Collection Patents [0/1] Periodical Articles [126/126] Books/Book Section [1/1] Conference Papers/Meeting Abstract [7/10] Siblings Gan-Guang Liou(2006-2014) [23/23] Hong-Hsing Liu [9/9] Chiou-Hwa Yuh [60/60] Y. Henry Sun [1/1] Chung-Ming Chang [30/31] Mingzi M. Zhang [14/14] Ya-Hsuan Chang [6/6] Wei-Che Hsu [7/7] Hsin-Ling Hsu [19/22] Hsiu-Ming Shih [35/39] Isao Matsuura [21/26] Chi-Ming Liang(2006-2007) [4/4] Yun-Jin Jiang [34/34] Shao-Win Wang [15/15] Lu-Hai Wang [35/36] Jyh-Lyh Juang [32/38] Huey-Herng Sheu [36/36] Chun-Hong Chen [16/16] Yi-Rong Chen [32/36] Shiu-Feng Kathy Huang [126/131] Li-Rung Huang [25/25] Hsing-Jien Kung [61/63] Others [154/158] Yuh-Shan Jou(1996-2005) [20/22] Ling-Mei Wang(2004-2008) [4/4] Shiou-Hwei Yeh(2001-2005) [21/22] King-Song Jeng(1997-2002) [6/6] Chi-Ying F. Huang(1998-2005) [32/34] Community Statistics Item counts issued in 3 years:15(10.87%) Items With Fulltext:134(97.10%) Download counts of the item Download times greater than 0:134(100.00%) Download times greater than 100:132(98.51%) Total Bitstream Download Counts:82488(1.54%) Last Update: 2024-11-28 15:56 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