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UnknownAURKAIP1 actuates tumor progression through stabilizing DDX5 in triple negative breast cancer.
Not available
S-EPMC10692340 | biostudies-literature
UnknownCYFIP1 coordinate with RNMT to induce osteosarcoma cuproptosis via AURKAIP1 m7G modification.
Not available
S-EPMC11846196 | biostudies-literature
UnknownAurora-A kinase interacting protein 1 (AURKAIP1) promotes Aurora-A degradation through an alternative ubiquitin-independent pathway.
Not available
S-EPMC1828899 | biostudies-literature
UnknownIdentification and characterization of CHCHD1, AURKAIP1, and CRIF1 as new members of the mammalian mitochondrial ribosome.
Not available
S-EPMC3726836 | biostudies-literature
UnknownIntegrative bioinformatics analyses of mitochondrial dysfunction-related genes in human non-obstructive azoospermia.
Not available
S-EPMC12923532 | biostudies-literature
UnknownCLPP Depletion Causes Diplotene Arrest; Underlying Testis Mitochondrial Dysfunction Occurs with Accumulation of Perrault Proteins ERAL1, PEO1, and HARS2.
Not available
S-EPMC9818230 | biostudies-literature
ProteomicsClpP-deletion causes azoospermia, with meiosis-I delay and insufficient biosynthesis of spermatid factors, due to mitochondrial dysfunction with accumulation of Perrault proteins ERAL1, PEO1, and HARS2.
Human Perrault syndrome (PRLTS) is defined by autosomal recessive inheritance with primary ovarian insufficiency and early hearing loss. Most PRLTS disease proteins modulate mitochondrial transcription or translation. Among the genetic causes are ClpP mutations, which trigger also complete azoosperm...
ORGANISM(S): Mus musculus (Mouse) 
2023-03-11 | PXD033388 | Pride
Meiosis-i  zygotene-pachytene  homologous recombination  h3k9ac  acetyl-tubulin  twinkle helicase  rmnd1  trna /rrna processing  cgas-sting signaling 
UnknownStratifying ALS Patients by Mode of Inheritance Reveals Transcriptomic Signatures Specific to sALS and fALS.
Not available
S-EPMC12470382 | biostudies-literature
ProteomicsAlternative start codon selection shapes mitochondrial function during evolution, homeostasis, and disease
Mitochondrial acquisition was a pivotal event in eukaryotic evolution, requiring core proteins adapt to function both within the mitochondria and in the host cell. Here, we systematically profile the localization of protein isoforms generated by alternative start codon selection. We identify hundred...
ORGANISM(S): Homo sapiens (Human) 
2025-10-28 | PXD062112 | Pride
Mrps38 Ribosomes Mitochondria Aurkaip1 
UnknownCo-expression analysis to identify key modules and hub genes associated with COVID-19 in platelets.
Not available
S-EPMC9008611 | biostudies-literature
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