Key Publications

Reviews focusing on specific disease areas with a selection of independent publications highlighting the advantages of using Transgenomic technologies.

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Reference	Links
Goldenberg O, Herrmann S, Marjoram G, Noyer-Weidner M, Hong G, Bereswill S, Gobel UB. (2007). Molecular monitoring of the intestinal flora by denaturing high performance liquid chromatography. J. Microbiol. Methods 68, 94-105.	Abstract
Cohen V, Agulnik JS, Jarry J, Batist G, Small D, Kreisman H, Adriana Tejada N, Miller WH Jr, Chong G. (2006). Evaluation of denaturing high-performance liquid chromatography as a rapid detection method for identification of epidermal growth factor receptor mutations in nonsmall-cell lung cancer. Cancer 107, 2858-2865.	Abstract
Chin TM, Anuar D, Soo R, Salto-Tellez M, Li WQ, Ahmad B, Lee SC, Goh BC, Kawakami K, Segal A, Iacopetta B, Soong R. (2007). Detection of epidermal growth factor receptor variations by partially denaturing HPLC. Clin. Chem. 53, 62-70.	Abstract
Xu L, Evans J, Ling T, Nye K, Hawkey P. (2007). Rapid genotyping of CTX-M extended-spectrum ß-lactamases by denaturing high-performance liquid chromatography (dHPLC). Antimicrob. Agents Chemother. 51, 1446-1454.	Abstract
Shi Y, Terry SF, Terry PF, Bercovitch LG, Gerard GF. (2007). Development of a rapid, reliable genetic test for pseudoxanthoma elasticum. J. Mol. Diagn. 9, 105–112.	Abstract
Thomas H, Ezzeldin H, Guarcello V, Mattison L, Fridley B, Diasio R (2008). Genetic regulation of beta-ureidopropionase and its possible implication in altered uracil catabolism Pharmacogenet. Genomics 18, 25-35.	Abstract
Mansour MR, Duke V, Foroni L, Patel B, Allen CG, Ancliff PJ, Gale RE, Linch DC. (2007). Notch-1 mutations are secondary events in some patients with T-cell acute lymphoblastic leukemia Clin. Cancer Res. 13, 6964-6969.	Abstract
Rose G, Passarino G, Scornaienchi V, Romeo G, Dato S, Bellizzi D, Mari V, Feraco E, Maletta R, Bruni A, Franceschi C, De Benedictis G. (2007). The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspring. BMC Genomics 8, 293.	Abstract
Bannwarth S, Procaccio V, Paquis-Flucklinger V. (2006). Rapid identification of unknown heteroplasmic mutations across the entire human mitochondrial genome with mismatch-specific Surveyor Nuclease Nat. Protoc. 1, 2037-2043.	Abstract
Bannwarth S, Procaccio V, Rouzier C, Fragaki K, Poole J, Chabrol B, Desnuelle C, Pouget J, Azulay JP, Attarian S, Pellissier JF, Gargus JJ, Abdenur JE, Mozaffar T, Calvas P, Labauge P, Pages M, Wallace DC, Lambert JC, Paquis-Flucklinger V. (2008). Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy Mitochondrion 8, 136-145.	Abstract