邻近类别 圖書 [1/1] 會議論文/會議摘要 [7/10] 專利 [0/1] 类别统计 近3年内发表的文件:14(11.11%) 含全文笔数:126(100.00%) 文件下载次数统计 下载大于0次:126(100.00%) 下载大于100次:125(99.21%) 全文下载总次数:76829(92.77%) 最后更新时间: 2024-12-01 13:11 上传排行 数据加载中..... 下载排行 数据加载中..... 最近上传 Next-generation integrated sequenci... 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 ... High-throughput sequencing of compl...

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日期	题名	關聯
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	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.
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.
2017-11-01	Hypermethylation of BEND5 contributes to cell proliferation and is a prognostic marker of colorectal cancer	Oncotarget. 2017 Nov 1;8(69):113431-113443.
2017-09	Novel mutations of the tetratricopeptide repeat domain 7A gene and phenotype/genotype comparison	Frontiers in Immunology. 2017 Sep;8:Article number 1066.

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