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Qing Ouyang, Ph.D. - Publications

Affiliations: 
2009- Molecular Biology, Cell Biology and Biochemistry Brown University, Providence, RI 
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9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Lizarraga SB, Ma L, Maguire AM, van Dyck LI, Wu Q, Ouyang Q, Kavanaugh BC, Nagda D, Livi LL, Pescosolido MF, Schmidt M, Alabi S, Cowen MH, Brito-Vargas P, Hoffman-Kim D, et al. Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13. PMID 33568516 DOI: 10.1126/scitranslmed.aaw0682  0.84
2019 Ouyang Q, Joesch-Cohen L, Mishra S, Riaz HA, Schmidt M, Morrow EM. Functional Assessment of the Mouse Homologue of the Human Ala-9-Ser NHE6 Variant. Eneuro. PMID 31676550 DOI: 10.1523/ENEURO.0046-19.2019  0.84
2019 Ouyang Q, Kavanaugh BC, Joesch-Cohen L, Dubois B, Wu Q, Schmidt M, Baytas O, Pastore SF, Harripaul R, Mishra S, Hussain A, Kim KH, Holler-Managan YF, Ayub M, Mir A, et al. GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates. Human Genetics. PMID 31471722 DOI: 10.1007/s00439-019-02057-x  0.84
2017 Xu M, Ouyang Q, Gong J, Pescosolido MF, Pruett BS, Mishra S, Schmidt M, Jones RN, Gamsiz Uzun ED, Lizarraga SB, Morrow EM. Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4. PMID 29349289 DOI: 10.1523/ENEURO.0388-17.2017  0.84
2017 Ma L, Ouyang Q, Werthmann GC, Thompson HM, Morrow EM. Live-cell Microscopy and Fluorescence-based Measurement of Luminal pH in Intracellular Organelles. Frontiers in Cell and Developmental Biology. 5: 71. PMID 28871281 DOI: 10.3389/fcell.2017.00071  0.84
2016 Ouyang Q, Nakayama T, Baytas O, Davidson SM, Yang C, Schmidt M, Lizarraga SB, Mishra S, Ei-Quessny M, Niaz S, Gul Butt M, Imran Murtaza S, Javed A, Chaudhry HR, Vaughan DJ, et al. Mutations in mitochondrial enzyme GPT2 cause metabolic dysfunction and neurological disease with developmental and progressive features. Proceedings of the National Academy of Sciences of the United States of America. PMID 27601654 DOI: 10.1073/pnas.1609221113  0.36
2015 Morrow EM, Lizarraga SB, Ouyang Q. REMOVED: Novel endosomal mechanisms in human axonal growth mediated by Christianson syndrome protein NHE6. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 20. PMID 29887063 DOI: 10.1016/j.ijdevneu.2015.04.063  0.84
2013 Ouyang Q, Lizarraga SB, Schmidt M, Yang U, Gong J, Ellisor D, Kauer JA, Morrow EM. Christianson syndrome protein NHE6 modulates TrkB endosomal signaling required for neuronal circuit development. Neuron. 80: 97-112. PMID 24035762 DOI: 10.1016/j.neuron.2013.07.043  0.36
2012 Gamsiz ED, Ouyang Q, Schmidt M, Nagpal S, Morrow EM. Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing. Genomics. 99: 44-51. PMID 22032952 DOI: 10.1016/j.ygeno.2011.09.003  0.36
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