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Annals of Clinical and Translational Neurology|February 11, 2023
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic featuresAmir Dori, Michael Arad, Yishay Wasserstrum, et al.Journal of the American Society of Nephrology : JASN|November 21, 2009
Homozygous SLC2A9 mutations cause severe renal hypouricemiaDganit Dinour, Nicola K Gray, Susan Campbell, et al.Plos One|August 23, 2016
Correction: Overcoming Resistance of Cancer Cells to PARP-1 Inhibitors with Three Different Drug CombinationsMichal Yalon, Liron Tuval-Kochen, David Castel, et al.Nature Genetics|February 27, 2007
A module of negative feedback regulators defines growth factor signalingIdo Amit, Ami Citri, Tal Shay, et al.Journal of Medical Genetics|April 16, 2011
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGNGal Maydan, Iris Noyman, Adi Har-Zahav, et al.Cancer|February 11, 2004
Reduced folate carrier mutations are not the mechanism underlying methotrexate resistance in childhood acute lymphoblastic leukemiaYotam Kaufman, Stavit Drori, Peter D Cole, et al.Genome Research|October 3, 2007
Altered adenosine-to-inosine RNA editing in human cancerNurit Paz, Erez Y Levanon, Ninette Amariglio, et al.Circulation|March 15, 2024
Small Extracellular Vesicles From Infarcted and Failing Heart Accelerate Tumor GrowthTal Caller, Itai Rotem, Olga Shaihov-Teper, et al.Clinical Chemistry and Laboratory Medicine|September 25, 2023
Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot studyRivka Goldis, Batia Kaplan, Michael Arad, et al.Acta Paediatrica (Oslo, Norway : 1992)|April 25, 2026
A Personalised Vaccination Program Based on Immune Reconstitution in Paediatric Cancer SurvivorsMenucha Jurkowicz, Raz Somech, Dan Dominissini, et al.Pageof 33