Ravia Y - Search Results

1

Novel DNA sequences at chromosome 10q26 are amplified in human gastric carcinoma cell lines: molecular cloning by competitive DNA reassociation.

Mor O, Messinger Y, Rotman G, Bar-Am I, Ravia Y, Eddy RL, Shows TB, Park JG, Gazdar AF, Shiloh Y. Mor O, et al. Among authors: ravia y. Nucleic Acids Res. 1991 Jan 11;19(1):117-23. doi: 10.1093/nar/19.1.117. Nucleic Acids Res. 1991. PMID: 2011492 Free PMC article.

2

DNA amplification in human gastric carcinomas.

Mor O, Ranzani GN, Ravia Y, Rotman G, Gutman M, Manor A, Amadori D, Houldsworth J, Hollstein M, Schwab M, Shiloh Y. Mor O, et al. Among authors: ravia y. Cancer Genet Cytogenet. 1993 Feb;65(2):111-4. doi: 10.1016/0165-4608(93)90217-a. Cancer Genet Cytogenet. 1993. PMID: 8453595

3

Cellular and molecular characteristics of an immortalized ataxia-telangiectasia (group AB) cell line.

Ziv Y, Jaspers NG, Etkin S, Danieli T, Trakhtenbrot L, Amiel A, Ravia Y, Shiloh Y. Ziv Y, et al. Among authors: ravia y. Cancer Res. 1989 May 1;49(9):2495-501. Cancer Res. 1989. PMID: 2539904

4

Amplification of c-myc and c-erbB-2 proto-oncogenes in human solid tumors: frequency and clinical significance.

Gutman M, Ravia Y, Assaf D, Yamamoto T, Rozin R, Shiloh Y. Gutman M, et al. Among authors: ravia y. Int J Cancer. 1989 Nov 15;44(5):802-5. doi: 10.1002/ijc.2910440509. Int J Cancer. 1989. PMID: 2573579

5

Modification in the inherent mode of allelic replication in lymphocytes of patients suffering from renal cell carcinoma: a novel genetic alteration associated with malignancy.

Dotan ZA, Dotan A, Litmanovitch T, Ravia Y, Oniashvili N, Leibovitch I, Ramon J, Avivi L. Dotan ZA, et al. Among authors: ravia y. Genes Chromosomes Cancer. 2000 Mar;27(3):270-7. Genes Chromosomes Cancer. 2000. PMID: 10679916

6

Increased spindle resistance to antimicrotubule agents in cells prone to chromosomal nondisjunction.

Avivi L, Dotan A, Ravia Y, Amiel A, Shacham H, Neumann Y. Avivi L, et al. Among authors: ravia y. Hum Genet. 1989 Sep;83(2):165-70. doi: 10.1007/BF00286711. Hum Genet. 1989. PMID: 2777256

7

High degree of satellite association and decreased nucleolar organizer activity in cystic fibrosis subjects.

Ravia Y, Lieberman I, Ravé A, Kremer M, Avivi L. Ravia Y, et al. Am J Med Genet. 1987 Nov;28(3):593-605. doi: 10.1002/ajmg.1320280307. Am J Med Genet. 1987. PMID: 3425629

8

Differences between cystic fibrosis and normal cells in the degree of satellite association.

Ravia Y, Avivi L, Goldman B. Ravia Y, et al. Hum Genet. 1985;71(4):294-300. doi: 10.1007/BF00388454. Hum Genet. 1985. PMID: 4077046

9

X-linked recessive primary retinal dysplasia is linked to the Norrie disease locus.

Ravia Y, Braier-Goldstein O, Bat-Miriam KM, Erlich S, Barkai G, Goldman B. Ravia Y, et al. Hum Mol Genet. 1993 Aug;2(8):1295-7. doi: 10.1093/hmg/2.8.1295. Hum Mol Genet. 1993. PMID: 8401512

10

No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome.

Pesso R, Barkai G, Ravia Y, Gak E, Frydman M, Goldman B, Friedman E. Pesso R, et al. Among authors: ravia y. Hum Genet. 1997 Dec;101(2):186-9. doi: 10.1007/s004390050611. Hum Genet. 1997. PMID: 9402966

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