| 臺大學術典藏 |
2020-03-06T08:25:03Z |
Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour
|
Lee J.-C.;Yung-Ming Jeng;Su S.-Y.;Wu C.-T.;Tsai K.-S.;Lee C.-H.;Lin C.-Y.;Carter J.M.;Huang J.-W.;Chen S.-H.;Shih S.-R.;Mari?o-Enr?quez A.;Chen C.-C.;Folpe A.L.;Chang Y.-L.;Liang C.-W.; Lee J.-C.; YUNG-MING JENG; Su S.-Y.; Wu C.-T.; Tsai K.-S.; Lee C.-H.; Lin C.-Y.; Carter J.M.; Huang J.-W.; Chen S.-H.; Shih S.-R.; Mariño-Enríquez A.; Chen C.-C.; Folpe A.L.; Chang Y.-L.; Liang C.-W. |
| 臺大學術典藏 |
2020-03-07T06:56:25Z |
Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour
|
Lee J.-C.;Jeng Y.-M.;Su S.-Y.;Wu C.-T.;Tsai K.-S.;Lee C.-H.;Lin C.-Y.;Carter J.M.;Huang J.-W.;Chen S.-H.;Shih S.-R.;Mari?o-Enr?quez A.;Chen C.-C.;Folpe A.L.;Yih-Leong Chang;Liang C.-W.; Lee J.-C.; Jeng Y.-M.; Su S.-Y.; Wu C.-T.; Tsai K.-S.; Lee C.-H.; Lin C.-Y.; Carter J.M.; Huang J.-W.; Chen S.-H.; Shih S.-R.; Mariño-Enríquez A.; Chen C.-C.; Folpe A.L.; YIH-LEONG CHANG; Liang C.-W. |
| 臺大學術典藏 |
2020-06-01T06:57:20Z |
Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour
|
Lee J.-C.;Jeng Y.-M.;Su S.-Y.;Wu C.-T.;Tsai K.-S.;Lee C.-H.;Lin C.-Y.;Carter J.M.;Huang J.-W.;Chen S.-H.;Shyang-Rong Shih;Mari?O-Enr?Quez A.;Chen C.-C.;Folpe A.L.;Chang Y.-L.;Liang C.-W.; Lee J.-C.; Jeng Y.-M.; Su S.-Y.; Wu C.-T.; Tsai K.-S.; Lee C.-H.; Lin C.-Y.; Carter J.M.; Huang J.-W.; Chen S.-H.; SHYANG-RONG SHIH; Mari?o-Enr?quez A.; Chen C.-C.; Folpe A.L.; Chang Y.-L.; Liang C.-W. |
| 國立臺灣大學 |
2015 |
Identification of a novel FN1-FGFR1 genetic fusion as a frequent event in phosphaturic mesenchymal tumour (vol 235, pg 539, 2015)
|
Chang, Yih-Leong; Liang, Cher-Wei; 張逸良; 梁哲維 |
| 國立成功大學 |
2024-05 |
Identification of a novel frameshift mutation in cathepsin C gene in a patient with coexisting Papillon-Lefevre syndrome and rheumatoid arthritis
|
Hsieh;Chang-Yu;Lin;Yu-Chen;Cheng;Hui-Ching;Chang;Chih-Yu;Tu;Wei-Ting;Hsu;Chao-Kai;Tsai;Tsen-Fang |
| 國立成功大學 |
2023 |
Identification of a novel frameshift mutation in cathepsin C gene in a patient with coexisting Papillon–Lefevre syndrome and rheumatoid arthritis
|
Hsieh, C.-Y.;Lin, Y.-C.;Cheng, H.-C.;Chang, Chang C.-Y.;Tu, W.-T.;Hsu, C.-K.;Tsai, Tsai T.-F. |
| 國立成功大學 |
2024 |
Identification of a novel frameshift mutation in cathepsin C gene in a patient with coexisting Papillon–Lefevre syndrome and rheumatoid arthritis
|
Hsieh;C, -Y.;Lin;Y, -C.;Cheng;H, -C.;Chang;C, -Y.;Tu;W, -T.;Hsu;C, -K.;Tsai;T, -F. |
| 中山醫學大學 |
2007 |
Identification of a Novel Frameshift Mutation in the ARSE Gene of a Newborn Boy Diagnosed with Chondrodysplasia Punctata 1 (CDPX1)
|
Su, Pen Hua; Chen, Jia Yuh; Yu, Ju Shan; Chen, Suh Jen; Hu, Jui Ming; Yang, Jia Min |
| 臺大學術典藏 |
2018-09-10T09:14:14Z |
Identification of a novel function of the clathrin-coated structure at the plasma membrane in facilitating GM-CSF receptor-mediated activation of JAK2
|
Chen, P.-H.;Chien, F.-C.;Lee, S.-P.;Chan, W.-E.;Lin, I.-H.;Liu, C.-S.;Lee, F.-J.;Lai, J.-S.;Chen, P.;Yang-Yen, H.-F.;Yen, J.J.-Y.; PING-HUNG, CHEN; FANG-JEN LEE |
| 臺大學術典藏 |
2021-07-02T07:27:55Z |
Identification of a novel function of the clathrin-coated structure at the plasma membrane in facilitating GM-CSF receptor-mediated activation of JAK2
|
Chen P.-H.; Chien F.-C.; Lee S.-P.; Chan W.-E.; Lin I.-H.; Liu C.-S.; Fang-Jen Scott Lee; Lai J.-S.; Chen P.; Yang-Yen H.-F.; Yen J.J.-Y. |
| 臺北醫學大學 |
2007 |
Identification of a novel gamete receptor involved in sperm-egg interaction.
|
黃彥華; Chio YY; Huang YH; Tsai MT; Yang RB |
| 臺大學術典藏 |
2020-04-24T01:34:20Z |
Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing
|
Lin Y.-H.; Chen-Chi Wu; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; Chen P.-L. |
| 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 |
2018-09-10T05:50:08Z |
Identification of a novel germline MET mutation in dogs
|
Liao, A.T.; McMahon, M.; London, C.A.; TAI-CHING LIAO |
| 國立臺灣大學 |
2006 |
Identification of a novel germline Met mutation in dogs; Short Communication
|
Liao, AT; McMahon, M; London, CA |
| 國立臺灣大學 |
2013 |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
|
Chen, P. -L.; Lai, S. -K.; Yang, W. -S.; Chang, T. -C.; Chu, C. -C.; 楊偉勛; 張天鈞; 陳沛隆 |
| 臺大學術典藏 |
2018-09-10T09:38:42Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
|
Chen, P.-L.;Lai, S.-K.;Yang, W.-S.;Chang, T.-C.;Chu, C.-C.; TIEN-CHUN CHANG; WEI-SHIUNG YANG; PEI-LUNG CHEN |
| 臺大學術典藏 |
2021-07-02T02:35:36Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
|
Chen P.-L.; Lai S.-K.; WEI-SHIUNG YANG; Chang T.-C.; Chu C.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:14Z |
Identification of a novel HLA-B allele, B*07:162, in a Taiwanese individual
|
PEI-LUNG CHEN; Lai S.-K.; Yang W.-S.; Chang T.-C.; Chu C.-C. |
| 臺大學術典藏 |
2021-07-06T02:04:04Z |
Identification of a novel HLA-B allele, HLA-B*40:238, in a Taiwanese individual
|
Lee H.-L.; Lai S.-K.; PEI-LUNG CHEN; Chu C.-C. |
| 中國文化大學 |
2022-12 |
Identification of a novel interaction site between the large hepatitis delta antigen and clathrin that regulates the assembly of genotype III hepatitis delta virus
|
Lai, Yu-Heng; 賴昱衡 |
| 臺大學術典藏 |
2020-09-28T02:47:25Z |
Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan
|
Hsiung Y.-C.; Lin P.-C.; Chen C.-S.; Tung Y.-C.; Yang W.-S.; Chen P.-L.; TA-CHEN SU |
| 臺大學術典藏 |
2021-01-08T06:17:19Z |
Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan
|
Hsiung Y.-C.; Hsiung Y.-C.;Lin P.-C.;Chen C.-S.;Yi-Ching Tung;Yang W.-S.;Chen P.-L.;Su T.-C.; Lin P.-C.; Chen C.-S.; YI-CHING TUNG; Yang W.-S.; Chen P.-L.; Su T.-C. |
| 臺大學術典藏 |
2021-07-02T02:35:15Z |
Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan
|
Hsiung Y.-C.; Lin P.-C.; Chen C.-S.; Tung Y.-C.; WEI-SHIUNG YANG; Chen P.-L.; Su T.-C. |
| 臺大學術典藏 |
2021-07-06T02:03:59Z |
Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan
|
Hsiung Y.-C.; Lin P.-C.; Chen C.-S.; Tung Y.-C.; Yang W.-S.; PEI-LUNG CHEN; Su T.-C. |
