Results 251 to 260 of about 3,391,200 (390)

Correlation between Protein and mRNA Abundance in Yeast

Molecular and Cellular Biology, 1999
S. Gygi, Yvan Rochon, B. Robert Franza, R. Aebersold   +3 more
semanticscholar   +1 more source

The E3 ubiquitin ligase, RNF219, suppresses CNOT6L expression to exhibit antiproliferative activity

FEBS Open Bio, EarlyView.
We identified RNF219 as a CCR4‐NOT complex‐interacting E3 ubiquitin ligase that targets the CCR4‐NOT subunit CNOT6L for ubiquitination. RNF219 directly binds to the DUF3819 domain of CNOT1 through its putative α‐helix spanning amino acids 521–542. Our findings also suggest that antiproliferative activity of RNF219 is at least partially mediated by ...
Shou Soeda, Melissa Montrose, Akinori Takahashi, Risa Ishida, Sandrine Burriel, Nao Ohmine, Tohru Natsume, Shungo Adachi, Minsoo Kim, Tadashi Yamamoto   +9 more
wiley   +1 more source

Immunogenicity and safety of mRNA-based seasonal influenza vaccines encoding hemagglutinin and neuraminidase. [PDF]

Nat Commun
Rudman Spergel AK, Lee IT, Koslovsky K, Schaefers K, Avanesov A, Logan DK, Hemmersmeier J, Ensz D, Stadlbauer D, Hu B, Pucci A, Vakil J, Paris R, Ananworanich J, Nachbagauer R.   +14 more
europepmc   +1 more source

Self-assembled mRNA vaccines

Advanced Drug Delivery Reviews, 2021
Jeonghwan Kim, Yulia Eygeris, Mohit Gupta, G. Sahay   +3 more
semanticscholar   +1 more source

A Novel CHMP2B Splicing Variant in Atypical Presentation of Familial Frontotemporal Lobar Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT C‐truncating variants in the charged multivesicular body protein 2B (CHMP2B) gene are a rare cause of frontotemporal lobar degeneration (FTLD), previously identified only in Denmark, Belgium, and China. We report a novel CHMP2B splice‐site variant (c.35‐1G>A) associated with familial FTLD in Spain. The cases were two monozygotic male twins who
Sara Rubio‐Guerra, Sara Bernal, David Almenta, Josefina Pérez‐Blanco, Valle Camacho, Isabel Sala, Mª Belén Sánchez‐Saudinós, Jesús García Castro, Judit Selma‐González, Miguel Ángel Santos‐Santos, Álvaro Carbayo, Janina Turon‐Sans, Ricard Rojas‐Garcia, Daniel Alcolea, Juan Fortea, Alberto Lleó, Oriol Dols‐Icardo, Ignacio Illán‐Gala   +17 more
wiley   +1 more source

On the Dependency of Cellular Protein Levels on mRNA Abundance

Cell, 2016
Yansheng Liu, A. Beyer, R. Aebersold
semanticscholar   +1 more source

Poly(4‐thiouridylic Acid) as Messenger RNA and Its Application for Photoaffinity Labelling of the Ribosomal mRNA Binding Site [PDF]

, 1977
I. Fiser, K.H. Scheit, Ernst Kuechler
openalex   +1 more source

Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT MRPS14 (uS14m) is a nuclear‐encoded ribosomal protein important for mitochondria‐specific translation. To date, only a single individual with a recessive MRPS14‐related disorder (also known as COXPD38) has been reported. We report an additional subject possessing novel compound heterozygous MRPS14 variants (p.Asp37Asn, p.Asn60Asp). The subject
Maria Gabriela Otero, Christina Freeman, Ruchi Shah, Renkui Bai, Hong Cui, Marian Castro, Zachary Myers, Eric Choy, Derek Chan, Molly Easter, Sophia Y. Zhao, Madeline Babros, Ruchi Garg, Matthew Deardorff, Franklin Moser, Tyler Mark Pierson   +15 more
wiley   +1 more source

p62 mRNA suppresses NLRP1 expression in cutaneous SCC cells through miR-34a-5p. [PDF]

Cell Death Dis
Hennig P, Turko P, Di Filippo M, Levesque MP, Kündig T, Beer HD.   +5 more
europepmc   +1 more source

Sinefungin, a potent inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viral multiplication.

, 1978
Charles Pugh, R. T. BORCHARDT, Henry O. Stone   +2 more
openalex   +1 more source