Results 221 to 230 of about 663,508 (269)
MetaTF is a new computational framework that uses single‐cell RNA sequencing (scRNA‐seq) data to infer transcription factor activity with the aim to help in deciphering cells identity starting from a heterogeneous population, and apply it to characterize mouse hematopoietic stem cells and breast cancer epithelial cells, thus identifying a novel subset ...
Yongfei Hu+15 more
wiley +1 more source
A CMTM6 Nanobody Overcomes EGFR‐TKI Resistance in Non‐Small Cell Lung Cancer
Overcoming EGFR‐TKI resistance remains a critical challenge in NSCLC treatment. This study identifies CMTM6 as a key regulator of EGFR stability and demonstrates that a novel anti‐CMTM6 nanobody disrupts the CMTM6‐EGFR interaction. Targeting CMTM6 restores EGFR degradation, suppresses tumor growth, and confers therapeutic benefit in both CDX and PDX ...
Lu Xia+18 more
wiley +1 more source
Protocol for the imputation of stimulus-induced single-cell gene expression trajectories from time-series scRNA-seq data. [PDF]
Sheu KM, Hoffmann A.
europepmc +1 more source
Schematic diagram showing the potential mechanism of bigelovin on the activation of NLRP3 inflammasome Bigelovin may inhibit activated protein C kinase 1 (RACK1) by directly binding with cys168 of RACK1. Bigelovin thus prevents oligomerization of NLRP3 (NLRP3 active conformation) and subsequent assembly of NLRP3 inflammasome, blocking the activation of
Jian Cui+17 more
wiley +1 more source
Two haplotype-resolved telomere-to-telomere genome assemblies of Xanthoceras sorbifolium. [PDF]
Liu Y+11 more
europepmc +1 more source
By studying the maturation mechanisms of vasopressin (AVP), this manuscript identifies FAM134B‐mediated ER‐phagy as a critical pathway for degrading both aggregated proAVP and the key ERAD component, HRD1. HRD1 induction mitigates proAVP aggregation and support AVP neuron function in the absence of autophagy.
Xuya Pan+16 more
wiley +1 more source
TIRE-seq simplifies transcriptomics via integrated RNA capture and library preparation. [PDF]
O'Keeffe P+22 more
europepmc +1 more source
Nonsyndromic orofacial clefts (NSOFCs) are the most common craniofacial defects. Exome sequencing of 214 sporadic cases sheds new light on its genetic architecture and identifies many candidate pathogenic variants. Furthermore, functional studies establish BOC as a novel causal gene and reveal an unusual two‐locus model of inheritance via the epistatic
Qing He+16 more
wiley +1 more source
A high-quality Chromosome-level reference genome assembly of white-lipped deer (Przewalskium albirostris). [PDF]
Yang Y+6 more
europepmc +1 more source
Exploring and mitigating shortcomings in single-cell differential expression analysis with a new statistical paradigm. [PDF]
Wu CH, Zhou X, Chen M.
europepmc +1 more source