Collection 專利 [0/1] 期刊論文 [126/126] 圖書 [1/1] 會議論文/會議摘要 [7/10] Siblings 劉淦光(2006-2014) [23/23] 劉鴻興 [9/9] 喻秋華 [60/60] 孫以瀚 [1/1] 張仲明 [30/31] 張明姿 [14/14] 張雅媗 [6/6] 徐唯哲 [7/7] 徐欣伶 [19/22] 施修明 [35/39] 松浦功 [21/26] 梁啟銘(2006-2007) [4/4] 江運金 [34/34] 王紹文 [15/15] 王陸海 [35/36] 莊志立 [32/38] 許惠恒 [36/36] 陳俊宏 [16/16] 陳怡榮 [32/36] 黃秀芬 [126/131] 黃麗蓉 [25/25] 龔行健 [61/63] 其他 [154/158] 周玉山(1996-2005) [20/22] 王玲美(2004-2008) [4/4] 葉秀慧(2001-2005) [21/22] 鄭金松(1997-2002) [6/6] 黃奇英(1998-2005) [32/34] Community Statistics 近3年內發表的文件:15(10.87%) 含全文筆數:134(97.10%) 文件下載次數統計 下載大於0次:134(100.00%) 下載大於100次:132(98.51%) 檔案下載總次數:82398(1.54%) 最後更新時間: 2024-11-28 12:10 Top Upload Loading... Top Download Loading... Recent Submissions Next-generation integrated sequenci... Trans-ethnic comprehensive genomic ... Genetic factors contribute to the p... HBV DNA integration into telomerase... Emergence and persistent dominance ... Lymphocyte disturbance and function... Protein O-fucosyltransferase-1 muta... Outbreak investigation in a COVID-1... Genomic profiling with whole-exome ... Disclosing an in-frame deletion of ...

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Showing items 1-25 of 138. (6 Page(s) Totally) 1 2 3 4 5 6 > >> View [10|25|50] records per page

Date	Title	Relation
2024-10-02	Next-generation integrated sequencing identifies poor prognostic factors in patients with MYD88-mutated chronic lymphocytic leukemia in Taiwan	Pathobiology. 2024 Oct 02;Article in press.
2023-11	Genetic factors contribute to the phenotypic variability in GJB2-related hearing impairment	Journal of Molecular Diagnostics. 2023 Nov;25(11):827-837.
2023-06	Outbreak investigation in a COVID-19 designated hospital: The combination of phylogenetic analysis and field epidemiology study suggesting airborne transmission	Journal of Microbiology, Immunology, and Infection. 2023 Jun;56(3):547-557.
2023-04-17	HBV DNA integration into telomerase or MLL4 genes and TERT promoter point mutation as three independent signatures in subgrouping HBV-related HCC with distinct features	Liver Cancer. 2023 Apr 17;13(1):41-55.
2023-02	Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation	Clinical Immunology. 2023 Feb;247:Article number 109236.
2023-02	Trans-ethnic comprehensive genomic cluster stratification of upper tract urothelial carcinoma	European Urology. 2023 Feb;83(Suppl. 1):S1695.
2023	Emergence and persistent dominance of SARS-CoV-2 omicron BA.2.3.7 variant, Taiwan	Emerging Infectious Diseases. 2023;29(4):792-796.
2022-12	Genomic profiling with whole-exome sequencing revealed distinct mutations and novel pathways in Asian melanoma	Journal of Dermatology. 2022 Dec;49(12):1299-1309.
2022-10	Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis	Dermatologica Sinica. 2022 Oct-Dec;40(4):251-252.
2022-08-17	Disclosing an in-frame deletion of the titin gene as the possible predisposing factor of anthracycline-induced cardiomyopathy: A case report	International Journal of Molecular Sciences. 2022 Aug 17;23(16):Article number 9261.
2022-05-25	High-throughput sequencing of complementarity determining region 3 in the heavy chain of B-cell receptor in renal transplant recipients: A preliminary Report	Journal of Clinical Medicine. 2022 May 25;11(11):Article number 2980.
2022-03-04	EGFR mutation-harboring lung cancer cells produce CLEC11A with endothelial trophic and tumor-promoting activities	Cancers. 2022 Mar 4;14(5):Article number 1356.
2022-03	A clinical and integrated genetic study of isolated and combined dystonia in Taiwan	Journal of Molecular Diagnostics. 2022 Mar;24(3):262-273.
2022-01	Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria	Journal of the European Academy of Dermatology and Venereology. 2022 Jan;36(1):e54-e57.
2022-01	Artificial-intelligence-assisted discovery of genetic factors for precision medicine of antiplatelet therapy in diabetic peripheral artery disease	Biomedicines. 2022 Jan;10:Article number 116.
2021-09-26	Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)	Journal of Biomedical Science. 2021 Sep 26;28:Article number 65.
2021-07	Complex movement disorders in a boy with PURA syndrome	Movement Disorders Clinical Practice. 2021 Jul 8;8(7):1137-1139.
2021-01-12	Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes	Scientific Reports. 2021 Jan 12;11:Article number 478.
2020-12	Diagnosis of Arboleda-Tham syndrome by whole genome sequencing in an Asian boy with severe developmental delay	Molecular Genetics and Metabolism Reports. 2020 Dec;25:Article number 100686.
2020-10	Increased mcr-1 in pathogenic Escherichia coli from diseased swine, Taiwan	Journal of Microbiology, Immunology and Infection. 2020 Oct;53(5):751-756.
2019-08-20	A novel BTK gene mutation in a child with atypical X-linked agammaglobulinemia and recurrent hemophagocytosis: A case report	Frontiers in Immunology. 2019 Aug 20;10:Article number 1953.
2018-07	Wild-type p53 upregulates an early onset breast cancer-associated gene GAS7 to suppress metastasis via GAS7-CYFIP1-mediated signaling pathway	Oncogene. 2018 Jul;37(30):4137-4150.
2018-07	GATA3 mutation of luminal-type breast cancer patients in Taiwan	Cancer Research. 2018 Jul;78(13, Suppl.):Meeting Abstract 3439.
2017-12	Shared IgG infection signatures vs. hemorrhage-restricted IgA clusters in human dengue: A phenotype of differential class-switch via TGF beta 1	Frontiers in Immunology. 2017 Dec;8:Article number 1726.
2017-11-21	CISD2 haploinsufficiency disrupts calcium homeostasis, causes nonalcoholic fatty liver disease, and promotes hepatocellular carcinoma	Cell Reports. 2017 Nov 21;21(8):2198-2211.

Showing items 1-25 of 138. (6 Page(s) Totally) 1 2 3 4 5 6 > >> View [10|25|50] records per page