Results 71 to 80 of about 13,308 (213)

Co‐translational protein targeting to mitochondria in the context of co‐translational protein maturation

open access: yesProtein Science, Volume 35, Issue 7, July 2026.
Abstract Mitochondria import the majority of their proteins from the cytosol, creating a fundamental challenge: precursor proteins must be synthesized, maintained in an import‐competent state, and delivered to mitochondrial translocases without premature folding or aggregation. While mitochondrial protein import has been considered a post‐translational
Nikita A. Kvasov, Yury S. Bykov
wiley   +1 more source

FMRP differentially regulates BK channels [PDF]

open access: yesJournal of General Physiology, 2020
Study suggests that the fragile X syndrome-associated protein FMRP can interact with different types of BK channels and modulate their kinetics in different ways.
openaire   +1 more source

EMSA binding of FMRP ISO1, FMRP S500D binding to miR-125a.

open access: yes, 2019
EMSA (15% non-denaturing gel) of miR-125a with FMRP ISO1 (A) and FMRP S500D (B). Free 200 nM miR-125a (lane 1) was incubated with a 1:1 (lane 2) and 1:2 (lane 3) RNA: protein ratio. (C) and (D).
Kathryn R. Moss (6719051)   +6 more
core   +1 more source

Characterization of Fragile X Mental Retardation Protein granules formation and dynamics in Drosophila

open access: yesBiology Open, 2012
Summary FMRP is an evolutionarily conserved protein that is highly expressed in neurons and its deficiency causes fragile X mental retardation syndrome.
Cristina Gareau   +4 more
doaj   +1 more source

Semaphorin-3A Promotes Degradation of Fragile X Mental Retardation Protein in Growth Cones via the Ubiquitin-Proteasome Pathway

open access: yesFrontiers in Neural Circuits, 2020
Fragile X mental retardation protein (FMRP) is an RNA-binding protein that regulates local translation in dendrites and spines for synaptic plasticity. In axons, FMRP is implicated in axonal extension and axon guidance.
Masaru Takabatake   +2 more
doaj   +1 more source

NSUN5 Attenuates Renal Injury and Ferroptosis in Hyperuricaemic Nephropathy Through YBX2‐Dependent Stabilisation of SCD1 m5C Methylation

open access: yesAdvanced Science, Volume 13, Issue 34, 19 June 2026.
NSUN5 is downregulated in hyperuricaemic nephropathy. Overexpression of NSUN5 enhances the stability of SCD1 mRNA through the m5C reader YBX2, ultimately inhibiting ferroptosis in renal tubular epithelial cells. Additionally, this axis suppresses the NF‐κB signaling pathway to alleviate inflammation and upregulates ABCG2 to promote uric acid excretion,
Xiu‐xiu Song   +12 more
wiley   +1 more source

NMDAR mediated translation at the synapse is regulated by MOV10 and FMRP

open access: yesMolecular Brain, 2019
Protein synthesis is crucial for maintaining synaptic plasticity and synaptic signalling. Here we have attempted to understand the role of RNA binding proteins, Fragile X Mental Retardation Protein (FMRP) and Moloney Leukemia Virus 10 (MOV10) protein in ...
Preeti Madhav Kute   +4 more
doaj   +1 more source

FMRP expression in primary breast tumor cells correlates with recurrence and specific site of metastasis.

open access: yesPLoS ONE, 2023
Breast cancer is the most common cancer among women worldwide. Molecular and clinical evidence indicated that Fragile X Messenger Ribonucleoprotein 1 (FMRP) plays a role in different types of cancer, including breast cancer.
E Caredda   +10 more
doaj   +1 more source

Familial p.(Ala73Thr) Variant in GNB2 Associated With Mild Neurodevelopmental Features and Pilocytic Astrocytoma

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Pathogenic variants in GNB2 have been associated with a neurodevelopmental disorder that includes global developmental delays and intellectual disability, hypotonia, increased risk for seizures, heart and renal anomalies, and characteristic facial features.
Megan Glassford   +2 more
wiley   +1 more source

Epitranscriptome and FMRP Regulated mRNA Translation [PDF]

open access: yesEpigenomes, 2017
An important regulatory mechanism affecting mRNA translation involves various covalent modifications of RNA, which establish distinct epitranscriptomic signatures that actively influence various physiological processes. Dendritic translation in mammalian neurons is a potent target for RNA modification-based regulation.
Pritha Majumder   +2 more
openaire   +2 more sources

Home - About - Disclaimer - Privacy