Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13

Por Toren, Amos, Amariglio, Ninette, Rozenfeld-Granot, Galit, Simon, Amos J., Brok-Simoni, Frida, Pras, Elon, Rechavi, Gideon
Publicado em 1999

The human granulocyte nucleus: unusual nuclear envelope and heterochromatin composition

Por Olins, Ada L., Zwerger, Monika, Herrmann, Harald, Zentgraf, Hanswalter, Simon, Amos J., Monestier, Marc, Olins, Donald E.
Publicado em 2008

The Kinetics of Early T and B Cell Immune Recovery after Bone Marrow Transplantation in RAG-2-Deficient SCID Patients

Por Lev, Atar, Simon, Amos J., Bareket, Mor, Bielorai, Bella, Hutt, Daphna, Amariglio, Ninette, Rechavi, Gideon, Somech, Raz
Publicado em 2012

Genome-wide analysis discloses reversal of the hypoxia-induced changes of gene expression in colon cancer cells by zinc supplementation

Por Sheffer, Michal, Simon, Amos J., Jacob-Hirsch, Jasmine, Rechavi, Gideon, Domany, Eytan, Givol, David, D’Orazi, Gabriella
Publicado em 2011

High metallothionein predicts poor survival in glioblastoma multiforme

Por Mehrian-Shai, Ruty, Yalon, Michal, Simon, Amos J., Eyal, Eran, Pismenyuk, Tatyana, Moshe, Itai, Constantini, Shlomi, Toren, Amos
Publicado no BMC Med Genomics (2015)

Characterizing T Cells in SCID Patients Presenting with Reactive or Residual T Lymphocytes

Por Lev, Atar, Simon, Amos J., Trakhtenbrot, Luba, Goldstein, Itamar, Nagar, Meital, Stepensky, Polina, Rechavi, Gideon, Amariglio, Ninette, Somech, Raz
Publicado em 2012

Elevated CO(2) levels affect development, motility, and fertility and extend life span in Caenorhabditis elegans

Por Sharabi, Kfir, Hurwitz, Anat, Simon, Amos J., Beitel, Greg J., Morimoto, Richard I., Rechavi, Gideon, Sznajder, Jacob I., Gruenbaum, Yosef
Publicado em 2009

Ex Vivo Treatment with a Novel Synthetic Aminoglycoside NB54 in Primary Fibroblasts from Rett Syndrome Patients Suppresses MECP2 Nonsense Mutations

Por Vecsler, Manuela, Ben Zeev, Bruria, Nudelman, Igor, Anikster, Yair, Simon, Amos J., Amariglio, Ninette, Rechavi, Gideon, Baasov, Timor, Gak, Eva
Publicado em 2011

G23D: Online tool for mapping and visualization of genomic variants on 3D protein structures

Por Solomon, Oz, Kunik, Vered, Simon, Amos, Kol, Nitzan, Barel, Ortal, Lev, Atar, Amariglio, Ninette, Somech, Raz, Rechavi, Gidi, Eyal, Eran
Publicado no BMC Genomics (2016)

The Effect of Gentamicin-Induced Readthrough on a Novel Premature Termination Codon of CD18 Leukocyte Adhesion Deficiency Patients

Por Simon, Amos J., Lev, Atar, Wolach, Baruch, Gavrieli, Ronit, Amariglio, Ninette, Rosenthal, Ester, Gazit, Ephraim, Eyal, Eran, Rechavi, Gideon, Somech, Raz
Publicado em 2010

Induction of polyploidy by nuclear fusion mechanism upon decreased expression of the nuclear envelope protein LAP2β in the human osteosarcoma cell line U2OS

Por Ben-Shoshan, Shirley Oren, Simon, Amos J, Jacob-Hirsch, Jasmine, Shaklai, Sigal, Paz-Yaacov, Nurit, Amariglio, Ninette, Rechavi, Gideon, Trakhtenbrot, Luba
Publicado em 2014

Leptin Locally Synthesized in Carotid Atherosclerotic Plaques Could Be Associated With Lesion Instability and Cerebral Emboli

Por Schneiderman, Jacob, Schaefer, Katrin, Kolodgie, Frank D., Savion, Naphtali, Kotev-Emeth, Shlomo, Dardik, Rima, Simon, Amos J., Halak, Moshe, Pariente, Clara, Engelberg, Isaac, Konstantinides, Stavros, Virmani, Renu
Publicado em 2012

Zinc enhances temozolomide cytotoxicity in glioblastoma multiforme model systems

Por Toren, Amos, Pismenyuk, Tatyana, Yalon, Michal, Freedman, Shani, Simon, Amos J., Fisher, Tamar, Moshe, Itai, Reichardt, Juergen K.V., Constantini, Shlomi, Mardor, Yael, Last, David, Guez, David, Daniels, Dianne, Assoulin, Moria, Mehrian-Shai, Ruty
Publicado no Oncotarget (2016)

A LAD-III syndrome is associated with defective expression of the Rap-1 activator CalDAG-GEFI in lymphocytes, neutrophils, and platelets

Por Pasvolsky, Ronit, Feigelson, Sara W., Kilic, Sara Sebnem, Simon, Amos J., Tal-Lapidot, Guy, Grabovsky, Valentin, Crittenden, Jill R., Amariglio, Ninette, Safran, Michal, Graybiel, Ann M., Rechavi, Gideon, Ben-Dor, Shifra, Etzioni, Amos, Alon, Ronen
Publicado em 2007

Local Application of Leptin Antagonist Attenuates Angiotensin II–Induced Ascending Aortic Aneurysm and Cardiac Remodeling

Por Ben‐Zvi, Danny, Savion, Naphtali, Kolodgie, Frank, Simon, Amos, Fisch, Sudeshna, Schäfer, Katrin, Bachner‐Hinenzon, Noa, Cao, Xin, Gertler, Arieh, Solomon, Gili, Kachel, Erez, Raanani, Ehud, Lavee, Jacob, Kotev Emeth, Shlomo, Virmani, Renu, Schoen, Frederick J., Schneiderman, Jacob
Publicado no J Am Heart Assoc (2016)

The isolation and characterization of renal cancer initiating cells from human Wilms' tumour xenografts unveils new therapeutic targets†

Por Pode-Shakked, Naomi, Shukrun, Rachel, Mark-Danieli, Michal, Tsvetkov, Peter, Bahar, Sarit, Pri-Chen, Sara, Goldstein, Ronald S, Rom-Gross, Eithan, Mor, Yoram, Fridman, Edward, Meir, Karen, Simon, Amos, Magister, Marcus, Kaminski, Naftali, Goldmacher, Victor S, Harari-Steinberg, Orit, Dekel, Benjamin
Publicado em 2013

Transient Infantile Hypertriglyceridemia, Fatty Liver, and Hepatic Fibrosis Caused by Mutated GPD1, Encoding Glycerol-3-Phosphate Dehydrogenase 1

Por Basel-Vanagaite, Lina, Zevit, Noam, Zahav, Adi Har, Guo, Liang, Parathath, Saj, Pasmanik-Chor, Metsada, McIntyre, Adam D., Wang, Jian, Albin-Kaplanski, Adi, Hartman, Corina, Marom, Daphna, Zeharia, Avraham, Badir, Abir, Shoerman, Oded, Simon, Amos J., Rechavi, Gideon, Shohat, Mordechai, Hegele, Robert A., Fisher, Edward A., Shamir, Raanan
Publicado em 2012

SOBP Is Mutated in Syndromic and Nonsyndromic Intellectual Disability and Is Highly Expressed in the Brain Limbic System

Por Birk, Efrat, Har-Zahav, Adi, Manzini, Chiara M., Pasmanik-Chor, Metsada, Kornreich, Liora, Walsh, Christopher A., Noben-Trauth, Konrad, Albin, Adi, Simon, Amos J., Colleaux, Laurence, Morad, Yair, Rainshtein, Limor, Tischfield, David J., Wang, Peter, Magal, Nurit, Maya, Idit, Shoshani, Noa, Rechavi, Gideon, Gothelf, Doron, Maydan, Gal, Shohat, Mordechai, Basel-Vanagaite, Lina
Publicado em 2010

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects

Por Simon, Amos J., Lev, Atar, Zhang, Yong, Weiss, Batia, Rylova, Anna, Eyal, Eran, Kol, Nitzan, Barel, Ortal, Cesarkas, Keren, Soudack, Michalle, Greenberg-Kushnir, Noa, Rhodes, Michele, Wiest, David L., Schiby, Ginette, Barshack, Iris, Katz, Shulamit, Pras, Elon, Poran, Hana, Reznik-Wolf, Haike, Ribakovsky, Elena, Simon, Carlos, Hazou, Wadi, Sidi, Yechezkel, Lahad, Avishay, Katzir, Hagar, Sagie, Shira, Aqeilan, Haifa A., Glousker, Galina, Amariglio, Ninette, Tzfati, Yehuda, Selig, Sara, Rechavi, Gideon, Somech, Raz
Publicado no J Exp Med (2016)

A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45

Por Vilboux, Thierry, Lev, Atar, Malicdan, May Christine V., Simon, Amos J., Järvinen, Päivi, Racek, Tomas, Puchalka, Jacek, Sood, Raman, Carrington, Blake, Bishop, Kevin, Mullikin, James, Huizing, Marjan, Garty, Ben Zion, Eyal, Eran, Wolach, Baruch, Gavrieli, Ronit, Toren, Amos, Soudack, Michalle, Atawneh, Osama M., Babushkin, Tatiana, Schiby, Ginette, Cullinane, Andrew, Avivi, Camila, Polak-Charcon, Sylvie, Barshack, Iris, Amariglio, Ninette, Rechavi, Gideon, van der Werff ten Bosch, Jutte, Anikster, Yair, Klein, Christoph, Gahl, William A., Somech, Raz
Publicado em 2013