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Cassandre Labelle-Dumais
Cassandre Labelle-Dumais
UCSF School of Medicine
Overená e-mailová adresa na: vision.ucsf.edu
Názov
Citované v
Citované v
Rok
COL4A1 and COL4A2 mutations and disease: insights into pathogenic mechanisms and potential therapeutic targets
DS Kuo, C Labelle-Dumais, DB Gould
Human molecular genetics 21 (R1), R97-R110, 2012
2972012
Uterine Wnt/β-catenin signaling is required for implantation
OA Mohamed, M Jonnaert, C Labelle-Dumais, K Kuroda, HJ Clarke, ...
Proceedings of the National Academy of Sciences 102 (24), 8579-8584, 2005
2872005
COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke
M Jeanne, C Labelle-Dumais, J Jorgensen, WB Kauffman, GM Mancini, ...
The American Journal of Human Genetics 90 (1), 91-101, 2012
2202012
COL4A1 mutations in patients with sporadic late‐onset intracerebral hemorrhage
YC Weng, A Sonni, C Labelle‐Dumais, M de Leau, WB Kauffman, ...
Annals of neurology 71 (4), 470-477, 2012
1392012
COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans
C Labelle-Dumais, DJ Dilworth, EP Harrington, M de Leau, D Lyons, ...
PLoS genetics 7 (5), e1002062, 2011
1392011
Type IV collagens and basement membrane diseases: cell biology and pathogenic mechanisms
M Mao, MV Alavi, C Labelle-Dumais, DB Gould
Current topics in membranes 76, 61-116, 2015
882015
Netrin‐1 receptor‐deficient mice show enhanced mesocortical dopamine transmission and blunted behavioural responses to amphetamine
A Grant, D Hoops, C Labelle‐Dumais, M Prévost, H Rajabi, B Kolb, ...
European Journal of Neuroscience 26 (11), 3215-3228, 2007
802007
Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
AM Slavotinek, SE Baranzini, D Schanze, C Labelle-Dumais, KM Short, ...
Journal of medical genetics 48 (6), 375-382, 2011
692011
Peri-pubertal emergence of UNC-5 homologue expression by dopamine neurons in rodents
C Manitt, C Labelle-Dumais, C Eng, A Grant, A Mimee, T Stroh, C Flores
PloS one 5 (7), e11463, 2010
682010
Allelic heterogeneity contributes to variability in ocular dysgenesis, myopathy and brain malformations caused by Col4a1 and Col4a2 mutations
DS Kuo, C Labelle-Dumais, M Mao, M Jeanne, WB Kauffman, J Allen, ...
Human molecular genetics 23 (7), 1709-1722, 2014
652014
Nuclear receptor NR5A2 is required for proper primitive streak morphogenesis
C Labelle‐Dumais, M Jacob‐Wagner, JF Paré, L Bélanger, D Dufort
Developmental dynamics: an official publication of the American Association …, 2006
572006
Regulation of netrin-1 receptors by amphetamine in the adult brain
L Yetnikoff, C Labelle-Dumais, C Flores
Neuroscience 150 (4), 764-773, 2007
532007
COL4A1 mutations cause neuromuscular disease with tissue-specific mechanistic heterogeneity
C Labelle-Dumais, V Schuitema, G Hayashi, K Hoff, W Gong, DQ Dao, ...
The American Journal of Human Genetics 104 (5), 847-860, 2019
432019
Post‐pubertal emergence of a dopamine phenotype in netrin‐1 receptor‐deficient mice
A Grant, Z Speed, C Labelle‐Dumais, C Flores
European Journal of Neuroscience 30 (7), 1318-1328, 2009
372009
Impaired Progesterone Production in Nr5a2+/− Mice Leads to a Reduction in Female Reproductive Function
C Labelle-Dumais, JF Paré, L Bélanger, R Farookhi, D Dufort
Biology of reproduction 77 (2), 217-225, 2007
372007
Müller glia-derived PRSS56 is required to sustain ocular axial growth and prevent refractive error
S Paylakhi, C Labelle-Dumais, NG Tolman, MA Sellarole, Y Seymens, ...
PLoS genetics 14 (3), e1007244, 2018
352018
Chronic phencyclidine treatment increases dendritic spine density in prefrontal cortex and nucleus accumbens neurons
C Flores, X Wen, C Labelle‐Dumais, B Kolb
Synapse 61 (12), 978-984, 2007
332007
Use of sodium 4-phenylbutyrate to define therapeutic parameters for reducing intracerebral hemorrhage and myopathy in Col4a1 mutant mice
G Hayashi, C Labelle-Dumais, DB Gould
Disease models & mechanisms 11 (7), dmm034157, 2018
272018
Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation
S Koli, C Labelle-Dumais, Y Zhao, S Paylakhi, KS Nair
PLoS Genetics 17 (3), e1009458, 2021
142021
Altered netrin‐1 receptor expression in dopamine terminal regions following neonatal ventral hippocampal lesions in the rat
C Flores, SK Bhardwaj, C Labelle‐Dumais, LK Srivastava
Synapse 63 (1), 54-60, 2009
142009
Systém momentálne nemôže vykonať operáciu. Skúste to neskôr.
Články 1–20