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Matrix Biology : Journal of the International Society for Matrix Biology|November 26, 2022
Elevated TGFβ signaling contributes to cerebral small vessel disease in mouse models of Gould syndromeKayla Branyan, Cassandre Labelle-Dumais, Xiaowei Wang, et al.American Journal of Human Genetics|May 4, 2019
COL4A1 Mutations Cause Neuromuscular Disease with Tissue-Specific Mechanistic HeterogeneityCassandre Labelle-Dumais, Vera Schuitema, Genki Hayashi, et al.Science Signaling|November 14, 2023
Impaired intracellular Ca<sup>2+</sup> signaling contributes to age-related cerebral small vessel disease in <i>Col4a1</i> mutant miceEvan Yamasaki, Pratish Thakore, Sher Ali, et al.American Journal of Human Genetics|January 3, 2012
COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic strokeMarion Jeanne, Cassandre Labelle-Dumais, Jeff Jorgensen, et al.Annals of Neurology|April 24, 2012
COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhageYi-Chinn Weng, Akshata Sonni, Cassandre Labelle-Dumais, et al.Biorxiv : the Preprint Server for Biology|February 6, 2026
PRSS56 acts as an intrinsic retinal signal driving postnatal ocular axial growth and myopia susceptibilityKiran Gangappa, Durairaj Duraikannu, Jayshree Advani, et al.The Journal of Cell Biology|April 25, 2025
A multifunction murine Col4a1 allele reveals potential gene therapy parameters for Gould syndromeMao Mao, Yoshihiro Ishikawa, Cassandre Labelle-Dumais, et al.Plos Genetics|March 13, 2018
Müller glia-derived PRSS56 is required to sustain ocular axial growth and prevent refractive errorSeyyedhassan Paylakhi, Cassandre Labelle-Dumais, Nicholas G Tolman, et al.Plos Genetics|June 1, 2011
COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humansCassandre Labelle-Dumais, David J Dilworth, Emily P Harrington, et al.Disease Models & Mechanisms|March 11, 2020
Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressureCassandre Labelle-Dumais, Goutham Pyatla, Seyyedhassan Paylakhi, et al.Pageof 4