Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Ayala Aviram-Goldring"'
Autor:
Shlomit, Rienstein, Ayala, Aviram-Goldring *, Michal, Daniely, Ninett, Amerigleo, Frida, Simoni, Boleslaw, Goldman, Gad, Barkai, Gideon, Rechavi, Shlomi, Constantini
Publikováno v:
In Cancer Genetics and Cytogenetics 2000 121(1):67-72
Autor:
Masha Brengauz, Boleslav Goldman, Shlomit Rienstein, Elon Pras, Jacob Levron, Hagith Yonath, Jehoshua Dor, Michal Dekel, Jana Shamash, Haike Wolf-Reznik, Ayala Aviram-Goldring, Talia Litmanovitch
Publikováno v:
Journal of Assisted Reproduction and Genetics. 28:77-83
Preimplantation genetic diagnosis using fluorescence in-situ hybridization (PGD-FISH) is currently the most common reproductive solution for translocation carriers. However, this technique usually does not differentiate between embryos carrying the b
Autor:
Shai Izraeli, Eitan Friedman, H. Frimer, M. Perlman, Pnina Yaron, W. Liao, Zohar Yakhini, Doron Lipson, David Simansky, Shlomit Rienstein, Amir Ben-Dor, E. Dehan, Meir Krupsky, Ayala Aviram-Goldring, Naftali Kaminski, G. Rechavi, M. Bittner
Publikováno v:
Lung Cancer. 56:175-184
Alterations in genomic content and changes in gene expression levels are central characteristics of tumors and pivotal to the tumorigenic process. We analyzed 23 non-small cell lung cancer (NSCLC) tumors by array comparative genomic hybridization (ar
Autor:
Keren Mammon-Daviko, Daphna Gordon, Gad Barkai, Michal J. Simchen, Nurit Rauchbach, Esther Guetta, Ayala Aviram-Goldring
Publikováno v:
Stem Cells and Development. 13:93-99
The invasive procedures amniocentesis and chorionic villus sampling (CVS) are routinely applied in pregnancies at risk for fetal abnormalities and the results obtained are the gold standard for prenatal diagnosis. Because these methods of fetal cell
Autor:
Shlomit Rienstein, Boleslaw Goldman, Gilad Ben-Baruch, Ayala Aviram-Goldring, Ofir Israeli, Eitan Friedman, Walter H. Gotlieb
Publikováno v:
Gynecologic Oncology. 90:629-636
Objective Our purpose was to get an overview of the genetic events leading to the development of familial and sporadic ovarian tumors and to identify chromosomal regions that may contain genes important in tumor progression. Methods The comparative g
Autor:
Dalit Modan-Moses, Shlomit Rienstein, Ayala Aviram-Goldring, Talia Litmanovitch, Boleslaw Goldman, Joseph Meyerovitch
Publikováno v:
American Journal of Medical Genetics. :300-303
Abnormal recombination between the X and Y chromosomes during meiosis, occurring outside the pseudoautosomal region, can result in translocation of the SRY gene from the Y to the X chromosome, and consequently in abnormal sexual differentiation, such
Autor:
Shlomit Rienstein, David Loven, Ayala Aviram-Goldring, Zvi H. Rappaport, Zvi Ram, Ofir Israeli, Eitan Friedman, Boleslaw Goldman, Gad Barkai
Publikováno v:
Cancer Genetics and Cytogenetics. 131:135-140
Ionizing irradiation to the skull is a known risk factor for meningioma development. To gain insight into the molecular mechanisms that underlie radiation-associated meningioma (RAM), we characterized the somatic genetic alterations in 16 RAMs by usi
Publikováno v:
Fertility and Sterility. 76:479-484
To investigate the potential paternal contribution to the risk of fetal chromosomal anomalies after intracytoplasmic sperm injection (ICSI).Spermatozoa isolated from testicular tissue and ejaculated specimens of consenting patients undergoing testicu
Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis
Autor:
Tamar Paperna, Ruth Gershoni-Baruch, Monica Epelman, Tatiana Smolkin, Shlomit Rienstein, Imad R. Makhoul, Polo Sujov, Ayala Aviram-Goldring
Publikováno v:
American Journal of Medical Genetics. 99:54-58
The clinical spectrum of caudal dysplasia sequence (CDS) is noted for its diversity. The origin of CDS remains unknown, though poorly controlled gestational diabetes has been implicated in some cases. Here we describe the case of a newborn with CDS a
Publikováno v:
Fertility and Sterility. 74:925-929
Objective: The aim of the study was to determine the potential risk for fetal chromosomal anomalies in non-mosaic Klinefelter's syndrome patients undergoing IVF and intracytoplasmic sperm injection. Design: Individually collected spermatozoa were iso