Joanna Pucilowska, Ph.D.

Affiliations: 
2012 Neurosciences Case Western Reserve University, Cleveland Heights, OH, United States 
Area:
Neuroscience Biology
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"Joanna Pucilowska"
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Gary Landreth grad student 2012 Case Western
 (Inactivation of ERK1 and ERK2 disrupts cortical progenitor proliferation leading to abnormal cytoarchitecture, circuitry and behavior, modeling human NCFC and related syndromes.)
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Publications

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Vithayathil J, Pucilowska J, Landreth GE. (2018) ERK/MAPK signaling and autism spectrum disorders. Progress in Brain Research. 241: 63-112
Pucilowska J, Vithayathil J, Pagani M, et al. (2018) Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Vithayathil J, Pucilowska J, Friel D, et al. (2017) Chronic impairment of ERK signaling in glutamatergic neurons of the forebrain does not affect spatial memory retention and LTP in the same manner as acute blockade of the ERK pathway. Hippocampus
Vithayathil J, Pucilowska J, Goodnough LH, et al. (2015) Dentate Gyrus Development Requires ERK Activity to Maintain Progenitor Population and MAPK Pathway Feedback Regulation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 6836-48
Pucilowska J, Vithayathil J, Tavares EJ, et al. (2015) The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 3190-200
Pucilowska J, Puzerey PA, Karlo JC, et al. (2012) Disrupted ERK signaling during cortical development leads to abnormal progenitor proliferation, neuronal and network excitability and behavior, modeling human neuro-cardio-facial-cutaneous and related syndromes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 8663-77
Higgins JJ, Lombardi RQ, Pucilowska J, et al. (2006) HS1-BP3 gene variant is common in familial essential tremor. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 306-9
Higgins JJ, Lombardi RQ, Pucilowska J, et al. (2005) A variant in the HS1-BP3 gene is associated with familial essential tremor Neurology. 64: 417-421
Higgins JJ, Lombardi RQ, Pucilowska J, et al. (2005) Reply from the authors [2] Neurology. 65: 1995
Higgins JJ, Pucilowska J, Lombardi RQ, et al. (2004) A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardation. Neurology. 63: 1927-31
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