Results 151 to 160 of about 15,243 (207)

Computational Analysis of Telomerase RNA Evolution in <i>Caenorhabditis</i> Species. [PDF]

Noncoding RNA
Klapproth C, Reinhardt F, Stadler PF, Findeiß S.   +3 more
europepmc   +1 more source

Leukoencephalopathy, brain calcifications, and cysts (LCC): Two unique cases. [PDF]

Rare
Grafstein J, Aoyama Y, Godfrey R, Howe C, Stephen J, Malicdan MC, Gahl WA, Toro C.   +7 more
europepmc   +1 more source

SnoBIRD: a tool to identify C/D box snoRNAs and refine their annotation across all eukaryotes. [PDF]

Nucleic Acids Res
Fafard-Couture É, Boulanger C, Faucher-Giguère L, Sinagoga V, Berthoumieux M, Hedjam J, Marcel V, Durand S, Bayfield MA, Bachand F, Abou Elela S, Jacques PÉ, Scott MS.   +12 more
europepmc   +1 more source

Yeast snoRNA accumulation relies on a cleavage-dependent/polyadenylation-independent 3'-processing apparatus

, 2000
Alessandro Fatica
openalex   +2 more sources

Helicase-mediated mechanism of SSU processome maturation and disassembly. [PDF]

Nature
Buzovetsky O, Klinge S.
europepmc   +1 more source

The human Imp3 and Imp4 proteins form a ternary complex with hMpp10, which only interacts with the U3 snoRNA in 60-80S ribonucleoprotein complexes [PDF]

, 2003
Sander Granneman
openalex   +1 more source

U3 snoRNA in a fission yeast

, 2007
U3 snoRNA is an essential trans-acting factor, which is required for rRNA processing in eukaryotic cells. This study examined the U3 snoRNA in ' S. pombe' in terms of its expression, which included the identification of the promoter elements and the processing/termination pathway, and its functional structure.
openaire   +1 more source

Unlocking the life code: a review of SnoRNA functional diversity and disease relevance. [PDF]

Cell Commun Signal
Li Y, Chen X, Xiao S, Wang H, Li B, Zhang M, Wang K.   +6 more
europepmc   +1 more source

A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism [PDF]

, 2009
Adam J. de Smith, Carolin Purmann, Robin Walters, Richard J. Ellis, Susan Holder, Mieke M. van Haelst, A. F. Brady, U. L. Fairbrother, Mehul Dattani, Julia M. Keogh, Elana Henning, Giles S.H. Yeo, Stephen O’Rahilly, Philippe Froguel, I. Sadaf Farooqi, Alexandra I. F. Blakemore   +15 more
openalex   +1 more source

A homozygous synonymous NOP58 variant causes a neurodevelopmental disorder by impairing maturation of pre-ribosomal RNAs. [PDF]

HGG Adv
Bonde LD, Holling T, Alawi M, El Beheiry AA, Mir Hassani Z, Bachand F, Abdelrazek IM, Kutsche K.   +7 more
europepmc   +1 more source