D
David R. Turner
Researcher at Flinders University
Publications - 31
Citations - 1208
David R. Turner is an academic researcher from Flinders University. The author has contributed to research in topics: Loss of heterozygosity & Mitotic crossover. The author has an hindex of 16, co-authored 30 publications receiving 1163 citations.
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Journal ArticleDOI
Isolation of fetal trophoblast cells from peripheral blood of pregnant women
U. W. Mueller,C.S. Hawes,A.E. Wright,E. DeBoni,W.R. Jones,Frank A. Firgaira,Alec Morley,David R. Turner +7 more
TL;DR: The fetal sex predicted by PCR analysis of the isolated trophoblast cells accorded with that ascertained by karyotyping of chorionic villus samples in eleven of twelve women studied in early pregnancy and with the sex of the baby on delivery in one woman studied at 34 weeks' gestation.
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Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
Ferdinando Squitieri,Cinzia Gellera,Milena Cannella,Caterina Mariotti,Giuliana Cislaghi,David C. Rubinsztein,E. Almqvist,David R. Turner,Anne-Catherine Bachoud-Lévi,Sheila A. Simpson,Martin B. Delatycki,Vittorio Maglione,Michael R. Hayden,Stefano Di Donato +13 more
TL;DR: Differences in the disease features between eight homozygotes and 75 heterozygotes for the Huntington disease mutation point to the possibility that the mechanisms underlying age at onset and disease progression in Huntington disease may differ, and suggest that the phenotype and the rate of disease progression may differ.
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Integrative analysis of RUNX1 downstream pathways and target genes
Joëlle Michaud,Joëlle Michaud,Joëlle Michaud,Ken M. Simpson,Robert Escher,Robert Escher,Karine Buchet-Poyau,Tim Beissbarth,Tim Beissbarth,Catherine Carmichael,Catherine Carmichael,Matthew E. Ritchie,Frédéric Schütz,Frédéric Schütz,Ping Cannon,Marjorie Liu,Xiaofeng Shen,Yoshiaki Ito,Wendy H. Raskind,Marshall S. Horwitz,Motomi Osato,David R. Turner,Terence P. Speed,Maria Kavallaris,Gordon K. Smyth,Hamish S. Scott,Hamish S. Scott +26 more
TL;DR: This work is the first large-scale study attempting to identify the genetic networks regulated by RUNX1, a master regulator in the development of the hematopoietic system and leukemia.
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Use of DNA polymorphisms and the polymerase chain reaction to examine the survival of a human limbal stem cell allograft.
Keryn A. Williams,Helen M. Brereton,Rajesh K. Aggarwal,Pamela J. Sykes,David R. Turner,Graeme R. Russ,Douglas J. Coster +6 more
TL;DR: In this article, the authors investigated the survival of donor-derived epithelial cells after limbal stem cell allotransplantation by using short tandem-repeat DNA polymorphisms to distinguish donor and recipient cells.
Journal ArticleDOI
Human lymphocytes aged in vivo have reduced levels of methylation in transcriptionally active and inactive DNA.
TL;DR: Results indicate that loss of genomic DNA methylation may be involved in aging in vivo and underscore the association of gene regulation with the distribution of methylation in DNA.