Labelle-Dumais C - Search Results

1

Faulty TRPM4 channels underlie age-dependent cerebral vascular dysfunction in Gould syndrome.

Yamasaki E, Ali S, Sanchez Solano A, Thakore P, Smith M, Wang X, Labelle-Dumais C, Gould DB, Earley S. Yamasaki E, et al. Among authors: labelle dumais c. Proc Natl Acad Sci U S A. 2023 Jan 31;120(5):e2217327120. doi: 10.1073/pnas.2217327120. Epub 2023 Jan 24. Proc Natl Acad Sci U S A. 2023. PMID: 36693102 Free PMC article.

2

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. Manitt C, et al. PLoS One. 2010 Jul 8;5(7):e11463. doi: 10.1371/journal.pone.0011463. PLoS One. 2010. PMID: 20628609 Free PMC article.

3

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. Slavotinek AM, et al. J Med Genet. 2011 Jun;48(6):375-82. doi: 10.1136/jmg.2011.089631. Epub 2011 Apr 20. J Med Genet. 2011. PMID: 21507892 Free PMC article.

4

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. Labelle-Dumais C, et al. PLoS Genet. 2011 May;7(5):e1002062. doi: 10.1371/journal.pgen.1002062. Epub 2011 May 19. PLoS Genet. 2011. PMID: 21625620 Free PMC article.

5

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. Jeanne M, et al. Am J Hum Genet. 2012 Jan 13;90(1):91-101. doi: 10.1016/j.ajhg.2011.11.022. Epub 2011 Dec 29. Am J Hum Genet. 2012. PMID: 22209247 Free PMC article.

6

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. Weng YC, et al. Ann Neurol. 2012 Apr;71(4):470-7. doi: 10.1002/ana.22682. Ann Neurol. 2012. PMID: 22522439 Free PMC article.

7

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

Kuo DS, Labelle-Dumais C, Gould DB. Kuo DS, et al. Hum Mol Genet. 2012 Oct 15;21(R1):R97-110. doi: 10.1093/hmg/dds346. Epub 2012 Aug 21. Hum Mol Genet. 2012. PMID: 22914737 Free PMC article. Review.

8

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. Kuo DS, et al. Hum Mol Genet. 2014 Apr 1;23(7):1709-22. doi: 10.1093/hmg/ddt560. Epub 2013 Nov 7. Hum Mol Genet. 2014. PMID: 24203695 Free PMC article.

9

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

Mao M, Alavi MV, Labelle-Dumais C, Gould DB. Mao M, et al. Curr Top Membr. 2015;76:61-116. doi: 10.1016/bs.ctm.2015.09.002. Epub 2015 Oct 20. Curr Top Membr. 2015. PMID: 26610912 Review.

10

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. Hayashi G, et al. Dis Model Mech. 2018 Jul 4;11(7):dmm034157. doi: 10.1242/dmm.034157. Dis Model Mech. 2018. PMID: 29895609 Free PMC article.

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