Xiangming Li

发表

SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct.

T. Shawker, A. Griffith, B. Choi, 2013, World journal of otorhinolaryngology.

Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teeth.

P. Wangemann, B. Zandieh-Doulabi, A. Bronckers, 2011, European journal of oral sciences.

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.

David S. Sharlin, D. Sharlin, D. Forrest, 2009, American journal of physiology. Renal physiology.

SLC 26 A 4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc 26 a 4 Mutant Mice

A. Griffith, R. Chambrey, P. Wangemann, 2013 .

Endolymphatic Na+ and K+ Concentrations during Cochlear Growth and Enlargement in Mice Lacking Slc26a4/pendrin

P. Wangemann, D. C. Marcus, Xiangming Li, 2013, PloS one.

SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice

A. Griffith, R. Chambrey, P. Wangemann, 2013, PLoS genetics.

Developmental expression of SLC26A4 (Pendrin) during amelogenesis in developing rodent teeth

P. Wangemann, B. Zandieh-Doulabi, A. Bronckers, 2012 .

Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.

R. Petralia, A. Griffith, T. Friedman, 2011, The Journal of clinical investigation.

Restoring hearing and balance in a mouse model of SLC26A4-related deafness

Xiangming Li, 2013 .

Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction

A. Griffith, B. Choi, P. Wangemann, 2014, Neurobiology of Disease.

Molecular architecture underlying fluid absorption by the developing inner ear

Michael C. Kelly, A. Griffith, M. Kelley, 2017, eLife.