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Items: 1 to 50 of 214

1.

Differential strain-specific diagnosis of the heartwater agent: Ehrlichia ruminantium.

Vachiery N, Maganga G, Lefrançois T, Kandassamy Y, Stachurski F, Adakal H, Ferraz C, Morgat A, Bensaid A, Coissac E, Boyer F, Demaille J, Viari A, Martinez D, Frutos R.

Infect Genet Evol. 2008 Jul;8(4):459-66. Epub 2007 Jun 19.

PMID:
17644446
2.

Comparative genomics of three strains of Ehrlichia ruminantium: a review.

Frutos R, Viari A, Ferraz C, Bensaid A, Morgat A, Boyer F, Coissac E, Vachiéry N, Demaille J, Martinez D.

Ann N Y Acad Sci. 2006 Oct;1081:417-33. Review.

PMID:
17135545
3.

Genome analysis of the smallest free-living eukaryote Ostreococcus tauri unveils many unique features.

Derelle E, Ferraz C, Rombauts S, Rouzé P, Worden AZ, Robbens S, Partensky F, Degroeve S, Echeynié S, Cooke R, Saeys Y, Wuyts J, Jabbari K, Bowler C, Panaud O, Piégu B, Ball SG, Ral JP, Bouget FY, Piganeau G, De Baets B, Picard A, Delseny M, Demaille J, Van de Peer Y, Moreau H.

Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11647-52. Epub 2006 Jul 25.

4.

Comparative genomic analysis of three strains of Ehrlichia ruminantium reveals an active process of genome size plasticity.

Frutos R, Viari A, Ferraz C, Morgat A, Eychenié S, Kandassamy Y, Chantal I, Bensaid A, Coissac E, Vachiery N, Demaille J, Martinez D.

J Bacteriol. 2006 Apr;188(7):2533-42.

5.

Comprehensive analysis of the renal transcriptional response to acute uranyl nitrate exposure.

Taulan M, Paquet F, Argiles A, Demaille J, Romey MC.

BMC Genomics. 2006 Jan 11;7:2.

6.

Binding of serum response factor to cystic fibrosis transmembrane conductance regulator CArG-like elements, as a new potential CFTR transcriptional regulation pathway.

René C, Taulan M, Iral F, Doudement J, L'Honoré A, Gerbon C, Demaille J, Claustres M, Romey MC.

Nucleic Acids Res. 2005 Sep 16;33(16):5271-90. Print 2005.

7.

Renal toxicogenomic response to chronic uranyl nitrate insult in mice.

Taulan M, Paquet F, Maubert C, Delissen O, Demaille J, Romey MC.

Environ Health Perspect. 2004 Nov;112(16):1628-35.

8.

Fluorescence in situ hybridization analysis of human oocytes: advantages of a double-labeling procedure.

Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J.

Fertil Steril. 2004 Oct;82(4):919-22.

PMID:
15482769
9.

Infevers: an evolving mutation database for auto-inflammatory syndromes.

Touitou I, Lesage S, McDermott M, Cuisset L, Hoffman H, Dode C, Shoham N, Aganna E, Hugot JP, Wise C, Waterham H, Pugnere D, Demaille J, Sarrauste de Menthiere C.

Hum Mutat. 2004 Sep;24(3):194-8.

PMID:
15300846
10.

The first green lineage cdc25 dual-specificity phosphatase.

Khadaroo B, Robbens S, Ferraz C, Derelle E, Eychenié S, Cooke R, Peaucellier G, Delseny M, Demaille J, Van de Peer Y, Picard A, Moreau H.

Cell Cycle. 2004 Apr;3(4):513-8. Epub 2004 Apr 1.

PMID:
15004533
11.

Fast multicolor primed in situ protocol for chromosome identification in isolated cells may be used for human oocytes and polar bodies.

Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J.

Fertil Steril. 2004 Feb;81(2):408-15.

PMID:
14967382
12.

Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting.

Anahory T, Andréo B, Régnier-Vigouroux G, Soulie JP, Baudouin M, Demaille J, Pellestor F.

Mol Hum Reprod. 2003 Oct;9(10):577-85.

PMID:
12970395
13.

Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis.

Molinari N, Koné Paut I, Manna R, Demaille J, Daures JP, Touitou I.

Am J Med Genet A. 2003 Oct 1;122A(2):115-8.

PMID:
12955762
14.

Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy.

Girardet A, Hamamah S, Déchaud H, Anahory T, Coubes C, Hédon B, Demaille J, Claustres M.

Mol Hum Reprod. 2003 Jul;9(7):421-7.

PMID:
12802049
15.

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F.

Am J Med Genet A. 2003 Apr 15;118A(2):333-8.

PMID:
12698965
16.

Genome-wide identification of in vivo Drosophila Engrailed-binding DNA fragments and related target genes.

Solano PJ, Mugat B, Martin D, Girard F, Huibant JM, Ferraz C, Jacq B, Demaille J, Maschat F.

Development. 2003 Apr;130(7):1243-54.

17.

First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.

Girardet A, Hamamah S, Anahory T, Déchaud H, Sarda P, Hédon B, Demaille J, Claustres M.

Mol Hum Reprod. 2003 Feb;9(2):111-6.

PMID:
12569181
18.

Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes.

Pellestor F, Andréo B, Arnal F, Humeau C, Demaille J.

Hum Genet. 2003 Feb;112(2):195-203. Epub 2002 Oct 29.

PMID:
12522562
19.

The MetaFMF website: a high quality tool for meta-analysis of FMF.

Pugnère D, Ruiz M, Sarrauste de Menthière C, Masdoua B, Demaille J, Touitou I.

Nucleic Acids Res. 2003 Jan 1;31(1):286-90.

20.

INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutations.

Sarrauste de Menthière C, Terrière S, Pugnère D, Ruiz M, Demaille J, Touitou I.

Nucleic Acids Res. 2003 Jan 1;31(1):282-5.

21.

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F.

Am J Med Genet. 2002 Dec 15;113(4):333-8. Corrected and republished in: Am J Med Genet A. 2003 Apr 15;118A(2):333-8.

PMID:
12457404
22.

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro.

Schmitt-Bernard CF, Chavanieu A, Herrada G, Subra G, Arnaud B, Demaille JG, Calas B, Argilés A.

Eur J Biochem. 2002 Nov;269(21):5149-56.

23.

Reduced MEFV messenger RNA expression in patients with familial Mediterranean fever.

Notarnicola C, Didelot MN, Koné-Paut I, Seguret F, Demaille J, Touitou I.

Arthritis Rheum. 2002 Oct;46(10):2785-93.

24.

Porcine odorant-binding protein selectively binds to a human olfactory receptor.

Matarazzo V, Zsürger N, Guillemot JC, Clot-Faybesse O, Botto JM, Dal Farra C, Crowe M, Demaille J, Vincent JP, Mazella J, Ronin C.

Chem Senses. 2002 Oct;27(8):691-701.

PMID:
12379593
25.

Transcriptome analysis of monocytic leukemia cell differentiation.

Piquemal D, Commes T, Manchon L, Lejeune M, Ferraz C, Pugnère D, Demaille J, Elalouf JM, Marti J.

Genomics. 2002 Sep;80(3):361-71.

PMID:
12213207
26.
27.

Multiplex fluorescent RT-PCR to quantify leukemic fusion transcripts.

Dupont M, Goldsborough A, Levayer T, Savare J, Rey JM, Rossi JF, Demaille J, Lavabre-Bertrand T.

Biotechniques. 2002 Jul;33(1):158-60, 162, 164.

28.

Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness.

Pallares-Ruiz N, Blanchet P, Mondain M, Low-Hong S, Demaille J, Claustres M, Roux AF.

Genet Test. 2001 Winter;5(4):339-43.

PMID:
11960582
29.

A single olfactory receptor specifically binds a set of odorant molecules.

Gaillard I, Rouquier S, Pin JP, Mollard P, Richard S, Barnabé C, Demaille J, Giorgi D.

Eur J Neurosci. 2002 Feb;15(3):409-18.

PMID:
11876768
30.

Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean fever.

Notarnicola C, Didelot MN, Seguret F, Demaille J, Touitou I.

Genes Immun. 2002 Feb;3(1):43-5.

31.

Mapping and identification of essential gene functions on the X chromosome of Drosophila.

Peter A, Schöttler P, Werner M, Beinert N, Dowe G, Burkert P, Mourkioti F, Dentzer L, He Y, Deak P, Benos PV, Gatt MK, Murphy L, Harris D, Barrell B, Ferraz C, Vidal S, Brun C, Demaille J, Cadieu E, Dreano S, Gloux S, Lelaure V, Mottier S, Galibert F, Borkova D, Miñana B, Kafatos FC, Bolshakov S, Sidén-Kiamos I, Papagiannakis G, Spanos L, Louis C, Madueño E, de Pablos B, Modolell J, Bucheton A, Callister D, Campbell L, Henderson NS, McMillan PJ, Salles C, Tait E, Valenti P, Saunders RD, Billaud A, Pachter L, Klapper R, Janning W, Glover DM, Ashburner M, Bellen HJ, Jäckle H, Schäfer U.

EMBO Rep. 2002 Jan;3(1):34-8. Epub 2001 Dec 19.

32.
33.

The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of Mylk.

Giorgi D, Ferraz C, Mattéi MG, Demaille J, Rouquier S.

Genomics. 2001 Jul;75(1-3):49-56.

PMID:
11472067
34.

Segregation of a mutation in CNGB1 encoding the beta-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa.

Bareil C, Hamel CP, Delague V, Arnaud B, Demaille J, Claustres M.

Hum Genet. 2001 Apr;108(4):328-34.

PMID:
11379879
35.

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation.

Lefort G, Blanchet P, Chaze AM, Girardet A, Sarda P, Demaille J, Pellestor F.

J Med Genet. 2001 Jan;38(1):67-73. No abstract available.

36.

From first base: the sequence of the tip of the X chromosome of Drosophila melanogaster, a comparison of two sequencing strategies.

Benos PV, Gatt MK, Murphy L, Harris D, Barrell B, Ferraz C, Vidal S, Brun C, Demaille J, Cadieu E, Dreano S, Gloux S, Lelaure V, Mottier S, Galibert F, Borkova D, Miñana B, Kafatos FC, Bolshakov S, Sidén-Kiamos I, Papagiannakis G, Spanos L, Louis C, Madueño E, de Pablos B, Modolell J, Peter A, Schöttler P, Werner M, Mourkioti F, Beinert N, Dowe G, Schäfer U, Jäckle H, Bucheton A, Callister D, Campbell L, Henderson NS, McMillan PJ, Salles C, Tait E, Valenti P, Saunders RD, Billaud A, Pachter L, Glover DM, Ashburner M.

Genome Res. 2001 May;11(5):710-30.

37.

The MICA region determines the first modifier locus in familial Mediterranean fever.

Touitou I, Picot MC, Domingo C, Notarnicola C, Cattan D, Demaille J, Koné-Paut I.

Arthritis Rheum. 2001 Jan;44(1):163-9.

38.

MEFV mutations in Behçet's disease.

Touitou I, Magne X, Molinari N, Navarro A, Quellec AL, Picco P, Seri M, Ozen S, Bakkaloglu A, Karaduman A, Garnier JM, Demaille J, Koné-Paut I.

Hum Mutat. 2000 Sep;16(3):271-2.

PMID:
10980540
39.

Lattice corneal dystrophy.

Schmitt-Bernard CF, Claustres M, Arnaud B, Demaille J, Argiles A.

Ophthalmology. 2000 Sep;107(9):1613-4. No abstract available.

PMID:
10964807
40.

Genomic sequencing reveals the structure of the Kcnk6 and map3k11 genes and their close vicinity to the sipa1 gene on mouse chromosome 19.

Saridaki A, Ferraz C, Demaille J, Scherer G, Roux AF.

Cytogenet Cell Genet. 2000;89(1-2):85-8.

PMID:
10894943
41.

In vitro creation of amyloid fibrils from native and Arg124Cys mutated betaIGH3((110-131)) peptides, and its relevance for lattice corneal amyloid dystrophy type I.

Schmitt-Bernard CF, Chavanieu A, Derancourt J, Arnaud B, Demaille JG, Calas B, Argiles A.

Biochem Biophys Res Commun. 2000 Jul 5;273(2):649-53.

PMID:
10873659
42.

W179R: a novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa.

Bareil C, Delague V, Arnaud B, Demaille J, Hamel C, Claustres M.

Hum Mutat. 2000 Jun;15(6):583-4. No abstract available.

PMID:
10862101
43.

Familial Mediterranean fever in the 'Chuetas' of Mallorca: a question of Jewish origin or genetic heterogeneity.

Domingo C, Touitou I, Bayou A, Ozen S, Notarnicola C, Dewalle M, Demaille J, Buades R, Sayadat C, Levy M, Ben-Chetrit E.

Eur J Hum Genet. 2000 Apr;8(4):242-6.

44.

Evolution of the Gypsy endogenous retrovirus in the Drosophila melanogaster subgroup.

Terzian C, Ferraz C, Demaille J, Bucheton A.

Mol Biol Evol. 2000 Jun;17(6):908-14.

PMID:
10833197
45.

BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.

Schmitt-Bernard CF, Guittard C, Arnaud B, Demaille J, Argiles A, Claustres M, Tuffery-Giraud S.

Invest Ophthalmol Vis Sci. 2000 May;41(6):1302-8.

PMID:
10798644
46.

Sequence, structure, and evolution of a complete human olfactory receptor gene cluster.

Glusman G, Sosinsky A, Ben-Asher E, Avidan N, Sonkin D, Bahar A, Rosenthal A, Clifton S, Roe B, Ferraz C, Demaille J, Lancet D.

Genomics. 2000 Jan 15;63(2):227-45.

PMID:
10673334
47.

A naturally occurring sequence variation that creates a YY1 element is associated with increased cystic fibrosis transmembrane conductance regulator gene expression.

Romey MC, Pallares-Ruiz N, Mange A, Mettling C, Peytavi R, Demaille J, Claustres M.

J Biol Chem. 2000 Feb 4;275(5):3561-7.

48.

Point mutations in the dystrophin gene: evidence for frequent use of cryptic splice sites as a result of splicing defects.

Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.

Hum Mutat. 1999;14(5):359-68.

PMID:
10533061
49.

Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4.

Bareil C, Hamel C, Pallarès-Ruiz N, Arnaud B, Demaille J, Claustres M.

Ophthalmic Genet. 1999 Sep;20(3):173-82.

PMID:
10521250
50.

Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone.

Romey MC, Guittard C, Chazalette JP, Frossard P, Dawson KP, Patton MA, Casals T, Bazarbachi T, Girodon E, Rault G, Bozon D, Seguret F, Demaille J, Claustres M.

Hum Genet. 1999 Jul-Aug;105(1-2):145-50.

PMID:
10480369

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