Search Results - "Ouellette, Gail"

Returning incidental findings from genetic research to children: views of parents of children affected by rare diseases by Kleiderman, Erika, Knoppers, Bartha Maria, Fernandez, Conrad V, Boycott, Kym M, Ouellette, Gail, Wong-Rieger, Durhane, Adam, Shelin, Richer, Julie, Avard, Denise

“…Purpose To explore parental perceptions and experiences regarding the return of genomic incidental research findings in children with rare diseases. Methods…”
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Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia by Chumakov, Ilya, Blumenfeld, Marta, Guerassimenko, Oxana, Cavarec, Laurent, Palicio, Marta, Abderrahim, Hadi, Bougueleret, Lydie, Barry, Caroline, Tanaka, Hiroaki, La Rosa, Philippe, Puech, Anne, Tahri, Nadia, Cohen-Akenine, Annick, Delabrosse, Sylvain, Lissarrague, Sébastien, Picard, Françoise-Pascaline, Maurice, Karelle, Essioux, Laurent, Millasseau, Philippe, Grel, Pascale, Debailleul, Virginie, Simon, Anne-Marie, Caterina, Dominique, Dufaure, Isabelle, Malekzadeh, Kattayoun, Belova, Maria, Luan, Jian-Jian, Bouillot, Michel, Sambucy, Jean-Luc, Primas, Gwenael, Saumier, Martial, Boubkiri, Nadia, Martin-Saumier, Sandrine, Nasroune, Myriam, Peixoto, Hélène, Delaye, Arnaud, Pinchot, Virginie, Bastucci, Mariam, Guillou, Sophie, Chevillon, Magali, Sainz-Fuertes, Ricardo, Meguenni, Said, Aurich-Costa, Joan, Cherif, Dorra, Gimalac, Anne, van Duijn, Cornelia, Gauvreau, Denis, Ouelette, Gail, Fortier, Isabel, Realson, John, Sherbatich, Tatiana, Riazanskaia, Nadejda, Rogaev, Evgeny, Raeymaekers, Peter, Aerssens, Jeroen, Konings, Frank, Luyten, Walter, Macciardi, Fabio, Sham, Pak C., Straub, Richard E., Weinberger, Daniel R., Cohen, Nadine, Cohen, Daniel

“…A map of 191 single-nucleotide polymorphism (SNPs) was built across a 5-Mb segment from chromosome 13q34 that has been genetically linked to schizophrenia. DNA…”
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A genealogical study of Alzheimer disease in the Saguenay region of Quebec by Vézina, Hélène, Heyer, Évelyne, Fortier, Isabel, Ouellette, Gail, Robitaille, Yves, Gauvreau, Denis

“…We performed an analysis of inbreeding and kinship among the ascending genealogies of 205 autopsy‐confirmed Alzheimer disease (AD) subjects recruited in the…”
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DNA methylation and genetic inactivation at thymidine kinase locus: two different mechanisms for silencing autosomal genes by DOBROVIC, A, GAREAU, J. L. P, OUELLETTE, G, BRADLEY, W. E. C

“…Patterns of methylation of CpG dinucleotides in the promoter region of the thymidine kinase (TK) gene in wild-type and TK-deficient Chinese hamster cell lines…”
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Phenotype reversal in induced mutants of CHO cells: analysis of the reversed cell lines by Ouellette, G, Bradley, W E

“…We have previously shown that descendants of CHO-derived hprt or aprt mutants induced by ethyl methanesulphonate usually undergo a rapid loss of the mutant…”
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