Beeri R - Search Results

1

Transcriptional regulation of the murine Presenilin-2 gene reveals similarities and differences to its human orthologue.

Ounallah-Saad H, Beeri R, Goshen I, Yirmiya R, Renbaum P, Levy-Lahad E. Ounallah-Saad H, et al. Among authors: beeri r. Gene. 2009 Oct 15;446(2):81-9. doi: 10.1016/j.gene.2009.06.015. Epub 2009 Jun 30. Gene. 2009. PMID: 19573580

2

Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells.

Renbaum P, Beeri R, Gabai E, Amiel M, Gal M, Ehrengruber MU, Levy-Lahad E. Renbaum P, et al. Among authors: beeri r. Gene. 2003 Oct 30;318:113-24. doi: 10.1016/s0378-1119(03)00766-2. Gene. 2003. PMID: 14585504

3

Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin.

Wolf I, Laitman Y, Rubinek T, Abramovitz L, Novikov I, Beeri R, Kuro-O M, Koeffler HP, Catane R, Freedman LS, Levy-Lahad E, Karlan BY, Friedman E, Kaufman B. Wolf I, et al. Among authors: beeri r. Oncogene. 2010 Jan 7;29(1):26-33. doi: 10.1038/onc.2009.301. Epub 2009 Oct 5. Oncogene. 2010. PMID: 19802015

4

Preimplantation genetic diagnosis (PGD) for a treatable disorder: Gaucher disease type 1 as a model.

Altarescu G, Renbaum P, Eldar-Geva T, Varshower I, Brooks B, Beeri R, Margalioth EJ, Levy-Lahad E, Elstein D, Zimran A. Altarescu G, et al. Among authors: beeri r. Blood Cells Mol Dis. 2011 Jan 15;46(1):15-8. doi: 10.1016/j.bcmd.2010.04.008. Epub 2010 Jun 1. Blood Cells Mol Dis. 2011. PMID: 20684885

5

The CYP17A1 -34T > C polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Kaufman B, Laitman Y, Ziv E, Hamann U, Torres D, Lahad EL, Beeri R, Renbaum P, Jakubowska A, Lubinski J, Huzarski T, Tołoczko-Grabarek A, Jaworska K, Durda K, Sprudle AB, Chenevix-Trench G, Simard J, Easton DF, Antonis A, Szabo C, Friedman E. Kaufman B, et al. Among authors: beeri r. Breast Cancer Res Treat. 2011 Apr;126(2):521-7. doi: 10.1007/s10549-010-1123-5. Epub 2010 Aug 27. Breast Cancer Res Treat. 2011. PMID: 20798986

6

Female sex bias in human embryonic stem cell lines.

Ben-Yosef D, Amit A, Malcov M, Frumkin T, Ben-Yehudah A, Eldar I, Mey-Raz N, Azem F, Altarescu G, Renbaum P, Beeri R, Varshaver I, Eldar-Geva T, Epsztejn-Litman S, Levy-Lahad E, Eiges R. Ben-Yosef D, et al. Among authors: beeri r. Stem Cells Dev. 2012 Feb 10;21(3):363-72. doi: 10.1089/scd.2011.0102. Epub 2011 Jun 24. Stem Cells Dev. 2012. PMID: 21585244 Free PMC article.

7

Preimplantation genetic diagnosis (PGD)--prevention of the birth of children affected with endocrine diseases.

Altarescu G, Barenholz O, Renbaum P, Beeri R, Levy-Lahad E, Margalioth EJ, Brooks B, Varshaver I, Eldar-Geva T. Altarescu G, et al. Among authors: beeri r. J Pediatr Endocrinol Metab. 2011;24(7-8):543-8. doi: 10.1515/jpem.2011.262. J Pediatr Endocrinol Metab. 2011. PMID: 21932595

8

X-inactivation in Fabry disease.

Elstein D, Schachamorov E, Beeri R, Altarescu G. Elstein D, et al. Among authors: beeri r. Gene. 2012 Sep 1;505(2):266-8. doi: 10.1016/j.gene.2012.06.013. Epub 2012 Jun 16. Gene. 2012. PMID: 22710134

9

PGD for germline mosaicism.

Altarescu G, Beeri R, Eldar-Geva T, Varshaver I, Margalioth EJ, Levy-Lahad E, Renbaum P. Altarescu G, et al. Among authors: beeri r. Reprod Biomed Online. 2012 Oct;25(4):390-5. doi: 10.1016/j.rbmo.2012.07.003. Epub 2012 Jul 20. Reprod Biomed Online. 2012. PMID: 22884613

10

Prevention of lysosomal storage diseases and derivation of mutant stem cell lines by preimplantation genetic diagnosis.

Altarescu G, Beeri R, Eiges R, Epsztejn-Litman S, Eldar-Geva T, Elstein D, Zimran A, Margalioth EJ, Levy-Lahad E, Renbaum P. Altarescu G, et al. Among authors: beeri r. Mol Biol Int. 2012;2012:797342. doi: 10.1155/2012/797342. Epub 2012 Dec 26. Mol Biol Int. 2012. PMID: 23320174 Free PMC article.

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