstra, Monica Rocha, Gerrit Jansen, Yehuda Assaraf, Inbal Lasry

J Cardiovasc Pharmacol· October 2017

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In situ dimerization of multiple wild type and mutant zinc transporters in live cells using bimolecular fluorescence complementation.
Inbal Lasry, Yarden Golan, Bluma Berman, Noy Amram, Fabian Glaser

J Biol Chem· March 2014

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A dominant negative heterozygous G87R mutation in the zinc transporter, ZnT-2 (SLC30A2), results in transient neonatal zinc deficiency.
Inbal Lasry, Young Ah Seo, Hadas Ityel, Nechama Shalva, Ben Pode-Shakked

J Biol Chem· August 2012

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Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
Inbal Lasry, Bluma Berman, Fabian Glaser, Gerrit Jansen, Yehuda G Assaraf

Biochem Biophys Res Commun· August 2009

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A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function.
Inbal Lasry, Bluma Berman, Rachel Straussberg, Yael Sofer, Hanna Bessler

Blood· September 2008

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