Results 131 to 140 of about 3,855 (167)

Selective 8-oxo-rG stalling occurs in the catalytic core of polynucleotide phosphorylase (PNPase) during degradation. [PDF]

Proc Natl Acad Sci U S A
Miller LG, Kim W, Schowe S, Taylor K, Han R, Jain V, Park R, Sherman M, Fang J, Ramirez H, Ellington A, Tamamis P, Resendiz MJE, Zhang YJ, Contreras L.   +14 more
europepmc   +1 more source

RNA degradation in human mitochondria: the journey is not finished. [PDF]

Hum Mol Genet
Santonoceto G, Jurkiewicz A, Szczesny RJ.   +2 more
europepmc   +1 more source

Rapid and scalable detection of synthetic mRNA byproducts using polynucleotide phosphorylase and polythymidine oligonucleotides. [PDF]

RNA Biol
Combes F, Bui TH, Pettersson FJ, Hak S.
europepmc   +1 more source

Cooperation of regulatory RNA and the RNA degradosome in transcript surveillance. [PDF]

Nucleic Acids Res
Bandyra KJ, Fröhlich KS, Vogel J, Rodnina M, Goyal A, Luisi BF.   +5 more
europepmc   +1 more source

Physiology, fast and slow: bacterial response to variable resource stoichiometry and dilution rate. [PDF]

mSystems
Peoples LM, Isanta-Navarro J, Bras B, Hand BK, Rosenzweig F, Elser JJ, Church MJ.   +6 more
europepmc   +1 more source

Biallelic mutations in SUPV3L1 cause an inherited neurodevelopmental disorder with variable leukodystrophy due to aberrant mitochondrial double stranded RNA processing

Green L, Hamilton N, Elpidorou M, Maroofian R, Douglas AG, Õunap K, Rose AM, Harris EL, Elworthy S, Renshaw SA, Low EC, Dockrell DH, Tveten K, Wells G, Harris SA, Al-Maawali A, Al-Thihli K, Al-Zuhaibi S, Futaisi AA, Calame D, Chinn I, Fisher KS, Sa M, Warren D, Zamani M, Sadeghian S, Azizimalamiri R, Galehdari H, Shariati G, Seifi T, Zaki MS, Afzal E, Tarnopolsky MA, Brady L, Zuchner SL, Efthymiou S, Scardamaglia A, Houlden H, Wakeling E, Prabhakar P, Roca-Bayerri C, Rice GI, Prouteau C, Bris C, Tessarech M, Sandvig I, Sheridan EG, Johnson CA, Livingston JH, Crow YJ, Poulter JA.   +50 more
europepmc   +1 more source

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does polyribonucleotide nucleotidyltransferase pnpase mutation affect the energetic metabolism and the microrna profile in cell and mitochondria

Journal of World Mitochondria Society, 2016
Objectives PNPase is a protein of the intermembrane space, encoded by PNPT1 and involved in RNA mitochondrial import [1]. PNPT1 mutations have been described in patients suffering from a severe neurological disease and combined respiratory chain defect [2]. We hypothesized that PNPAse could play a role in miRNA import [3].
Barrey, Eric, Beinat, Marine, Le Moyec, L., Rotig, A.   +3 more
openaire   +4 more sources

Polyribonucleotide nucleotidyltransferase

, 2007
Antje Chang, Ida Schomburg, Professor Diethmar Schomburg   +2 more
openaire   +2 more sources

Polyribonucleotide nucleotidyltransferase

, 1997
Dietmar Schomburg, Dörte Stephan
openaire   +2 more sources

Structure of an uncharacterized domain in polyribonucleotide nucleotidyltransferase from Streptococcus mutans UA159

, 2009
M.E. Cuff, C. Hatzos, R. Jedrzejczak, A. Joachimiak   +3 more
openalex   +2 more sources