A5047150449- Forensic and Genetic Research
- Molecular Biology Techniques and Applications
- Environmental DNA in Biodiversity Studies
- Genomics and Phylogenetic Studies
- Fermentation and Sensory Analysis
- Yersinia bacterium, plague, ectoparasites research
- Metabolomics and Mass Spectrometry Studies
- RNA and protein synthesis mechanisms
- Animal Diversity and Health Studies
- Fungal and yeast genetics research
- Race, Genetics, and Society
- Plant Pathogens and Fungal Diseases
- Genetic diversity and population structure
- CRISPR and Genetic Engineering
- Mass Spectrometry Techniques and Applications
- Autism Spectrum Disorder Research
- Rangeland Management and Livestock Ecology
- Radioactive contamination and transfer
- Pluripotent Stem Cells Research
- Bone and Dental Protein Studies
- Plant Gene Expression Analysis
- Biofuel production and bioconversion
Laboratoire National de Santé
2022-2025
Institut de Médecine et d'Epidémiologie Africaines
2004-2007
DNA markers used for individual identification in forensic sciences are based on repeat sequences nuclear and the mitochondrial hypervariable regions 1 2. An alternative to these is use of single nucleotide polymorphisms (SNPs). These have a particular advantage analysis degraded or poor samples, which often all that available forensics anthropology. In order study potential SNP fields, 41 SNPs were selected basis following criteria: conservation, lack phenotypic expression, frequency...
Abstract The ReAct (Recovery, Activity) project is an ENFSI (European Network of Forensic Science Institutes) supported initiative comprising a large consortium laboratories. Here, the results from more than 23 laboratories are presented. primary purpose was to design experiments simulating typical casework circumstances; collect data and implement Bayesian networks assess value (i.e., likelihood ratio) DNA given activity level propositions. Two different experimental designs were used...
We describe the generation of an isogenic control cell line DJ-1-delP GC13 from induced pluripotent stem (iPSC) LCSBi008-A that was derived fibroblasts obtained a Parkinson's disease (PD) patient. Using CRISPR/Cas9 technology, we corrected causing c.471_473delGCC homozygous mutation in PARK7 gene leading to p.158P deletion encoded protein DJ-1. The generated pair will be used for phenotypic analysis PD-patient neurons and astrocytes.