Mesenchymal stem cells with high telomerase expression do not actively restore their chromosome arm specific telomere length pattern after exposure to ionizing radiation

Por Graakjaer, Jesper, Christensen, Rikke, Kolvraa, Steen, Serakinci, Nedime
Publicado em 2007

A New Approach for Screening for Y Microdeletions: Capillary Electrophoresis Combined with Fluorescent Multiplex PCR

Por Bor, Pinar, Hindkjær, Johnny, Kølvraa, Steen, Ingerslev, Hans Jakob
Publicado em 2003

Genetics: Multiplex PCR for Screening of Microdeletions on the Y Chromosome

Por Bor, Pinar, Hindkjær, Johnny, Ingerslev, Hans Jakob, Kølvraa, Steen
Publicado em 2001

Y-Chromosome Microdeletions and Cytogenetic Findings in Unselected ICSI Candidates at a Danish Fertility Clinic

Por Bor, Pinar, Hindkjær, Johnny, Kølvraa, Steen, Ingerslev, Hans Jakob
Publicado em 2002

Gene expression profiling in Werner syndrome closely resembles that of normal aging

Por Kyng, Kasper J., May, Alfred, Kølvraa, Steen, Bohr, Vilhelm A.
Publicado em 2003

Microselection – affinity selecting antibodies against a single rare cell in a heterogeneous population

Por Sørensen, Morten Dræby, Agerholm, Inge Errebo, Christensen, Britta, Kølvraa, Steen, Kristensen, Peter
Publicado em 2010

Reduced heat shock response in human mononuclear cells during aging and its association with polymorphisms in HSP70 genes

Por Singh, Ripudaman, Kølvraa, Steen, Bross, Peter, Jensen, Uffe Birk, Gregersen, Niels, Tan, Qihua, Knudsen, Christian, Rattan, Suresh I.S.
Publicado em 2006

Telomere Fluorescence Measurements in Granulocytes and T Lymphocyte Subsets Point to a High Turnover of Hematopoietic Stem Cells and Memory T Cells in Early Childhood

Por Rufer, Nathalie, Brümmendorf, Tim H., Kolvraa, Steen, Bischoff, Claus, Christensen, Kaare, Wadsworth, Louis, Schulzer, Michael, Lansdorp, Peter M.
Publicado em 1999

Epsilon Haemoglobin Specific Antibodies with Applications in Noninvasive Prenatal Diagnosis

Por Sørensen, Morten Dræby, Gonzalez Dosal, Regina, Jensen, Kim Bak, Christensen, Britta, Kølvraa, Steen, Jensen, Uffe Birk, Kristensen, Peter
Publicado em 2009

The Prognostic Value of Haplotypes in the Vascular Endothelial Growth Factor A Gene in Colorectal Cancer

Por Hansen, Torben F., Spindler, Karen-Lise G., Andersen, Rikke F., Lindebjerg, Jan, Kølvraa, Steen, Brandslund, Ivan, Jakobsen, Anders
Publicado em 2010

Telomere shortening correlates to dysplasia but not to DNA aneuploidy in longstanding ulcerative colitis

Por Friis-Ottessen, Mariann, Bendix, Laila, Kølvraa, Steen, Norheim-Andersen, Solveig, De Angelis, Paula M, Clausen, Ole Petter F
Publicado em 2014

Microarray-Based Analysis of Methylation Status of CpGs in Placental DNA and Maternal Blood DNA – Potential New Epigenetic Biomarkers for Cell Free Fetal DNA-Based Diagnosis

Por Hatt, Lotte, Aagaard, Mads M., Graakjaer, Jesper, Bach, Cathrine, Sommer, Steffen, Agerholm, Inge E., Kølvraa, Steen, Bojesen, Anders
Publicado no PLoS One (2015)

Microarray-Based Analysis of Methylation of 1st Trimester Trisomic Placentas from Down Syndrome, Edwards Syndrome and Patau Syndrome

Por Hatt, Lotte, Aagaard, Mads M., Bach, Cathrine, Graakjaer, Jesper, Sommer, Steffen, Agerholm, Inge E., Kølvraa, Steen, Bojesen, Anders
Publicado no PLoS One (2016)

Fetal Gender and Several Cytokines Are Associated with the Number of Fetal Cells in Maternal Blood – An Observational Study

Por Schlütter, Jacob Mørup, Kirkegaard, Ida, Petersen, Olav Bjørn, Larsen, Nanna, Christensen, Britta, Hougaard, David M., Kølvraa, Steen, Uldbjerg, Niels
Publicado em 2014

Screening for Y microdeletions in men with testicular cancer and undescended testis

Por Bor, Pinar, Hindkjær, Johnny, Kølvraa, Steen, Rossen, Philip, von der Maase, Hans, Jørgensen, Troels Munch, Sørensen, Viggo Tønning, Eiberg, Hans, Ingerslev, Hans Jakob
Publicado em 2006

Are Keratoacanthomas Variants of Squamous Cell Carcinomas? A Comparison of Chromosomal Aberrations by Comparative Genomic Hybridization

Por Clausen, Ole Petter F., Aass, Hans Christian D., Beigi, Marzieh, Purdie, Karin J., Proby, Charlotte M., Brown, Victoria L., Mattingsdal, Morten, Micci, Francesca, Kølvraa, Steen, Bolund, Lars, DeAngelis, Paula M.
Publicado em 2006

A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain...

Por Andresen, Brage Storstein, Bross, Peter, Jensen, Thomas G., Winter, Vibeke, Knudsen, Inga, Kølvraa, Steen, Jensen, Uffe Birk, Bolund, Lars, Duran, Marinus, Kim, Jung-Ja, Curtis, Diana, Divry, Priscille, Vianey-Saban, Christine, Gregersen, Niels
Publicado em 1993

Disease-causing Mutations in Exon 11 of the Medium-Chain Acyl-CoA Dehydrogenase Gene

Por Andresen, Brage Storstein, Jensen, Thomas G., Bross, Peter, Knudsen, Inga, Winter, Vibeke, Kølvraa, Steen, Bolund, Lars, Ding, Jia-Huan, Chen, Yuan-Tsong, Van Hove, Johan L. K., Curtis, Diana, Yokota, Ichiro, Tanaka, Kay, Kim, Jung-Ja Park, Gregersen, Niels
Publicado em 1994