Anne C. Hart

Affiliations: 
Harvard Medical School, Boston, MA, United States 
 Neuroscience Brown University, Providence, RI 
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"Anne Hart"
Mean distance: 15.29 (cluster 11)
 
SNBCP

Children

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Ivan C. Alcantara research assistant Brown
Lukas Lu Skuja research assistant 2014-2017 Brown
Gal Haspel post-doc 2004- Harvard Medical School
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Publications

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Walsh MB, Janzen E, Wingrove E, et al. (2020) Genetic modifiers ameliorate endocytic and neuromuscular defects in a model of spinal muscular atrophy. Bmc Biology. 18: 127
Schuch KN, Govindarajan LN, Guo Y, et al. (2020) Discriminating between sleep and exercise-induced fatigue using computer vision and behavioral genetics. Journal of Neurogenetics. 1-13
Huang H, Hayden DJ, Zhu CT, et al. (2018) Gap Junctions and NCA Cation Channels Are Critical for Developmentally-Timed Sleep and Arousal in . Genetics
Baskoylu SN, Yersak J, O'Hern P, et al. (2018) Single copy/knock-in models of ALS SOD1 in C. elegans suggest loss and gain of function have different contributions to cholinergic and glutamatergic neurodegeneration. Plos Genetics. 14: e1007682
Bennett HL, Khoruzhik Y, Hayden D, et al. (2018) Normal sleep bouts are not essential for C. elegans survival and FoxO is important for compensatory changes in sleep. Bmc Neuroscience. 19: 10
Huang H, Zhu CT, Skuja LL, et al. (2017) Genome-Wide Screen for Genes Involved in Caenorhabditis elegans Developmentally Timed Sleep. G3 (Bethesda, Md.)
O'Hern PJ, do Carmo G Gonçalves I, Brecht J, et al. (2017) Decreased microRNA levels lead to deleterious increases in neuronal M2 muscarinic receptors in Spinal Muscular Atrophy models. Elife. 6
Huang H, Zhu Y, Eliot MN, et al. (2017) Combining Human Epigenetics and Sleep Studies in C. elegans: A Cross-species Approach for Finding Conserved Genes Regulating Sleep. Sleep
Riessland M, Kaczmarek A, Schneider S, et al. (2017) Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis. American Journal of Human Genetics
Sorkaç A, Alcantara IC, Hart AC. (2016) In Vivo Modelling of ATP1A3 G316S-Induced Ataxia in C. elegans Using CRISPR/Cas9-Mediated Homologous Recombination Reveals Dominant Loss of Function Defects. Plos One. 11: e0167963
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