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Items: 1 to 20 of 118

1.

Increased TERC gene copy number in amniocytes from fetuses with trisomy 18 or a sex chromosome aneuploidy.

Biron-Shental T, Kitay-Cohen Y, Tene T, Sharony R, Amiel A.

Gene. 2012 Sep 10;506(1):46-9. doi: 10.1016/j.gene.2012.06.072. Epub 2012 Jul 5.

PMID:
22772461
2.

Increased TERC gene copy number and cells in senescence in primary sclerosing cholangitis compared to colitis and control patients.

Laish I, Katz H, Sulayev Y, Liberman M, Naftali T, Benjaminov F, Stein A, Kitay-Cohen Y, Biron-Shental T, Konikoff F, Amiel A.

Gene. 2013 Oct 25;529(2):245-9. doi: 10.1016/j.gene.2013.07.098. Epub 2013 Aug 8.

PMID:
23933276
3.

Telomeres in trisomy 21 amniocytes.

Sukenik-Halevy R, Biron-Shental T, Sharony R, Fejgin MD, Amiel A.

Cytogenet Genome Res. 2011;135(1):12-8. doi: 10.1159/000329714. Epub 2011 Jul 6.

PMID:
21734364
4.

Genomic integration of oncogenic HPV and gain of the human telomerase gene TERC at 3q26 are strongly associated events in the progression of uterine cervical dysplasia to invasive cancer.

Hopman AH, Theelen W, Hommelberg PP, Kamps MA, Herrington CS, Morrison LE, Speel EJ, Smedts F, Ramaekers FC.

J Pathol. 2006 Dec;210(4):412-9.

PMID:
17054308
5.

[Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization].

Xiao HM, Tan YQ, Li LY, Lu GX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):608-10. Chinese.

PMID:
15583993
6.

Fluorescence in situ hybridization in uncultured amniocytes for detection of aneuploidy in 4210 prenatal cases.

Jia CW, Wang SY, Ma YM, Lan YL, Si YM, Yu L, Zhou LY.

Chin Med J (Engl). 2011 Apr;124(8):1164-8.

PMID:
21542989
7.
8.

Evaluation of X, Y, 18, and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization.

Cacheux V, Tachdjian G, Druart L, Oury JF, Sérero S, Blot P, Nessmann C.

Prenat Diagn. 1994 Feb;14(2):79-86.

PMID:
8183853
9.

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.

Prenat Diagn. 2002 Jan;22(1):29-33.

PMID:
11810646
10.

Amniocytes from aneuploidy embryos have enhanced random aneuploidy and signs of senescence - can these findings be related to medical problems?

Biron-Shental T, Liberman M, Sharvit M, Sukenik-Halevy R, Amiel A.

Gene. 2015 May 15;562(2):232-5. doi: 10.1016/j.gene.2015.02.075. Epub 2015 Feb 28.

PMID:
25735571
11.

Role of FISH on uncultured amniocytes for the diagnosis of aneuploidies in the presence of fetal anomalies.

Locatelli A, Mariani S, Ciriello E, Dalprà L, Villa N, Sala E, Vergani P.

Fetal Diagn Ther. 2005 Jan-Feb;20(1):1-4.

PMID:
15608449
12.

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA).

Hochstenbach R, Meijer J, van de Brug J, Vossebeld-Hoff I, Jansen R, van der Luijt RB, Sinke RJ, Page-Christiaens GC, Ploos van Amstel JK, de Pater JM.

Prenat Diagn. 2005 Nov;25(11):1032-9.

PMID:
16231311
13.
14.

TERC telomerase subunit gene copy number in placentas from pregnancies complicated with intrauterine growth restriction.

Biron-Shental T, Kidron D, Sukenik-Halevy R, Goldberg-Bittman L, Sharony R, Fejgin MD, Amiel A.

Early Hum Dev. 2011 Feb;87(2):73-5. doi: 10.1016/j.earlhumdev.2010.08.024. Epub 2010 Dec 17.

PMID:
21168289
15.

[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].

Ulmer R, Pfeiffer RA, Kollert A, Beinder E.

Z Geburtshilfe Neonatol. 2000 Jan-Feb;204(1):1-7. German.

PMID:
10721179
16.

TERC telomerase subunit gene copy number in different disease stages of non-hodgkin lymphoma and in hepatitis C.

Goldberg-Bittman L, Kitay-Cohen Y, Fejgin MD, Hadary R, Quitt M, Amiel A.

Cancer Invest. 2010 Feb;28(2):181-5. doi: 10.3109/07357900903095748.

PMID:
20121548
17.

Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer.

Munné S, Sultan KM, Weier HU, Grifo JA, Cohen J, Rosenwaks Z.

Am J Obstet Gynecol. 1995 Apr;172(4 Pt 1):1191-9; discussion 1199-201.

PMID:
7726256
18.

A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis.

Eiben B, Trawicki W, Hammans W, Goebel R, Epplen JT.

Prenat Diagn. 1998 Sep;18(9):901-6.

PMID:
9793971
19.

Increased copy number of the TERT and TERC telomerase subunit genes in cancer cells.

Cao Y, Bryan TM, Reddel RR.

Cancer Sci. 2008 Jun;99(6):1092-9. doi: 10.1111/j.1349-7006.2008.00815.x. Review.

20.

Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimens.

Ward BE, Gersen SL, Carelli MP, McGuire NM, Dackowski WR, Weinstein M, Sandlin C, Warren R, Klinger KW.

Am J Hum Genet. 1993 May;52(5):854-65.

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