Results 211 to 220 of about 400,889 (317)
In macrophage‐myofibroblast transition, upregulated NNMT depletes S‐Adenosylmethionine (SAM) and nicotinamide adenine dinucleotide(NAD+), thereby triggering epigenetic reprogramming via Histone H3 Lysine 27 acetylation (H3K27ac) accumulation at the promoter region of master transcription factor Prrx1.
Xiwen Dong +11 more
wiley +1 more source
Single-cell lineage tracing techniques in hematology: unraveling the cellular narrative. [PDF]
Deng LH, Li MZ, Huang XJ, Zhao XY.
europepmc +1 more source
This study successfully establishes adamantinomatous craniopharyngioma (ACP) patient‐derived organoids (PDOs) that preserve the histopathological and genetic features of the original tumors. Through drug sensitivity assays and subsequent mechanistic analyses, the study demonstrates that Ceritinib exerts its inhibitory effects on ACP PDO growth by ...
Huarong Zhang +15 more
wiley +1 more source
TimeFlow 2: an unsupervised cell lineage detection method for flow cytometry data
Liarou M, Matthes T, Marchand-Maillet S.
europepmc +1 more source
The CFII components PCF11 and Cbc change subnuclear localization as cells differentiate in an adult stem cell lineage. [PDF]
Nava I, Fuller MT, Gallicchio L.
europepmc +1 more source
This research conducts an in‐depth investigation of cell‐type‐specific regulatory mechanisms underlying molecular and complex phenotypes through integrative analysis of multitissue single‐nucleus RNA sequencing, bulk RNA‐seq, and genome‐wide association study (GWAS) data in pigs.
Lijuan Chen +31 more
wiley +1 more source
Maximum likelihood inference of time-scaled cell lineage trees with mixed-type missing data using LAML. [PDF]
Chu G, Mai U, Schmidt H, Raphael BJ.
europepmc +1 more source
Figure S3 from Single-Cell Clonal Lineage Tracing Identifies the Transcriptional Program Controlling the Cell-Fate Decisions by Neoantigen-Specific CD8<sup>+</sup> T Cells [PDF]
Ying Luo, Taidou Hu, Chen Yao, Tuoqi Wu
openalex +1 more source
Sabotaged Integral HSC Heterogeneity Underlies Essential Thrombocythemia Development
Single‐cell RNA sequencing (scRNA‐seq) maps how distinct driver mutations remodel hematopoietic stem cell (HSC) programs across essential thrombocythemia (ET). Comparative analysis uncovers both shared and subtype‐specific molecular signatures, identifies a triple‐negative (TN)‐associated HSC population enriched with malignant traits, and reveals the ...
Jingyuan Tong +21 more
wiley +1 more source

