☰

Chun Hu, Ph.D.

Affiliations: 
2016- Pharmacology Yale University, New Haven, CT 
Google:
"Chun Hu"
Mean distance: (not calculated yet)
 
Tree Publications Grants Similar researchers PubMed Report error

Parents

Sign in to add mentor
Evan P. Lebois research assistant 2012-2015 Emory
Joseph R. Manns research assistant 2012-2015 Emory
Stephen F. Traynelis research assistant 2015-2016 Emory
Minhong Yan research assistant 2017-2017 Genentech, Inc.
Mark A. Lemmon grad student 2017-2022 Yale (Chemistry Tree)

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Mudumbi KC, Burns EA, Schodt DJ, et al. (2023) Distinct interactions stabilize EGFR dimers and higher-order oligomers in cell membranes. Cell Reports. 43: 113603
Mudumbi KC, Burns EA, Schodt DJ, et al. (2023) Distinct interactions stabilize EGFR dimers and higher-order oligomers in cell membranes. Biorxiv : the Preprint Server For Biology
Hu C, Leche CA, Kiyatkin A, et al. (2022) Glioblastoma mutations alter EGFR dimer structure to prevent ligand bias. Nature. 602: 518-522
Ferguson KM, Hu C, Lemmon MA. (2020) Insulin and EGF receptor family members share parallel activation mechanisms. Protein Science : a Publication of the Protein Society
Li J, Zhang J, Tang W, et al. (2019) De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases. Human Mutation
Fry AE, Fawcett KA, Zelnik N, et al. (2018) De novo mutations in GRIN1 cause extensive bilateral polymicrogyria. Brain : a Journal of Neurology
Hu C, Chen W, Myers SJ, et al. (2017) Corrigendum to "Human GRIN2B variants in neurodevelopmental disorders" [J Pharmacol Sci 132 (2) 115-121]. Journal of Pharmacological Sciences
Platzer K, Yuan H, Schütz H, et al. (2017) GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects. Journal of Medical Genetics
Gao K, Tankovic A, Zhang Y, et al. (2017) A de novo loss-of-function GRIN2A mutation associated with childhood focal epilepsy and acquired epileptic aphasia. Plos One. 12: e0170818
Ogden KK, Chen W, Swanger SA, et al. (2017) Molecular Mechanism of Disease-Associated Mutations in the Pre-M1 Helix of NMDA Receptors and Potential Rescue Pharmacology. Plos Genetics. 13: e1006536
See more...