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21 results
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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. Chumakov I, et al. Among authors: millasseau p. Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13675-80. doi: 10.1073/pnas.182412499. Epub 2002 Oct 3. Proc Natl Acad Sci U S A. 2002. PMID: 12364586 Free PMC article.
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. Weissenbach J, et al. Among authors: millasseau p. Nature. 1992 Oct 29;359(6398):794-801. doi: 10.1038/359794a0. Nature. 1992. PMID: 1436057
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. Gyapay G, et al. Among authors: millasseau p. Nat Genet. 1994 Jun;7(2 Spec No):246-339. doi: 10.1038/ng0694supp-246. Nat Genet. 1994. PMID: 7545953
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. Berthon P, et al. Among authors: millasseau p. Am J Hum Genet. 1998 Jun;62(6):1416-24. doi: 10.1086/301879. Am J Hum Genet. 1998. PMID: 9585607 Free PMC article.
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. Amson RB, et al. Among authors: millasseau p. Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):3953-7. doi: 10.1073/pnas.93.9.3953. Proc Natl Acad Sci U S A. 1996. PMID: 8632996 Free PMC article.
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. Plassart E, et al. Among authors: millasseau p. Eur J Hum Genet. 1994;2(2):110-24. doi: 10.1159/000472351. Eur J Hum Genet. 1994. PMID: 8044656
21 results