McKenzie O - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Page 1

Patient-reported barriers and drivers of adherence to antiretrovirals in sub-Saharan Africa: a meta-ethnography.

Merten S, Kenter E, McKenzie O, Musheke M, Ntalasha H, Martin-Hilber A. Merten S, et al. Among authors: mckenzie o. Trop Med Int Health. 2010 Jun;15 Suppl 1:16-33. doi: 10.1111/j.1365-3156.2010.02510.x. Trop Med Int Health. 2010. PMID: 20586957 Free article. Review.

A systematic review of qualitative findings on factors enabling and deterring uptake of HIV testing in Sub-Saharan Africa.

Musheke M, Ntalasha H, Gari S, McKenzie O, Bond V, Martin-Hilber A, Merten S. Musheke M, et al. Among authors: mckenzie o. BMC Public Health. 2013 Mar 11;13:220. doi: 10.1186/1471-2458-13-220. BMC Public Health. 2013. PMID: 23497196 Free PMC article. Review.

Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor.

McKenzie O, Ponte I, Mangelsdorf M, Finnis M, Colasante G, Shoubridge C, Stifani S, Gécz J, Broccoli V. McKenzie O, et al. Neuroscience. 2007 Apr 25;146(1):236-47. doi: 10.1016/j.neuroscience.2007.01.038. Epub 2007 Feb 27. Neuroscience. 2007. PMID: 17331656

Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation.

Weaving LS, Christodoulou J, Williamson SL, Friend KL, McKenzie OL, Archer H, Evans J, Clarke A, Pelka GJ, Tam PP, Watson C, Lahooti H, Ellaway CJ, Bennetts B, Leonard H, Gécz J. Weaving LS, et al. Among authors: mckenzie ol. Am J Hum Genet. 2004 Dec;75(6):1079-93. doi: 10.1086/426462. Epub 2004 Oct 18. Am J Hum Genet. 2004. PMID: 15492925 Free PMC article.

Aberrant CBFA2T3B gene promoter methylation in breast tumors.

Bais AJ, Gardner AE, McKenzie OL, Callen DF, Sutherland GR, Kremmidiotis G. Bais AJ, et al. Among authors: mckenzie ol. Mol Cancer. 2004 Aug 10;3:22. doi: 10.1186/1476-4598-3-22. Mol Cancer. 2004. PMID: 15301688 Free PMC article.

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.

Bhalla K, Phillips HA, Crawford J, McKenzie OLD, Mulley JC, Eyre H, Gardner AE, Kremmidiotis G, Callen DF. Bhalla K, et al. Among authors: mckenzie old. J Hum Genet. 2004;49(6):308-311. doi: 10.1007/s10038-004-0145-4. Epub 2004 May 18. J Hum Genet. 2004. PMID: 15148587

CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3.

Kochetkova M, McKenzie OL, Bais AJ, Martin JM, Secker GA, Seshadri R, Powell JA, Hinze SJ, Gardner AE, Spendlove HE, O'Callaghan NJ, Cleton-Jansen AM, Cornelisse C, Whitmore SA, Crawford J, Kremmidiotis G, Sutherland GR, Callen DF. Kochetkova M, et al. Among authors: mckenzie ol. Cancer Res. 2002 Aug 15;62(16):4599-604. Cancer Res. 2002. PMID: 12183414

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results