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RNA Seq in Patients with Primordial Dwarfism
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创建时间：
2013-08-07
相关数据集
Additional file 1: Table S1. of A novel joint analysis framework improves identification of differentially expressed genes in cross disease transcriptomic analysis
Comparison of average sensitivity and FDR between single and joint analysis. (XLSX 16Â kb)
Figshare2023-05-30 更新80
Additional file 6: of Transcriptome analysis of human heart failure reveals dysregulated cell adhesion in dilated cardiomyopathy and activated immune pathways in ischemic heart failure
Table S5. Enriched IPA Canonical Pathways. IPA canonical pathways for p ≤ 0.05 for Analysis 1 (HF-DEGs), Analysis 2 (DCM-specific and ICM-specific), and Analysis 3 (DCM vs ICM). (XLSX 56 kb)
Figshare2018-11-13 更新70
Additional file 10 of Transcriptomic analysis identifies diagnostic genes in polycystic ovary syndrome and periodontitis
Additional file 10: Table S4. Results of GO enrichment.
Figshare2024-08-14 更新40
温阳化积法与非自发缓解性膜性肾病疗效相关性的双向队列研究组学信息数据
2019-2022年温阳化积法与非自发缓解性膜性肾病疗效相关性的双向队列研究临床定位为多中心双向队列临床试验，在试验研究过程中采用基础研究方式协助验证组学信息，通过制备主动和被动膜性肾病大鼠模型并进行中药干预，干预结束后选择大鼠的肾脏进行转录组测序，获得部分基因数据集，格式为.xlsx。在使用或对本课题科学数据再加工时，应在成果中标注数据来源，按照要求规范、准确的引用数据。 其他：符合NMPA-C
国家人口健康科学数据中心70
Structure of OCNDS-related CK2alpha variant F197I
The Okur-Chung neurodevelopment syndrome is a rare disease caused by mutations of the CSNK2A1 gene, which encodes for the catalytic subunit of protein kinase CK2. in this study, we analyzed the most c
DataCite Commons2026-05-14 更新40
