Publications

  1. Towfic, F., Funt, J. M., Fowler, K. D., Bakshi, S., Blaugrund, E., Artyomov, M. N., Hayden, M. R., Ladkani, D., Schwartz, R., and Zeskind, B. (2014) Comparing the biological impact of glatiramer acetate with the biological impact of a generic. PLoS One 9, e83757
  2. Nardone, S., Sams, D. S., Reuveni, E., Getselter, D., Oron, O., Karpuj, M., and Elliott, E. (2014) DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways. Transl Psychiatry 4, e433
  3. Isakov, E., Weisman-Shomer, P., and Benhar, M. (2014) Suppression of the pro-inflammatory NLRP3/interleukin-1beta pathway in macrophages by the thioredoxin reductase inhibitor auranofin. Biochim Biophys Acta 1840, 3153-3161
  4. Barash, U., Zohar, Y., Wildbaum, G., Beider, K., Nagler, A., Karin, N., Ilan, N., and Vlodavsky, I. (2014) Heparanase enhances myeloma progression via CXCL10 downregulation. Leukemia 28, 2178-2187
  5. Seroussi, E., Glick, G., Shirak, A., Ezra, E., Zeron, Y., Ron, M., and Weller, J. I. (2013) Maternity validation using sire-only BovineSNP50 BeadChip data. Anim Genet 44, 754-757
  6. Scheinman, E. J., Rostoker, R., and Leroith, D. (2013) Cholesterol affects gene expression of the Jun family in colon carcinoma cells using different signaling pathways. Mol Cell Endocrinol 374, 101-107
  7. Sarig, O., Goldsher, D., Nousbeck, J., Fuchs-Telem, D., Cohen-Katsenelson, K., Iancu, T. C., Manov, I., Saada, A., Sprecher, E., and Mandel, H. (2013) 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. Am J Med Genet A 161A, 2204-2215
  8. Henig, N., Avidan, N., Mandel, I., Staun-Ram, E., Ginzburg, E., Paperna, T., Pinter, R. Y., and Miller, A. (2013) Interferon-beta induces distinct gene expression response patterns in human monocytes versus T cells. PLoS One 8, e62366
  9. Abelson, S., Shamai, Y., Berger, L., Skorecki, K., and Tzukerman, M. (2013) Niche-dependent gene expression profile of intratumoral heterogeneous ovarian cancer stem cell populations. PLoS One 8, e83651
  10. Sukhotnik, I., Mogilner, J. G., Pollak, Y., Blumenfeld, S., Bejar, J., and Coran, A. G. (2012) PDGF-alpha stimulates intestinal epithelial cell turnover after massive small bowel resection in a rat. Am J Physiol Gastrointest Liver Physiol 302, G1274-1281
  11. Sarig, O., Nahum, S., Rapaport, D., Ishida-Yamamoto, A., Fuchs-Telem, D., Qiaoli, L., Cohen-Katsenelson, K., Spiegel, R., Nousbeck, J., Israeli, S., Borochowitz, Z. U., Padalon-Brauch, G., Uitto, J., Horowitz, M., Shalev, S., and Sprecher, E. (2012) Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation. Am J Hum Genet 91, 337-342
  12. Sarig, O., Bercovici, S., Zoller, L., Goldberg, I., Indelman, M., Nahum, S., Israeli, S., Sagiv, N., Martinez de Morentin, H., Katz, O., Baum, S., Barzilai, A., Trau, H., Murrell, D. F., Bergman, R., Hertl, M., Rosenberg, S., Nothen, M. M., Skorecki, K., Schmidt, E., Zillikens, D., Darvasi, A., Geiger, D., Rosset, S., Ibrahim, S. M., and Sprecher, E. (2012) Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. J Invest Dermatol 132, 1798-1805
  13. Fuchs-Telem, D., Sarig, O., van Steensel, M. A., Isakov, O., Israeli, S., Nousbeck, J., Richard, K., Winnepenninckx, V., Vernooij, M., Shomron, N., Uitto, J., Fleckman, P., Richard, G., and Sprecher, E. (2012) Familial pityriasis rubra pilaris is caused by mutations in CARD14. Am J Hum Genet 91, 163-170
  14. Nousbeck, J., Burger, B., Fuchs-Telem, D., Pavlovsky, M., Fenig, S., Sarig, O., Itin, P., and Sprecher, E. (2011) A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia. Am J Hum Genet 89, 302-307
  15. Nousbeck, J., Sarig, O., Avidan, N., Indelman, M., Bergman, R., Ramon, M., Enk, C. D., and Sprecher, E. (2010) Insulin-like growth factor-binding protein 7 regulates keratinocyte proliferation, differentiation and apoptosis. J Invest Dermatol 130, 378-387
  16. Basel-Vanagaite, L., Sarig, O., Hershkovitz, D., Fuchs-Telem, D., Rapaport, D., Gat, A., Isman, G., Shirazi, I., Shohat, M., Enk, C. D., Birk, E., Kohlhase, J., Matysiak-Scholze, U., Maya, I., Knopf, C., Peffekoven, A., Hennies, H. C., Bergman, R., Horowitz, M., Ishida-Yamamoto, A., and Sprecher, E. (2009) RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome. Am J Hum Genet 85, 254-263