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Cancer Genetics and Cytogenetics|May 18, 2010
Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNAInas A Ahmed, Carsten M Pusch, Thanaa Hamed, et al.
International Journal of Molecular Medicine|March 25, 2008
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mappingGudrun Nürnberg, Felix K Jacobi, Martina Broghammer, et al.
Plos One|April 9, 2013
Molecular identification of falciparum malaria and human tuberculosis co-infections in mummies from the Fayum depression (Lower Egypt)Albert Lalremruata, Markus Ball, Raffaella Bianucci, et al.
Molecular Pharmacology|August 23, 2000
Pharmacological characterization of chloride channels belonging to the ClC family by the use of chiral clofibric acid derivativesM Pusch, A Liantonio, L Bertorello, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
International Journal of Molecular Medicine|June 16, 2001
Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disordersK Pesch, J Tomiuk, M Broghammer, et al.
American Journal of Human Genetics|May 2, 2000
Genomic differentiation of Neanderthals and anatomically modern man allows a fossil-DNA-based classification of morphologically indistinguishable hominid bonesM Scholz, L Bachmann, G J Nicholson, et al.
Molecular Biology and Evolution|July 16, 2004
PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutationsC M Pusch, M Broghammer, G J Nicholson, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma casesKathrin Riemann, Karl Sotlar, Susan Kupka, et al.
American Journal of Ophthalmology|April 30, 2003
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindnessFelix Karl Jacobi, Christian P Hamel, Bernard Arnaud, et al.
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