Publications

1              Flint Brodsly, N. et al. The transcription factor Hey and nuclear lamins specify and maintain cell identity. eLife 8, doi:10.7554/eLife.44745 (2019).

2              Barash, U. et al. Heparanase promotes glioma progression via enhancing CD24 expression. International journal of cancer 145, 1596-1608, doi:10.1002/ijc.32375 (2019).

3              Shamai, Y., Alperovich, D. C., Yakhini, Z., Skorecki, K. & Tzukerman, M. Reciprocal Reprogramming of Cancer Cells and Associated Mesenchymal Stem Cells in Gastric Cancer. Stem cells, doi:10.1002/stem.2942 (2018).

4              Kaplan, E. et al. ASCT1 (Slc1a4) transporter is a physiologic regulator of brain d-serine and neurodevelopment. Proceedings of the National Academy of Sciences of the United States of America 115, 9628-9633, doi:10.1073/pnas.1722677115 (2018).

5              Journo, G. et al. Modulation of Cellular CpG DNA Methylation by Kaposi’s Sarcoma-Associated Herpesvirus. Journal of virology 92, doi:10.1128/JVI.00008-18 (2018).

6              Ben Jehuda, R., Shemer, Y. & Binah, O. Genome Editing in Induced Pluripotent Stem Cells using CRISPR/Cas9. Stem cell reviews 14, 323-336, doi:10.1007/s12015-018-9811-3 (2018).

7              Yasin, N. et al. Classical and Novel TSPO Ligands for the Mitochondrial TSPO Can Modulate Nuclear Gene Expression: Implications for Mitochondrial Retrograde Signaling. International journal of molecular sciences 18, doi:10.3390/ijms18040786 (2017).

8              Simanovich, E. et al. Inhibition of tumor growth and metastasis by EMMPRIN multiple antigenic peptide (MAP) vaccination is mediated by immune modulation. Oncoimmunology 6, e1261778, doi:10.1080/2162402X.2016.1261778 (2017).

9              Mamrut, S. et al. Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins. Journal of autoimmunity 82, 62-73, doi:10.1016/j.jaut.2017.05.005 (2017).

10           Kalfon, R. et al. c-Jun dimerization protein 2 (JDP2) deficiency promotes cardiac hypertrophy and dysfunction in response to pressure overload. International journal of cardiology 249, 357-363, doi:10.1016/j.ijcard.2017.08.074 (2017).

11           Towfic, F. et al. Comparing the biological impact of glatiramer acetate with the biological impact of a generic. PloS one 9, e83757, doi:10.1371/journal.pone.0083757 (2014).

12           Nardone, S. et al. DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways. Translational psychiatry 4, e433, doi:10.1038/tp.2014.70 (2014).

13           Isakov, E., Weisman-Shomer, P. & Benhar, M. Suppression of the pro-inflammatory NLRP3/interleukin-1beta pathway in macrophages by the thioredoxin reductase inhibitor auranofin. Biochimica et biophysica acta 1840, 3153-3161, doi:10.1016/j.bbagen.2014.07.012 (2014).

14           Barash, U. et al. Heparanase enhances myeloma progression via CXCL10 downregulation. Leukemia 28, 2178-2187, doi:10.1038/leu.2014.121 (2014).

15           Seroussi, E. et al. Maternity validation using sire-only BovineSNP50 BeadChip data. Animal genetics 44, 754-757, doi:10.1111/age.12062 (2013).

16           Scheinman, E. J., Rostoker, R. & Leroith, D. Cholesterol affects gene expression of the Jun family in colon carcinoma cells using different signaling pathways. Molecular and cellular endocrinology 374, 101-107, doi:10.1016/j.mce.2013.04.011 (2013).

17           Sarig, O. et al. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome (3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome) caused by novel mutations in SERAC1. American journal of medical genetics. Part A 161A, 2204-2215, doi:10.1002/ajmg.a.36059 (2013).

18           Henig, N. et al. Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells. PloS one 8, e62366, doi:10.1371/journal.pone.0062366 (2013).

19           Abelson, S., Shamai, Y., Berger, L., Skorecki, K. & Tzukerman, M. Niche-dependent gene expression profile of intratumoral heterogeneous ovarian cancer stem cell populations. PloS one 8, e83651, doi:10.1371/journal.pone.0083651 (2013).

20           Sukhotnik, I. et al. PDGF-alpha stimulates intestinal epithelial cell turnover after massive small bowel resection in a rat. American journal of physiology. Gastrointestinal and liver physiology 302, G1274-1281, doi:10.1152/ajpgi.00532.2011 (2012).

21           Sarig, O. et al. Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation. American journal of human genetics 91, 337-342, doi:10.1016/j.ajhg.2012.06.003 (2012).

22           Sarig, O. et al. Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. The Journal of investigative dermatology 132, 1798-1805, doi:10.1038/jid.2012.46 (2012).

23           Fuchs-Telem, D. et al. Familial pityriasis rubra pilaris is caused by mutations in CARD14. American journal of human genetics 91, 163-170, doi:10.1016/j.ajhg.2012.05.010 (2012).

24           Nousbeck, J. et al. A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. American journal of human genetics 89, 302-307, doi:10.1016/j.ajhg.2011.07.004 (2011).

25           Nousbeck, J. et al. Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis. The Journal of investigative dermatology 130, 378-387, doi:10.1038/jid.2009.265 (2010).

26           Basel-Vanagaite, L. et al. RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome. American journal of human genetics 85, 254-263, doi:10.1016/j.ajhg.2009.07.001 (2009).