Pikarsky E - Search Results

1

Oct-3/4 is a dose-dependent oncogenic fate determinant.

Gidekel S, Pizov G, Bergman Y, Pikarsky E. Gidekel S, et al. Among authors: pikarsky e. Cancer Cell. 2003 Nov;4(5):361-70. doi: 10.1016/s1535-6108(03)00270-8. Cancer Cell. 2003. PMID: 14667503 Free article.

2

Extinction of Oct-3/4 gene expression in embryonal carcinoma x fibroblast somatic cell hybrids is accompanied by changes in the methylation status, chromatin structure, and transcriptional activity of the Oct-3/4 upstream region.

Ben-Shushan E, Pikarsky E, Klar A, Bergman Y. Ben-Shushan E, et al. Among authors: pikarsky e. Mol Cell Biol. 1993 Feb;13(2):891-901. doi: 10.1128/mcb.13.2.891-901.1993. Mol Cell Biol. 1993. PMID: 7678695 Free PMC article.

3

A dynamic balance between ARP-1/COUP-TFII, EAR-3/COUP-TFI, and retinoic acid receptor:retinoid X receptor heterodimers regulates Oct-3/4 expression in embryonal carcinoma cells.

Ben-Shushan E, Sharir H, Pikarsky E, Bergman Y. Ben-Shushan E, et al. Among authors: pikarsky e. Mol Cell Biol. 1995 Feb;15(2):1034-48. doi: 10.1128/MCB.15.2.1034. Mol Cell Biol. 1995. PMID: 7823919 Free PMC article.

4

Retinoic acid represses Oct-3/4 gene expression through several retinoic acid-responsive elements located in the promoter-enhancer region.

Pikarsky E, Sharir H, Ben-Shushan E, Bergman Y. Pikarsky E, et al. Mol Cell Biol. 1994 Feb;14(2):1026-38. doi: 10.1128/mcb.14.2.1026-1038.1994. Mol Cell Biol. 1994. PMID: 8289783 Free PMC article.

5

Pregnancy restores the regenerative capacity of the aged liver via activation of an mTORC1-controlled hyperplasia/hypertrophy switch.

Gielchinsky Y, Laufer N, Weitman E, Abramovitch R, Granot Z, Bergman Y, Pikarsky E. Gielchinsky Y, et al. Among authors: pikarsky e. Genes Dev. 2010 Mar 15;24(6):543-8. doi: 10.1101/gad.563110. Genes Dev. 2010. PMID: 20231314 Free PMC article.

6

The rejuvenating effect of pregnancy on muscle regeneration.

Falick Michaeli T, Laufer N, Sagiv JY, Dreazen A, Granot Z, Pikarsky E, Bergman Y, Gielchinsky Y. Falick Michaeli T, et al. Among authors: pikarsky e. Aging Cell. 2015 Aug;14(4):698-700. doi: 10.1111/acel.12286. Epub 2015 Mar 13. Aging Cell. 2015. PMID: 25773509 Free PMC article.

7

Chronic inflammation induces a novel epigenetic program that is conserved in intestinal adenomas and in colorectal cancer.

Abu-Remaileh M, Bender S, Raddatz G, Ansari I, Cohen D, Gutekunst J, Musch T, Linhart H, Breiling A, Pikarsky E, Bergman Y, Lyko F. Abu-Remaileh M, et al. Among authors: pikarsky e. Cancer Res. 2015 May 15;75(10):2120-30. doi: 10.1158/0008-5472.CAN-14-3295. Epub 2015 Mar 25. Cancer Res. 2015. PMID: 25808873

8

The microbiota programs DNA methylation to control intestinal homeostasis and inflammation.

Ansari I, Raddatz G, Gutekunst J, Ridnik M, Cohen D, Abu-Remaileh M, Tuganbaev T, Shapiro H, Pikarsky E, Elinav E, Lyko F, Bergman Y. Ansari I, et al. Among authors: pikarsky e. Nat Microbiol. 2020 Apr;5(4):610-619. doi: 10.1038/s41564-019-0659-3. Epub 2020 Feb 3. Nat Microbiol. 2020. PMID: 32015497

9

The NF-ĸB p50 subunit generated by KPC1-mediated ubiquitination and limited proteasomal processing, suppresses tumor growth.

Kravtsova-Ivantsiv Y, Goldhirsh G, Tomuleasa C, Pikarsky E, Ciechanover A. Kravtsova-Ivantsiv Y, et al. Among authors: pikarsky e. Cancer Cell Int. 2023 Apr 13;23(1):67. doi: 10.1186/s12935-023-02919-5. Cancer Cell Int. 2023. PMID: 37055826 Free PMC article. Review.

10

TET2 and TET3 loss disrupts small intestine differentiation and homeostasis.

Ansari I, Solé-Boldo L, Ridnik M, Gutekunst J, Gilliam O, Korshko M, Liwinski T, Jickeli B, Weinberg-Corem N, Shoshkes-Carmel M, Pikarsky E, Elinav E, Lyko F, Bergman Y. Ansari I, et al. Among authors: pikarsky e. Nat Commun. 2023 Jul 6;14(1):4005. doi: 10.1038/s41467-023-39512-3. Nat Commun. 2023. PMID: 37414790 Free PMC article.

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