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Items: 18


Use of sodium 4-phenylbutyrate to define therapeutic parameters for reducing intracerebral hemorrhage and myopathy in Col4a1 mutant mice.

Hayashi G, Labelle-Dumais C, Gould DB.

Dis Model Mech. 2018 Jul 4;11(7). pii: dmm034157. doi: 10.1242/dmm.034157.


Müller glia-derived PRSS56 is required to sustain ocular axial growth and prevent refractive error.

Paylakhi S, Labelle-Dumais C, Tolman NG, Sellarole MA, Seymens Y, Saunders J, Lakosha H, deVries WN, Orr AC, Topilko P, John SW, Nair KS.

PLoS Genet. 2018 Mar 12;14(3):e1007244. doi: 10.1371/journal.pgen.1007244. eCollection 2018 Mar.


Type IV Collagens and Basement Membrane Diseases: Cell Biology and Pathogenic Mechanisms.

Mao M, Alavi MV, Labelle-Dumais C, Gould DB.

Curr Top Membr. 2015;76:61-116. doi: 10.1016/bs.ctm.2015.09.002. Epub 2015 Oct 20. Review.


Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations.

Kuo DS, Labelle-Dumais C, Mao M, Jeanne M, Kauffman WB, Allen J, Favor J, Gould DB.

Hum Mol Genet. 2014 Apr 1;23(7):1709-22. doi: 10.1093/hmg/ddt560. Epub 2013 Nov 7.


COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets.

Kuo DS, Labelle-Dumais C, Gould DB.

Hum Mol Genet. 2012 Oct 15;21(R1):R97-110. Epub 2012 Aug 21. Review.


COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage.

Weng YC, Sonni A, Labelle-Dumais C, de Leau M, Kauffman WB, Jeanne M, Biffi A, Greenberg SM, Rosand J, Gould DB.

Ann Neurol. 2012 Apr;71(4):470-7. doi: 10.1002/ana.22682.


COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke.

Jeanne M, Labelle-Dumais C, Jorgensen J, Kauffman WB, Mancini GM, Favor J, Valant V, Greenberg SM, Rosand J, Gould DB.

Am J Hum Genet. 2012 Jan 13;90(1):91-101. doi: 10.1016/j.ajhg.2011.11.022. Epub 2011 Dec 29.


COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans.

Labelle-Dumais C, Dilworth DJ, Harrington EP, de Leau M, Lyons D, Kabaeva Z, Manzini MC, Dobyns WB, Walsh CA, Michele DE, Gould DB.

PLoS Genet. 2011 May;7(5):e1002062. doi: 10.1371/journal.pgen.1002062. Epub 2011 May 19.


Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.

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, Hassan MG, Gould DB, Madireddy L, Li C, Cox TC, Smyth I, Chudley AE, Zenker M.

J Med Genet. 2011 Jun;48(6):375-82. doi: 10.1136/jmg.2011.089631. Epub 2011 Apr 20.


Peri-pubertal emergence of UNC-5 homologue expression by dopamine neurons in rodents.

Manitt C, Labelle-Dumais C, Eng C, Grant A, Mimee A, Stroh T, Flores C.

PLoS One. 2010 Jul 8;5(7):e11463. doi: 10.1371/journal.pone.0011463.


Post-pubertal emergence of a dopamine phenotype in netrin-1 receptor-deficient mice.

Grant A, Speed Z, Labelle-Dumais C, Flores C.

Eur J Neurosci. 2009 Oct;30(7):1318-28. doi: 10.1111/j.1460-9568.2009.06919.x. Epub 2009 Sep 24.


Altered netrin-1 receptor expression in dopamine terminal regions following neonatal ventral hippocampal lesions in the rat.

Flores C, Bhardwaj SK, Labelle-Dumais C, Srivastava LK.

Synapse. 2009 Jan;63(1):54-60. doi: 10.1002/syn.20584.


Netrin-1 receptor-deficient mice show enhanced mesocortical dopamine transmission and blunted behavioural responses to amphetamine.

Grant A, Hoops D, Labelle-Dumais C, Prévost M, Rajabi H, Kolb B, Stewart J, Arvanitogiannis A, Flores C.

Eur J Neurosci. 2007 Dec;26(11):3215-28. Epub 2007 Nov 14.


Regulation of netrin-1 receptors by amphetamine in the adult brain.

Yetnikoff L, Labelle-Dumais C, Flores C.

Neuroscience. 2007 Dec 19;150(4):764-73. Epub 2007 Oct 10.


Chronic phencyclidine treatment increases dendritic spine density in prefrontal cortex and nucleus accumbens neurons.

Flores C, Wen X, Labelle-Dumais C, Kolb B.

Synapse. 2007 Dec;61(12):978-84.


Impaired progesterone production in Nr5a2+/- mice leads to a reduction in female reproductive function.

Labelle-Dumais C, Paré JF, Bélanger L, Farookhi R, Dufort D.

Biol Reprod. 2007 Aug;77(2):217-25. Epub 2007 Apr 4.


Nuclear receptor NR5A2 is required for proper primitive streak morphogenesis.

Labelle-Dumais C, Jacob-Wagner M, Paré JF, Bélanger L, Dufort D.

Dev Dyn. 2006 Dec;235(12):3359-69.


Uterine Wnt/beta-catenin signaling is required for implantation.

Mohamed OA, Jonnaert M, Labelle-Dumais C, Kuroda K, Clarke HJ, Dufort D.

Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8579-84. Epub 2005 Jun 1.

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