Bannwarth S - Search Results

1

DNA extraction by FTA technology: application for rapid detection of 1p/19q deletions in gliomas.

Fontaine D, Monnot S, Vandenbos F, Paquis P, Michiels JF, Bannwarth S; Nice Brain Tumor Study Group; Paquis-Flucklinger V. Fontaine D, et al. Among authors: bannwarth s. Neuropathol Appl Neurobiol. 2007 Jun;33(3):360-3. doi: 10.1111/j.1365-2990.2007.00835.x. Neuropathol Appl Neurobiol. 2007. PMID: 17493015 No abstract available.

2

Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.

Giuliano F, Bannwarth S, Monnot S, Cano A, Chabrol B, Vialettes B, Delobel B, Paquis-Flucklinger V; French Group of WS. Giuliano F, et al. Among authors: bannwarth s. Hum Mutat. 2005 Jan;25(1):99-100. doi: 10.1002/humu.9300. Hum Mutat. 2005. PMID: 15605410

3

Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects.

Bannwarth S, Procaccio V, Paquis-Flucklinger V. Bannwarth S, et al. Hum Mutat. 2005 Jun;25(6):575-82. doi: 10.1002/humu.20177. Hum Mutat. 2005. PMID: 15880407

4

A novel homozygous MMP2 mutation in a family with Winchester syndrome.

Rouzier C, Vanatka R, Bannwarth S, Philip N, Coussement A, Paquis-Flucklinger V, Lambert JC. Rouzier C, et al. Among authors: bannwarth s. Clin Genet. 2006 Mar;69(3):271-6. doi: 10.1111/j.1399-0004.2006.00584.x. Clin Genet. 2006. PMID: 16542393

5

Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.

Procaccio V, Neckelmann N, Paquis-Flucklinger V, Bannwarth S, Jimenez R, Davila A, Poole JC, Wallace DC. Procaccio V, et al. Among authors: bannwarth s. Mol Diagn Ther. 2006;10(6):381-9. doi: 10.1007/BF03256215. Mol Diagn Ther. 2006. PMID: 17154655

6

Rapid identification of unknown heteroplasmic mutations across the entire human mitochondrial genome with mismatch-specific Surveyor Nuclease.

Bannwarth S, Procaccio V, Paquis-Flucklinger V. Bannwarth S, et al. Nat Protoc. 2006;1(4):2037-47. doi: 10.1038/nprot.2006.318. Nat Protoc. 2006. PMID: 17487193

7

Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene.

Valéro R, Bannwarth S, Roman S, Paquis-Flucklinger V, Vialettes B. Valéro R, et al. Among authors: bannwarth s. Diabet Med. 2008 Jun;25(6):657-61. doi: 10.1111/j.1464-5491.2008.02448.x. Diabet Med. 2008. PMID: 18544103

8

Rapid identification of unknown heteroplasmic mitochondrial DNA mutations with mismatch-specific surveyor nuclease.

Bannwarth S, Procaccio V, Paquis-Flucklinger V. Bannwarth S, et al. Methods Mol Biol. 2009;554:301-13. doi: 10.1007/978-1-59745-521-3_19. Methods Mol Biol. 2009. PMID: 19513682

9

eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data.

Goudenège D, Bris C, Hoffmann V, Desquiret-Dumas V, Jardel C, Rucheton B, Bannwarth S, Paquis-Flucklinger V, Lebre AS, Colin E, Amati-Bonneau P, Bonneau D, Reynier P, Lenaers G, Procaccio V. Goudenège D, et al. Among authors: bannwarth s. Genet Med. 2019 Jun;21(6):1407-1416. doi: 10.1038/s41436-018-0350-8. Epub 2018 Nov 5. Genet Med. 2019. PMID: 30393377 Free article.

10

Expression of LSLCL, a new C-type lectin, is closely restricted, in bone marrow, to immature neutrophils.

Perrin C, Bayle J, Bannwarth S, Michiels JF, Heudier P, Lefebvre JC, Giordanengo V. Perrin C, et al. Among authors: bannwarth s. C R Acad Sci III. 2001 Dec;324(12):1125-32. doi: 10.1016/s0764-4469(01)01392-0. C R Acad Sci III. 2001. PMID: 11803813

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