Letourneur F - Search Results

1

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.

Dodé C, Le Dû N, Cuisset L, Letourneur F, Berthelot JM, Vaudour G, Meyrier A, Watts RA, Scott DG, Nicholls A, Granel B, Frances C, Garcier F, Edery P, Boulinguez S, Domergues JP, Delpech M, Grateau G. Dodé C, et al. Among authors: letourneur f. Am J Hum Genet. 2002 Jun;70(6):1498-506. doi: 10.1086/340786. Epub 2002 Apr 25. Am J Hum Genet. 2002. PMID: 11992256 Free PMC article.

2

Metachromatic leukodystrophy: identification of the first deletion in exon 1 and of nine novel point mutations in the arylsulfatase A gene.

Draghia R, Letourneur F, Drugan C, Manicom J, Blanchot C, Kahn A, Poenaru L, Caillaud C. Draghia R, et al. Among authors: letourneur f. Hum Mutat. 1997;9(3):234-42. doi: 10.1002/(SICI)1098-1004(1997)9:3<234::AID-HUMU4>3.0.CO;2-7. Hum Mutat. 1997. PMID: 9090526

3

Glycogen-storage disease type II (acid maltase deficiency): identification of a novel small deletion (delCC482+483) in French patients.

Nicolino M, Puech JP, Letourneur F, Fardeau M, Kahn A, Poenaru L. Nicolino M, et al. Among authors: letourneur f. Biochem Biophys Res Commun. 1997 Jun 9;235(1):138-41. doi: 10.1006/bbrc.1997.6749. Biochem Biophys Res Commun. 1997. PMID: 9196050

4

Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysis.

Quelin C, Saillour Y, Poirier K, Roubertie A, Boddaert N, Desguerre I, Letourneur F, Beldjord C, Chelly J, Bahi-Buisson N. Quelin C, et al. Among authors: letourneur f. Eur J Med Genet. 2012 Oct;55(10):527-30. doi: 10.1016/j.ejmg.2012.06.004. Epub 2012 Jul 2. Eur J Med Genet. 2012. PMID: 22766001

5

Cholestasis is a marker for hepatocellular carcinomas displaying beta-catenin mutations.

Audard V, Grimber G, Elie C, Radenen B, Audebourg A, Letourneur F, Soubrane O, Vacher-Lavenu MC, Perret C, Cavard C, Terris B. Audard V, et al. Among authors: letourneur f. J Pathol. 2007 Jul;212(3):345-52. doi: 10.1002/path.2169. J Pathol. 2007. PMID: 17487939

6

Identification of susceptibility genes for peritoneal, ovarian, and deep infiltrating endometriosis using a pooled sample-based genome-wide association study.

Borghese B, Tost J, de Surville M, Busato F, Letourneur F, Mondon F, Vaiman D, Chapron C. Borghese B, et al. Among authors: letourneur f. Biomed Res Int. 2015;2015:461024. doi: 10.1155/2015/461024. Epub 2015 Feb 4. Biomed Res Int. 2015. PMID: 25722978 Free PMC article.

7

A comparative analysis of cDNA-derived sequences for rat and mouse beta 3 integrins (GPIIIA) with their human counterpart.

Cieutat AM, Rosa JP, Letourneur F, Poncz M, Rifat S. Cieutat AM, et al. Among authors: letourneur f. Biochem Biophys Res Commun. 1993 Jun 15;193(2):771-8. doi: 10.1006/bbrc.1993.1692. Biochem Biophys Res Commun. 1993. PMID: 8512576

8

Impaired alveolarization and intra-uterine growth restriction in rats: a postnatal genome-wide analysis.

Zana-Taieb E, Pham H, Franco-Montoya ML, Jacques S, Letourneur F, Baud O, Jarreau PH, Vaiman D. Zana-Taieb E, et al. Among authors: letourneur f. J Pathol. 2015 Feb;235(3):420-30. doi: 10.1002/path.4470. J Pathol. 2015. PMID: 25347958

9

AhR-deficiency as a cause of demyelinating disease and inflammation.

Juricek L, Carcaud J, Pelhaitre A, Riday TT, Chevallier A, Lanzini J, Auzeil N, Laprévote O, Dumont F, Jacques S, Letourneur F, Massaad C, Agulhon C, Barouki R, Beraneck M, Coumoul X. Juricek L, et al. Among authors: letourneur f. Sci Rep. 2017 Aug 29;7(1):9794. doi: 10.1038/s41598-017-09621-3. Sci Rep. 2017. PMID: 28851966 Free PMC article.

10

Insights into the P. y. yoelii hepatic stage transcriptome reveal complex transcriptional patterns.

Grüner AC, Hez-Deroubaix S, Snounou G, Hall N, Bouchier C, Letourneur F, Landau I, Druilhe P. Grüner AC, et al. Among authors: letourneur f. Mol Biochem Parasitol. 2005 Aug;142(2):184-92. doi: 10.1016/j.molbiopara.2005.03.019. Mol Biochem Parasitol. 2005. PMID: 15913805

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