about
Multidisciplinary Identification of the Controversial Freedom Fighter Jörg Jenatsch, Assassinated 1639 in Chur, SwitzerlandA global analysis of Y-chromosomal haplotype diversity for 23 STR lociToward male individualization with rapidly mutating y-chromosomal short tandem repeats.Sarcomeric gene mutations in sudden infant death syndrome (SIDS).Post mortem DNA degradation of human tissue experimentally mummified in salt.Y-chromosome STR haplotypes in a population sample from Switzerland (Zurich area).Forensic ancestry analysis with two capillary electrophoresis ancestry informative marker (AIM) panels: Results of a collaborative EDNAP exercise.Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.A collaborative EDNAP exercise on SNaPshot™-based mtDNA control region typing.Forensic interlaboratory evaluation of the ForFLUID kit for vaginal fluids identification.Specific and sensitive mRNA biomarkers for the identification of skin in 'touch DNA' evidence.A collaborative European exercise on mRNA-based body fluid/skin typing and interpretation of DNA and RNA results.mRNA profiling using a minimum of five mRNA markers per body fluid and a novel scoring method for body fluid identification.Y-chromosomal analysis identifies the skeletal remains of Swiss national hero Jörg Jenatsch (1596-1639).No association of serotonin transporter gene variation with sudden infant death syndrome (SIDS) in Caucasians.Aquaporin-4 polymorphisms and brain/body weight ratio in sudden infant death syndrome (SIDS).2,000 Year old β-thalassemia case in Sardinia suggests malaria was endemic by the Roman period.Detection of painted-over traces of blood and seminal fluid.Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling.Body fluid identification using a targeted mRNA massively parallel sequencing approach - results of a EUROFORGEN/EDNAP collaborative exercise.Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.RNA/DNA co-analysis from human skin and contact traces--results of a sixth collaborative EDNAP exercise.The combined inactivation of tumor necrosis factor and interleukin-6 prevents induction of the major acute phase proteins by endotoxin.Predicting the origin of stains from next generation sequencing mRNA data.Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour.A syndrome resembling human systemic sclerosis (scleroderma) in MRL/lpr mice lacking interferon-gamma (IFN-gamma) receptor (MRL/lprgammaR-/-).Tyrosine hydroxylase TH01 9.3 allele in the occurrence of sudden infant death syndrome in Swiss Caucasians.Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.Messenger RNA biomarker signatures for forensic body fluid identification revealed by targeted RNA sequencing.Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases.Body Fluid Identification Using mRNA Profiling.Recovery of Trace DNA on Clothing: A Comparison of Mini-tape Lifting and Three Other Forensic Evidence Collection Techniques.RNA/DNA co-analysis from human saliva and semen stains--results of a third collaborative EDNAP exercise.Development and optimization of a PCR assay for detection of Dobrava and Puumala hantaviruses in Bosnia and Herzegovina.RNA/DNA co-analysis from blood stains--results of a second collaborative EDNAP exercise.mRNA profiling for the identification of blood--results of a collaborative EDNAP exercise.RNA/DNA co-analysis from human menstrual blood and vaginal secretion stains: results of a fourth and fifth collaborative EDNAP exercise.mRNA profiling for body fluid identification by reverse transcription endpoint PCR and realtime PCR.Lipopolysaccharide-induced glomerulonephritis develops in the absence of interferon-gamma signaling.Functional implications of a rare variant in the sodium channel β1B subunit (SCN1B) in a 5-month-old male sudden infant death syndrome case.
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