Results 241 to 250 of about 6,113,563 (357)

Generation of ribosomal protein S1 mutants for improving of expression of difficult to translate mRNAs. [PDF]

Appl Microbiol Biotechnol
Niemelä LRK, Pásztor A, Frey AD.
europepmc   +1 more source

Assembly of ribosomal proteins L7, L10, L11, and L12, on the 50 S subunit of Escherichia coli.

, 1975
Joseph H. Highland, Guy A. Howard
openalex   +1 more source

RPS27L Enhances Myogenesis and Muscle Mass by Targeting IGF1 Through Liquid‐Liquid Phase Separation

Advanced Science, EarlyView.
Muscle‐specific RPS27L knock‐in mice exhibit increased body weight, muscle mass, and enhanced muscle regenerative capacity. RPS27L drives myogenesis by promoting myoblast proliferation, while inhibiting myogenic differentiation. Mechanistically, RPS27L targets IGF1 protein by liquid‐liquid phase separation through its N‐terminal intrinsically ...
Xiaoqin Liu, Yilong Yao, Junyu Yan, Mu Zeng, Xinhao Fan, Yijie Tang, Jiju Li, Yanwen Liu, Shanying Yan, Wei Wang, Lijuan Chen, Ruipu Chen, Yuxin Huang, Honor Calnan, Heng Wang, Graham Gardner, Yalan Yang, Zhonglin Tang   +17 more
wiley   +1 more source

Oxydifficidin, a potent <i>Neisseria gonorrhoeae</i> antibiotic due to DedA-assisted uptake and ribosomal protein RplL sensitivity. [PDF]

Elife
Kan J, Morales-Amador A, Hernandez Y, Ternei MA, Lemetre C, Maclntyre LW, Biais N, Brady SF.   +7 more
europepmc   +1 more source

Emetine resistance in Chinese hamster cells. Analysis of ribosomal proteins prepared from mutant cells.

, 1979
David P. Boersma, S. McGill, J. W. Mollenkamp, Donald J. Roufa   +3 more
openalex   +1 more source

ABERRANT INTRANUCLEOLAR MATURATION OF RIBOSOMAL PRECURSORS IN THE ABSENCE OF PROTEIN SYNTHESIS [PDF]

, 1970
Nessly Craig, Robert P. Perry
openalex   +1 more source

A Splice‐Region Variant Causes an Atypical Presentation of GNAS Inactivation Disorder

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in GNAS can cause a wide range of diseases including pseudohypoparathyroidism, pseudopseudohypoparathyroidism, McCune‐Albright syndrome, among others. The specific phenotypic features that may be seen are influenced by the variant type and location in the gene, whether it causes loss or gain of function, and whether it is ...
Brandon S. Stone, Swetha Ramadesikan, Regan McGinley, Scott E. Hickey, Leeran B. Dublin‐Ryan, Steven I. Estes, Victoria A. Elliott, Benjamin Karabasz, Jesse M. Hunter, Bimal P. Chaudhari, Richard K. Wilson, Daniel C. Koboldt   +11 more
wiley   +1 more source

JNK signaling coordinates epithelial cell turnover through exocytosis in <i>Drosophila</i> ribosomal protein mutants. [PDF]

iScience
Akai N, Yagi Y, Igaki T, Ohsawa S.
europepmc   +1 more source

Ethionine and the phosphorylation of ribosomal protein S6.

, 1977
Margaret A. Treloar, M E Treloar, Robert Kisilevsky   +2 more
openalex   +1 more source

Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia

Science, 2013
A. Bolze, N. Mahlaoui, M. Byun, B. Turner, N. Trede, S. Ellis, A. Abhyankar, Y. Itan, E. Patin, S. Brebner, P. Sackstein, A. Puel, C. Picard, L. Abel, L. Quintana-Murci, S. Faust, A. Williams, R. Baretto, M. Duddridge, U. Kini, A. Pollard, C. Gaud, P. Frange, D. Orbach, J. Emile, J. Stéphan, R. Sorensen, A. Plebani, Lennart Hammarstrom, M. Conley, L. Selleri, J. Casanova   +31 more
semanticscholar   +1 more source