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Journal of Immunology Research|June 29, 2018
NMO-IgG and AQP4 Peptide Can Induce Aggravation of EAMG and Immune-Mediated Muscle WeaknessTehila Mizrachi, Livnat Brill, Malcolm Rabie, et al.International Journal of Clinical and Experimental Medicine|May 9, 2012
Transcriptional targeting of glioblastoma by diphtheria toxin-A driven by both H19 and IGF2-P4 promotersDoron Amit, Imad J Matouk, Iris Lavon, et al.Journal of Neuroinflammation|October 24, 2023
Complement-membrane regulatory proteins are absent from the nodes of Ranvier in the peripheral nervous systemNetanel Karbian, Yael Eshed-Eisenbach, Marian Zeibak, et al.Molecular Genetics & Genomic Medicine|December 31, 2021
Congenital Hypotonia: Cracking a SAGA of consanguineous kindred harboring four genetic variantsLimor Kalfon, Meirav Baydany, Nadra Samra, et al.Oncotarget|May 8, 2018
Androgen receptor: a potential therapeutic target for glioblastomaNomi Zalcman, Tamar Canello, Haim Ovadia, et al.Neurogenetics|April 3, 2021
Multi-system neurological disorder associated with a CRYAB variantMenachem Sadeh, Dolev Rahat, Vardiella Meiner, et al.Neuromolecular Medicine|December 15, 2012
Variable phenotypes of knockin mice carrying the M712T Gne mutationIlan Sela, Lena Yakovlev, Michal Becker Cohen, et al.Plos One|July 30, 2013
Variable myopathic presentation in a single family with novel skeletal RYR1 mutationRuben Attali, Sharon Aharoni, Susan Treves, et al.Human Molecular Genetics|August 13, 2013
Congenital myopathy is caused by mutation of HACD1Emad Muhammad, Orit Reish, Yusuke Ohno, et al.Journal of Neuromuscular Diseases|June 14, 2024
Induced Muscle and Liver Absence of Gne in Postnatal Mice Does Not Result in Structural or Functional Muscle ImpairmentAvi Harazi, Lena Yakovlev, Nili Ilouz, et al.Pageof 7