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Current HIV Research|January 11, 2005
HIV-1 TAR RNA: the target of molecular interactions between the virus and its hostSylvie Bannwarth, Anne Gatignol
Methods in Molecular Biology (Clifton, N.J.)|June 11, 2009
Rapid identification of unknown heteroplasmic mitochondrial DNA mutations with mismatch-specific surveyor nucleaseSylvie Bannwarth, Vincent Procaccio, Véronique Paquis-Flucklinger
Nature Protocols|May 10, 2007
Rapid identification of unknown heteroplasmic mutations across the entire human mitochondrial genome with mismatch-specific Surveyor NucleaseSylvie Bannwarth, Vincent Procaccio, Veronique Paquis-Flucklinger
Human Mutation|May 10, 2005
Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defectsSylvie Bannwarth, Vincent Procaccio, Veronique Paquis-Flucklinger
Medecine Sciences : M/S|March 3, 2025
["Mitochondrial medicine" in the light of the fourth national plan for rare diseases (PNMR4): The example of the MITOMICS project]Clémence Guillermain, Stéphane Tirard, Sylvie Bannwarth, et al.
International Journal of Molecular Sciences|October 13, 2021
A Survey of Autoencoder Algorithms to Pave the Diagnosis of Rare DiseasesDavid Pratella, Samira Ait-El-Mkadem Saadi, Sylvie Bannwarth, et al.
The Journal of Biological Chemistry|December 12, 2002
The TAR RNA-binding protein, TRBP, stimulates the expression of TAR-containing RNAs in vitro and in vivo independently of its ability to inhibit the dsRNA-dependent kinase PKRDominique Dorin, Marion C Bonnet, Sylvie Bannwarth, et al.
Molecular Genetics and Metabolism|May 23, 2017
Assembly defects of multiple respiratory chain complexes in a child with cardiac hypertrophy associated with a novel ACAD9 mutationKonstantina Fragaki, Annabelle Chaussenot, Audrey Boutron, et al.
Frontiers in Molecular Biosciences|November 26, 2020
Multi-Omics Approaches to Improve Mitochondrial Disease Diagnosis: Challenges, Advances, and PerspectivesJustine Labory, Morgane Fierville, Samira Ait-El-Mkadem, et al.
Diabetes Care|October 14, 2011
A novel unstable mutation in mitochondrial DNA responsible for maternally inherited diabetes and deafnessSylvie Bannwarth, Meriame Abbassi, René Valéro, et al.
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