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Sharon Zeligson

Research Profile

Procedures

Concepts & Ideas

Physiology

Mutation

Living Beings

Devices

Oligonucleotide Array Sequence Analysis

Disorders

46,XX Gonadal Dysgenesis

Chemicals & Drugs

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Publications

TOP 3
Eran Cohen; Oren S Cohen; Kati Frid; Esther Kahana; Iris Lavon; Ephrat Levy Lahad; Shira Perlberg; Sharon Zeligson; Dana Avrahami; Tamar Canello; Joab Chapman; Ruth Gabizon
Snord 3A: a molecular marker and modulator of prion disease progression.
Oded Breuer; Hila Fridman; Ephrat Levy-Lahad; Paul Renbaum; Maha Abdulhadi-Atwan; Sharon Zeligson; David H Zangen
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.
Sarah B Pierce; Cailyn H Spurrell; Sunday M Stray; Sharon Zeligson; Michael S Bereman; Siv Fokstuen; Mary-Claire King; Ming K Lee; Ephrat Levy-Lahad; Michael J MacCoss; Jessica B Mandell; Arno G Motulsky
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.

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All Publications

2013: Eran Cohen; Oren S Cohen; Kati Frid; Esther Kahana; Iris Lavon; Ephrat Levy Lahad; Shira Perlberg; Sharon Zeligson; Dana Avrahami; Tamar Canello; Joab Chapman; Ruth Gabizon
Snord 3A: a molecular marker and modulator of prion disease progression.
PloS one 2013;8(1):e54433.
2012: Oded Breuer; Hila Fridman; Ephrat Levy-Lahad; Paul Renbaum; Maha Abdulhadi-Atwan; Sharon Zeligson; David H Zangen
A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.
European journal of endocrinology / European Federation of Endocrine Societies 2012;167(2):209-16.
2011: Sarah B Pierce; Cailyn H Spurrell; Sunday M Stray; Sharon Zeligson; Michael S Bereman; Siv Fokstuen; Mary-Claire King; Ming K Lee; Ephrat Levy-Lahad; Michael J MacCoss; Jessica B Mandell; Arno G Motulsky
Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria.
Proceedings of the National Academy of Sciences of the United States of America 2011;108(45):18313-7.
2011: Ziva Ben-Neriah; Orly Elpeleg; Michal Inbar-Feigenberg; Rachel Michaelson-Cohen; Michael Nadjari; Avraham Shaag; Sharon Zeligson; Shamir Zenvirt; Ephrat Levy-Lahad
A deleterious founder mutation in the BMPER gene causes diaphanospondylodysostosis (DSD).
American journal of medical genetics. Part A 2011;155A(11):2801-6.
2011: David Zangen; Sharon Zeligson; Shira Perlberg; Paul Renbaum; Maha Abdulhadi-Atwan; Abdulsalam Abu Libdeh; Liran Carmel; Hila Fridman; Ayal Gussow; Moein Kanaan; Yotam Kaufman; Irit Kisslov; Ephrat Levy-Lahad
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.
American journal of human genetics 2011;89(4):572-9.
2011: Ruth Belostotsky; Efrat Ben-Shalom; Choni Rinat; Rachel Becker-Cohen; Sofia Feinstein; Sharon Zeligson; Reeval Segel; Orly Elpeleg; Suheir Nassar; Yaacov Frishberg
Mutations in the mitochondrial seryl-tRNA synthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome.
American journal of human genetics 2011;88(2):193-200.
2010: Libi Hertzberg; Elena Vendramini; Ithamar Ganmore; Gianni Cazzaniga; Maike Schmitz; Jane Chalker; Ruth Shiloh; Ilaria Iacobucci; Chen Shochat; Sharon Zeligson; Gunnar Cario; Martin Stanulla; Sabine Strehl; Lisa J Russell; Christine J Harrison; Beat Bornhauser; Akinori Yoda; Gideon Rechavi; Dani Bercovich; Arndt Borkhardt; Helena Kempski; Geertruy Te Kronnie; Jean-Pierre Bourquin; Eytan Domany; Shai Izraeli
Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group.
Blood 2010;115(5):1006-17.
2007: Tamar Fisher; Gil Galanti; Gad Lavie; Jasmine Jacob-Hirsch; Iris Kventsel; Sharon Zeligson; Robert Winkler; Amos J Simon; Ninette Amariglio; Gideon Rechavi; Amos Toren
Mechanisms operative in the antitumor activity of temozolomide in glioblastoma multiforme.
Cancer journal (Sudbury, Mass.) 2007;13(5):335-44.
2007: Itzhak Binderman; Hila Bahar; Jasmine Jacob-Hirsch; Sharon Zeligson; Ninette Amariglio; Gideon Rechavi; Sheryl Shoham; Avinoam Yaffe
P2X4 is up-regulated in gingival fibroblasts after periodontal surgery.
Journal of dental research 2007;86(2):181-5.
2007: Natalie Dror; Michal Alter-Koltunoff; Aviva Azriel; Ninette Amariglio; Jasmine Jacob-Hirsch; Sharon Zeligson; Avigail Morgenstern; Tomohiko Tamura; Hansjörg Hauser; Gideon Rechavi; Keiko Ozato; Ben-Zion Levi
Identification of IRF-8 and IRF-1 target genes in activated macrophages.
Molecular immunology 2007;44(4):338-46.
2006: Dan Piestun; Bose S Kochupurakkal; Jasmine Jacob-Hirsch; Sharon Zeligson; Mark Koudritsky; Eytan Domany; Ninette Amariglio; Gideon Rechavi; David Givol
Nanog transforms NIH3T3 cells and targets cell-type restricted genes.
Biochemical and biophysical research communications 2006;343(1):279-85.
2005: Leonid Brodsky; Jasmine Jacob-Hirsch; Aaron Avivi; Luba Trakhtenbrot; Sharon Zeligson; Ninette Amariglio; Arnon Paz; Abraham Korol; M Band; Gideon Rechavi; Eviatar Nevo
Evolutionary regulation of the blind subterranean mole rat, Spalax, revealed by genome-wide gene expression.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(47):17047-52.
2005: Amos Toren; Bella Bielorai; Jasmine Jacob-Hirsch; Tamar Fisher; Doron Kreiser; Orit Moran; Sharon Zeligson; David Givol; Assif Yitzhaky; Joseph Itskovitz-Eldor; Iris Kventsel; Eti Rosenthal; Ninette Amariglio; Gideon Rechavi
CD133-positive hematopoietic stem cell "stemness" genes contain many genes mutated or abnormally expressed in leukemia.
Stem cells (Dayton, Ohio) 2005;23(8):1142-53.
2004: Edna Grünblatt; Silvia Mandel; Jasmine Jacob-Hirsch; Sharon Zeligson; N Amariglo; G Rechavi; J Li; Rivka Ravid; Wolfgang Roggendorf; Peter Riederer; Moussa B H Youdim
Gene expression profiling of parkinsonian substantia nigra pars compacta; alterations in ubiquitin-proteasome, heat shock protein, iron and oxidative stress regulated proteins, cell adhesion/cellular matrix and vesicle trafficking genes.
Journal of neural transmission (Vienna, Austria : 1996) 2004;111(12):1543-73.