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Inhibition of oxygen-induced retinopathy in RTP801-deficient mice.
Brafman A, Mett I, Shafir M, Gottlieb H, Damari G, Gozlan-Kelner S, Vishnevskia-Dai V, Skaliter R, Einat P, Faerman A, Feinstein E, Shoshani T.
Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3796-805.
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The role of organ vascularization and lipoplex-serum initial contact in intravenous murine lipofection.
Simberg D, Weisman S, Talmon Y, Faerman A, Shoshani T, Barenholz Y.
J Biol Chem. 2003 Oct 10;278(41):39858-65. Epub 2003 Jul 17.
Identification of a novel stress-responsive gene Hi95 involved in regulation of cell viability.
Budanov AV, Shoshani T, Faerman A, Zelin E, Kamer I, Kalinski H, Gorodin S, Fishman A, Chajut A, Einat P, Skaliter R, Gudkov AV, Chumakov PM, Feinstein E.
Oncogene. 2002 Sep 5;21(39):6017-31.
Identification of a novel hypoxia-inducible factor 1-responsive gene, RTP801, involved in apoptosis.
Shoshani T, Faerman A, Mett I, Zelin E, Tenne T, Gorodin S, Moshel Y, Elbaz S, Budanov A, Chajut A, Kalinski H, Kamer I, Rozen A, Mor O, Keshet E, Leshkowitz D, Einat P, Skaliter R, Feinstein E.
Mol Cell Biol. 2002 Apr;22(7):2283-93.
The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation.
Chiba-Falek O, Kerem E, Shoshani T, Aviram M, Augarten A, Bentur L, Tal A, Tullis E, Rahat A, Kerem B.
Genomics. 1998 Nov 1;53(3):276-83.
Analysis of random recombination between human MDR1 and mouse mdr1a cDNA in a pHaMDR-dihydrofolate reductase bicistronic expression system.
Shoshani T, Zhang S, Dey S, Pastan I, Gottesman MM.
Mol Pharmacol. 1998 Oct;54(4):623-30.
pHaMDR-DHFR bicistronic expression system for mutational analysis of P-glycoprotein.
Zhang S, Sugimoto Y, Shoshani T, Pastan I, Gottesman MM.
Methods Enzymol. 1998;292:474-80. No abstract available.
Highly variable incidence of cystic fibrosis and different mutation distribution among different Jewish ethnic groups in Israel.
Kerem E, Kalman YM, Yahav Y, Shoshani T, Abeliovich D, Szeinberg A, Rivlin J, Blau H, Tal A, Ben-Tur L, et al.
Hum Genet. 1995 Aug;96(2):193-7.
Two novel mutations in the CFTR gene: W1089X in exon 17B and 4010delTATT in exon 21.
Shoshani T, Augarten A, Yahav J, Gazit E, Kerem B.
Hum Mol Genet. 1994 Apr;3(4):657-8. No abstract available.
Similar levels of mRNA from the W1282X and the delta F508 cystic fibrosis alleles, in nasal epithelial cells.
Shoshani T, Kerem E, Szeinberg A, Augarten A, Yahav Y, Cohen D, Rivlin J, Tal A, Kerem B.
J Clin Invest. 1994 Apr;93(4):1502-7.
Extended haplotype analysis of cystic fibrosis mutations and its implications for the selective advantage hypothesis.
Sereth H, Shoshani T, Bashan N, Kerem BS.
Hum Genet. 1993 Oct 1;92(3):289-95.
A new mutation in the CFTR gene, composed of two adjacent DNA alterations, is a common cause of cystic fibrosis among Georgian Jews.
Shoshani T, Berkun Y, Yahav Y, Augarten A, Bashan N, Rivlin Y, Gazit E, Sereth H, Kerem E, Kerem BS.
Genomics. 1993 Jan;15(1):236-7. No abstract available.
Cystic fibrosis manifested as undescended testis and absence of vas deferens.
Goshen R, Kerem E, Shoshani T, Kerem BS, Feigin E, Zamir O, Yahav Y.
Pediatrics. 1992 Dec;90(6):982-3. No abstract available.
Association of a nonsense mutation (W1282X), the most common mutation in the Ashkenazi Jewish cystic fibrosis patients in Israel, with presentation of severe disease.
Shoshani T, Augarten A, Gazit E, Bashan N, Yahav Y, Rivlin Y, Tal A, Seret H, Yaar L, Kerem E, et al.
Am J Hum Genet. 1992 Jan;50(1):222-8.
Cis-regulatory elements that confer differential expression upon the rat gene encoding phosphoenolpyruvate carboxykinase in kidney and liver.
Shoshani T, Benvenisty N, Trus M, Reshef L.
Gene. 1991 May 30;101(2):279-83.
trans activation of rat phosphoenolpyruvate carboxykinase (GTP) gene expression by micro-coinjection of rat liver mRNA in Xenopus laevis oocytes.
Benvenisty N, Shoshani T, Farkash Y, Soreq H, Reshef L.
Mol Cell Biol. 1989 Nov;9(11):5244-7.
Turnover of purine nucleotides in rabbit erythrocytes. II. Studies in vitro.
Hershko A, Razin A, Shoshani T, Mager J.
Biochim Biophys Acta. 1967 Nov 21;149(1):59-73. No abstract available.
Turnover of purine nucleotides in rabbit erythrocytes. I. Studies in vivo.
Mager J, Hershko A, Zeitlin-Beck R, Shoshani T, Razin A.
Biochim Biophys Acta. 1967 Nov 21;149(1):50-8. No abstract available.
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