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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
臺大學術典藏 2021-08-05T02:41:21Z A novel synthesis of sulfurized magnetic biochar for aqueous Hg(II) capture as a potential method for environmental remediation in water Hsu C.-J;Cheng Y.-H;Huang Y.-P;Atkinson J.D;Hsi H.-C.; Hsu C.-J; Cheng Y.-H; Huang Y.-P; Atkinson J.D; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-08-05T02:41:20Z Adsorption of aqueous Hg2+ and inhibition of Hg0 re-emission from actual seawater flue gas desulfurization wastewater by using sulfurized activated carbon and NaClO Hsu C.-J;Chen Y.-H;Hsi H.-C.; Hsu C.-J; Chen Y.-H; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-08-05T02:41:20Z A simulation study of mercury immobilization in estuary sediment microcosm by activated carbon/clay-based thin-layer capping under artificial flow and turbation Ting Y;Ch'ng B.-L;Chen C;Ou M.-Y;Cheng Y.-H;Hsu C.-J;Hsi H.-C.; Ting Y; Ch'ng B.-L; Chen C; Ou M.-Y; Cheng Y.-H; Hsu C.-J; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-07-26T10:01:32Z A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss Lin Y.-H;Lin Y.-H;Lu Y.-C;Liu T.-C;Chen C.-Y;Hsu C.-J;Chen P.-L;Wu C.-C.; Lin Y.-H; Lin Y.-H; Lu Y.-C; Liu T.-C; Chen C.-Y; Hsu C.-J; Chen P.-L; Wu C.-C.; CHIEN-YU CHEN
臺大學術典藏 2021-07-06T02:04:15Z Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:11Z Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:09Z Identifying children with poor cochlear implantation outcomes using massively parallel sequencing Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏 2021-07-06T02:04:02Z A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏 2021-07-06T02:04:02Z Prediction Model for Audiological Outcomes in Patients with GJB2 Mutations Chen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Hsu C.-J.
臺大學術典藏 2021-07-06T02:03:57Z Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct Lin Y.-H.;Wu C.-C.;Lin Y.-H.;Lu Y.-C.;Chen C.-S.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Lin Y.-H.; Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.
臺大學術典藏 2021-07-06T02:03:57Z Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations Erdenechuluun J.; Lin Y.-H.; Ganbat K.; Bataakhuu D.; Makhbal Z.; Tsai C.-Y.; Lin Y.-H.; Chan Y.-H.; Hsu C.-J.; Hsu W.-C.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏 2021-07-06T02:03:53Z Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population Wu C.-C.;Tsai C.-Y.;Lin Y.-H.;Chen P.-Y.;Lin P.-H.;Cheng Y.-F.;Wu C.-M.;Lin Y.-H.;Lee C.-Y.;Erdenechuluun J.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Wu C.-C.; Tsai C.-Y.; Lin Y.-H.; Chen P.-Y.; Lin P.-H.; Cheng Y.-F.; Wu C.-M.; Lin Y.-H.; Lee C.-Y.; Erdenechuluun J.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.
臺大學術典藏 2021-07-06T02:03:49Z An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response Lin P.-H.; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Yang S.-Y.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Liu T.-C.
臺大學術典藏 2021-07-03T03:35:26Z Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations Wu C.-C.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:25Z Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: A unique spectrum of mutations in Taiwan, including a frequent founder mutation Wu C.-C.; Yeh T.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:23Z Common clinical features of children with enlarged vestibular aqueduct and mondini dysplasia Wu C.-C.; Chen Y.-S.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:08Z Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families Wu C.-C.; Chiu Y.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:03Z Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children Wu C.-C.; Lee Y.-C.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:01Z Prospective mutation screening of three common deafness genes in a large Taiwanese cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities Wu C.-C.; PEI-JER CHEN; Chiu Y.-H.; Lu Y.-C.; Wu M.-C.; Hsu C.-J.
臺大學術典藏 2021-07-03T03:34:55Z Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Liu A.Y.-Z.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏 2021-07-03T03:34:48Z Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy Chiu Y.-H.; Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Lee W.-Y.; Liu A.Y.-Z.; Hsu C.-J.
臺大學術典藏 2021-07-03T03:34:45Z Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or pendred syndrome Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Yeh P.-L.; Su Y.-N.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏 2021-07-03T03:34:39Z Establishment of a knock-in mouse model with the SLC26A4 c.919-2a>G mutation and characterization of its pathology Lu Y.-C.; Wu C.-C.; Shen W.-S.; Yang T.-H.; Yeh T.-H.; PEI-JER CHEN; Yu I.-S.; Lin S.-W.; Wong J.-M.; Chang Q.; Lin X.; Hsu C.-J.
臺大學術典藏 2021-07-03T03:34:17Z Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment Wu C.-C.; Lin Y.-H.; Lu Y.-C.; PEI-JER CHEN; Yang W.-S.; Hsu C.-J.; Chen P.-L.
臺大學術典藏 2021-07-03T03:34:00Z Contribution of adiponectin and its type 1 receptor to age-related hearing impairment Wu C.-C.; Tsai C.-H.; Lu Y.-C.; Lin H.-C.; Hwang J.-H.; Lin Y.-H.; Yang W.-S.; PEI-JER CHEN; Liao W.-C.; Lee Y.L.; Liu T.-C.; Hsu C.-J.

顯示項目 101-125 / 419 (共17頁)
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