Siblings 圖書 [1/1] 會議論文/會議摘要 [7/10] 專利 [0/1] Collection Statistics 近3年內發表的文件:14(11.11%) 含全文筆數:126(100.00%) 文件下載次數統計 下載大於0次:126(100.00%) 下載大於100次:125(99.21%) 檔案下載總次數:76789(92.76%) 最後更新時間: 2024-12-01 10:56 Top Upload Loading... Top Download Loading... Recent Submissions 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...

Jump to a point in the index: (Choose year) 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 2001 2000 1999 1998 1997 1996 1995 1994 1993 1992 1991 1990 1985 1980 1975 1970 1960 1950 (Choose month) January February March April May June July August September October November December Or type in a year:

Ordering With Most Recent First Show Oldest First

Showing items 1-50 of 126. (3 Page(s) Totally) 1 2 3 > >> 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	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.
2017-08	DNA adenine methylation modulates pathogenicity of Klebsiella pneumoniae genotype K1	Journal of Microbiology, Immunology and Infection. 2017 Aug;50(4):471-477.
2017-06	Functional and biochemical characterization of a T cell-associated anti-apoptotic protein, GIMAP6	Journal of Biological Chemistry. 2017 Jun;292(22):9305-9319.
2017-05-03	Lineage-specific SNPs for genotyping of Mycobacterium tuberculosis clinical isolates	Scientific Reports. 2017 May 03;7:Article number 1425.
2016-11-25	Epigenetic enhancement of the post-replicative DNA mismatch repair of mammalian genomes by a Hemi-mCpG-Np95-Dnmt1 axis	Scientific Reports. 2016 Nov 25;6:Article number 37490.
2016-09-27	Genomics study of mycobacterium tuberculosis strains from different ethnic populations in Taiwan	Evolutionary Bioinformatics. 2016 Sep 27;12:213-221.
2016-05-25	Network signatures of IgG immune repertoires in hepatitis B associated chronic infection and vaccination responses	Scientific Reports. 2016 May 25;6:Article number 26556.
2016-05	Selective retention of an inactive allele of the DKK2 tumor suppressor gene in hepatocellular carcinoma	PLoS Genetics. 2016 May;12(5):Article number e1006051.
2016-01	Comparative phosphoproteomics reveals the role of AmpC beta-lactamase phosphorylation in the clinical imipenem-resistant strain acinetobacter baumannii SK17	Molecular and Cellular Proteomics. 2016 Jan;15(1):12-25.
2015-12-17	Complete genome sequence of Xanthomonas campestris pv. campestris Strain 17 from Taiwan	Genome Announcements. 2015 Dec 17;3:Article number e01466-15.
2015-12	Clinical relevance of plasma DNA methylation in colorectal cancer patients identified by using a genome-wide high-resolution array	Annals of Surgical Oncology. 2015 Dec;22(Suppl. 3):1419-1427.
2015-10	Effective transfer of a 47 kb NDM-1-positive plasmid among Acinetobacter species	Journal of Antimicrobial Chemotherapy. 2015 Oct;70(10):2734-2738.
2015-07	EGFR over-expression in non-small cell lung cancers harboring EGFR mutations is associated with marked down-regulation of CD82	Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2015 Jul;1852(7):1540-1549.
2014-11	A mutation of the Col2alpha1 gene (G1170S) alters the transgenic murine phenotype and cartilage matrix homeostasis	Journal of the Formosan Medical Association. 2014 Nov;113(11):803-812.
2014-08	Genetic variants associated with phenytoin-related severe cutaneous adverse reactions	JAMA. 2014 Aug;312(5):525-534.
2014-05-07	Manipulation Therapy prior to diagnosis induced primary osteosarcoma metastasis—From clinical to basic research	PLoS ONE. 2014 May 7;9(5):Article number e96571.
2014-04	Detection of common mutations in sporadic primary localized cutaneous amyloidosis by DNA mass spectrometry	British Journal of Dermatology. 2014 Apr;170(4):974-976.
2014-04	High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry	Molecular Genetics and Metabolism. 2014 Apr;111(4):507-512.
2014-02	SitA contributes to the virulence of Klebsiella pneumoniae in a mouse infection model	Microbes and Infection. 2014 Feb;16(2):161-170.
2014-01-08	Capsule deletion via a lambda-Red knockout system perturbs biofilm formation and fimbriae expression in Klebsiella pneumoniae MGH 78578	BMC Research Notes. 2014 Jan 8;7(1):Article number 13.
2013-08	Complete sequences of two plasmids in a blaNDM-1-positive Klebsiella oxytoca isolated from Taiwan	Antimicrobial Agents and Chemotherapy. 2013 Aug;57(8):4072-4076.
2013-05	MCP-1 as an effector of IL-31 signaling in familial primary cutaneous amyloidosis	Journal of Investigative Dermatology. 2013 May;133(5):1375-1378.
2013-04-29	Copy number change of the NDM-1 sequence in a multidrug-resistant Klebsiella pneumoniae clinical isolate	PLoS ONE. 2013 Apr 29;8(4):Article number e62774.
2013-04	ALPK1 genetic regulation and risk in relation to gout	International Journal of Epidemiology. 2013 Apr;42(2):466-474.
2013-01	Decoding the disease-associated proteins encoded in the human chromosome 4	Journal of Proteome Research. 2013 Jan;12(1):33-44.
2012-11-29	Multiple-omic data analysis of Klebsiella pneumoniae MGH 78578 reveals its transcriptional architecture and regulatory features	BMC Genomics. 2012 Nov 29;13:Article number 679.

Showing items 1-50 of 126. (3 Page(s) Totally) 1 2 3 > >> View [10|25|50] records per page