Paquis-Flucklinger V - Search Results

1

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

2

Early-onset fatal encephalomyopathy associated with severe mtDNA depletion.

Paquis-Flucklinger V, Pellissier JF, Camboulives J, Chabrol B, Saunières A, Monfort MF, Giudicelli H, Desnuelle C. Paquis-Flucklinger V, et al. Eur J Pediatr. 1995 Jul;154(7):557-62. doi: 10.1007/BF02074834. Eur J Pediatr. 1995. PMID: 7556323

3

Rapid mapping of mitochondrial dna deletions by large-fragment PCR.

Paul R, Santucci S, Saunières A, Desnuelle C, Paquis-Flucklinger V. Paul R, et al. Trends Genet. 1996 Apr;12(4):131-2. Trends Genet. 1996. PMID: 8901416 No abstract available.

4

Clinical aspects of mitochondrial diabetes.

Vialettes B, Paquis-Flucklinger V, Bendahan D. Vialettes B, et al. Diabetes Metab. 1997 Mar;23 Suppl 2:52-6. Diabetes Metab. 1997. PMID: 9105784 Review.

5

[Detection and prevalence of mitochondrial genome mutations in diabetes].

Paquis-Flucklinger V, Vialettes B, Canivet B, Freychet P, Hieronimus S, Vague P, Saunières A, Desnuelle C. Paquis-Flucklinger V, et al. Journ Annu Diabetol Hotel Dieu. 1997:25-31. Journ Annu Diabetol Hotel Dieu. 1997. PMID: 9296981 Review. French. No abstract available.

6

Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions.

Paul R, Desnuelle C, Pouget J, Pellissier JF, Richelme C, Monfort MF, Butori C, Saunieres A, Paquis-Flucklinger V. Paul R, et al. Eur J Hum Genet. 2000 May;8(5):331-8. doi: 10.1038/sj.ejhg.5200463. Eur J Hum Genet. 2000. PMID: 10854092

7

Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.

Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C. Perucca-Lostanlen D, et al. Biochem Biophys Res Commun. 2000 Nov 2;277(3):771-5. doi: 10.1006/bbrc.2000.3751. Biochem Biophys Res Commun. 2000. PMID: 11062027

8

The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.

Santucci-Darmanin S, Neyton S, Lespinasse F, Saunières A, Gaudray P, Paquis-Flucklinger V. Santucci-Darmanin S, et al. Hum Mol Genet. 2002 Jul 15;11(15):1697-706. doi: 10.1093/hmg/11.15.1697. Hum Mol Genet. 2002. PMID: 12095912

9

Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness.

Perucca-Lostanlen D, Taylor RW, Narbonne H, Mousson de Camaret B, Hayes CM, Saunieres A, Paquis-Flucklinger V, Turnbull DM, Vialettes B, Desnuelle C. Perucca-Lostanlen D, et al. Biochim Biophys Acta. 2002 Dec 12;1588(3):210-6. doi: 10.1016/s0925-4439(02)00167-9. Biochim Biophys Acta. 2002. PMID: 12393175

10

Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).

Guillausseau PJ, Dubois-Laforgue D, Massin P, Laloi-Michelin M, Bellanné-Chantelot C, Gin H, Bertin E, Blickle JF, Bauduceau B, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Derrien C, Grimaldi A, Guerci B, Kaloustian E, Lorenzini F, Murat A, Olivier F, Paques M, Paquis-Flucklinger V, Tielmans A, Vincenot M, Vialettes B, Timsit J; GEDIAM, Mitochondrial Diabetes French Study Group. Guillausseau PJ, et al. Diabetes Metab. 2004 Apr;30(2):181-6. doi: 10.1016/s1262-3636(07)70105-2. Diabetes Metab. 2004. PMID: 15223991

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