Clinical Chemistry Link to Randox Laboratories Web Site
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 47: 1577-1578, 2001;
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (7)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hahn, S.
Right arrow Articles by Holzgreve, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hahn, S.
Right arrow Articles by Holzgreve, W.
Related Collections
Right arrow Molecular Diagnostics and Genetics
(Clinical Chemistry. 2001;47:1577-1578.)
© 2001 American Association for Clinical Chemistry, Inc.


Editorial

Quantification of Circulating DNA: In the Preparation Lies the Rub

Sinuhe Hahna1, Xiao Yan Zhong1 and Wolfgang Holzgreve1

1 Laboratory for Prenatal Medicine, Department of Obstetrics and Gynaecology, University of Basel, CH 4031 Basel, Switzerland

aAddress correspondence to this author at: Laboratory for Prenatal Medicine, Department of Obstetrics and Gynecology, University of Basel, Schanzenstrasse 46, CH 4031 Basel, Switzerland. Fax 41-61-325-9399; e-mail shahn@uhbs.ch.

Although cell-free nucleic acids were first described in the 1940s (1), it was not until tumor-specific DNA sequences were detected in the plasma of cancer patients (2) that they started to attract the interest of the wider scientific community. Because the placenta shares numerous features with malignant tissues, such as a high rate of cell turnover and the expression of certain protooncogenes, these seminal reports prompted Lo and colleagues to examine whether fetal DNA could be detected in an analogous manner in the plasma of pregnant women. This hypothesis indeed proved to be true, and in 1997 Lo et al. (3) described the presence of fetal DNA circulating in maternal plasma and serum. This observation has been one of the most important for those attempting to develop safe and efficacious methods for prenatal diagnosis of fetal genetic traits. The reason for this interest is that current methods of obtaining fetal material for prenatal diagnosis rely on invasive procedures such as amniocentesis or chorionic villus sampling, both of which are associated with a procedure-related fetal loss rate of almost 1% (4). Although concerted efforts had been made to develop noninvasive, and hence risk-free, alternative prenatal diagnostic methods using fetal cells enriched from the blood of pregnant women, . . . [Full Text of this Article]


References




The following articles in journals at HighWire Press have cited this article:


Home page
Clin. Chem.Home page
S. K. R. Chinnapapagari, W. Holzgreve, O. Lapaire, B. Zimmermann, and S. Hahn
Treatment of Maternal Blood Samples with Formaldehyde Does Not Alter the Proportion of Circulatory Fetal Nucleic Acids (DNA and mRNA) in Maternal Plasma
Clin. Chem., March 1, 2005; 51(3): 652 - 655.
[Full Text] [PDF]


Home page
Mol Hum ReprodHome page
X. Y. Zhong, W. Holzgreve, and S. Hahn
Cell-free fetal DNA in the maternal circulation does not stem from the transplacental passage of fetal erythroblasts
Mol. Hum. Reprod., September 1, 2002; 8(9): 864 - 870.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2001 by the American Association for Clinical Chemistry.