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Items: 21

1.

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H, Bougueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, Van Duijn C, Gauvreau D, Ouellette G, Fortier I, Raelson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D.

Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13675-80. Epub 2002 Oct 3. Erratum in: Proc Natl Acad Sci U S A 2002 Dec 24;99(26):17221. Ouelette, G [corrected to Ouellette, G]; Realson, J [corrected to Raelson, J].

2.

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43.

Berthon P, Valeri A, Cohen-Akenine A, Drelon E, Paiss T, Wöhr G, Latil A, Millasseau P, Mellah I, Cohen N, Blanché H, Bellané-Chantelot C, Demenais F, Teillac P, Le Duc A, de Petriconi R, Hautmann R, Chumakov I, Bachner L, Maitland NJ, Lidereau R, Vogel W, Fournier G, Mangin P, Cussenot O, et al.

Am J Hum Genet. 1998 Jun;62(6):1416-24.

3.

Survey of CAG/CTG repeats in human cDNAs representing new genes: candidates for inherited neurological disorders.

Néri C, Albanèse V, Lebre AS, Holbert S, Saada C, Bougueleret L, Meier-Ewert S, Le Gall I, Millasseau P, Bui H, Giudicelli C, Massart C, Guillou S, Gervy P, Poullier E, Rigault P, Weissenbach J, Lennon G, Chumakov I, Dausset J, Lehrach H, Cohen D, Cann HM.

Hum Mol Genet. 1996 Jul;5(7):1001-9.

PMID:
8817338
4.

Isolation of 10 differentially expressed cDNAs in p53-induced apoptosis: activation of the vertebrate homologue of the drosophila seven in absentia gene.

Amson RB, Nemani M, Roperch JP, Israeli D, Bougueleret L, Le Gall I, Medhioub M, Linares-Cruz G, Lethrosne F, Pasturaud P, Piouffre L, Prieur S, Susini L, Alvaro V, Millasseau P, Guidicelli C, Bui H, Massart C, Cazes L, Dufour F, Bruzzoni-Giovanelli H, Owadi H, Hennion C, Charpak G, Telerman A, et al.

Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):3953-7.

5.

A comprehensive genetic map of the human genome based on 5,264 microsatellites.

Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J.

Nature. 1996 Mar 14;380(6570):152-4.

PMID:
8600387
6.

Down-regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophy.

Gannoun-Zaki L, Fournier-Bidoz S, Le Cam G, Chambon C, Millasseau P, Léger JJ, Dechesne CA.

FEBS Lett. 1995 Nov 20;375(3):268-72.

7.

Identification and characterization of a spinal muscular atrophy-determining gene.

Lefebvre S, Bürglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, Cruaud C, Millasseau P, Zeviani M, et al.

Cell. 1995 Jan 13;80(1):155-65.

8.

E-box- and MEF-2-independent muscle-specific expression, positive autoregulation, and cross-activation of the chicken MyoD (CMD1) promoter reveal an indirect regulatory pathway.

Dechesne CA, Wei Q, Eldridge J, Gannoun-Zaki L, Millasseau P, Bougueleret L, Caterina D, Paterson BM.

Mol Cell Biol. 1994 Aug;14(8):5474-86.

9.

De novo and inherited deletions of the 5q13 region in spinal muscular atrophies.

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboullet S, Bénichou B, Zeviani M, Le Paslier D, et al.

Science. 1994 Jun 3;264(5164):1474-7.

PMID:
7910982
10.

The 1993-94 Généthon human genetic linkage map.

Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J.

Nat Genet. 1994 Jun;7(2 Spec No):246-339.

PMID:
7545953
11.

Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3.

Gecz J, Pollard H, Consalez G, Villard L, Stayton C, Millasseau P, Khrestchatisky M, Fontes M.

Hum Mol Genet. 1994 Jan;3(1):39-44.

PMID:
8162050
12.

Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.

Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Eymard B, Pelletier J, Thomas C, Chapon F, Desnuelle C, et al.

Eur J Hum Genet. 1994;2(2):110-24.

PMID:
8044656
13.

[Physical study of big fragments and search strategy of genes. Application to locus of infant spinal muscular atrophies].

Melki J, Lefebvre S, Burglen L, Burlet P, Clermont O, Millasseau P, Reboulet S, Benichou B, Zeviani M, Le Paslier D, et al.

C R Seances Soc Biol Fil. 1994;188(5-6):495-8. Review. French.

PMID:
7780792
14.

Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts.

Gecz J, Villard L, Lossi AM, Millasseau P, Djabali M, Fontes M.

Hum Mol Genet. 1993 Sep;2(9):1389-96.

PMID:
8242062
15.

Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria.

Abadie V, Jaruzelska J, Lyonnet S, Millasseau P, Berthelon M, Rey F, Munnich A, Rey J.

Hum Mol Genet. 1993 Jan;2(1):31-4.

PMID:
8098245
16.

A second-generation linkage map of the human genome.

Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M.

Nature. 1992 Oct 29;359(6398):794-801.

PMID:
1436057
17.

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

Legouis R, Hardelin JP, Levilliers J, Claverie JM, Compain S, Wunderle V, Millasseau P, Le Paslier D, Cohen D, Caterina D, et al.

Cell. 1991 Oct 18;67(2):423-35.

PMID:
1913827
18.

Use of synthetic oligonucleotides for genomic DNA dot hybridization to split the DQw3 haplotype.

Martell M, Le Gall I, Millasseau P, Dausset J, Cohen D.

Proc Natl Acad Sci U S A. 1988 Apr;85(8):2682-5.

19.

Two DR beta allelic series defined by exon II-specific synthetic oligonucleotide genomic hybridization: a method of HLA typing?

Le Gall I, Millasseau P, Dausset J, Cohen D.

Proc Natl Acad Sci U S A. 1986 Oct;83(20):7836-40.

20.

New methods for detection of HLA genes polymorphism useful for associated diseases studies.

Le Gall I, Chausse AM, Marcadet A, Millasseau P, Beaud'Huy-Lancelin D, Font MP, Paul P, Sayagh B, Masse M, Massart C, et al.

Pathol Biol (Paris). 1986 Jun;34(6):801-7.

PMID:
3531998
21.

[Detection of polymorphism of HLA class II genes using synthetic oligonucleotides].

Le Gall I, Millasseau P, Dausset J, Cohen D.

C R Acad Sci III. 1985;301(15):669-73. French.

PMID:
3935278

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