Yaohui Chai

University of Tennessee Health Science Center — United States

Neuroscience · Life Sciences

10h-index2.1kcitations13works0.02yr avg
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Research Topics

Genetic Neurodegenerative Diseases(7), Mitochondrial Function and Pathology(6), Inflammatory Myopathies and Dermatomyositis(3), Muscle Physiology and Disorders(2), Neurological disorders and treatments(2)

Publications13 total

Dermatomyositis Presenting With Focal Scleroderma-Like Skin Changes
Journal of Clinical Neuromuscular Disease·2012· 1 cited
Limb edema and anasarca associated with severe dermatomyositis: Report of four cases
Neuromuscular Disorders·2011· 23 cited
Hereditary inclusion‐body myopathy associated with cardiomyopathy: Report of two siblings
Muscle & Nerve·2010· 29 cited
A Female With Progressive Four-Limb Paresthesias and Gait Difficulty
Journal of Clinical Neuromuscular Disease·2010· 4 cited
Cryptogenic Gelastic Epilepsy Originating from the Right Temporal Lobe
Medical Principles and Practice·2010· 10 citedOpen Access
Defining the Role of Ubiquitin-interacting Motifs in the Polyglutamine Disease Protein, Ataxin-3
Journal of Biological Chemistry·2005· 102 citedOpen Access
Poly-ubiquitin Binding by the Polyglutamine Disease Protein Ataxin-3 Links Its Normal Function to Protein Surveillance Pathways
Journal of Biological Chemistry·2004· 170 citedOpen Access
Live-cell imaging reveals divergent intracellular dynamics of polyglutamine disease proteins and supports a sequestration model of pathogenesis
Proceedings of the National Academy of Sciences·2002· 203 citedOpen Access
The Role of Protein Composition in Specifying Nuclear Inclusion Formation in Polyglutamine Disease
Journal of Biological Chemistry·2001· 116 citedOpen Access
Suppression of polyglutamine-mediated neurodegeneration in Drosophila by the molecular chaperone HSP70
Nature Genetics·1999· 832 cited
Analysis of the Role of Heat Shock Protein (Hsp) Molecular Chaperones in Polyglutamine Disease
Journal of Neuroscience·1999· 428 citedOpen Access
Association of Gonadotropin Receptor Precursors with the Protein Folding Chaperone Calnexin<sup>1</sup>
Endocrinology·1998· 68 citedOpen Access
A Homozygous Microdeletion in Helix 7 of the Luteinizing Hormone Receptor Associated with Familial Testicular and Ovarian Resistance Is Due to Both Decreased Cell Surface Expression and Impaired Effector Activation by the Cell Surface Receptor
Molecular Endocrinology·1998· 122 citedOpen Access

Frequent Co-authors

Henry L. Paulson(6), Tulio E. Bertorini(4), Nancy M. Bonini(2), Deborah L. Segaloff(2), John M. Warrick(1), Ho Yin Edwin Chan(1), Gladys L. Gray-Board(1), Stacia L. Koppenhafer(1), Jianqiang Shao(1), Victor M. Miller(1), Aislinn Williams(1), Sarah Shoesmith Berke(1), Robert E. Cohen(1), Ana Cláudia Latronico(1), Ivo J.P. Arnhold(1), Xuebo Liu(1), Berenice B. Mendonça(1), Lizi Wu(1), James D. Griffin(1), Sarah J Shoesmith Berke(1)