Fang He, Ph.D.

Affiliations: 
1999-2001 Biology Jiangxi Institute of Education 
 2001-2004 Biochemistry and Molecular Biology Nanjing University, Nanjing Shi, Jiangsu Sheng, China 
 2004-2011 Biological Sciences Louisiana State University, Baton Rouge, LA, United States 
 2011- Neurology University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Fly Genetics, Neurodegeneration
Website:
https://www.linkedin.com/pub/fang-he/95/812/8b0
Google:
"Fang He"
Bio:

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Publications

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He F, Flores BN, Krans A, et al. (2020) The carboxyl termini of RAN translated GGGGCC nucleotide repeat expansions modulate toxicity in models of ALS/FTD. Acta Neuropathologica Communications. 8: 122
Linsalata AE, He F, Malik AM, et al. (2019) DDX3X and specific initiation factors modulate FMR1 repeat-associated non-AUG-initiated translation. Embo Reports. e47498
Sellier C, Buijsen RA, He F, et al. (2017) Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome. Neuron
Yang WY, He F, Strack RL, et al. (2016) Small Molecule Recognition and Tools to Study Modulation of r(CGG)exp in Fragile X-Associated Tremor Ataxia Syndrome. Acs Chemical Biology
He F, Jones JM, Figueroa-Romero C, et al. (2016) Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci. Neurology. Genetics. 2: e71
Oh SY, He F, Krans A, et al. (2015) RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome. Human Molecular Genetics. 24: 4317-26
He F, James A, Raje H, et al. (2015) Deletion of Drosophila Nopp140 induces subcellular ribosomopathies. Chromosoma. 124: 191-208
He F, Krans A, Freibaum BD, et al. (2014) TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1. Human Molecular Genetics. 23: 5036-51
Todd PK, Oh SY, Krans A, et al. (2013) CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome. Neuron. 78: 440-55
Meisler MH, Grant AE, Jones JM, et al. (2013) C9ORF72 expansion in a family with bipolar disorder. Bipolar Disorders. 15: 326-32
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