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Xiaofei Du

TitleResearch Associate Professor
InstitutionUniversity of Chicago
DepartmentNeurology
AddressChicago IL 60637
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Wei C, Benzow K, Koob MD, Gomez CM, Du X. Correction: The Transcription Factor, a1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development. Cerebellum. 2024 Apr; 23(2):876. PMID: 37198370; PMCID: PMC10950944.
      Citations:    Fields:    
    2. Busch SE, Simmons DH, Gama E, Du X, Longo F, Gomez CM, Klann E, Hansel C. Overexpression of the autism candidate gene Cyfip1 pathologically enhances olivo-cerebellar signaling in mice. Front Cell Neurosci. 2023; 17:1219270. PMID: 37545882; PMCID: PMC10399232.
      Citations: 1     
    3. Godfrey JD, Hejazi D, Du X, Wei C, Rao E, Gomez CM. HER2 c-Terminal Fragments Are Expressed via Internal Translation of the HER2 mRNA. Int J Mol Sci. 2022 Aug 23; 23(17). PMID: 36076950; PMCID: PMC9455161.
      Citations:    Fields:    Translation:Humans
    4. Wei C, Benzow K, Koob MD, Gomez CM, Du X. The Transcription Factor, a1ACT, Acts Through a MicroRNA Network to Regulate Neurogenesis and Cell Death During Neonatal Cerebellar Development. Cerebellum. 2023 Aug; 22(4):651-662. PMID: 35729466; PMCID: PMC10307715.
      Citations:    Fields:    Translation:Animals
    5. Simmons DH, Busch SE, Titley HK, Grasselli G, Shih J, Du X, Wei C, Gomez CM, Piochon C, Hansel C. Sensory Over-responsivity and Aberrant Plasticity in Cerebellar Cortex in a Mouse Model of Syndromic Autism. Biol Psychiatry Glob Open Sci. 2022 Oct; 2(4):450-459. PMID: 36324646; PMCID: PMC9616247.
      Citations: 2     
    6. Du X, Carvalho-de-Souza JL, Wei C, Kubota T, Staisch J, Hain T, Petrossian N, Xu M, Bezanilla F, Gomez CM, Carrasquel-Ursulaez W, Lorenzo Y, Gonzalez N, Latorre R. Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia. Proc Natl Acad Sci U S A. 2020 03 17; 117(11):6023-6034. PMID: 32132200; PMCID: PMC7084159.
      Citations: 29     Fields:    Translation:HumansAnimalsCells
    7. Du X, Wei C, Hejazi Pastor DP, Rao ER, Li Y, Grasselli G, Godfrey J, Palmenberg AC, Andrade J, Hansel C, Gomez CM. a1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window. Neuron. 2019 05 22; 102(4):770-785.e7. PMID: 30922876; PMCID: PMC6533132.
      Citations: 13     Fields:    Translation:HumansAnimalsCells
    8. Pastor PDH, Du X, Fazal S, Davies AN, Gomez CM. Targeting the CACNA1A IRES as a Treatment for Spinocerebellar Ataxia Type 6. Cerebellum. 2018 02; 17(1):72-77. PMID: 29374372; PMCID: PMC5809202.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    9. Du X, Gomez CM. Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics. Adv Exp Med Biol. 2018; 1049:147-173. PMID: 29427102.
      Citations: 10     Fields:    Translation:HumansAnimalsCells
    10. Du X, Gomez CM. Erratum to: Spinocerebellar Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics. Adv Exp Med Biol. 2018; 1049:E1. PMID: 29637516.
      Citations:    Fields:    
    11. Miyazaki Y, Du X, Muramatsu S, Gomez CM. An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron. Sci Transl Med. 2016 07 13; 8(347):347ra94. PMID: 27412786; PMCID: PMC5241274.
      Citations: 28     Fields:    Translation:HumansAnimalsCells
    12. McMurray KM, Du X, Brownlee M, Palmer AA. Neuronal overexpression of Glo1 or amygdalar microinjection of methylglyoxal is sufficient to regulate anxiety-like behavior in mice. Behav Brain Res. 2016 Mar 15; 301:119-23. PMID: 26711908; PMCID: PMC4728018.
      Citations: 11     Fields:    Translation:HumansAnimalsCells
    13. Du X, Semler BL, Gomez CM. Revelations from a bicistronic calcium channel gene. Cell Cycle. 2014; 13(6):875-6. PMID: 24552819; PMCID: PMC3984306.
      Citations: 2     Fields:    Translation:HumansAnimals
    14. Du X, Wang J, Zhu H, Rinaldo L, Lamar KM, Palmenberg AC, Hansel C, Gomez CM. Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6. Cell. 2013 Jul 03; 154(1):118-33. PMID: 23827678; PMCID: PMC3939801.
      Citations: 86     Fields:    Translation:HumansAnimalsCells
    15. Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM. A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult. Hum Mol Genet. 2012 Dec 15; 21(26):5472-83. PMID: 23001565; PMCID: PMC3516132.
      Citations: 33     Fields:    Translation:HumansAnimalsCells
    16. Du X, Rosenfield RL, Qin K. KLF15 Is a transcriptional regulator of the human 17beta-hydroxysteroid dehydrogenase type 5 gene. A potential link between regulation of testosterone production and fat stores in women. J Clin Endocrinol Metab. 2009 Jul; 94(7):2594-601. PMID: 19366843; PMCID: PMC2708951.
      Citations: 29     Fields:    Translation:HumansAnimalsCells
    17. Qin K, Du X, Rich BH. An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome. Mol Genet Metab. 2007 Dec; 92(4):359-63. PMID: 17911039.
      Citations: 4     Fields:    Translation:HumansCells
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