Publications

  1. W. Yaseen et al., Fibroblast fusion to the muscle fiber regulates myotendinous junction formation. Nat Commun 12, (Jun 22, 2021).
  2. Y. Shemer et al., Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. International journal of molecular sciences 22, (Aug, 2021).
  3. A. Altshuler et al., Discrete limbal epithelial stem cell populations mediate corneal homeostasis and wound healing. Cell stem cell, (May 8, 2021).
  4. G. Hevroni, J. Flores-Uribe, O. Beja, A. Philosof, Seasonal and diel patterns of abundance and activity of viruses in the Red Sea. Proceedings of the National Academy of Sciences of the United States of America 117, 29738 (Nov 24, 2020).
  5. R. Gabay Yehezkely et al., Intracellular Role for the Matrix-Modifying Enzyme Lox in Regulating Transcription Factor Subcellular Localization and Activity in Muscle Regeneration. Developmental cell 53, 406 (May 18, 2020).
  6. M. Carmel et al., Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry, 1 (Apr 14, 2020).
  7. S. Avraham et al., Early Cardiac Remodeling Promotes Tumor Growth and Metastasis. Circulation 142, 670 (Aug 18, 2020).
  8. N. Flint Brodsly et al., The transcription factor Hey and nuclear lamins specify and maintain cell identity. eLife 8, (Jul 16, 2019).
  9. U. Barash et al., Heparanase promotes glioma progression via enhancing CD24 expression. International journal of cancer 145, 1596 (Sep 15, 2019).
  10. Y. Shamai, D. C. Alperovich, Z. Yakhini, K. Skorecki, M. Tzukerman, Reciprocal Reprogramming of Cancer Cells and Associated Mesenchymal Stem Cells in Gastric Cancer. Stem cells, (Oct 31, 2018).
  11. E. Kaplan 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 (Sep 18, 2018).
  12. G. Journo et al., Modulation of Cellular CpG DNA Methylation by Kaposi’s Sarcoma-Associated Herpesvirus. Journal of virology 92, (Aug 15, 2018).
  13. R. Ben Jehuda, Y. Shemer, O. Binah, Genome Editing in Induced Pluripotent Stem Cells using CRISPR/Cas9. Stem cell reviews 14, 323 (Jun, 2018).
  14. N. Yasin 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, (Apr 7, 2017).
  15. E. Simanovich et al., Inhibition of tumor growth and metastasis by EMMPRIN multiple antigenic peptide (MAP) vaccination is mediated by immune modulation. Oncoimmunology 6, e1261778 (2017).
  16. S. Mamrut et al., Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins. Journal of autoimmunity 82, 62 (Aug, 2017).
  17. R. Kalfon 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 (Dec 15, 2017).
  18. F. Towfic et al., Comparing the biological impact of glatiramer acetate with the biological impact of a generic. PloS one 9, e83757 (2014).
  19. S. Nardone et al., DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways. Translational psychiatry 4, e433 (Sep 2, 2014).
  20. E. Isakov, P. Weisman-Shomer, M. Benhar, Suppression of the pro-inflammatory NLRP3/interleukin-1beta pathway in macrophages by the thioredoxin reductase inhibitor auranofin. Biochimica et biophysica acta 1840, 3153 (Oct, 2014).
  21. U. Barash et al., Heparanase enhances myeloma progression via CXCL10 downregulation. Leukemia 28, 2178 (Nov, 2014).
  22. E. Seroussi et al., Maternity validation using sire-only BovineSNP50 BeadChip data. Animal genetics 44, 754 (Dec, 2013).
  23. E. J. Scheinman, R. Rostoker, D. Leroith, Cholesterol affects gene expression of the Jun family in colon carcinoma cells using different signaling pathways. Molecular and cellular endocrinology 374, 101 (Jul 15, 2013).
  24. O. Sarig 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 (Sep, 2013).
  25. N. Henig et al., Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells. PloS one 8, e62366 (2013).
  26. S. Abelson, Y. Shamai, L. Berger, K. Skorecki, M. Tzukerman, Niche-dependent gene expression profile of intratumoral heterogeneous ovarian cancer stem cell populations. PloS one 8, e83651 (2013).
  27. I. Sukhotnik 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 (Jun 1, 2012).
  28. O. Sarig et al., Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation. American journal of human genetics 91, 337 (Aug 10, 2012).
  29. O. Sarig 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 (Jul, 2012).
  30. D. Fuchs-Telem et al., Familial pityriasis rubra pilaris is caused by mutations in CARD14. American journal of human genetics 91, 163 (Jul 13, 2012).
  31. J. Nousbeck et al., A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. American journal of human genetics 89, 302 (Aug 12, 2011).
  32. J. Nousbeck et al., Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis. The Journal of investigative dermatology 130, 378 (Feb, 2010).
  33. L. Basel-Vanagaite et al., RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome. American journal of human genetics 85, 254 (Aug, 2009).