Karen Thatcher - Publications

Affiliations: 
University of California, Davis, Davis, CA 

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 Wang NJ, Parokonny AS, Thatcher KN, Driscoll J, Malone BM, Dorrani N, Sigman M, LaSalle JM, Schanen NC. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15. Bmc Genetics. 9: 2. PMID 18177502 DOI: 10.1186/1471-2156-9-2  0.68
2007 Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21. PMID 18042715 DOI: 10.1073/Pnas.0707442104  0.68
2006 Thatcher KN, LaSalle JM. Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. Epigenetics : Official Journal of the Dna Methylation Society. 1: 24-31. PMID 17464364 DOI: 10.4161/epi.1.1.2339  0.68
2006 Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. Bmc Medical Genetics. 7: 61. PMID 16859563 DOI: 10.1186/1471-2350-7-61  0.68
2005 LaSalle JM, Hogart A, Thatcher KN. Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism. International Review of Neurobiology. 71: 131-65. PMID 16512349 DOI: 10.1016/S0074-7742(05)71006-0  0.68
2005 Thatcher KN, Peddada S, Yasui DH, Lasalle JM. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Human Molecular Genetics. 14: 785-97. PMID 15689352 DOI: 10.1093/Hmg/Ddi073  0.68
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