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A-Z Articles Index by First Author's Last Name |
| Ma L et al. The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome. J Biol Chem. 2004 Oct 22;279(43):44394-9. Epub 2004 Aug 10. |
| reference 3 (Magnus) |
| Maher CA et al. Transcriptome sequencing to detect gene fusions in cancer. Nature. 2009 Mar 5;458(7234):97-101. Epub 2009 Jan 11. |
| Mak W et al. Reactivation of the paternal X chromosome in early mouse embryos. Science. 2004 Jan 30;303(5658):666-9. |
| Malone FD et al. First-trimester or second-trimester screening, or both, for Down's syndrome. N Engl J Med. 2005 Nov 10;353(19):2001-11. |
| Mandel H et al. The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA. Nature Genetics 29:337-341, 2001. |
| Manfredi G & Beal MF. Merging mitochondria for neuronal survival. Nat Med. 2007 Oct;13(10):1140-1. |
| Manno CS et al. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response. Nat Med. 2006 Mar;12(3):342-347. Epub 2006 Feb 12. |
| Marchuk et al. Vascular morphogenesis: tales of two syndromes. Hum Mol Genet 2003;12(Suppl 1):R97-R112. |
| Martinowich et al. DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science. 2003 Oct 31;302(5646):890-3. |
| Matoba S et al. p53 regulates mitochondrial respiration. Science. 2006 Jun 16;312 (5780):1650-3. Epub 2006 May 25. |
| Matzke M, Matzke AJ.RNAi extends its reach. Science. 2003 Aug 22;301(5636):1060-1. |
McCarroll SA et al. Common deletion polymorphisms in the human genome Nat Genet. 2006 Jan;38(1):86-92. |
| Meier U. Dissecting dyskeratosis. Nat Genet. 2003;33(2):116-7. |
| Meissner A and Jaenisch R. Generation of nuclear transfer-derived pluripotent ES cells from cloned Cdx2-deficient blastocysts. Nature. 2005 Oct 16; [Epub ahead of print] |
| Menashe et al. Population differences in haplotype structure within a human olfactory receptor gene cluster. Hum Mol Genet. 2002;11:1381-1390. |
| Merz Jon F et al. (2002) Diagnostic Testing Fails the Test: The Pitfalls of Patents Are Demonstrated by the Case of Haemochromatosis. Nature 415:577-579. |
| Mill J et al. Epigenomic Profiling Reveals DNA-methylation Changes Associated with Major Psychosis. Am J Hum Genet. 2008 Mar;82(3):696-711. |
| Miller G. Medicine. Rett symptoms reversed in mice. Science. 2007 Feb 9;315(5813):749. |
| Mitrasinovic, O et al. On possible mechanisms for reactive oxygen species (ROS)-mediated cross-talk between NF-kB and JNK: A system biology view". GESTS International Transactions on Computer Science and Engineering, Vol. 27, No. 1, pp. 41-52, 2006 |
Mizuguchi T et al. Heterozygous TGFBR2 mutations in Marfan syndrome. Nat Genet. 2004 Aug;36(8):855-60. Epub 2004 Jul 04. |
| Moberg KH et al. Archipelago regulates Cyclin E levels in Drosophila and is mutated in human cancer cell lines. Nature. 2001; 413:311-316. |
| Mochizuki K et al. Analysis of a piwi-related gene implicates small RNAs in genome rearrangement in tetrahymena. Cell. 2002 Sep 20;110(6):689-99. |
| Moller T., et al. (2002) Hfq: a bacterial Sm-like protein that mediates RNA-RNA interaction. Molecular Cell 9:23-30. |
| Morais VA et al. Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function. EMBO Mol Med. 2009 May;1(2):99-111. |
Morley M et al.Genetic analysis of genome-wide variation in human gene expression.Nature. 2004 Aug 12;430(7001):743-7. Epub 2004 Jul 21. |
Morris CA, et al. GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region. Am J Med Genet A. 2003 Nov 15;123(1):45-59 |
| Mostoslavsky R et al. Genomic instability and aging-like phenotype in the absence of mammalian SIRT6. Cell. 2006 Jan 27;124(2):315-29. |
| Muenke M. The pit, the cleft and the web. Nat Genet 2002 Oct;32:219-220. |
| Murata T et al. Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein-Taybi syndrome. Hum Mol Genet 2001;10(10):1071-1076. |
| Murdoch S, et al. Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans. Nat Genet. 2006 Mar;38(3):300-2. Epub 2006 Feb 5. |
| Murphy WJ et al. The origin of human chromosome 1 and its homologs in placental mammals. Genome Res. 2003 Aug;13(8):1880-8. Epub 2003 Jul 17. |
| Musante L et al. Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome. Eur J Hum Genet. 2003 Feb;11(2):201-6. |
| Musio A et al, Recapitulation of the Roberts syndrome cellular phenotype by inhibition of INCENP, ZWINT-1 and ZW10 genes. Gene. 2004 Apr 28;331:33-40. |