Micro-editing mistake translates into a devastating brain tumor

Por Dominissini, Dan, Amariglio, Ninette, Rechavi, Gideon
Publicado em 2012

F11R Expression upon Hypoxia Is Regulated by RNA Editing

Por Ben-Zvi, Michal, Amariglio, Ninette, Paret, Gideon, Nevo-Caspi, Yael
Publicado em 2013

Mutation analysis of the ferritin L-chain gene in age-related cataract

Por Assia, Nurit, Goldenberg-Cohen, Nitza, Rechavi, Gideon, Amariglio, Ninette, Cohen, Yoram
Publicado em 2010

ADAR1 is vital for B cell lineage development in the mouse bone marrow

Por Marcu-Malina, Victoria, Goldberg, Sanja, Vax, Einav, Amariglio, Ninette, Goldstein, Itamar, Rechavi, Gideon
Publicado no Oncotarget (2016)

Mutagen-Specific Mutation Signature Determines Global microRNA Binding

Por Greenberg, Eyal, Rechavi, Gideon, Amariglio, Ninette, Solomon, Oz, Schachter, Jacob, Markel, Gal, Eyal, Eran
Publicado em 2011

Identification of RNA editing sites in the SNP database

Por Eisenberg, Eli, Adamsky, Konstantin, Cohen, Lital, Amariglio, Ninette, Hirshberg, Abraham, Rechavi, Gideon, Levanon, Erez Y.
Publicado em 2005

Genome-wide activation of latent donor splice sites in stress and disease

Por Nevo, Yuval, Kamhi, Eyal, Jacob-Hirsch, Jasmine, Amariglio, Ninette, Rechavi, Gideon, Sperling, Joseph, Sperling, Ruth
Publicado em 2012

Inhibition of p53-induced apoptosis without affecting expression of p53-regulated genes

Por Lotem, Joseph, Gal, Hilah, Kama, Rachel, Amariglio, Ninette, Rechavi, Gideon, Domany, Eytan, Sachs, Leo, Givol, David
Publicado em 2003

Clone clusters in autoreactive CD4 T-cell lines from probable multiple sclerosis patients form disease-characteristic signatures

Por Mandel, Mathilda, Achiron, Anat, Tuller, Tamir, Barliya, Tilda, Rechavi, Gideon, Amariglio, Ninette, Loewenthal, Ron, Lavie, Gad
Publicado em 2009

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

Two Faces of Chondroitin Sulfate Proteoglycan in Spinal Cord Repair: A Role in Microglia/Macrophage Activation

Por Rolls, Asya, Shechter, Ravid, London, Anat, Segev, Yifat, Jacob-Hirsch, Jasmin, Amariglio, Ninette, Rechavi, Gidon, Schwartz, Michal
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

Dual Role of CD38 in Microglial Activation and Activation-induced Cell Death

Por Mayo, Lior, Jacob-Hirsch, Jasmine, Amariglio, Ninette, Rechavi, Gideon, Moutin, Marie-Jo, Lund, Frances E., Stein, Reuven
Publicado em 2008

Nm-seq maps 2′-O-methylation sites in human mRNA with base precision

Por Dai, Qing, Moshitch-Moshkovitz, Sharon, Han, Dali, Kol, Nitzan, Amariglio, Ninette, Rechavi, Gideon, Dominissini, Dan, He, Chuan
Publicado no Nat Methods (2017)

Profiling of Discrete Gynecological Cancers Reveals Novel Transcriptional Modules and Common Features Shared by Other Cancer Types and Embryonic Stem Cells

Por Pappa, Kalliopi I., Polyzos, Alexander, Jacob-Hirsch, Jasmine, Amariglio, Ninette, Vlachos, George D., Loutradis, Dimitrios, Anagnou, Nicholas P.
Publicado no PLoS One (2015)

Dissection of a DNA-damage-induced transcriptional network using a combination of microarrays, RNA interference and computational promoter analysis

Por Elkon, Ran, Rashi-Elkeles, Sharon, Lerenthal, Yaniv, Linhart, Chaim, Tenne, Tamar, Amariglio, Ninette, Rechavi, Gideon, Shamir, Ron, Shiloh, Yosef
Publicado em 2005

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

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

Consistent levels of A-to-I RNA editing across individuals in coding sequences and non-conserved Alu repeats

Por Greenberger, Shoshana, Levanon, Erez Y, Paz-Yaacov, Nurit, Barzilai, Aviv, Safran, Michal, Osenberg, Sivan, Amariglio, Ninette, Rechavi, Gideon, Eisenberg, Eli
Publicado em 2010

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)