Cassandre Labelle-Dumais

发表

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

C. Labelle-Dumais, Debbie S Kuo, D. Gould, 2012, Human molecular genetics.

Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation.

C. Labelle-Dumais, Yin-yin Zhao, K. S. Nair, 2021, PLoS genetics.

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

S. Greenberg, J. Rosand, J. Favor, 2012, American journal of human genetics.

Netrin-1 receptor deficiency protects against psychostimulant-induced behaviours in mice

Daniel S. Hoops, C. Flores, D. Hoops, 2008, McGill Science Undergraduate Research Journal.

Uterine Wnt/β-catenin signaling is required for implantation

D. Dufort, H. Clarke, C. Labelle-Dumais, 2005 .

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

D. Dufort, H. Clarke, C. Labelle-Dumais, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Elevated TGFβ signaling contributes to ocular anterior segment dysgenesis in Col4a1 mutant mice.

D. Keene, D. B. Gould, C. Labelle-Dumais, 2022, Matrix biology : journal of the International Society for Matrix Biology.

COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans

C. Walsh, D. Dilworth, W. Dobyns, 2011, PLoS genetics.

Identification of ADAMTS19 as a novel retinal factor involved in ocular growth regulation

C. Labelle-Dumais, Yin-yin Zhao, K. S. Nair, 2020, bioRxiv.

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

S. John, S. John, P. Topilko, 2018, PLoS genetics.

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

Mohamed G. Hassan, P. Kwok, S. Baranzini, 2011, Journal of Medical Genetics.

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

Genki Hayashi, C. Labelle-Dumais, D. Gould, 2018, Disease Models & Mechanisms.

COL4A1 mutations in patients with sporadic late‐onset intracerebral hemorrhage

S. Greenberg, A. Biffi, J. Rosand, 2012, Annals of neurology.

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

D. B. Gould, C. Labelle-Dumais, Mao Mao, 2015, Current topics in membranes.

Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure

R. Khanna, S. John, S. Senthil, 2020, Disease Models & Mechanisms.

PRSS56 is required for the developmental positioning of ocular angle structures

S. John, C. Labelle-Dumais, Nicholas G. Tolman, 2018, bioRxiv.

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

B. Kolb, C. Flores, C. Labelle-Dumais, 2007, Synapse.

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

Daniel S. Hoops, B. Kolb, A. Arvanitogiannis, 2007, The European journal of neuroscience.

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

C. Flores, C. Labelle-Dumais, A. Grant, 2009, The European journal of neuroscience.

Elevated TGFβ Signaling Contributes to Cerebral Small Vessel Disease in Mouse Models of Gould Syndrome.

Genki Hayashi, D. B. Gould, C. Labelle-Dumais, 2022, Matrix biology : journal of the International Society for Matrix Biology.

Impaired Progesterone Production in Nr5a2+/− Mice Leads to a Reduction in Female Reproductive Function1

J. Paré, D. Dufort, C. Labelle-Dumais, 2007, Biology of reproduction.

Nuclear receptor NR5A2 is required for proper primitive streak morphogenesis

J. Paré, D. Dufort, C. Labelle-Dumais, 2006, Developmental dynamics : an official publication of the American Association of Anatomists.

Impaired intracellular Ca2+ signaling contributes to age-related cerebral small vessel disease in Col4a1 mutant mice

M. Chaumeil, S. Earley, C. Labelle-Dumais, 2023, bioRxiv.

COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic Heterogeneity.

E. Ullian, Genki Hayashi, C. Labelle-Dumais, 2019, American journal of human genetics.

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

J. Favor, D. B. Gould, M. Jeanne, 2013, Human molecular genetics.

Defective Ca 2+ - dependent activation of TRPM4 channels contributes to age-related cerebral small vessel disease in Col4a1 mutant mice

M. Chaumeil, D. B. Gould, S. Earley, 2022 .

Peri-Pubertal Emergence of UNC-5 Homologue Expression by Dopamine Neurons in Rodents

C. Flores, T. Stroh, C. Labelle-Dumais, 2010, PloS one.

PI3K block restores age-dependent neurovascular coupling defects associated with cerebral small vessel disease

M. Chaumeil, S. Earley, Xiao Gao, 2023, Proceedings of the National Academy of Sciences of the United States of America.

PI3K block restores age-dependent neurovascular coupling defects associated with cerebral small vessel disease

M. Chaumeil, S. Earley, Xiao Gao, 2023, bioRxiv.

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

C. Flores, L. Srivastava, S. Bhardwaj, 2009, Synapse.

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

L. Yetnikoff, C. Flores, C. Labelle-Dumais, 2007, Neuroscience.

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

Genki Hayashi, D. Gould, Cassandre Labelle-Dumais, 2018, Disease Models & Mechanisms.

Skeletal pathology in mouse models of Gould syndrome is partially alleviated by genetically reducing TGFβ signaling.

Serra Kaya, Bryson Lee, Cassandre Labelle-Dumais, 2024, Matrix biology : journal of the International Society for Matrix Biology.