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Sabrina Yum

Research Profile

Chemicals & Drugs

Anatomy

Procedures

Disorders

Physiology

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Electrophysiology

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Quaternary Protein Structure

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Publications

TOP 3
Sabrina W Yum; Junxian Zhang; Steven S Scherer
Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30.
Sabrina W Yum; Junxian Zhang; Katie Mo; Jian Li; Steven S Scherer
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.
Sabrina W Yum; Junxian Zhang; Virginijus Valiunas; Giedrius Kanaporis; Peter R Brink; Thomas W White; Steven S Scherer
Human connexin26 and connexin30 form functional heteromeric and heterotypic channels.

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All Publications

2010: Sabrina W Yum; Junxian Zhang; Steven S Scherer
Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30.
Neurobiology of disease 2010;38(2):226-36.
2009: Sabrina W Yum; Junxian Zhang; Katie Mo; Jian Li; Steven S Scherer
A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy.
Annals of neurology 2009;66(6):759-70.
2007: Sabrina W Yum; Junxian Zhang; Virginijus Valiunas; Giedrius Kanaporis; Peter R Brink; Thomas W White; Steven S Scherer
Human connexin26 and connexin30 form functional heteromeric and heterotypic channels.
American journal of physiology. Cell physiology 2007;293(3):C1032-48.
2002: Sabrina W Yum; Kleopas A Kleopa; Susan Shumas; Steven S Scherer
Diverse trafficking abnormalities of connexin32 mutants causing CMTX.
Neurobiology of disease 2002;11(1):43-52.
2002: Kleopas A Kleopa; Sabrina W Yum; Steven S Scherer
Cellular mechanisms of connexin32 mutations associated with CNS manifestations.
Journal of neuroscience research 2002;68(5):522-34.
1997: David R Lynch; H Hara; Sabrina W Yum; Phillip F Chance; Steven S Scherer; Shawn J Bird; Kenneth H Fischbeck
Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III).
Neurology 1997;49(2):601-3.

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