Results 171 to 180 of about 34,718 (253)

Coordinated alternative splicing decisions via stepwise exon definition. [PDF]

Nucleic Acids Res
Kristofori P, Xiao Z, Braun S, Busch A, Zarnack K, König J, Legewie S, Li C.   +7 more
europepmc   +1 more source

Loss of U11/U12 spliceosome gene <i>ZCRB1</i> leads to aberrant ciliogenesis and WNT signaling. [PDF]

Life Sci Alliance
Pirzada MUR, Powell-Rodgers G, Richee J, Norppa AJ, Jungers CF, Colijn S, Frilander MJ, Stratman AN, Djuranovic S.   +8 more
europepmc   +1 more source

Phosphorylation of SF3B1 by CDK11 orchestrates spliceosome activation via SNIP1-dependent RES complex recruitment. [PDF]

Nat Commun
Gajdušková P, Ruiz de Los Mozos I, Hluchý M, Myšková A, Zábrady K, Maník P, Dragišić N, Hanáková K, Potěšil D, Bologna S, Nováček J, Friedel CC, Tripsianes K, Zdráhal Z, Blazek D.   +14 more
europepmc   +1 more source

The "cutting edge" of non-canonical RNA splicing. [PDF]

Front Mol Biosci
Guo J.
europepmc   +1 more source

Exploring Disordered Regions of Human Spliceosome Proteins. [PDF]

J Phys Chem Lett
Santos BPO, Bera K, Grisanti L, Felli IC, Pierattelli R, Magistrato A.   +5 more
europepmc   +1 more source

G-patch proteins: important regulators of pre-mRNA splicing and ribosome biogenesis. [PDF]

Front Cell Dev Biol
Karika LO, Cipakova I, Hronska L, Cipak L.   +3 more
europepmc   +1 more source

The human DBR1 interactome reveals coupling between intron lariat turnover, pre-mRNA splicing, and RNA quality control pathways. [PDF]

Cell Stress Chaperones
Barwell T, Gautam D, Nitika, Zheng B, Truman AW, Chakrabarti K.   +5 more
europepmc   +1 more source

Spliceosome induction is a druggable dependency of RAS-driven senescence and cancer. [PDF]

Nat Commun
Wagner V, Bousset L, Ascensão-Ferreira M, Sun B, Barragan Avila JE, Kaizeler A, Martins-Silva R, Rahbari M, Fernández-Vaquero M, Haston S, Tinti M, Pombo J, Khadayate S, Roth S, Schürch CM, Martínez-Barbera JP, Bahat A, Wee KB, Morton JP, Malek N, Innes AJ, Vernia S, Barbosa-Morais NL, Gallage S, Heikenwalder M, Gil J.   +25 more
europepmc   +1 more source

Bi-allelic variants in the non-protein-coding minor spliceosome components RNU6ATAC and RNU4ATAC cause syndromic monogenic autoimmune diabetes. [PDF]

Am J Hum Genet
Johnson MB, Russ-Silsby J, Blair PA, Govier M, Bonfield G, Domingo-Vila C, EXE-T1D consortium, ATAC clinical consortium, Wakeling MN, Oram RA, Flanagan SE, Tree TIM, Patel KA, Hattersley AT, De Franco E.   +14 more
europepmc   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source