Εμφανίζονται 1 - 20 Αποτελέσματα από 187.067 για την αναζήτηση 'Small interfering RNA - Data processing*', χρόνος αναζήτησης: 1,49δλ Περιορισμός αποτελεσμάτων
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    Academic Journal

    Συγγραφείς: Jarva T; Developmental Biology Program, Sloan Kettering Institute, New York, New York 10065, USA., Baugh C; The ATM Solution, Hattiesburg, Mississippi 30403, USA., Zhang J; Department of Mathematics and Statistics, Mississippi State University, Starkville, Mississippi 39762, USA., Lai EC; Developmental Biology Program, Sloan Kettering Institute, New York, New York 10065, USA., Flynt A; Department of Biomedical Engineering, University of Mississippi, Oxford, Mississippi 38655, USA asflynt@olemiss.edu.

    Πηγή: RNA (New York, N.Y.) [RNA] 2026 Apr 16; Vol. 32 (5), pp. 584-595. Date of Electronic Publication: 2026 Apr 16.

    Τύπος έκδοσης: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.

    Στοιχεία περιοδικού: Publisher: Cold Spring Harbor Laboratory Press Country of Publication: United States NLM ID: 9509184 Publication Model: Electronic Cited Medium: Internet ISSN: 1469-9001 (Electronic) Linking ISSN: 13558382 NLM ISO Abbreviation: RNA Subsets: MEDLINE

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    Academic Journal

    Alternate Title: CHARACTERISTICS OF WHITE SPOT SYNDROME VIRUS-DERIVED SMALL RNAS IN CRUSTACEANS AND THE STRUCTURAL BASIS OF THEIR CONSERVED ENRICHMENT. (English)

    Συγγραφείς: 亓玉华, 何嘉乐, 刘萍萍, 高杰, 孙磊, 王显伟

    Πηγή: Journal of Hydrobiology / Shuisheng Shengwu Xuebao; Jun2026, Vol. 50 Issue 6, p1-10, 10p

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    Academic Journal

    Πηγή: Science (pre-March 2025); 12/20/2024, Vol. 386 Issue 6728, p1427-1434, 8p, 5 Diagrams

    Θεματικοί όροι: Small interfering RNA, Heme, Biosynthesis, Liver cells

    Εταιρία/Οντότητα: United States. Food & Drug Administration

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    Mixed Materials

    Additional Titles: Inhibition of GSL (glycosphingolipid) synthesis reduces Aβ (amyloid β-peptide) production in vitro. Previous studies indicate that GCS (glucosylceramide synthase) inhibitors modulate phosphorylation of ERK1/2 (extracellular-signal-regulated kinase 1/2) and that the ERK pathway may regulate some aspects of Aβ production. It is not clear whether there is a causative relationship linking GSL synthesis inhibition, ERK phosphorylation and Aβ production. In the present study, we treated CHO cells (Chinese-hamster ovary cells) and SH-SY5Y neuroblastoma cells, that both constitutively express human wild-type APP (amyloid precursor protein) and process this to produce Aβ, with GSL-modulating agents to explore this relationship. We found that three related ceramide analogue GSL inhibitors, based on the PDMP (D-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol) structure, reduced cellular Aβ production and in all cases this was correlated with inhibition of pERK (phosphorylated ERK) formation. Importantly, the L-threo enantiomers of these compounds (that are inferior GSL synthesis inhibitors compared with the D-threo-enantiomers) also reduced ERK phosphorylation to a similar extent without altering Aβ production. Inhibition of ERK activation using either PD98059 [2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one] or U0126 (1,4-diamino-2,3-dicyano-1,4-bis[2-aminophenylthio] butadiene) had no impact on Aβ production, and knockdown of endogenous GCS using small interfering RNA reduced cellular GSL levels without suppressing Aβ production or pERK formation. Our data suggest that the alteration in pERK levels following treatment with these ceramide analogues is not the principal mechanism involved in the inhibition of Aβ generation and that the ERK signalling pathway does not play a crucial role in processing APP through the amyloidogenic pathway.

    Συγγραφείς: Li, H, Evin, G, Hill, AF, Hung, YH, Bush, AI, Garner, B

    Όροι ευρετηρίου: Journal Article

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    Mixed Materials

    Additional Titles: Inhibition of GSL (glycosphingolipid) synthesis reduces Aβ (amyloid β-peptide) production in vitro. Previous studies indicate that GCS (glucosylceramide synthase) inhibitors modulate phosphorylation of ERK1/2 (extracellular-signal-regulated kinase 1/2) and that the ERK pathway may regulate some aspects of Aβ production. It is not clear whether there is a causative relationship linking GSL synthesis inhibition, ERK phosphorylation and Aβ production. In the present study, we treated CHO cells (Chinese-hamster ovary cells) and SH-SY5Y neuroblastoma cells, that both constitutively express human wild-type APP (amyloid precursor protein) and process this to produce Aβ, with GSL-modulating agents to explore this relationship. We found that three related ceramide analogue GSL inhibitors, based on the PDMP (D-threo-1-phenyl-2-decanoylamino- 3-morpholino-1-propanol) structure, reduced cellular Aβ production and in all cases this was correlated with inhibition of pERK (phosphorylated ERK) formation. Importantly, the L-threo enantiomers of these compounds (that are inferior GSL synthesis inhibitors compared with the D-threo-enantiomers) also reduced ERK phosphorylation to a similar extent without altering Aβ production. Inhibition of ERK activation using either PD98059 [2-(2-amino-3-methoxyphenyl)-4H- 1-benzopyran-4-one] or U0126 (1,4-diamino-2,3-dicyano-1,4-bis[2-aminophenylthio] butadiene) had no impact on Aβ production, and knockdown of endogenous GCS using small interfering RNA reduced cellular GSL levels without suppressing Aβ production or pERK formation. Our data suggest that the alteration in pERK levels following treatment with these ceramide analogues is not the principal mechanism involved in the inhibition of Aβ generation and that the ERK signalling pathway does not play a crucial role in processing APP through the amyloidogenic pathway.

    Πηγή: Faculty of Science - Papers (Archive)

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    Academic Journal

    Συγγραφείς: Schlösser, Verena1 (AUTHOR), Lightfoot, Helen Louise1 (AUTHOR), Leemann, Christine2,3 (AUTHOR), Bejoy, Aathma Merin4 (AUTHOR), Tiwari, Shashank4 (AUTHOR), Schloßhauer, Jeffrey L.4 (AUTHOR), Vongrad, Valentina2,3 (AUTHOR), Brunschweiger, Andreas1,5 (AUTHOR), Hall, Jonathan1 (AUTHOR), Metzner, Karin J.2,3 (AUTHOR) karin.metzner@usz.ch, Imig, Jochen1,4 (AUTHOR) jochen.imig@mpi-dortmund.mpg.de

    Πηγή: Non-Coding RNA. Feb2025, Vol. 11 Issue 1, p8. 21p.

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