Imprinting Articles : 2003
Below are selected articles on genomic imprinting organized by year. Select a year by clicking its tab. Hover over each article's title to view its abstract, and click the title to view its full PubMed record. Corresponding authors follow the author list, and fulltext PDFs are available for some articles and reviews.
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An Early Cretaceous tribosphenic mammal and metatherian evolution
Luo ZX, Ji Q, Wible JR, Yuan CX [ZX Luo]
Science 302:1934-40 (2003)
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Review: The monotreme genome: a patchwork of reptile, mammal and unique features?
Grützner F, Deakin J, Rens W, El-Mogharbel N, Marshall Graves JA [F Grützner] [JA Marshall Graves]
Comp Biochem Physiol A Mol Integr Physiol 136:867-81 (2003)
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The evolution of tribospheny and the antiquity of mammalian clades
Woodburne MO, Rich TH, Springer MS [MO Woodburne]
Mol Phylogenet Evol 28:360-85 (2003)
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Epigenetic detection of human chromosome 14 uniparental disomy
Murphy SK, Wylie AA, Coveler KJ, Cotter PD, Papenhausen PR, Sutton VR, Shaffer LG, Jirtle RL
Hum Mutat 22:92-7 (2003)
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In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene
Gicquel C, Gaston V, Mandelbaum J, Siffroi JP, Flahault A, Le Bouc Y [C Gicquel]
Am J Hum Genet 72:1338-41 (2003)
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Review: Imprinting evolution and the price of silence
Murphy SK, Jirtle RL [RL Jirtle]
Bioessays 25:577-88 (2003)
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M6P/IGF2R loss of heterozygosity in head and neck cancer associated with poor patient prognosis
Jamieson TA, Brizel DM, Killian JK, Oka Y, Jang HS, Fu X, Clough RW, Vollmer RT, Anscher MS, Jirtle RL [RL Jirtle]
BMC Cancer 3:4 (2003)
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Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay
Dietz LG, Wylie AA, Rauen KA, Murphy SK, Jirtle RL, Cotter PD
J Med Genet 40:e46 (2003)
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Genome imprinting regulated by the mouse Polycomb group protein Eed
Mager J, Montgomery ND, de Villena FP, Magnuson T [T Magnuson]
Nat Genet 33:502-7 (2003)
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Review: The need for Eed
Ferguson-Smith AC, Reik W [W Reik]
Nat Genet 33:433-4 (2003)
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Loss of IGF2 imprinting: a potential marker of colorectal cancer risk
Cui H, Cruz-Correa M, Giardiello FM, Hutcheon DF, Kafonek DR, Brandenburg S, Wu Y, He X, Powe NR, Feinberg AP [AP Feinberg]
Science 299:1753-5 (2003)
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Review: Mannose 6-phosphate receptors: new twists in the tale
Ghosh P, Dahms NM, Kornfeld S [S Kornfeld]
Nat Rev Mol Cell Biol 4:202-12 (2003)
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Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection
Ørstavik KH, Eiklid K, van der Hagen CB, Spetalen S, Kierulf K, Skjeldal O, Buiting K [KH Ørstavik]
Am J Hum Genet 72:218-9 (2003)
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Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)
Maher ER, Brueton LA, Bowdin SC, Luharia A, Cooper W, Cole TR, Macdonald F, Sampson JR, Barratt CL, Reik W, Hawkins MM [ER Maher]
J Med Genet 40:62-4 (2003)
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Tissue-specific inactivation of murine M6P/IGF2R
Wylie AA, Pulford DJ, McVie-Wylie AJ, Waterland RA, Evans HK, Chen YT, Nolan CM, Orton TC, Jirtle RL [RL Jirtle]
Am J Pathol 162:321-8 (2003)
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Review: H19 and Igf2--enhancing the confusion?
Arney KL [KL Arney]
Trends Genet 19:17-23 (2003)
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Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19
DeBaun MR, Niemitz EL, Feinberg AP [AP Feinberg]
Am J Hum Genet 72:156-60 (2003)
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Transposable elements: targets for early nutritional effects on epigenetic gene regulation
Waterland RA, Jirtle RL
Mol Cell Biol 23:5293-300 (2003)
