Inbal Lasry

USP1 deubiquitinates Akt to inhibit PI3K‐Akt‐FoxO signaling in muscle during prolonged starvation

Dana Goldbraikh, Danielle Neufeld, Yara Eid‐Mutlak et al. · EMBO Reports · 2020 · 118 citations · Full text

Life Sciences, Biochemistry, Cell Biology +9

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 et al. · Journal of Biological Chemistry · 2012 · 91 citations · Full text

Medicine, Genetics, Molecular Genetics +13

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 et al. · Blood · 2008 · 76 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

In Situ Dimerization of Multiple Wild Type and Mutant Zinc Transporters in Live Cells Using Bimolecular Fluorescence Complementation

Inbal Lasry, Yarden Golan, Bluma Berman et al. · Journal of Biological Chemistry · 2014 · 61 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +7

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 et al. · Biochemical and Biophysical Research Communications · 2009 · 29 citations

Life Sciences, Genetics, Molecular Biology +16