A biobank management model applicable to biomedical research

Por Patenaude Johane, Auray-Blais Christiane
Publicado em 2006-04-01

A biobank management model applicable to biomedical research

Por Auray-Blais, Christiane, Patenaude, Johane
Publicado em 2006

Relative distribution of Gb(3) isoforms/analogs in NOD/SCID/Fabry mice tissues determined by tandem mass spectrometry

Por Provençal, Philippe, Boutin, Michel, Dworski, Shaalee, Au, Bryan, Medin, Jeffrey A, Auray-Blais, Christiane
Publicado no Bioanalysis (2016)

Variations in the GLA gene correlate with globotriaosylceramide and globotriaosylsphingosine analog levels in urine and plasma

Por Ferreira, Susana, Auray-Blais, Christiane, Boutin, Michel, Lavoie, Pamela, Nunes, José Pedro, Martins, Elisabete, Garman, Scott, Oliveira, João Paulo
Publicado no Clin Chim Acta (2015)

The lysosomal enzyme alpha-Galactosidase A is deficient in Parkinson’s disease brain in association with the pathologic accumulation of alpha-synuclein

Por Nelson, Michael P., Boutin, Michel, Tse, Tonia E., Lu, Hailin, Haley, Emily D., Ouyang, Xiaosen, Zhang, Jianhua, Auray-Blais, Christiane, Shacka, John J.
Publicado no Neurobiol Dis (2017)

Sulfatide Analysis by Mass Spectrometry for Screening of Metachromatic Leukodystrophy in Dried Blood and Urine Samples

Por Spacil, Zdenek, Kumar, Arun Babu, Liao, Hsuan-Chieh, Auray-Blais, Christiane, Stark, Samantha, Suhr, Teryn R., Scott, C. Ronald, Turecek, Frantisek, Gelb, Michael H.
Publicado no Clin Chem (2015)

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Por Bröer, Stefan, Bailey, Charles G., Kowalczuk, Sonja, Ng, Cynthia, Vanslambrouck, Jessica M., Rodgers, Helen, Auray-Blais, Christiane, Cavanaugh, Juleen A., Bröer, Angelika, Rasko, John E.J.
Publicado em 2008

Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria

Por Bailey, Charles G., Ryan, Renae M., Thoeng, Annora D., Ng, Cynthia, King, Kara, Vanslambrouck, Jessica M., Auray-Blais, Christiane, Vandenberg, Robert J., Bröer, Stefan, Rasko, John E.J.
Publicado em 2010

Glycosphingolipid storage in Fabry mice extends beyond globotriaosylceramide and is affected by ABCB1 depletion

Por Kamani, Mustafa A, Provençal, Philippe, Boutin, Michel, Pacienza, Natalia, Fan, Xin, Novak, Anton, Huang, Tonny C, Binnington, Beth, Au, Bryan C, Auray-Blais, Christiane, Lingwood, Clifford A, Medin, Jeffrey A
Publicado no Future Sci OA (2016)

Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment

Por Waters, Paula J., Kitzler, Thomas M., Feigenbaum, Annette, Geraghty, Michael T., Al-Dirbashi, Osama, Bherer, Patrick, Auray-Blais, Christiane, Gravel, Serge, McIntosh, Nathan, Siriwardena, Komudi, Trakadis, Yannis, Brunel-Guitton, Catherine, Al-Hertani, Walla
Publicado no JIMD Rep (2017)

Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing

Por Lévesque, Sébastien, Auray-Blais, Christiane, Gravel, Elaine, Boutin, Michel, Dempsey-Nunez, Laura, Jacques, Pierre-Etienne, Chenier, Sébastien, Larue, Sandrine, Rioux, Marie-France, Al-Hertani, Walla, Nadeau, Amelie, Mathieu, Jean, Maranda, Bruno, Désilets, Valérie, Waters, Paula J., Keutzer, Joan, Austin, Stephanie, Kishnani, Priya
Publicado no Orphanet J Rare Dis (2016)

Lentivector Iterations and Pre-Clinical Scale-Up/Toxicity Testing: Targeting Mobilized CD34(+) Cells for Correction of Fabry Disease

Por Huang, Ju, Khan, Aneal, Au, Bryan C., Barber, Dwayne L., López-Vásquez, Lucía, Prokopishyn, Nicole L., Boutin, Michel, Rothe, Michael, Rip, Jack W., Abaoui, Mona, Nagree, Murtaza S., Dworski, Shaalee, Schambach, Axel, Keating, Armand, West, Michael L., Klassen, John, Turner, Patricia V., Sirrs, Sandra, Rupar, C. Anthony, Auray-Blais, Christiane, Foley, Ronan, Medin, Jeffrey A.
Publicado no Mol Ther Methods Clin Dev (2017)