ENVIRONMENT: THE REBUILDING AND GREENING OF THE WORLD TRADE CENTER SITE WHY GREEN BUILDING IS PLAYING A ROLE IN THE DEVELOPMENT DISCUSSIONS IN LOWER MANHATTAN von Drury, Allison, Rosenberg, Ariella

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Natural Killer Cell-Mediated Host Defense against Uropathogenic E. coli Is Counteracted by Bacterial HemolysinA-Dependent Killing of NK Cells von Gur, Chamutal, Coppenhagen-Glazer, Shunit, Rosenberg, Shilo, Yamin, Rachel, Enk, Jonatan, Glasner, Ariella, Bar-On, Yotam, Fleissig, Omer, Naor, Ronit, Abed, Jawad, Mevorach, Dror, Granot, Zvi, Bachrach, Gilad, Mandelboim, Ofer

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Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome von Mor-Cohen, Ronit, Zivelin, Ariella, Rosenberg, Nurit, Shani, Mordechai, Muallem, Shmuel, Seligsohn, Uri

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No Evidence from Genome-Wide Data of a Khazar Origin for the Ashkenazi Jews von Behar, Doron M., Metspalu, Mait, Baran, Yael, Kopelman, Naama M., Yunusbayev, Bayazit, Gladstein, Ariella, Tzur, Shay, Sahakyan, Hovhannes, Bahmanimehr, Ardeshir, Yepiskoposyan, Levon, Tambets, Kristiina, Khusnutdinova, Elza K., Kushniarevich, Alena, Balanovsky, Oleg, Balanovsky, Elena, Kovacevic, Lejla, Marjanovic, Damir, Mihailov, Evelin, Kouvatsi, Anastasia, Triantaphyllidis, Costas, King, Roy J., Semino, Ornella, Torroni, Antonio, Hammer, Michael F., Metspalu, Ene, Skorecki, Karl, Rosset, Saharon, Halperin, Eran, Villems, Richard, Rosenberg, Noah A.

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The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans von Rosenberg, Nurit, Murata, Mitsuru, Ikeda, Yasuo, Opare-Sem, Ohene, Zivelin, Ariella, Geffen, Eli, Seligsohn, Uri

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Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene von Zivelin, Ariella, Bauduer, Frederic, Ducout, Louis, Peretz, Hava, Rosenberg, Nurit, Yatuv, Rivka, Seligsohn, Uri

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene von Zivelin, Ariella, Rosenberg, Nurit, Faier, Shlomit, Kornbrot, Nurit, Peretz, Hava, Mannhalter, Christine, Horellou, Marie Helene, Seligsohn, Uri

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Single and Combined Prothrombotic Factors in Patients With Idiopathic Venous Thromboembolism: Prevalence and Risk Assessment von Salomon, Ophira, Steinberg, David M, Zivelin, Ariella, Gitel, Sanford, Dardik, Rima, Rosenberg, Nurit, Berliner, Shlomo, Inbal, Aida, Many, Amira, Lubetsky, Aharon, Varon, David, Martinowitz, Uriel, Seligsohn, Uri

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A novel ancestral splicing mutation in the multidrug resistance protein 2 gene causes Dubin-Johnson syndrome in Ashkenazi Jewish patients von Mor-Cohen, Ronit, Zivelin, Ariella, Rosenberg, Nurit, Goldberg, Iris, Seligsohn, Uri

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Improved method for genotyping apolipoprotein E polymorphisms by a PCR-based assay simultaneously utilizing two distinct restriction enzymes von ZIVELIN, A, ROSENBERG, N, PERETZ, H, AMIT, Y, KORNBROT, N, SELIGSOHN, U

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Analysis of prothrombotic and vascular risk factors in patients with nonarteritic anterior ischemic optic neuropathy von Salomon, Ophira, Huna-Baron, Ruth, Kurtz, Shimon, Steinberg, David M, Moisseiev, Joseph, Rosenberg, Nurit, Yassur, Iftach, Vidne, Orit, Zivelin, Ariella, Gitel, Sanford, Davidson, Jacqueline, Ravid, Bruria, Seligsohn, Uri

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Major mutations in calf-1 and calf-2 domains of glycoprotein IIb in patients with Glanzmann thrombasthenia enable GPIIb/IIIa complex formation, but impair its transport from the en... von Rosenberg, Nurit, Yatuv, Rivka, Sobolev, Vladimir, Peretz, Hava, Zivelin, Ariella, Seligsohn, Uri

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A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene von Zivelin, Ariella, Rosenberg, Nurit, Faier, Shlomit, Kornbrot, Nurit, Peretz, Hava, Mannhalter, Christine, Horellou, Marie Helene, Seligsohn, Uri

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A mutation in LMAN1 (ERGIC-53) causing combined factor V and factor VIII deficiency is prevalent in Jews originating from the island of Djerba in Tunisia von Segal, Avichai, Zivelin, Ariella, Rosenberg, Nurit, Ginsburg, David, Shpilberg, Ofer, Seligsohn, Uri

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No Evidence from Genome-wide Data of a Khazar Origin for the Ashkenazi Jews von Behar, Doron M., Metspalu, Mait, Baran, Yael, Kopelman, Naama M., Yunusbayen, Bayazit, Gladstein, Ariella, Tzur, Shay, Sahakyan, Hovhannes, Bahmanimehr, Ardeshir, Yepiskoposyan, Levon, Tambets, Kristiina, Khusnutdinova, Elza K., Kushniarevich, Alena, Balanovsky, Oleg, Balanovsky, Elena, Kovacevic, Lejla, Marjanovic, Damir, Mihailov, Evelin, Kouvatsi, Anastasia, Triantaphyllidis, Costas, King, Roy J., Semino, Ornella, Torroni, Antonio, Hammer, Michael F., Metspalu, Ene, Skorecki, Karl, Rosset, Saharon, Halperin, Eran, Villems, Richard, Rosenberg, Noah A.

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No Evidence from Genome-wide Data of a Khazar Origin fo the Ashkenazi Jews von Doron M. Behar, Mait Metspalu, Yael Baran, Naama M. Kopelman, Bayazit Yunusbayev, Ariella Gladstein, Shay Tzur, Hovhannes Sahakyan, Ardeshir Bahmanimehr, Levon Yepiskoposyan, Kristiina Tambets, Elza K. Khusnutdinova, Alena Kushniarevich, Oleg Balanovsky, Elena Balanovsky, Lejla Kovacevic, Damir Marjanovic, Evelin Mohailov, Anastasia Kouvatsi, Costas Triantaphyllidis, Roy J. King, Ornella Semino, Antonio Torroni, Michael F. Hammer, Ene Metspalu, Karl Skorecki, Saharon Rosset, Eran Halperin, Richard Villems, Noah A. Rosenberg

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High prevalences of vitamin B-12 and folic acid deficiency in elderly subjects in Israel von Figlin, Elizabeth, Chetrit, Angela, Shahar, Avner, Shpilberg, Ofer, Zivelin, Ariella, Rosenberg, Nurit, Brok-Simoni, Frida, Gadoth, Nathan, Sela, Ben-Ami, Seligsohn, Uri

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Age estimates of ancestral mutations causing factor VII deficiency and Dubin–Johnson syndrome in Iranian and Moroccan Jews are consistent with ancient Jewish migrations von Mor-Cohen, Ronit, Zivelin, Ariella, Fromovich-Amit, Yonit, Kovalski, Victoria, Rosenberg, Nurit, Seligsohn, Uri

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Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia von Yatuv, Rivka, Rosenberg, Nurit, Zivelin, Ariella, Peretz, Hava, Dardik, Rima, Trakhtenbrot, Luba, Seligsohn, Uri

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Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation von Fromovich-Amit, Yonit, Zivelin, Ariella, Rosenberg, Nurit, Landau, Meytal, Rosa, Jean-Philippe, Seligsohn, Uri

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