Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Hsiao-Yuan Tang"'
Publikováno v:
PLoS ONE, Vol 4, Iss 6, p e5762 (2009)
Prestin, encoded by the gene SLC26A5, is a transmembrane protein of the cochlear outer hair cell (OHC). Prestin is required for the somatic electromotile activity of OHCs, which is absent in OHCs and causes severe hearing impairment in mice lacking p
Externí odkaz:
https://doaj.org/article/e380ca7617854219b3eacc459b49b748
Autor:
Hsiao-Yuan Tang, 唐筱媛
103
The aims of the present study were to establish a Framework of Elementary English Teacher’s Professional Knowledge and Ability, and to use expertise of English subject, knowledge and ability of professional occupation enrichment to analyze
The aims of the present study were to establish a Framework of Elementary English Teacher’s Professional Knowledge and Ability, and to use expertise of English subject, knowledge and ability of professional occupation enrichment to analyze
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/82825462421779936987
Autor:
Minor, Jacob S.1,2, Hsiao-Yuan Tang1, Pereira, Fred A.1,3, Alford, Raye Lynn1 ralford@bcm.edu
Publikováno v:
PLoS ONE. 2009, Vol. 4 Issue 6, p1-8. 8p. 1 Diagram, 5 Charts.
Autor:
Hsiao-Yuan Tang1 tang@bcm.tmc.edu, Anping Xia1 axia@bcm.tmc.edu, Oghalai, John S1 jso@bcm.tmc.edu, Pereira, Fred A1,2 fpereira@bcm.tmc.edu, Alford, Raye L1 ralford@bcm.tmc.edu
Publikováno v:
BMC Medical Genetics. 2005, Vol. 6, p1-7. 7p. 1 Diagram, 3 Charts.
Autor:
Brooke T. Osborne, Ping Fang, Jerry W. Lin, Hsiao Yuan Tang, John S. Oghalai, Sandra Darilek, Benjamin B. Roa, Jo Ann Haymond, Raye L. Alford, Spiros Manolidis
Publikováno v:
BMJ Open
Objectives Aetiological assessment of 71 probands whose clinical presentation suggested a genetic syndrome or auditory neuropathy. Methods Sanger sequencing was performed on DNA isolated from peripheral blood or lymphoblastoid cell lines. Genes were
Autor:
Ping Fang, Hsiao-Yuan Tang, Eric S. Schmitt, Sandra Darilek, John S. Oghalai, Benjamin B. Roa, Patricia A. Ward, Raye L. Alford, Spiros Manolidis
Publikováno v:
American Journal of Medical Genetics Part A. :2401-2415
Mutations in GJB2 are associated with hereditary hearing loss. DNA sequencing of GJB2 in a cohort of hearing impaired patients and a multi-ethnic control group is reported. Among 610 hearing impaired cases, 43 DNA sequence variations were identified
Autor:
Michael E. Speer, Hsiao-Yuan Tang, Eldridge Hutcheson, Margaret Drummond-Borg, Susan Neill, Raye L. Alford
Publikováno v:
Genetics in Medicine. 4:336-345
Purpose: To assess the occurrence of two mutations associated with susceptibility to aminoglycoside ototoxicity. Methods: Genetic analysis of anonymized, residual diagnostic specimens. Results: One occurrence of the A1555G mutation and seven occurren
Autor:
Hsiao-Yuan Tang, Larry I. Lipshultz, Rahul K. Nath, Edward D. Kim, Dov Kadmon, Thomas M. Wheeler, Peter T. Scardino, Brian J. Miles, Kevin M. Slawin
Publikováno v:
The Journal of Urology. :1950-1956
With the interposition of a sural nerve graft to replace resected cavernous nerves at radical retropubic prostatectomy, we have previously reported the return of effective erectile function. We determine the efficacy of this procedure in a series of
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1473:363-375
Cyanothece sp. ATCC 51142 is a unicellular, diazotrophic cyanobacterium that demonstrates diurnal rhythms for photosynthesis and N2 fixation, with peaks of O2 evolution and nitrogenase activity approximately 12 h out of phase. We cloned and sequenced
Publikováno v:
Journal of Biological Chemistry. 271:9716-9722
The bullous pemphigoid antigen BPAG1 is required for keratin filament linkage to the hemidesmosome, an adhesion complex in epithelial basal cells. BPAG1 structural organization is similar to the intermediate filament-associated proteins desmoplakin I