子类别 會議論文/會議摘要 [3/3] 期刊論文 [23/23] 邻近社群 于重元 [19/19] 劉柯俊 [85/98] 劉滄梧 [119/125] 劉界元(2003-2010) [3/3] 夏和雄(1996-2012) [26/31] 夏興國 [51/54] 姜乃榕 [82/94] 常慧如 [39/44] 張俊彥 [234/254] 張光裕 [69/79] 張憶壽 [103/106] 張文祥 [52/53] 張書銘 [89/91] 彭汪嘉康(1996-2007) [120/126] 施能耀 [37/43] 李家惠 [29/29] 李岳倫 [48/49] 林素芳 [32/32] 楊奕馨 [41/42] 江士昇 [88/90] 沈哲宏 [14/16] 洪文俊 [88/88] 莊雙恩 [82/91] 蔡坤志 [32/34] 蔡慧珍 [66/71] 蘇勇曄 [40/40] 蘇振良 [24/25] 郭靜娟 [71/76] 陳尚鴻 [45/48] 陳振陽 [72/72] 陳立宗 [443/510] 陳美霞(2002-2009) [1/1] 陳詩政 [2/2] 陳雅雯 [38/39] 黃智興 [55/55] 丁兆治(2000-2004) [5/5] 其他 [464/471] 劉敏(1996-2007) [60/62] 劉玫英(2004-2006) [2/2] 吳成文(1996-2008) [53/55] 曾思文(1997-2007) [4/4] 李冠德(1997-2004) [4/6] 林景太(1999-2007) [5/5] 楊文光(1996-1999) [21/21] 王全正(1996-2003) [4/4] 莊聲宏(1997-2004) [11/11] 詹宗晃(2000-2008) [2/2] 賴基銘(2004-2008) [41/47] 阮麗蓉(2000-2006) [6/7] 陳俊叡(2003-2007) [6/6] 馬彥英(1997-1999) [1/1] 黃奇英(2005-2007) [9/10] 社群统计 近3年内发表的文件:21(80.77%) 含全文笔数:26(100.00%) 文件下载次数统计 下载大于0次:26(100.00%) 下载大于100次:15(57.69%) 全文下载总次数:3732(0.07%) 最后更新时间: 2024-12-01 08:28 上传排行 数据加载中..... 下载排行 数据加载中..... 最近上传 Comparison of single-cell transcrip... PKD2 founder mutation is the most c... Discordant phenotypes of nephritis ... CXCR7 activation evokes the anti-PD... Kidney cysts in children with alpor... NTRK3 exhibits a pro-oncogenic func... Dominant dystrophic epidermolysis b... Germline mutations of homologous re... Profibrotic subsets of SPP1(+) macr... Single-cell RNA sequencing via Endo...

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显示项目11-20 / 26. (共3页) << < 1 2 3 > >> 每页显示[10|25|50]项目

日期	题名	關聯
2023-02	The association between UGT1A1 polymorphisms and treatment toxicities of liposomal irinotecan	ESMO Open. 2023 Feb;8(1):Article number 100746.
2023-01	TRPM1 promotes tumor progression in acral melanoma by activating the Ca2+/CaMKIIdelta/AKT pathway	Journal of Advanced Research. 2023 Jan;43:45-57.
2022-12-01	Methylation of TET2 promoter is associated with global hypomethylation and hypohydroxymethylation in peripheral blood mononuclear cells of systemic lupus erythematosus patients	Diagnostics. 2022 Dec 1;12(12):Article number 3006.
2022-11	PKD2 founder mutation is the most common mutation of polycystic kidney disease in Taiwan	Journal of the American Society of Nephrology. 2022 Nov;33(11S):150.
2022-11	Comparison of single-cell transcriptomic profiles of early and late peritoneal dialysis	Journal of the American Society of Nephrology. 2022 Nov;33(11S):449.
2022-09-13	UMOD mutations in chronic kidney disease in Taiwan	Biomedicines. 2022 Sep 13;10(9):Article number 2265.
2022-07-21	Whole-exome sequencing identified mutational profiles of urothelial carcinoma post kidney transplantation	Journal of Translational Medicine. 2022 Jul 21;20:Article number 324.
2022-07-13	SH3GLB1-related autophagy mediates mitochondrial metabolism to acquire resistance against temozolomide in glioblastoma	Journal of Experimental and Clinical Cancer Research. 2022 Jul 13;41:Article number 220.
2022-07-01	PKD2 founder mutation is the most common mutation of polycystic kidney disease in Taiwan	npj Genomic Medicine. 2022 Jul 01;7:Article number 40.
2022-04-27	Single-cell RNA sequencing analysis for oncogenic mechanisms underlying oral squamous cell carcinoma carcinogenesis with Candida albicans infection	International Journal of Molecular Sciences. 2022 Apr 27;23(9):Article number 4833.

显示项目11-20 / 26. (共3页) << < 1 2 3 > >> 每页显示[10|25|50]项目