1. A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds. Issue 5 (7th March 2020) Authors: Marek‐Yagel, Dina; Bolkier, Yoav; Barel, Ortal; Vardi, Amir; Mishali, David; Katz, Uriel; Salem, Yishay; Abudi, Shachar; Nayshool, Omri; Kol, Nitzan; Raas‐Rothschild, Annick; Rechavi, Gideon; Anikster, Yair; Pode‐Shakked, Ben Journal: American journal of medical genetics Issue: Volume 182:Issue 5(2020) Page Start: 987 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. ADAR1 deletion induces NFκB and interferon signaling dependent liver inflammation and fibrosis. Issue 5 (4th May 2017) Authors: Ben-Shoshan, Shirley Oren; Kagan, Polina; Sultan, Maya; Barabash, Zohar; Dor, Chen; Jacob-Hirsch, Jasmine; Harmelin, Alon; Pappo, Orit; Marcu-Malina, Victoria; Ben-Ari, Ziv; Amariglio, Ninette; Rechavi, Gideon; Goldstein, Itamar; Safran, Michal Journal: RNA biology Issue: Volume 14:Issue 5(2017) Page Start: 587 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Breaking the Ceiling of Human Maximal Life span. (7th November 2017) Authors: Ben-Haim, Moshe Shay; Kanfi, Yariv; Mitchell, Sarah J; Maoz, Noam; Vaughan, Kelli L; Amariglio, Ninette; Lerrer, Batia; de Cabo, Rafael; Rechavi, Gideon; Cohen, Haim Y Journal: Journals of gerontology Issue: Volume 73:Number 11(2018:Nov.) Page Start: 1465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Characterizing of functional human coding RNA editing from evolutionary, structural, and dynamic perspectives. Issue 11 (3rd September 2014) Authors: Solomon, Oz; Bazak, Lily; Levanon, Erez Y.; Amariglio, Ninette; Unger, Ron; Rechavi, Gideon; Eyal, Eran Journal: Proteins Issue: Volume 82:Issue 11(2014) Page Start: 3117 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Characterizing T Cells in SCID Patients Presenting with Reactive or Residual T Lymphocytes. (19th November 2012) Authors: Lev, Atar; Simon, Amos J.; Trakhtenbrot, Luba; Goldstein, Itamar; Nagar, Meital; Stepensky, Polina; Rechavi, Gideon; Amariglio, Ninette; Somech, Raz Other Names: Goulielmos George N. Academic Editor. Journal: Clinical & developmental immunology Issue: Volume 2012(2012) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Characterizing T Cells in SCID Patients Presenting with Reactive or Residual T Lymphocytes. (20th November 2012) Authors: Lev, Atar; Simon, Amos J.; Trakhtenbrot, Luba; Goldstein, Itamar; Nagar, Meital; Stepensky, Polina; Rechavi, Gideon; Amariglio, Ninette; Somech, Raz Other Names: Goulielmos George N. Academic Editor. Journal: Clinical & developmental immunology Issue: Volume 2012(2012) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene. Issue 6 (11th April 2020) Authors: Goldberg, Lior; Simon, Amos J.; Rechavi, Gideon; Lev, Atar; Barel, Ortal; Kunik, Vered; Toren, Amos; Schiby, Ginette; Tamary, Hannah; Steinberg‐Shemer, Orna; Somech, Raz Journal: Pediatric blood & cancer Issue: Volume 67:Issue 6(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Congenital Sucrase-isomaltase Deficiency: A Novel Compound Heterozygous Mutation Causing Aberrant Protein Localization. Issue 5 (May 2017) Authors: Haberman, Yael; Di Segni, Ayelet; Loberman-Nachum, Nurit; Barel, Ortal; Kunik, Vered; Eyal, Eran; Kol, Nitzan; Hout-Siloni, Goni; Kochavi, Brigitte; Avivi, Camila; Schvimer, Michael; Rechavi, Gideon; Anikster, Yair; Barshack, Iris; Weiss, Batia Journal: Journal of pediatric gastroenterology and nutrition Issue: Volume 64:Issue 5(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Correlation between 'ACKR1/DARC null' polymorphism and benign neutropenia in Yemenite Jews. (26th March 2015) Authors: Rappoport, Naama; Simon, Amos J.; Lev, Atar; Yacobi, Michal; Kaplinsky, Chaim; Weingarten, Michael; Somech, Raz; Amariglio, Ninette; Rechavi, Gideon Journal: British journal of haematology Issue: Volume 170:Number 6(2015:Sep.) Page Start: 892 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Detection of BCR‐ABL1 mutations in chronic myeloid leukaemia by massive parallel sequencing. (17th December 2012) Authors: Eyal, Eran; Tohami, Tali; Amir, Amnon; Cesarkas, Karen; Jacob‐Hirsch, Jasmine; Volchek, Yuliya; Nagler, Arnon; Rechavi, Gideon; Amariglio, Ninette Journal: British journal of haematology Issue: Volume 160:Number 4(2013:Feb.) Page Start: 477 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗