Results 151 to 160 of about 12,504 (200)

Exploring the role of readthrough-inducing molecule 2,6-diaminopurine to increase immune response against cancer cells. [PDF]

Mol Ther
Sandoval Pacheco C, Leroy AM, Derhourhi M, Cardon T, Leroy C, Jouy N, Com E, Guevel B, Bourette R, Carrard J, Barros D, Duchêne B, Toussaint B, Froguel P, Jonckheere N, Chassat T, Van Seuningen I, Lavigne R, Pineau C, Pierre P, Soncin F, Salzet M, Bonnefond A, Lejeune F.   +23 more
europepmc   +1 more source

What Peroxisomes (Don't) do to Mitochondria. [PDF]

Contact (Thousand Oaks)
Bülow MH, Thoms S.
europepmc   +1 more source

The dual luciferase assay does not support claims of stop codon readthrough on the AGO1 mRNA. [PDF]

EMBO J
Suresh AN, Atkins JF, Loughran G.
europepmc   +1 more source

<i>KCNJ11</i> readthrough variant in a patient with congenital hyperinsulinism. [PDF]

Clin Pediatr Endocrinol
Uehara E, Sugihara K, Hata I, Akiba K, Hattori A, Kageyama I, Matsubara K, Fukami M.   +7 more
europepmc   +1 more source

Omics-Based Expression Cassette for Heterologous Protein Production in <i>Y. lipolytica</i>. [PDF]

ACS Synth Biol
Elemosho R, Zhang C, Karyolaimos A, Brambor A, Pasadas Castilla R, Asmund Arnesen J, Jahn LJ, Sommer MOA.   +7 more
europepmc   +1 more source

Therapeutic Potential of Translational Readthrough at Disease-Associated Premature Termination Codons From Tumor Suppressor Genes. [PDF]

IUBMB Life
Torices L, Nunes-Xavier CE, Pulido R.
europepmc   +1 more source

CRISPR-free RNA base editing mediated PTC-readthrough restores hearing in mice with Otof nonsense mutation. [PDF]

Nat Commun
Sun H, Teng Q, Liu W, Guo R, Li M, Xiong W, Huang Q, Yu Q, Luo N, Li Y, Song J, Gong S, Shi X, Yi C, Liu K.   +14 more
europepmc   +1 more source

High-fidelity and differential nonsense suppression in live cells and a frontotemporal dementia allele with human transfer RNAs. [PDF]

Nucleic Acids Res
Beharry A, Ward C, Moore H, Hoffman KS, Chan PP, Lowe TM, O'Donoghue P.   +6 more
europepmc   +1 more source

Genotype-phenotype characterization and functional reconstitution of pathogenic β-catenin variants from CTNNB1 syndrome patients. [PDF]

PLoS Genet
Nunes-Xavier CE, Pallarès-Sastre M, Rodríguez-Ramos A, Bañuelos S, Cortajarena I, Cavaliere F, Ruiz-Espinoza C, Llano-Rivas I, García M, Amayra I, Pulido R.   +10 more
europepmc   +1 more source

Comprehensive resource for transcription readthrough events in healthy human tissues. [PDF]

Sci Data
Mei Y, Cheng Z, Lu Y, Wu S, Chen X.
europepmc   +1 more source