Cassandre Labelle-Dumais - Publications

Affiliations: 
McGill University, Montreal, QC, Canada 
Area:
dopamine development

16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Mao M, Alavi MV, Labelle-Dumais C, Gould DB. Type IV Collagens and Basement Membrane Diseases: Cell Biology and Pathogenic Mechanisms. Current Topics in Membranes. 76: 61-116. PMID 26610912 DOI: 10.1016/bs.ctm.2015.09.002  0.72
2014 Kuo DS, Labelle-Dumais C, Mao M, Jeanne M, Kauffman WB, Allen J, Favor J, Gould DB. Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations. Human Molecular Genetics. 23: 1709-22. PMID 24203695 DOI: 10.1093/hmg/ddt560  0.72
2012 Kuo DS, Labelle-Dumais C, Gould DB. COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets. Human Molecular Genetics. 21: R97-110. PMID 22914737 DOI: 10.1093/hmg/dds346  0.72
2012 Weng YC, Sonni A, Labelle-Dumais C, de Leau M, Kauffman WB, Jeanne M, Biffi A, Greenberg SM, Rosand J, Gould DB. COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage. Annals of Neurology. 71: 470-7. PMID 22522439 DOI: 10.1002/ana.22682  0.72
2012 Jeanne M, Labelle-Dumais C, Jorgensen J, Kauffman WB, Mancini GM, Favor J, Valant V, Greenberg SM, Rosand J, Gould DB. COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke. American Journal of Human Genetics. 90: 91-101. PMID 22209247 DOI: 10.1016/j.ajhg.2011.11.022  0.72
2011 Labelle-Dumais C, Dilworth DJ, Harrington EP, de Leau M, Lyons D, Kabaeva Z, Manzini MC, Dobyns WB, Walsh CA, Michele DE, Gould DB. COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. Plos Genetics. 7: e1002062. PMID 21625620 DOI: 10.1371/journal.pgen.1002062  0.72
2011 Slavotinek AM, Baranzini SE, Schanze D, Labelle-Dumais C, Short KM, Chao R, Yahyavi M, Bijlsma EK, Chu C, Musone S, Wheatley A, Kwok PY, Marles S, Fryns JP, Maga AM, et al. Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. Journal of Medical Genetics. 48: 375-82. PMID 21507892 DOI: 10.1136/jmg.2011.089631  0.72
2010 Manitt C, Labelle-Dumais C, Eng C, Grant A, Mimee A, Stroh T, Flores C. Peri-pubertal emergence of UNC-5 homologue expression by dopamine neurons in rodents. Plos One. 5: e11463. PMID 20628609 DOI: 10.1371/journal.pone.0011463  0.72
2009 Grant A, Speed Z, Labelle-Dumais C, Flores C. Post-pubertal emergence of a dopamine phenotype in netrin-1 receptor-deficient mice. The European Journal of Neuroscience. 30: 1318-28. PMID 19788579 DOI: 10.1111/j.1460-9568.2009.06919.x  0.72
2009 Flores C, Bhardwaj SK, Labelle-Dumais C, Srivastava LK. Altered netrin-1 receptor expression in dopamine terminal regions following neonatal ventral hippocampal lesions in the rat. Synapse (New York, N.Y.). 63: 54-60. PMID 18932228 DOI: 10.1002/syn.20584  0.72
2007 Grant A, Hoops D, Labelle-Dumais C, Prévost M, Rajabi H, Kolb B, Stewart J, Arvanitogiannis A, Flores C. Netrin-1 receptor-deficient mice show enhanced mesocortical dopamine transmission and blunted behavioural responses to amphetamine. The European Journal of Neuroscience. 26: 3215-28. PMID 18005074 DOI: 10.1111/j.1460-9568.2007.05888.x  0.72
2007 Yetnikoff L, Labelle-Dumais C, Flores C. Regulation of netrin-1 receptors by amphetamine in the adult brain. Neuroscience. 150: 764-73. PMID 17996376 DOI: 10.1016/j.neuroscience.2007.09.069  0.72
2007 Flores C, Wen X, Labelle-Dumais C, Kolb B. Chronic phencyclidine treatment increases dendritic spine density in prefrontal cortex and nucleus accumbens neurons. Synapse (New York, N.Y.). 61: 978-84. PMID 17879264 DOI: 10.1002/syn.20452  0.72
2007 Labelle-Dumais C, Paré JF, Bélanger L, Farookhi R, Dufort D. Impaired progesterone production in Nr5a2+/- mice leads to a reduction in female reproductive function. Biology of Reproduction. 77: 217-25. PMID 17409375 DOI: 10.1095/biolreprod.106.059121  0.72
2006 Labelle-Dumais C, Jacob-Wagner M, Paré JF, Bélanger L, Dufort D. Nuclear receptor NR5A2 is required for proper primitive streak morphogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 235: 3359-69. PMID 17075876 DOI: 10.1002/dvdy.20996  0.72
2005 Mohamed OA, Jonnaert M, Labelle-Dumais C, Kuroda K, Clarke HJ, Dufort D. Uterine Wnt/beta-catenin signaling is required for implantation. Proceedings of the National Academy of Sciences of the United States of America. 102: 8579-84. PMID 15930138 DOI: 10.1073/pnas.0500612102  0.72
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