Erasmus Schneider
Affiliations: | State University of New York, Albany, Albany, NY, United States |
Area:
Cell Biology, Molecular Biology, OncologyGoogle:
"Erasmus Schneider"
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Publications
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| Cho S, Lu M, He X, et al. (2011) Notch1 regulates the expression of the multidrug resistance gene ABCC1/MRP1 in cultured cancer cells. Proceedings of the National Academy of Sciences of the United States of America. 108: 20778-83 |
| Yao R, Schneider E. (2007) Detection of B- and T-cell-specific gene rearrangements in 13 cell lines and 50 clinical specimens using the BIOMED-2 and the original InVivoScribe primers. Leukemia & Lymphoma. 48: 837-40 |
| Schneider E, Ryan TJ. (2006) Gamma-glutamyl hydrolase and drug resistance. Clinica Chimica Acta; International Journal of Clinical Chemistry. 374: 25-32 |
| Marshall LA, Rhee MS, Hofmann L, et al. (2005) Increased lysosomal uptake of methotrexate-polyglutamates in two methotrexate-resistant cell lines with distinct mechanisms of resistance. Biochemical Pharmacology. 71: 203-13 |
| Rhee MS, Schneider E. (2005) Lack of an effect of breast cancer resistance protein (BCRP/ABCG2) overexpression on methotrexate polyglutamate export and folate accumulation in a human breast cancer cell line. Biochemical Pharmacology. 69: 123-32 |
| Kowalski P, Farley KM, Lage H, et al. (2004) Effective knock down of very high ABCG2 expression by a hammerhead ribozyme Anticancer Research. 24: 2231-2235 |
| Volk EL, Pankuch JJ, Chave KJ, et al. (2003) A rapid assay for the quantitation of gamma-glutamyl hydrolase using a fluorogenic peptide as substrate. Biotechniques. 35: 926-8, 930, 932 |
| Volk EL, Schneider E. (2003) Wild-type breast cancer resistance protein (BCRP/ABCG2) is a methotrexate polyglutamate transporter. Cancer Research. 63: 5538-43 |
| Volk EL, Farley KM, Wu Y, et al. (2002) Overexpression of wild-type breast cancer resistance protein mediates methotrexate resistance. Cancer Research. 62: 5035-40 |
| Yao R, Rich SA, Schneider E. (2002) Validation of sixteen leukemia and lymphoma cell lines as controls for molecular gene rearrangement assays. Clinical Chemistry. 48: 1344-51 |