Search Results - "Zheng, Q.Y"

Tauroursodeoxycholic acid prevents hearing loss and hair cell death in Cdh23erl/erl mice by Hu, J, Xu, M, Yuan, J, Li, B, Entenman, S, Yu, H, Zheng, Q.Y

“…Highlights • Cdh23erl/erl mutant mouse is an established model of genetic hearing loss. • Tauroursodeoxycholic acid (TUDCA) has been used in diseases related…”
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Otoprotective effects of erythropoietin on Cdh23erl/erl mice by Han, F, Yu, H, Zheng, T, Ma, X, Zhao, X, Li, P, Le, L, Su, Y, Zheng, Q.Y

“…Highlights ► The Cdh23erl/erl mice are a novel mouse model for progressive hearing loss. ► We evaluated EPO as an effective as an otoprotectant on the…”
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A new spontaneous mutation in the mouse protocadherin 15 gene by Zheng, Q.Y., Yu, H., Washington, J.L., Kisley, L.B., Kikkawa, Y.S., Pawlowski, K.S., Wright, C.G., Alagramam, K.N.

“…We have characterized a new allele of the protocadherin 15 gene (designated Pcdh15 av-6 J ) that arose as a spontaneous, recessive mutation in the C57BL/6J…”
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The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC by JOHNSON, K. R, ZHENG, Q. Y, WESTON, M. D, PTACEK, L. J, NOBEN-TRAUTH, K

“…The human ortholog of the gene responsible for audiogenic seizure susceptibility in Frings and BUB/BnJ mice (mouse gene symbol Mass1) recently was shown to…”
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new spontaneous mouse mutation in the Kcne1 gene by Letts, V.A, Valenzuela, A, Dunbar, C, Zheng, Q.Y, Johnson, K.R, Frankel, W.N

“…A new mouse mutant, punk rocker (allele symbol Kcne1 ᵖᵏʳ ), arose spontaneously on a C57BL/10J inbred strain background and is characterized by a distinctive…”
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POS-825 LIGHT-HEVEM/LTβR pathway mediates the ischemic acute kidney injury by promoting oxidative stress and mitochondria dysfunction by ZHANG, K.Q., Zheng, Q.Y., Li, Y., Xu, G.L.

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Tauroursodeoxycholic acid prevents hearing loss and hair cell death in Cdh23(erl/erl) mice by Hu, J, Xu, M, Yuan, J, Li, B, Entenman, S, Yu, H, Zheng, Q Y

“…Sensorineural hearing loss has long been the subject of experimental and clinical research for many years. The recently identified novel mutation of the…”
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Alms1-disrupted mice recapitulate human Alström syndrome by Collin, G B, Cyr, E, Bronson, R, Marshall, J D, Gifford, E J, Hicks, W, Murray, S A, Zheng, Q Y, Smith, R S, Nishina, P M, Naggert, J K

“…Mutations in the human ALMS1 gene cause Alström syndrome (AS), a progressive disease characterized by neurosensory deficits and by metabolic defects including…”
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Imidazole alkaloids from Lepidium meyenii by Cui, B, Zheng, B.L, He, K, Zheng, Q.Y

“…Two new imidazole alkaloids (lepidiline A and lepidiline B) have been isolated from a root extract of Lepidium meyenii with the common name Maca and identified…”
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A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs by Han, F, Yu, H, Tian, C, Chen, H E, Benedict-Alderfer, C, Zheng, Y, Wang, Q, Han, X, Zheng, Q Y

“…We report a novel mutation (erlong, erl) of the cadherin 23 ( Cdh23 ) gene in a mouse model for DFNB12 characterized by progressive hearing loss beginning from…”
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Electronic and transport properties of a biased multilayer hexagonal boron nitride by Tang, K., Ni, Z. Y., Liu, Q. H., Quhe, R. G., Zheng, Q. Y., Zheng, J. X., Fei, R. X., Gao, Z. X., Lu, J.

“…We explore the electronic and transport properties out of a biased multilayer hexagonal boron nitride (h-BN) by first-principles calculations. The band gaps of…”
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Hyperactivity, startle reactivity and cell‐proliferation deficits are resistant to chronic lithium treatment in adult Nr2e1 frc/frc mice by Wong, B. K. Y., Hossain, S. M., Trinh, E., Ottmann, G. A., Budaghzadeh, S., Zheng, Q.Y., Simpson, E. M.

“…The NR2E1 region on Chromosome 6q21‐22 has been repeatedly linked to bipolar disorder (BP) and NR2E1 has been associated with BP, and more specifically bipolar…”
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Hyperactivity, startle reactivity and cell‐proliferation deficits are resistant to chronic lithium treatment in adult Nr2e1frc/frc mice by Wong, B. K. Y., Hossain, S. M., Trinh, E., Ottmann, G. A., Budaghzadeh, S., Zheng, Q.Y., Simpson, E. M.

“…The NR2E1 region on Chromosome 6q21‐22 has been repeatedly linked to bipolar disorder (BP) and NR2E1 has been associated with BP, and more specifically bipolar…”
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The Mass1 frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC by Johnson, K.R., Zheng, Q.Y., Weston, M.D., Ptacek, L.J., Noben-Trauth, K.

“…The human ortholog of the gene responsible for audiogenic seizure susceptibility in Frings and BUB/BnJ mice (mouse gene symbol Mass1) recently was shown to…”
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Alms1-disrupted mice recapitulate human Alström syndrome by Collin, G.B., Cyr, E., Bronson, R., Marshall, J.D., Gifford, E.J., Hicks, W., Murray, S.A., Zheng, Q.Y., Smith, R.S., Nishina, P.M., Naggert, J.K.

“…Mutations in the human ALMS1 gene cause Alström syndrome (AS), a progressive disease characterized by neurosensory deficits and by metabolic defects including…”
Get full text