Friedman E - Search Results

1

Chromosomal aberrations and gene expression profiles in non-small cell lung cancer.

Dehan E, Ben-Dor A, Liao W, Lipson D, Frimer H, Rienstein S, Simansky D, Krupsky M, Yaron P, Friedman E, Rechavi G, Perlman M, Aviram-Goldring A, Izraeli S, Bittner M, Yakhini Z, Kaminski N. Dehan E, et al. Among authors: friedman e. Lung Cancer. 2007 May;56(2):175-84. doi: 10.1016/j.lungcan.2006.12.010. Epub 2007 Jan 25. Lung Cancer. 2007. PMID: 17258348

2

Genomic analyses of primary and metastatic serous epithelial ovarian cancer.

Israeli O, Gotlieb WH, Friedman E, Korach J, Friedman E, Goldman B, Zeltzer A, Ben-Baruch G, Rienstein S, Aviram-Goldring A. Israeli O, et al. Among authors: friedman e. Cancer Genet Cytogenet. 2004 Oct 1;154(1):16-21. doi: 10.1016/j.cancergencyto.2004.02.006. Cancer Genet Cytogenet. 2004. PMID: 15381367

3

Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas.

Rienstein S, Loven D, Israeli O, Ram Z, Rappaport ZH, Barkai G, Goldman B, Aviram-Goldring A, Friedman E. Rienstein S, et al. Among authors: friedman e. Cancer Genet Cytogenet. 2001 Dec;131(2):135-40. doi: 10.1016/s0165-4608(01)00506-4. Cancer Genet Cytogenet. 2001. PMID: 11750053

4

Carcinoid tumors frequently display genetic abnormalities involving chromosome 11.

Jakobovitz O, Nass D, DeMarco L, Barbosa AJ, Simoni FB, Rechavi G, Friedman E. Jakobovitz O, et al. Among authors: friedman e. J Clin Endocrinol Metab. 1996 Sep;81(9):3164-7. doi: 10.1210/jcem.81.9.8784062. J Clin Endocrinol Metab. 1996. PMID: 8784062

5

Analysis of microsatellite repeats in pediatric brain tumors.

Amariglio N, Friedman E, Mor O, Stiebel H, Phelan C, Collins P, Nordenskjold M, Brok-Simoni F, Rechavi G. Amariglio N, et al. Among authors: friedman e. Cancer Genet Cytogenet. 1995 Oct 1;84(1):56-9. doi: 10.1016/0165-4608(95)00085-2. Cancer Genet Cytogenet. 1995. PMID: 7497444

6

An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews.

Theodor L, Bar-Sade R, Kruglikova A, Ben-Baruch G, Risel S, Shiri-Sverdlov R, Hirsh Yechezkel G, Modan B, Papa MZ, Rechavi G, Friedman E. Theodor L, et al. Among authors: friedman e. Br J Cancer. 1998 Jun;77(11):1880-3. doi: 10.1038/bjc.1998.313. Br J Cancer. 1998. PMID: 9667663 Free PMC article.

7

Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: possible role in risk modification for cancer development.

Koren-Michowitz M, Friedman E, Gershoni-Baruch R, Brok-Simoni F, Patael Y, Rechavi G, Amariglio N. Koren-Michowitz M, et al. Among authors: friedman e. Am J Hematol. 2005 Mar;78(3):203-6. doi: 10.1002/ajh.20310. Am J Hematol. 2005. PMID: 15726604 Free article.

8

Ubiquitous expression of a cloned murine thymopoietin cDNA.

Theodor L, Shoham J, Berger R, Gokkel E, Trachtenbrot L, Simon AJ, Brok-Simon F, Nir U, Ilan E, Zevin-Sonkin D, Friedman E, Rechavi G. Theodor L, et al. Among authors: friedman e. Acta Haematol. 1997;97(3):153-63. doi: 10.1159/000203673. Acta Haematol. 1997. PMID: 9066710

9

A germline mutation in the von Hippel-Lindau disease gene (L178Q) detected by denaturing gradient gel electrophoresis in a large Jewish-Yemenite family.

Jakobovitz-Picard O, Olchovsky D, Nativ O, Resnick MB, Rechavi G, Karasik A, Friedman E. Jakobovitz-Picard O, et al. Among authors: friedman e. Hum Mutat. 1999 Nov;14(5):448. doi: 10.1002/(SICI)1098-1004(199911)14:5<448::AID-HUMU16>3.0.CO;2-N. Hum Mutat. 1999. PMID: 10533077 No abstract available.

10

Mutation analysis of the MEN1 gene in Israeli patients with MEN1 and familial isolated hyperprolactinemia.

Jakobovitz-Picard O, Olchovsky D, Berezin M, Ghodsizade A, Zahavi Z, Karasik A, Rechavi G, Friedman E. Jakobovitz-Picard O, et al. Among authors: friedman e. Hum Mutat. 2000 Sep;16(3):269. doi: 10.1002/1098-1004(200009)16:3<269::AID-HUMU11>3.0.CO;2-2. Hum Mutat. 2000. PMID: 10980535

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