Search Results - "Lolas, I."

Quantitative proteomic analysis of ibuprofen-degrading Patulibacter sp. strain I11 by Almeida, B., Kjeldal, H., Lolas, I., Knudsen, A. D., Carvalho, G., Nielsen, K. L., Barreto Crespo, M. T., Stensballe, A., Nielsen, J. L.

“…Ibuprofen is the third most consumed pharmaceutical drug in the world. Several isolates have been shown to degrade ibuprofen, but very little is known about…”
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A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis by Lolas, I.B., Sommerlund, M., Okkels, H., Ramsing, M., Petersen, M.B.

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SO-29 Dihydropyrimidine dehydrogenase (DPD) genotype and phenotype among Danish cancer patients: Prevalence and correlation between DPYD-genotype mutations and P-uracil concentrations by Paulsen, N., Ewertz, M., Bergmann, T., Holm, H., Feddersen, S., Fruekilde, P., Vojdeman, F., Nielsen, H., Qvortrup, C., Plomgaard, P., Bertelsen, B., Rossing, C., Andersen, S., Greibe, E., Hoffmann-Lücke, E., Ramlov, A., Nielsen, C., Lolas, I., Bøttger, P., Bergmann, M., Pfeiffer, P., Damkier, P.

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Detection of PMS2 Mutations by Screening Hereditary Nonpolyposis Colon Cancer Families from Denmark and Sweden by Okkels, Henrik, Lagerstedt-Robinsson, Kristina, Wikman, Friedrik P, Hansen, Thomas V O, Lolas, Ihab, Lindberg, Lars Joachim, Krarup, Henrik B

“…Hereditary nonpolyposis colon cancer (HNPCC) and Lynch syndrome (LS) are characterized by defects in the mismatch repair (MMR) system, which protects the…”
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A novel deletion mutation in the ALOX12B gene in a Kurdish family with autosomal recessive congenital ichthyosis by Lolas, I B, Sommerlund, M, Okkels, H, Ramsing, M, Petersen, M B

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