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"weng hy"的相關文件
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| 國家衛生研究院 |
2025-04 |
Rare APOE p.Gly4Glu: A putative disease-causing variant for early-onset Alzheimer's disease identified by next-generation sequencing
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Wu, CT;Hu, LH;Weng, HY;Liu, YM;Lin, YF;Tsai, SF;Lo, RY;Ching, YH |
| 國家衛生研究院 |
2023-01-16 |
Outbreak investigation in a COVID-19 designated hospital: The combination of phylogenetic analysis and field epidemiology study suggesting airborne transmission
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Huang, YC;Tu, HC;Kuo, HY;Shao, PL;Gong, YN;Weng, HY;Shu, HY;Kuo, CH;Kuo, PH;Chien, CH;Wu, CC;Chan, DD;Tsai, MK;Tsai, SF;Yu, CJ |
| 國家衛生研究院 |
2023 |
Emergence and persistent dominance of SARS-CoV-2 omicron BA.2.3.7 variant, Taiwan
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Shao, PL;Tu, HC;Gong, YN;Shu, HY;Kirby, R;Hsu, LY;Yeo, HY;Kuo, HY;Huang, YC;Lin, YF;Weng, HY;Wu, YL;Chen, CC;Chen, TW;Lee, KM;Huang, CG;Shih, SR;Chen, WJ;Wu, CC;Yu, CJ;Tsai, SF |
| 國家衛生研究院 |
2022-10-02 |
Genomic profiling with whole-exome sequencing revealed distinct mutations and novel pathways in Asian melanoma
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Chiu, YJ;Weng, HY;Lin, YY;Lin, YF;Yeh, YC;Perng, CK;Ma, H;Tsai, SF;Chou, TY |
| 國家衛生研究院 |
2022-10 |
Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis
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Wu, RW;Weng, HY;Huang, WP;Lin, YF;Liu, YM;Tsai, SF;Chang, CH |
| 國家衛生研究院 |
2022-08-17 |
Disclosing an in-frame deletion of the titin gene as the possible predisposing factor of anthracycline-induced cardiomyopathy: A case report
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Chang, YW;Weng, HY;Tsai, SF;Fan, FS |
| 國家衛生研究院 |
2021-08-21 |
Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria
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Weng, HY;Wu, RW;Chen, YT;Lin, YF;Liu, YM;Tsai, SF;Chang, CH |
| 國家衛生研究院 |
2020-12 |
Diagnosis of Arboleda-Tham syndrome by whole genome sequencing in an Asian boy with severe developmental delay
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Lin, YF;Lin, TC;Kirby, R;Weng, HY;Liu, YM;Niu, DM;Tsai, SF;Yang, CF |
| 國家衛生研究院 |
2019-08-20 |
A novel BTK gene mutation in a child with atypical X-linked agammaglobulinemia and recurrent hemophagocytosis: A case report
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Han, SP;Lin, YF;Weng, HY;Tsai, SF;Fu, LS |
| 國家衛生研究院 |
2019-07 |
Elucidating unique axonal dysfunction between nitrous oxide abuse and vitamin B12 deficiency
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Tani, J;Weng, HY;Chen, HJ;Chang, TS;Sung, JY;Lin, CSY |
| 國家衛生研究院 |
2019-07 |
Identify the predisposition genes to endometrial cancer
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Chiang, YC;Lee, TF;Lin, YF;Weng, HY;Tsai, SF;Wu, CW |
| 國家衛生研究院 |
2017-09 |
Novel mutations of the tetratricopeptide repeat domain 7A gene and phenotype/genotype comparison
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Lien, R;Lin, YF;Lai, MW;Weng, HY;Wu, RC;Jaing, TH;Huang, JL;Tsai, SF;Lee, WI |
| 臺北醫學大學 |
2013 |
Denbinobin induces human glioblastoma multiforme cell apoptosis through the IKKα-Akt-FKHR signaling cascade
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Weng, HY;Hsu, MJ;Chen, CC;Chen, BC;Hong, CY;Teng;CM;Pan;SL;Chiu;WT;Lin;CH |
| 臺北醫學大學 |
2012 |
Zerumbone suppresses IKKα, Akt, and FOXO1 activation, resulting in apoptosis of GBM 8401 cells
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Weng, HY;Hsu, MJ;Wang, CC;Chen, BC;Hong, CY;Chen, MC;Chiu, WT;Lin, CH |
| 國家衛生研究院 |
2010-01 |
Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis
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Lin, MW;Lee, DD;Liu, TT;Lin, YF;Chen, SY;Huang, CC;Weng, HY;Liu, YF;Tanaka, A;Arita, K;Lai-Cheong, J;Palisson, F;Chang, YT;Wong, CK;Matsuura, I;McGrath, JA;Tsai, SF |
| 高雄醫學大學 |
2007 |
於急性缺血性中風五小時內使用一新型血栓溶解劑的有效度之初報
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趙雅琴;鄧木火;鍾芷萍;翁興裕;陳彥宇;楊馥依;王立敏;胡漢華; Chao, AC;Teng, MM;Chung, CP;Weng, HY;Chen, YY;Yang, FY;Wang, LM;HH , Hu |
| 南亞技術學院 |
2003-07-22 |
Chemistry of dimolybdenum complexes containing anions of N,N '-di(6-methyl-2-pyridyl)formamidine (HDMepyF) and carboxylate ligands
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Weng, HY;Lee, CW;Chuang, YY;Suen, MC;Chen, JD;Hung, CH |
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