Searching for evidence of disease and malignant cell contamination in ovarian tissue stored from hematologic cancer patients von Meirow, Dror, Hardan, Izhar, Dor, Jehoshua, Fridman, Eduard, Elizur, Shai, Ra'anani, Hila, Slyusarevsky, Elena, Amariglio, Ninette, Schiff, Eyal, Rechavi, Gideon, Nagler, Arnon, Yehuda, Dina Ben

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Correction: Modeling invasive breast cancer: growth factors propel progression of HER2-positive premalignant lesions von Pradeep, C. -R, Zeisel, A., Köstler, W. J., Lauriola, M., Jacob-Hirsch, J., Haibe-Kains, B., Amariglio, N., Ben-Chetrit, N., Emde, A., Solomonov, I., Neufeld, G., Piccart, M., Sagi, I., Sotiriou, C., Rechavi, G., Domany, E., Desmedt, C., Yarden, Y.

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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum von Heimer, G., Marek-Yagel, D., Eyal, E., Barel, O., Oz Levi, D., Hoffmann, C., Ruzzo, E.K., Ganelin-Cohen, E., Lancet, D., Pras, E., Rechavi, G., Nissenkorn, A., Anikster, Y., Goldstein, D.B., Ben Zeev, B.

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Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN von Maydan, Gal, Noyman, Iris, Har-Zahav, Adi, Neriah, Ziva Ben, Pasmanik-Chor, Metsada, Yeheskel, Adva, Albin-Kaplanski, Adi, Maya, Idit, Magal, Nurit, Birk, Efrat, Simon, Amos J, Halevy, Ayelet, Rechavi, Gideon, Shohat, Mordechai, Straussberg, Rachel, Basel-Vanagaite, Lina

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Gene expression profiling of parkinsonian substantia nigra pars compacta; alterations in ubiquitin-proteasome, heat shock protein, iron and oxidative stress regulated proteins, cel... von Grünblatt, E, Mandel, S, Jacob-Hirsch, J, Zeligson, S, Amariglo, N, Rechavi, G, Li, J, Ravid, R, Roggendorf, W, Riederer, P, Youdim, M B H

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A Possible Role for CXCR4 and Its Ligand, the CXC Chemokine Stromal Cell-Derived Factor-1, in the Development of Bone Marrow Metastases in Neuroblastoma von Geminder, Hila, Sagi-Assif, Orit, Goldberg, Lilach, Meshel, Tsipi, Rechavi, Gideon, Witz, Isaac P, Ben-Baruch, Adit

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Chromosomal aberrations and gene expression profiles in non-small cell lung cancer von Dehan, E, Ben-Dor, A, Liao, W, Lipson, D, Frimer, H, Rienstein, S, Simansky, D, Krupsky, M, Yaron, P, Friedman, E, Rechavi, G, Perlman, M, Aviram-Goldring, A, Izraeli, S, Bittner, M, Yakhini, Z, Kaminski, N

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Modeling invasive breast cancer: growth factors propel progression of HER2-positive premalignant lesions von Pradeep, C-R, Zeisel, A, Köstler, W J, Lauriola, M, Jacob-Hirsch, J, Haibe-Kains, B, Amariglio, N, Ben-Chetrit, N, Emde, A, Solomonov, I, Neufeld, G, Piccart, M, Sagi, I, Sotiriou, C, Rechavi, G, Domany, E, Desmedt, C, Yarden, Y

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Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children von Kenet, G, Sadetzki, S, Murad, H, Martinowitz, U, Rosenberg, N, Gitel, S, Rechavi, G, Inbal, A

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The CXCR4 antagonist AMD3100 impairs survival of human AML cells and induces their differentiation von Tavor, S, Eisenbach, M, Jacob-Hirsch, J, Golan, T, Petit, I, BenZion, K, Kay, S, Baron, S, Amariglio, N, Deutsch, V, Naparstek, E, Rechavi, G

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Gene expression profiles of AML derived stem cells; similarity to hematopoietic stem cells von GAL, H, AMARIGLIO, N, DOMANY, E, RECHAVI, G, GIVOL, D, TRAKHTENBROT, L, JACOB-HIRSH, J, MARGALIT, O, AVIGDOR, A, NAGLER, A, TAVOR, S, EIN-DOR, L, LAPIDOT, T

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Modeling ductal carcinoma in situ: a HER2–Notch3 collaboration enables luminal filling von Pradeep, C-R, Köstler, W J, Lauriola, M, Granit, R Z, Zhang, F, Jacob-Hirsch, J, Rechavi, G, Nair, H B, Hennessy, B T, Gonzalez-Angulo, A M, Tekmal, R R, Ben-Porath, I, Mills, G B, Domany, E, Yarden, Y

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Cancer cells suppress p53 in adjacent fibroblasts von Bar, J, Feniger-Barish, R, Lukashchuk, N, Shaham, H, Moskovits, N, Goldfinger, N, Simansky, D, Perlman, M, Papa, M, Yosepovich, A, Rechavi, G, Rotter, V, Oren, M

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610 RNA editing meets cancer von Rechavi, G

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The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation von Basel-Vanagaite, L, Attia, R, Yahav, M, Ferland, R J, Anteki, L, Walsh, C A, Olender, T, Straussberg, R, Magal, N, Taub, E, Drasinover, V, Alkelai, A, Bercovich, D, Rechavi, G, Simon, A J, Shohat, M

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Analysis of gene expression array in TSC2-deficient AML cells reveals IRF7 as a pivotal factor in the Rheb/mTOR pathway von Makovski, V, Jacob-Hirsch, J, Gefen-Dor, C, Shai, B, Ehrlich, M, Rechavi, G, Kloog, Y

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The UVB-induced gene expression profile of human epidermis in vivo is different from that of cultured keratinocytes von ENK, C. D, JACOB-HIRSCH, J, GAL, H, VERBOVETSKI, I, AMARIGLIO, N, MEVORACH, D, INGBER, A, GIVOL, D, RECHAVI, G, HOCHBERG, M

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Nuclear membrane protein LAP2β mediates transcriptional repression alone and together with its binding partner GCL (germ-cell-less) von Nili, Einav, Cojocaru, Gady S., Kalma, Yael, Ginsberg, Doron, Copeland, Neal G., Gilbert, Debra J., Jenkins, Nancy A., Berger, Raanan, Shaklai, Sigal, Amariglio, Ninette, Brok-Simoni, Frida, Simon, Amos J., Rechavi, Gideon

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Co‐existence of clonal expanded autologous and transplacental‐acquired maternal T cells in recombination activating gene‐deficient severe combined immunodeficiency von Lev, A., Simon, A. J., Ben‐Ari, J., Takagi, D., Stauber, T., Trakhtenbrot, L., Rosenthal, E., Rechavi, G., Amariglio, N., Somech, R.

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Chromosomal Numerical Aberrations in Oral Lichen Planus von Yarom, N., Shani, T., Amariglio, N., Taicher, S., Kaplan, I., Vered, M., Rechavi, G., Trakhtenbrot, L., Hirshberg, A.

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