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Genes & Development|December 21, 2018
PRC1 preserves epidermal tissue integrity independently of PRC2Idan Cohen, Dejian Zhao, Gopinathan Menon, et al.Human Mutation|May 22, 2012
Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1Barak Markus, Ginat Narkis, Daniella Landau, et al.Cell Reports|July 4, 2019
Polycomb Repressive Complex 1 Controls Maintenance of Fungiform Papillae by Repressing Sonic Hedgehog ExpressionCarmit Bar, Idan Cohen, Dejian Zhao, et al.American Journal of Medical Genetics. Part A|December 12, 2017
A novel homozygous SLC25A1 mutation with impaired mitochondrial complex V: Possible phenotypic expansionIdan Cohen, Orna Staretz-Chacham, Ohad Wormser, et al.The Journal of Investigative Dermatology|March 21, 2016
Dissecting the Roles of Polycomb Repressive Complex 2 Subunits in the Control of Skin DevelopmentKatherine L Dauber, Carolina N Perdigoto, Victor J Valdes, et al.Experimental Dermatology|February 14, 2019
Dissection of Merkel cell formation in hairy and glabrous skin reveals a common requirement for FGFR2-mediated signallingMinh Binh Nguyen, Victor Julian Valdes, Idan Cohen, et al.The Journal of Biological Chemistry|December 18, 2003
RNA binding activity of the ribulose-1,5-bisphosphate carboxylase/oxygenase large subunit from Chlamydomonas reinhardtiiIdo Yosef, Vered Irihimovitch, Joel A Knopf, et al.Human Mutation|January 15, 2013
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfectaMichael Volodarsky, Barak Markus, Idan Cohen, et al.European Journal of Human Genetics : EJHG|September 19, 2013
Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutationYonatan Perez, Libe Gradstein, Hagit Flusser, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 21, 2011
IL-1α and IL-1β recruit different myeloid cells and promote different stages of sterile inflammationPeleg Rider, Yaron Carmi, Ofer Guttman, et al.Pageof 8