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Melanie Ehrlich
Human Genetics Program
Tulane Medical School
New Orleans
USA
Name/email consistency: high
- Gene expression during normal and FSHD myogenesis. Tsumagari, K., Chang, S.C., Lacey, M., Baribault, C., Chittur, S.V., Sowden, J., Tawil, R., Crawford, G.E., Ehrlich, M. BMC. Med. Genomics (2011)
- ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation. Ehrlich, M., Sanchez, C., Shao, C., Nishiyama, R., Kehrl, J., Kuick, R., Kubota, T., Hanash, S.M. Autoimmunity (2008)
- Hybridization analysis of D4Z4 repeat arrays linked to FSHD. Ehrlich, M., Jackson, K., Tsumagari, K., Camaño, P., Lemmers, R.J. Chromosoma (2007)
- Quantitative analysis of associations between DNA hypermethylation, hypomethylation, and DNMT RNA levels in ovarian tumors. Ehrlich, M., Woods, C.B., Yu, M.C., Dubeau, L., Yang, F., Campan, M., Weisenberger, D.J., Long, T., Youn, B., Fiala, E.S., Laird, P.W. Oncogene (2006)
- Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF). Ehrlich, M., Jackson, K., Weemaes, C. Orphanet J. Rare Diseases (2006)
- Cancer-linked DNA hypomethylation and its relationship to hypermethylation. Ehrlich, M. Curr. Top. Microbiol. Immunol. (2006)
- The controversial denouement of vertebrate DNA methylation research. Ehrlich, M. Biochemistry Mosc. (2005)
- Satellite DNA hypomethylation in karyotyped Wilms tumors. Ehrlich, M., Hopkins, N.E., Jiang, G., Dome, J.S., Yu, M.C., Woods, C.B., Tomlinson, G.E., Chintagumpala, M., Champagne, M., Dillerg, L., Parham, D.M., Sawyer, J. Cancer Genet. Cytogenet. (2003)
- Expression of various genes is controlled by DNA methylation during mammalian development. Ehrlich, M. J. Cell. Biochem. (2003)
- The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease. Ehrlich, M. Clin. Immunol. (2003)
- DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements. Ehrlich, M. J. Nutr. (2002)
- Hypomethylation and hypermethylation of DNA in Wilms tumors. Ehrlich, M., Jiang, G., Fiala, E., Dome, J.S., Yu, M.C., Long, T.I., Youn, B., Sohn, O.S., Widschwendter, M., Tomlinson, G.E., Chintagumpala, M., Champagne, M., Parham, D., Liang, G., Malik, K., Laird, P.W. Oncogene (2002)
- DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes. Ehrlich, M., Buchanan, K.L., Tsien, F., Jiang, G., Sun, B., Uicker, W., Weemaes, C.M., Smeets, D., Sperling, K., Belohradsky, B.H., Tommerup, N., Misek, D.E., Rouillard, J.M., Kuick, R., Hanash, S.M. Hum. Mol. Genet. (2001)
