Results 151 to 160 of about 114,739 (248)

In vivo partial cellular reprogramming enhances liver plasticity and regeneration. [PDF]

open access: yesCell Rep, 2022
Hishida T   +35 more
europepmc   +1 more source

Regulation of Pluripotency and Cellular Reprogramming by the Ubiquitin-Proteasome System

open access: bronze, 2012
Shannon M. Buckley   +13 more
openalex   +1 more source

H3K36me3‐Guided m6A Modification of Oncogenic L1CAM‐AS1 Drives Macrophage Polarization and Immunotherapy Resistance in Hepatocellular Carcinoma

open access: yesAdvanced Science, EarlyView.
L1CAM‐AS1 is identified as a novel H3K36me3‐guided, m6A‐modified long noncoding RNA (lncRNA) in hepatocellular carcinoma (HCC) cells. L1CAM‐AS1 stabilizes RAN protein, enhances M2 macrophages‐released CCL5‐induced nuclear import of RELA, activates the NF‐κB signaling, up‐regulates CCL2 expression and secretion from HCC cells, and enhances M2 ...
Teng Wang   +6 more
wiley   +1 more source

Generation of induced pluripotent stem cells (CSSi017-A)(12862) from an ALS patient carrying a repeat expansion in the C9orf72 gene

open access: yesStem Cell Research
Genetic expansions of the hexanucleotide repeats (GGGGCC) in the C9orf72 gene appear in approximately 40% of patients with familial ALS and 7% of patients with sporadic ALS in the European population, making this mutation one of the most prevalent ...
G. Ruotolo   +14 more
doaj  

Single influenza A viruses induce nanoscale cellular reprogramming at the virus-cell interface. [PDF]

open access: yesNat Commun
Broich L   +7 more
europepmc   +1 more source

Molecular Roadblocks for Cellular Reprogramming

open access: bronze, 2012
Thomas Vierbuchen, Marius Wernig
openalex   +1 more source

Cellular reprogramming of human monocytes is regulated by time-dependent IL4 signalling and NCOR2 [PDF]

open access: green, 2017
Jil Sander   +36 more
openalex   +1 more source

The Non‐Coding Regulatory Variant rs2863002 at chr11p11.2 Increases Neuroblastoma Risk by Affecting HSD17B12 Expression and Lipid Metabolism

open access: yesAdvanced Science, EarlyView.
The SNP rs2863002 at the 11p11.2 locus, identified through GWAS, is associated with an increased risk of neuroblastoma. The rs2863002‐C allele impairs the binding of the transcription factor GATA3, resulting in upregulation of the HSD17B12 gene.
Teresa Maiorino   +20 more
wiley   +1 more source

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