Xiangming Li, Ph.D. - Publications

Affiliations: 
2013 Department of Biochemistry Kansas State University, Manhattan, KS, United States 
Area:
Biochemistry, Physiology Biology

9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Honda K, Kim SH, Kelly MC, Burns JC, Constance L, Li X, Zhou F, Hoa M, Kelley MW, Wangemann P, Morell RJ, Griffith AJ. Molecular architecture underlying fluid absorption by the developing inner ear. Elife. 6. PMID 28994389 DOI: 10.7554/Elife.26851  0.648
2017 Honda K, Kim SH, Kelly MC, Burns JC, Constance L, Li X, Zhou F, Hoa M, Kelley MW, Wangemann P, Morell RJ, Griffith AJ. Author response: Molecular architecture underlying fluid absorption by the developing inner ear Elife. DOI: 10.7554/Elife.26851.034  0.566
2014 Ito T, Li X, Kurima K, Choi BY, Wangemann P, Griffith AJ. Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction. Neurobiology of Disease. 66: 53-65. PMID 24561068 DOI: 10.1016/J.Nbd.2014.02.002  0.647
2013 Ito T, Muskett J, Chattaraj P, Choi BY, Lee KY, Zalewski CK, King KA, Li X, Wangemann P, Shawker T, Brewer CC, Alper SL, Griffith AJ. SLC26A4 mutation testing for hearing loss associated with enlargement of the vestibular aqueduct. World Journal of Otorhinolaryngology. 3: 26-34. PMID 25960948 DOI: 10.5319/wjo.v3.i2.26  0.591
2013 Li X, Sanneman JD, Harbidge DG, Zhou F, Ito T, Nelson R, Picard N, Chambrey R, Eladari D, Miesner T, Griffith AJ, Marcus DC, Wangemann P. SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice. Plos Genetics. 9: e1003641. PMID 23874234 DOI: 10.1371/Journal.Pgen.1003641  0.664
2013 Li X, Zhou F, Marcus DC, Wangemann P. Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin. Plos One. 8: e65977. PMID 23741519 DOI: 10.1371/Journal.Pone.0065977  0.611
2011 Bronckers AL, Guo J, Zandieh-Doulabi B, Bervoets TJ, Lyaruu DM, Li X, Wangemann P, DenBesten P. Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teeth. European Journal of Oral Sciences. 119: 185-92. PMID 22243245 DOI: 10.1111/J.1600-0722.2011.00901.X  0.603
2011 Choi BY, Kim HM, Ito T, Lee KY, Li X, Monahan K, Wen Y, Wilson E, Kurima K, Saunders TL, Petralia RS, Wangemann P, Friedman TB, Griffith AJ. Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition. The Journal of Clinical Investigation. 121: 4516-25. PMID 21965328 DOI: 10.1172/Jci59353  0.661
2009 Wangemann P, Kim HM, Billings S, Nakaya K, Li X, Singh R, Sharlin DS, Forrest D, Marcus DC, Fong P. Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression. American Journal of Physiology. Renal Physiology. 297: F1435-47. PMID 19692489 DOI: 10.1152/Ajprenal.00011.2009  0.662
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